Repairing trauma to the central nervous system by replacement of glial support cells is an increasingly attractive therapeutic strategy. We have focused on the less-studied replacement of astrocytes, the major support cell in the central nervous system, by generating astrocytes from embryonic human glial precursor cells using two different astrocyte differentiation inducing factors. The resulting astrocytes differed in expression of multiple proteins thought to either promote or inhibit central nervous system homeostasis and regeneration. When transplanted into acute transection injuries of the adult rat spinal cord, astrocytes generated by exposing human glial precursor cells to bone morphogenetic protein promoted significant recovery of volitional foot placement, axonal growth and notably robust increases in neuronal survival in multiple spinal cord laminae. In marked contrast, human glial precursor cells and astrocytes generated from these cells by exposure to ciliary neurotrophic factor both failed to promote significant behavioral recovery or similarly robust neuronal survival and support of axon growth at sites of injury. Our studies thus demonstrate functional differences between human astrocyte populations and suggest that pre-differentiation of precursor cells into a specific astrocyte subtype is required to optimize astrocyte replacement therapies. To our knowledge, this study is the first to show functional differences in ability to promote repair of the injured adult central nervous system between two distinct subtypes of human astrocytes derived from a common fetal glial precursor population. These findings are consistent with our previous studies of transplanting specific subtypes of rodent glial precursor derived astrocytes into sites of spinal cord injury, and indicate a remarkable conservation from rat to human of functional differences between astrocyte subtypes. In addition, our studies provide a specific population of human astrocytes that appears to be particularly suitable for further development towards clinical application in treating the traumatically injured or diseased human central nervous system.
Citation: Davies SJA, Shih C-H, Noble M, Mayer-Proschel M, Davies JE, et al. (2011) Transplantation of Specific Human Astrocytes Promotes Functional Recovery after Spinal Cord Injury. PLoS ONE 6(3): e17328. doi:10.1371/journal.pone.0017328
Editor: Colin Combs, University of North Dakota, United States of America
Received: November 26, 2010; Accepted: January 24, 2011; Published: March 2, 2011
This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
Funding: This work was supported by funding from the National Institutes of Health [grant numbers RO1-NS046442, RO1-NS42820]; the Carlson Stem Cell Trust and the CareCure SCI community. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The recognition that astrocyte dysfunction may play an important role in a wide range of neurological disorders raises the question of whether astrocyte transplantation could be of therapeutic value in treating the injured or diseased human central nervous system (CNS). For example, it has long been known that astrocytes within glial scar tissue contribute to the failure of axon regeneration across sites of traumatic brain or spinal cord injury –. A failure of normal astrocyte generation by CNS precursor cells has been discovered to be a consequence of the mutations that cause Vanishing White Matter leukodystrophy , and dysfunction of astrocytes has also been suggested to be of importance in models of amyotrophic lateral sclerosis , forebrain ischemic injury , epileptic seizures , Huntington's disease , tuberous sclerosis  and Rett syndrome . We therefore have proposed that enhancing astrocyte function through transplantation of specific subtypes of astrocytes derived from glial precursors will promote repair and functional recovery after CNS injury .
There are a number of challenges inherent in the development of astrocyte-based treatments for human disease. One of the most important of these is the question of whether all astrocytes are equivalent in their ability to promote repair, or whether specific populations of astrocytes are more useful than others. While previous studies had demonstrated a synergistic effect of BMP and LIF on the astrocytic differentiation of human neural stem cells , it remains unclear whether BMP and LIF induce distinct types of astrocytes and if so, what the functional properties of these astrocytes may be with respect to repairing CNS injuries. The recent description of considerable astrocyte heterogeneity in the human CNS raises the question whether distinct astrocytes can also be derived from single populations of human glial precursors, and more importantly whether different human astrocyte populations exhibit distinct functional properties . Further challenges include the identification of signaling molecules that promote the generation of beneficial populations of astrocytes, identification of appropriate stem and/or progenitor cell populations that can be the source of such cells, and determination of whether there are situations in which it is more useful to transplant astrocytes themselves rather than to transplant stem or progenitor cells that might generate astrocytes in vivo in response to signals present in the host environment.
We now show that astrocytes generated from the same population of human fetal glial precursor cells, by exposure to either bone morphogenetic protein (BMP) or ciliary neurotrophic factor (CNTF), promote widely divergent outcomes with respect to repairing the injured adult spinal cord. Transplantation of astrocytes generated by exposure of human glial progenitor cells (hGPCs) to BMP (hGDAsBMP) promoted robust behavioral recovery and multi-laminae protection of spinal cord neurons following spinal cord injury (SCI), while transplantation of undifferentiated hGPCs or astrocytes generated by hGPC exposure to CNTF (hGDAsCNTF) failed to provide such benefits. These results provide a defined population of human astrocytes suitable for further pre-clinical development for treatment of SCI, and demonstrate that pre-differentiation into astrocytes prior to transplantation provides a much greater functional recovery than transplantation of precursor cells themselves. Our results also underscore the importance of function-based analysis of astrocyte diversity as a foundation for the development of astrocyte transplantation-based therapies.
Human glial precursors give rise to two distinct astrocyte populations in vitro
As a first step towards determining whether human glial progenitor cells (hGPCs) can generate functionally distinct astrocyte populations, we exposed embryonic hGPCs isolated from spinal cords of 9.5 week old abortuses to BMP or CNTF. Both BMP and CNTF-induced astrocyte populations express GFAP (Fig. 1 A–C), AQP4 and S100β (Fig. 1 D), three widely used markers of astrocyte differentiation –. hGDAsBMP also expressed connexin 43 (CX43), glutamate transporter 1 (GLT-1), AKAP12 and glia-derived neurotrophic factor (GDNF), all of which are expressed in the astroglial lineage –. In contrast, CNTF treatment did not induce expression of GLT-1, connexin 43, AKAP12, or GDNF. Instead, hGDAsCNTF – but not hGDAsBMP – expressed several antigens expressed in astrocytes generated in response to injury (Fig. 1 E and F), including the transcription factor OLIG2 and the chondroitin sulphate proteogylcans (CSPGs) phosphacan and CSPG4/NG2 , –. Thus, induction of differentiation of human spinal cord derived glial precursors with BMP or CNTF induces the generation of two phenotypically distinct astrocyte populations.
Both BMP and CNTF promote the differentiation of hGPCs into GFAP-positive astrocytes expressing S100b but with otherwise distinct morphological and antigenic phenotypes. hGDAsBMP express lower levels of GFAP and exhibit a more compact morphology. hGDAsCNTF have a more elongated morphology and expressed high levels of GFAP. hGDAsCNTF also expressed high levels of neurite-outgrowth inhibitory chondroitin sulfate proteoglycans, phosphacan and CSPG4, as well as the transcription factor Olig2 - all of which have been found to be upregulated in glial scar associated astrocytes. (A–C) Human GPCs grown in bFGF (A) were induced to differentiate into astrocytes using BMP-4 (B) or CNTF (C). Labeling with anti-GFAP (Alexa-488) demonstrates that both BMP4 and CNTF induce differentiation of human glial precursors into GFAP-expressing astrocytes, while Olig2 expression (Alexa-568) is repressed in hGDAsBMP. Scale bar = 50 µm. (D) RT-QPCR analysis of hGPC, hGDABMP and hGDACNTF populations reveals induction of AQP4 and S100β in both hGDAsBMP and hGDAsCNTF. Induction of CX43, GLT1, AKAP12 and GDNF however are restricted to hGDAsBMP. Average fold change and SD of expression levels is shown for three independent experiments using 9W-1 hGPCs. (E and F) Phosphacan and CSPG4 remain elevated in hGDAsCNTF and are reduced in hGDAsBMP derived from both 9W-1 (E) and 9W-2 (F) glial precursors. Mean relative protein expression and SD from three independent experiments are shown. Values were normalized to β-actin and expression in hGPCs.
To test the functional properties of these distinct astrocyte populations in vivo, hGDAsBMP, hGDAsCNTF or undifferentiated hGPCs were transplanted into the injury site of adult Sprague-Dawley rats that had received unilateral transections of the right-side dorso-lateral funiculus (DLF), including the rubrospinal pathway, at the C3/C4 intervertebral spinal cord level.
Serial section analysis of transplants using antibodies to human mitochondria (hMito) showed that the majority of hGDABMP transplants (4 out of 6) and half of the hGDACNTF transplants (3 out of 6) that under went histological analysis had robust survival of hMito+ cells at 5 weeks post transplantation within dorsolateral funiculus (DLF) injury sites. Surviving transplants spanned the rostral to caudal extent of injury sites to effectively provide continuous substrates for potential growth of host axons across sites of injury. Qualitative assessment of transplant size showed that all surviving hGDACNTF transplants were larger than hGDABMP transplants in terms of both their rostral to caudal and lateral to medial extents (Fig. 2 A–D).
Immuno-staining for human mitochondrial marker (red channel) of histological cross sections at sites of injury revealed hGDAsBMP (A, C, E) and hGDAsCNTF (B, D, F) transplant masses spanning the dorsal-ventral and lateral-medial margins of injury sites. Arrowheads in C and D indicate accumulations of hGDAsBMP and hGDAsCNTF respectively at the pial surface of lateral funiculus white matter (see also Fig. 4 A, B). Co-labeling for neurofilament (NF: green) and human mitochondrial marker (hMito: red) shows a markedly higher density of axons within hGDAsBMP treated injury sites (A, E) compared to hGDAsCNTF treated injury sites (B, F). Greater numbers of NF+ axons within hGDAsBMP transplants aligned with the normal rostral/caudal trajectory of DLF white matter (E) compared to NF+ axons within hGDAsCNTF transplants (F). Survival = 5 weeks post injury/transplantation. Scale bars: A, B, C, D = 200 µm; E, F = 100 µm.
We next found that hGDABMP grafted injury sites exhibited higher densities of axons than hGDACNTF grafted injury sites. As shown in figure 2, hGDABMP grafts contained many 200 kD neurofilament+ axons (Fig. 2 A and E), while relatively few axons were observed in hGDACNTF grafts (Fig. 2 B and F). Quantification of neurofilament immuno-reactivity within hGDAsBMP and hGDAsCNTF treated injury sites revealed that the injury centers of hGDABMP treated spinal cords contained almost double the density of NF+ axon profiles (1.91 fold more: average 14.79 units2 +/− 3.05 st. dev.) than measured in hGDACNTF treated injury centers (average 7.75 units2 +/− 2.28 st. dev.; p = 0.003). Notably the profiles of the majority of NF+ axons, particularly within the rostral and caudal margins of hGDABMP grafted injuries, were end on to the transverse plane of section indicating that, as previously observed for axons within spinal cord injury sites bridged with rodent GDAsBMP , these axons were aligned with the normal rostral/caudal trajectory of the DLF white matter (Fig. 2 A and E).
hGDA migration and cell morphology
Analysis of the migration of transplanted hMito+ hGDAs revealed similar patterns of distribution within spinal cord gray matter. The highest densities of both types of hGDAs were observed within laminae 4, 5 and 6 of gray matter directly adjacent to sites of injury (Fig. 2 A–D). In contrast, relatively few hMito+ hGDA cells of either type were observed within laminae 7, 8 and 9 (Fig. 2 A–D) directly adjacent to injury sites. No hMito+ cells of either type of hGDA were observed to have migrated medially in either gray or white matter beyond the central canal i.e. into the contra-lateral side of the spinal cord. Significantly, in all hGDA treated cords analyzed, neither type of hGDA was found in the contra-lateral side of the spinal cord or within gray matter rostral or caudal to the injury site. Migration of hGDAs in white matter was more extensive than in gray matter, with both types of hGDAs showing extensive migration both rostral and caudal to the injury site, with maximum rostral/caudal migration distances of 3.24 mm/3.96 mm recorded for hGDAsCNTF and 2.52 mm/2.16 mm recorded for hGDAsBMP respectively.
High power imaging of the centers of both types of hGDA grafts showed comparable densities of hMito positive cell bodies and processes that contained GFAP+ intermediate filaments (Fig. 3). Similar densities of hGDAsBMP and hGDAsCNTF had migrated to the pial surface of lateral funiculus white matter both rostral and caudal to the injury site (Figs. 2 C and D; Fig. 4 A and B). The distribution and density of hMito+ mitochondria within individual hGDAs was sufficient to identify their cell bodies and show that both types of hGDA often displayed similar typical astrocytic “stellate” arrangements of their processes within transplant parenchyma, gray matter and white matter (Fig. 2 E and F, Fig. 3 A and B, Fig. 4 C).
Images of hMito+ (red) and GFAP (green) immuno-reactivity within hGDAsBMP (A, C, E, F) and hGDAsCNTF (B, D, G, H) transplants at the center of injury sites showing comparable densities of GFAP+ intermediate filaments (green) within hMito immuno-positive cell bodies and process of both types of hGDAs. Arrowheads indicate some examples of GFAP+/hMito+ hGDA cell bodies at low and high magnification. Images are maximum projections of apotome (Zeiss) optical sections captured through a depth of 3.5 µm of tissue. Survival = 5 weeks post injury/transplantation. All scale bars = 20 µm.
(A, B) High power images showing hMito+ hGDAsBMP in the process of migrating and accumulating at the pial surface within lateral funniculus white matter. Note the elongated radially orientated processes displayed by some hMito+ hGDAsBMP within white matter (B: arrowheads), a glial morphology indicative of tangential migration of these cells towards the adjacent pial surface (hMito: red; NF+ axons: green). (C) hGDAsBMP displaying typical astrocytic “stellate” arrangements of their processes within white matter immediately ventral to the injury site. Survival = 5 weeks post injury/transplantation. Scale bars: A, B = 100 µm; C = 20 µm.
hGDAsBMP promote locomotor recovery while hGDAsCNTF do not
Despite the similar ability of transplanted hGDAsBMP and hGDAsCNTF to span the rostral to caudal extent of injury sites and migrate into adjacent tissues, only hGDAsBMP promoted locomotor recovery following transplantation into the transected dorsolateral funiculus (DLF). This injury severs descending, supraspinal axons and causes chronic deficits in both fore- and hind-limb motor function , which can be detected by the grid-walk behavioral test . A similar average number of mistakes were seen in each group at 3 days post injury/transplantation (Fig. 5 A). At day 7 the hGDABMP group improved from an average 7.7±0.7 mistakes per crossing to 4.7±0.8, and further improved by day 28 to only 2.4±0.2 mistakes, comparable to uninjured controls. By comparison, by day 28 the untreated injury group and animals receiving hGDAsCNTF transplants made 6.7±0.5 and 6.5±0.5 mistakes respectively. The number of mistakes made by rats in the hGDACNTF group was not significantly different from those in the media-injected DLF injured control group and did not improve statistically over time. Persistent survival of the transplant was not required in order to obtain benefit after transplantation, as behavioral recovery was as extensive in animals in which transplanted cells were still present at 5 weeks as in those in which no human cells were detected at this time point.
Graphs show the average number of mistakes per experimental group made during Grid walk testing of locomotor recovery at 1 day before injury to 28 days after injury. In two separate experiments, hGDABMP transplanted animals (closed circles) performed significantly better than hGDACNTF (A) or hGPC (B) transplanted animals at all time points from 7 to 28 days post injury/transplantation. Note that the performance of hGDACNTF or hGPC transplanted animals was not significantly different from control injured rats at all time points (two-way repeated measures ANOVA, *p< 0.05).
Pre-differentiation of hGPCs to hGDAsBMP is required for robust functional recovery
We next examined the question of whether the precursor cells from which hGDAsBMP were derived were also capable of promoting behavioral recovery after DLF transection and found that pre-differentiation of these precursor cells into astrocytes was essential to promote significant functional recovery. Rats that received hGDABMP transplants performed significantly better on the grid-walk test than either the hGPC transplanted group or the media-injected control injury group at all time points from 7 to 28 days post injury/transplantation (Fig. 5 B). The number of mistakes made by the hGPC treated group was not different from the injury control group at all post-injury time points and did not improve statistically over time. Specifically, at 3 days after injury/transplantation the average number of mistakes for each group were 8.2+/−1.3 (media-injected control injury), 7.9+/−1.6 (hGPCs), and 8.2+/−1.4 (9W-1 hGDAsBMP), which are not significantly different from each other (as also seen for 9W-2 hGDAsBMP). However by day 7 the hGDABMP group showed a robust improvement to 3.75+/−1.5 mistakes, and by 28 days post injury/transplantation, the last time point tested, the 9W-1 hGDABMP group made an average of only 3.0+/−0.7 mistakes, compared to 5.5+/−1.0 and 5.1+/−0.8 mistakes for hGPC treated and control groups respectively (p<0.05, Fig. 5 B).
hGDAsBMP are more effective at providing neuroprotection than hGDAsCNTF and hGPCs
Differences in behavioral recovery were mirrored by marked differences in promotion of neuronal survival within ipsilateral gray matter immediately adjacent to sites of injury (Fig. 6 and Fig. 7) and even within rostral and caudal gray matter in which no transplanted hGDAsBMP were observed. Previous studies of neuron survival by the Priestley lab have confirmed with toluidine blue histochemistry that NeuN immuno-reactivity is a reliable marker of neuron survival after spinal cord injury . At 5 weeks post injury/transplantation, NeuN+ neuron cell bodies were counted in laminae 4 to 9 on the injured, right hand side of the spinal cord (Tables 1 and 2). These regions of the spinal cord were chosen because they are either post synaptic targets of the corticospinal (laminae 3–7, dense terminations; laminae 8 and 9, sparse terminations), rubrospinal (laminae 5–7), and raphe (laminae 7–9) supra-spinal motor systems; contain interneurons, propriospinal neurons (laminae 4–8), or commissural neurons (lamina 8) involved in motor control; or primary motor neurons (lamina 9) –.
Montaged images of NeuN immuno-histochemistry at the C5 spinal level of normal (A) and untreated injured (control) spinal cords (B) show that the unilateral DLF transection injury causes loss of NeuN+ neurons in multiple spinal cord laminae adjacent to the transected white matter. Transplantation of hGDAsBMP (C) promotes significant protection of neurons in laminae 7, 8, and 9 at the injury center. In contrast, transplantation of hGDAsCNTF (D) or hGPCs (E) did not promote significant levels of neuroprotection. (F) Schematic showing gray matter laminae at the C5 level of the rat spinal cord (adapted from ). All scale bars = 200 µm.
(A) hGDABMP transplantation led to significant increases in numbers of NeuN+ neurons counted in a 1.8mm length of spinal cord encompassing the injury site. Graphs show percentage changes in numbers of NeuN+ neurons in laminae 4 to 9; laminae 4, 5, and 6; 7; and 8 and 9 in spinal cords from animals that received transplants of 9W2 or 9W1 hGDAsBMP, hGDAsCNTF or hGPCs and untreated control injuries. (B) Analysis of neuron survival within laminae immediately adjacent to the site of injury shows that hGDABMP transplantation promoted significant protection of neurons when all laminae were considered (4 to 9), with the most robust increases in neuron numbers in intermediate (7) and ventral (8 and 9) gray matter laminae. Numbers of NeuN+ neurons in spinal cords of rats transplanted with GDAsCNTF or hGPCs were not significantly different from each other or untreated spinal cord injuries. * ANOVA and Pairwise Multiple Comparison (Holm-Sidak), p<0.05. + t-test comparison with untreated spinal cord injuries, p<0.05.
Significant improvements in neuronal survival in all laminae studied were seen in a 1.8 mm length of spinal cord encompassing the injury site of hGDABMP-treated animals. Combined neuron counts for all laminae (4 to 9) showed that hGDABMP transplantation promoted increases of 40% and 32%, in two separate experiments, of surviving neurons compared to untreated injured spinal cords (Fig. 7 A; Table 1), with significant increases seen in all laminae. Analysis of a region closer to the site of injury, through 750 µm of tissue spanning the injury center, revealed notably robust increases in numbers of neurons for lamina 7 (35% and 32%) and laminae 8 and 9 (70% and 54%) above control injured cords (Fig. 7 B; Table 2). As with behavioral recovery, continued graft survival was not required for promotion of neuronal survival. Significant increases in neuron numbers were not observed in lamina 4, 5, 6 adjacent to injury centers, despite rescue of neurons more distal to the zone of injury; an outcome most likely due to neuron loss resulting from direct trauma to these laminae at time of injury.
The present studies provide multiple novel findings relevant to the development of astrocyte transplantation therapies for treatment of the injured or diseased central nervous system. We show that subpopulations of human astrocytes, generated by activation of different signaling pathways in the same population of human glial precursor cells, have markedly different effects when transplanted into the injured spinal cord. hGDAsBMP provided extensive benefit, including robust protection of spinal cord neurons, increased support of axon growth and locomotor recovery. In contrast, transplantation of either undifferentiated hGPCs or hGDAsCNTF failed to provide significant benefits. The major gains in behavioral recovery and neuronal survival achieved by pre-differentiation of glial precursors to specific, beneficial astrocytic cell types prior to transplantation stresses the need to consider such manipulations as a critical component in the optimization of stem/precursor cell transplantation based therapies.
The development of astrocyte transplantation represents a new avenue for the treatment of CNS injury, as contrasted with the extensive research that has been conducted on replacement of oligodendrocytes. Starting with transplants of human oligodendrocytes in the late 1980s , and more recently with populations of human oligodendrocyte progenitor cells isolated from the developing or adult CNS, or from human embryonic stem cells, it has been possible to generate extensive myelination upon transplantation into spinal cord injury or into congenital mouse models of hypomyelination –. In contrast, much less is known about the potential utility of astrocyte-based therapies. Moreover, initial studies showed only modest benefits of astrocyte transplantation for treatment of traumatic injury to the spinal cord –.
One of the striking differences in outcome between our studies and work on oligodendrocyte and oligodendrocyte-precursor replacement lies in the finding that differentiation of precursor cells into a specific astrocyte subtype prior to transplantation provides a much greater level of benefit than transplantation of the precursor cells themselves. This is the opposite situation to that reported in the oligodendrocyte lineage, for which a greater degree of pre-transplant differentiation is associated with less effective repair , . While it may be that precursor cell transplantation is of potential use in astrocyte replacement in neurological disorders such as ALS , our results demonstrate the importance of determining whether direct transplantation of astrocytes themselves provides greater benefit. In light of the modest benefits obtained with transplantation of rodent astrocytes isolated directly from the immature CNS –, however, our present and earlier studies ,  suggest that it is necessary instead to transplant astrocytes generated from precursor cells in vitro in order to optimize benefit.
Along with demonstrating the marked benefits from astrocyte transplantation in experimental injuries of the spinal cord, our studies also demonstrate that obtaining benefit may require transplanting very specific populations of human astrocytes. The significant difference in outcome achieved by transplantation of hGDAsBMP versus hGDAsCNTF demonstrates clearly that not all astrocytes are equivalent in respect to their therapeutic value, and this appears to be the first study demonstrating functional differences between different human astrocyte populations with respect to repairing the adult central nervous system. It is also interesting to note the similarity between the outcomes obtained with human cells and with our prior studies on rat cells , . In a similar fashion to that observed for rodent GDAs transplanted hGDAsBMP were more supportive of axon growth than hGDAsCNTF at sites of spinal cord injury. Like the human GDAsBMP, rodent derived GDAsBMP promote robust functional recovery, while GDAsCNTF did not . The conservation of the phenotypic and functional properties of GDAsBMP and GDAsCNTF between human astrocytes and rat astrocytes suggests that such properties are fundamental to the biology of these cells. The one difference observed in these studies was that hGDABMP transplantation showed a slightly longer delay (7 days versus 3 days) in providing significant behavioral recovery. Whether this is due to differences in cell properties or a consequence of the xenograft itself remains to be investigated.
It was also of interest to observe that prolonged survival of the grafted astrocytes was not required to obtain durable improvements in behavior and neuronal survival. This also demonstrates a conservation of outcomes between human cells and rat cells, which also did not require prolonged survival to provide durable benefit , , suggesting that this too might be a conserved aspect of GDABMP function.
This is also the first study, to our knowledge, in which transplanted astrocytes (rodent or human) have been shown to promote extensive neuroprotection of spinal cord neurons following spinal cord injury, an observation consistent with the robust neuroprotective effects of intra-spinal rodent GDABMP transplants on axotomized neurons of the red nucleus , . While future studies will reveal whether transplantation of hGDAsBMP to DLF injuries provide protection of red nucleus neurons, hGDAsBMP provided robust neuron protection in multiple spinal cord laminae, even in more distant gray matter in which there was no evidence of hGDAsBMP migration. hGDAsBMP were able to promote survival of multiple neuronal populations within multiple gray matter laminae with notably robust increases of up to 69% in neuronal survival in laminae 8 and 9 containing motor neurons. In contrast, although SCI rats that were treated with hGPCs and hGDAsCNTF showed positive trends in neuron protection for laminae 8 and 9, this did not translate to improvements in grid-walk performance and these cells failed to promote statistically significant increases in neuronal survival even in laminae into which they had migrated.
The underlying mechanisms accounting for why hGDAsBMP are so much more beneficial in terms of neuroprotection and functional recovery than either hGDAsCNTF or undifferentiated precursor cells when transplanted into spinal cord injured rats remain to be investigated, but it is likely that multiple cellular functions are involved. For example, hGDAsBMP express higher levels of such astrocyte-related genes as glutamate transporter 1, connexin 43, and AKAP12, which are relevant to maintaining tissue homeostasis in the CNS as well as reducing astrogliosis and neuronal death after injury, mediating glutamate uptake and promoting blood-brain barrier formation , , –. These and other differences between hGDAsBMP and undifferentiated hGPCs and hGDAsCNTF, such as the marked differences in expression of axon growth inhibitory CSPGs and the expression of GDNF, may all contribute to creating a particularly effective cell type for promoting functional recovery in the traumatically injured adult central nervous system.
In brief our present studies provide the first demonstration of the utility of human astrocyte transplantation as a therapy for central nervous system injuries. Moreover, our studies provide a specific population of human astrocytes that appear to be particularly suitable for further development towards clinical applications.
Materials and Methods
The University of Rochester RSRB has reviewed this study and determined that based on federal (45 CFR 46.102) and University criteria, the study does not qualify as human subjects research and has waived the need for consent (RSRB#00024759). All animal procedures were performed under guidelines of the National Institutes of Health and approved by the Institutional Animal Care and Utilization Committee (IACUC) of University of Colorado Denver, Aurora, CO (UCAR# 80710(05)1E). or the IACUC of University of Rochester Medical Center, Rochester, NY (UCAR# 2008-075).
Preparation of human cells
Human spinal cord tissues were obtained from two nine week old, de-identified abortus samples collected in the course of medically prescribed procedures using the Safe-Harbor Method. Spinal cord-derived glial precursors were grown and isolated as previously described –. Spinal cord tissue was dissected from the rostral neural tube of two 9 week old samples (referred to here as 9W1 and 9W2). After removal of the meninges, tissue was digested at 37°C with 59 U/ml papain (Worthington) in Hanks balanced salt solution (HBSS, Invitrogen) supplemented with 10 mM Hepes (EMD), pH 8.0 and 125 U/ml Dnase I (Sigma), and triturated in 0.3%(w/v) BSA/HBSS (Sigma), 250 U/ml Dnase I. A2B5+PSA-NCAM− glial progenitor cells were isolated by step-wise immunopurification using anti-PSA-NCAM and A2B5-bound magnetic beads (Miltenyi). and cultured in 5% O2/7% CO2 in Bottenstein-Sato F12 medium with 10 ng/ml human recombinant basic fibroblast growth factor (Peprotech) on a substrate of 1 µg/cm2 fibronectin (Chemicon) and 0.5 µg/cm2 laminin (Invitrogen). Differentiation of hGPCs was induced at 2500 cells/cm2 by replacing bFGF with either 20 ng/ml BMP-4 (R&D) or 10 ng/ml CNTF (Peprotech) and allowed to differentiate for 7 days prior to harvest.
RNA and protein expression analysis
Characterization of hGPC and hGDA cultures was performed by reverse-transcriptase semi-quantitative polymerase chain reaction (RT-QPCR), Western blot and immunofluorescent labeling as previously described , . Multiplex QPCR reactions of RT product were performed using FAM-labeled probes for aquaporin 4, S100b, CX43, GLT-1 and AKAP12, in combination with VIC-labeled, primer limited GAPDH probe and Taqman mastermix (all Applied Biosystems). DDCt analysis was performed using Microsoft Excel software as previously described . Independent experiments were performed in triplicate and average fold change expression normalized to expression in undifferentiated hGPCs grown in bFGF. Western blot analysis of chondroitin sulfate proteoglycans and Olig2 was performed as previously described , using anti-phosphacan monoclonal (1:1000, 3F8, Developmental Studies Hybridoma Bank), anti-CSPG4/NG2 monoclonal (1:2000, Chemicon), anti-Olig2 polyclonal (1:4000, Chemicon) and anti-b-tubulin monoclonal antibody (1:1000, Santa Cruz). Expression levels of phosphacan (320–340 kDa band) NG2 (270–300 kDa band) and Olig2 (32 kDa band), respectively, were normalized for each sample to β-tubulin (52 kDa) expression. All Western blot experiments were conducted in triplicate and results were compared using the Student's t-test, p<0.05. Immunofluorescent labeling was performed using anti-Olig2 (1:4000, Chemicon) and anti-GFAP (1:400, Cell Signaling) followed by fluorescently labeled, secondary anti-Ig antibodies (Alexa 488 and 568 conjugates, Invitrogen) at a 1:2000 dilution. Monochrome images of parallel samples were captured using identical exposure times and gain settings, and merged as pseudo-colored images.
Spinal cord injury model
Adult female Sprague Dawley rats (3 months old, Harlan) were used in all in vivo spinal cord injury experiments and were anesthetized by injection of a cocktail containing ketamine and xylazine. Unilateral transections of the right-side dorso-lateral funiculus (DLF) including the rubrospinal pathway were conducted at the C3/C4 intervertebral spinal cord level (Supplemental Fig. S1A and S1B). The dorsal surface of the spinal cord was exposed by opening the intervertebral space between the C3 and C4 vertebrae. After opening the dura, a 1 mm deep transection was made lateral to the midline using micro-scissors. To ensure that the injury was complete and that the depth was uniformly 1 mm, a 30 gauge needle was again inserted into the transection site to a depth of 1 mm and slowly passed through the medial to lateral extent of the injury. The use of an inter-vertebral surgery approach in combination with discreet transection injuries of the dorsolateral funiculus results in highly consistent deficits in grid-walk locomotor performance , .
A total of 6 µl of hGDABMP, hGDACNTF or hGPC suspensions (30,000 cells/µl; 180,000 cells total) per animal were acutely transplanted into six different sites at the injury site on the right side of the spinal cord: medial and lateral of the rostral and caudal injury margins, and medial and lateral of the injury center (Supplemental Fig. S1C). Control injured rats were injected with 6 µl HBSS. All control or cell transplanted rats were immune suppressed. Rats in the 9W2 groups were given daily injections of cyclosporine (1 mg/100 g body weight) beginning the day before injury/transplantation through the duration of the experiment. Due to a temporary unavailability of injectable cyclosporine, rats in the 9W1 group were given a bolus injection of methyl prednisolone (30 mg/kg body weight) 1 hour prior to injury/transplantation.
At 5 weeks post-surgery animals were deeply anesthetized and transcardially perfused with 0.1 M PBS followed by 4% paraformaldehyde in 0.1M PBS. Dissected spinal cords were cryosectioned and immunofluorescently labeled as previously described , . The following primary antibodies were used: mouse anti-GFAP (Sigma), rabbit polyclonal anti-GFAP (Sigma) or goat anti GFAP (Lifespan Biosciences); mouse anti-NeuN (Millipore); rabbit anti- 200 kD neurofilament (Serotec); mouse anti-human mitochondrial antigen (Millipore). Alexa-488, Alexa-594, and Alexa-647 conjugated secondary antibodies (Invitrogen) were used to visualize primary antibody binding. All secondary antibodies were pre-absorbed against rat serum. To control for nonspecific secondary antibody binding, adjacent sections were also processed as described above without primary antibodies. Some sections were counterstained with DAPI to show nuclei. Labeled sections were examined and imaged using a Zeiss 510 Meta confocal microscope. Antigen co-localization and cellular associations were determined with Zeiss Confocal image analysis software.
Quantification of axon growth into GDA treated injury sites
The relative density of axons within the centers of hGDABMP or hGDACNTF transplanted injury sites was determined by quantifying neurofilament-immunoreactive pixels in 4 tissue sections per spinal cord from 5 animals per experimental group. Images were captured (Zeiss-Z1 microscope) of the right-side dorsolateral funiculus from every sixth histological cross section (4 sections in total per spinal cord) from tissue at injury centers. Using Image-J analysis software, a 465 µm×465 µm square region of interest was drawn on each image with the upper right corner located on the dorso-lateral outer edge of the transplant mass such that the region of interest was contained within injury sites/transplant parenchyma (Supplemental Fig. S2). The area within the region of interest filled with NF+ pixels was determined. The sum total of NF+ areas of each region of interest per spinal cord was calculated, and then the average area per experimental group was determined. A two-sample T-test was applied to assess statistical significance (alpha = 0.05).
Quantification of neuron survival
Neuronal survival within spinal cord gray matter was determined using NeuN immuno-reactivity as a marker of surviving spinal cord neurons after spinal cord injury . To quantify surviving NeuN+ neurons, 15 sections per spinal cord at 5 weeks post injury were sampled from a 1.8 mm length of spinal cord encompassing the injury site. 5 spinal cords per experimental group were analyzed. Starting 400 µm rostral to the injury site, the right side of every sixth serial section was imaged (Zeiss-Z1 microscope). Using AxioVision software the gray matter was subdivided into 3 regions: laminae 4-6; lamina 7; laminae 8–9. NeuN+ neurons were counted within each region per section. The average number of neurons (+/− one standard deviaton) per total number of neurons was determined per region (tables 1 and 2). The percent change was calculated by dividing the average number of neurons per group by the average number of neurons in the injury control group. A second set of calculations was conducted on 6 sections per spinal cord through 750 µm of tissue spanning the injury center. One way ANOVA and Holm-Sidak multiple comparisons post hoc tests were applied to determine statistical significance (p<0.05). The power of these tests, with an alpha of 0.05, was 0.996 when all sections are considered, and 0.702 when only the 6 sections spanning the injury center are considered.
Analysis of Locomotor Recovery
Behavioral analysis of volitional foot placement was tested using a grid-walk behavioral test (Foot Misplacement Apparatus, Columbus Instruments) as previously described , . Two weeks before surgery, rats were trained to walk across a horizontal ladder and those that consistently crossed without stopping were used in experiments. Baseline gridwalk scores were obtained one day prior to surgery and rats were randomly assigned into experimental groups. One experiment included the following three groups: DLF injury + media injection (n = 8), DLF injury + 9W-1 hGPCs (n = 8), and DLF injury + 9W-1 hGDAsBMP (n = 8). The second experiment included DLF injury + media injection (n = 6), DLF injury + 9W-2 hGDAsCNTF (n = 6) and DLF injury + 9W-2 hGDAsBMP (n = 7). At 3, 7, 10, 14, 21, and 28 days post-surgery, each rat was tested three times and the number of mistakes from each trial was averaged to generate a daily score for each animal. Two-way repeated measures ANOVA and Holm-Sidak post hoc (p<0.05) were applied to assess statistical significance using Sigma Stat 3.5 (Systat Software Inc.). The power of these tests for each independent behavior study, with an alpha of 0.05, was equal to 1.0.
Schematic illustrations of the adult rat dorso-lateral funiculus (DLF) transection spinal cord injury model and cell injections at injury sites. Dorsal (A) and cross section (B) schematics of the rat cervical spinal cord showing right side unilateral transection injury (red shaded area) conducted at the level of the C3/C4 intervertebral junction. (C) Injections (six in total) of either hGDAs or hGPCs were made at sites if injury, two into injury centers and two further injections each to rostral and caudal injury margins respectively (black diamonds represent injection sites). C3/C4, junction of the third and fourth cervical vertebrae; DLF, dorsolateral funiculus; Cf, cuneate fasciculus; Gf, gracile fasciculus; GM, gray matter. (Cross section schematic (B) adapted from Grant and Koerber ).
Schematic illustration of neurofilament sampling region at injury/transplantation sites. Image-J analysis software has been used to draw a 465 µm×465 µm square region of interest (ROI, white box) on a representative image of an NF immuno-stained tissue section at the center of hGDACNTF treated DLF injury site. The upper right corner of the ROI is located on the dorso-lateral outer edge of the transplant mass such that that the region of interest is contained within the injury site/transplant mass. Scale bar = 200 µm.
We thank K. Saul, D. Harlow and K. Ellison for conducting histology and behavioral testing (Department of Neurosurgery, UC Denver) and Michelle Lacagnina (Department for Biomedical Genetics, University of Rochester, NY) and Laurie Baxter (Surgical Pathology, University of Rochester, NY) for assistance with human cell cultures, and Brendan Carlin for assistance with RT-PCR analysis (Department for Biomedical Genetics, University of Rochester, NY). The 3F8 anti-phosphacan antibody was obtained from the Developmental Hybridoma Bank developed under the auspices of the NICHID and maintained by the University of Iowa, Department of Biological Sciences.
Conceived and designed the experiments: SJAD MN MM-P JED CP. Performed the experiments: SJAD C-HS JED CP. Analyzed the data: SJAD JED CP. Contributed reagents/materials/analysis tools: SJAD MM-P JED CP. Wrote the paper: SJAD MN JED CP.
- 1. Windle WF, Clemente CD, Chambers WW (1952) Inhibition of formation of a glial barrier as a means of permitting a peripheral nerve to grow into the brain. J Comp Neurol 96: 359–369.
- 2. McKeon RJ, Hoke A, Silver J (1995) Injury-induced proteoglycans inhibit the potential for laminin-mediated axon growth on astrocytic scars. Exp Neurol 136: 32–43.
- 3. Davies SJ, Field PM, Raisman G (1996) Regeneration of cut adult axons fails even in the presence of continuous aligned glial pathways. Exp Neurol 142: 203–216.
- 4. Zuo J, Neubauer D, Dyess K, Ferguson TA, Muir D (1998) Degradation of chondroitin sulfate proteoglycan enhances the neurite-promoting potential of spinal cord tissue. Exp Neurol 154: 654–662.
- 5. McKeon RJ, Jurynec MJ, Buck CR (1999) The chondroitin sulfate proteoglycans neurocan and phosphacan are expressed by reactive astrocytes in the chronic CNS glial scar. J Neurosci 19: 10778–10788.
- 6. Davies S, Goucher D, Doller C, Silver J (1999) Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord. J Neurosci 19: 5810–5822.
- 7. Dietrich J, Lacagnina M, Gass D, Richfield E, Mayer-Proschel M, et al. (2005) EIF2B5 mutations compromise GFAP(+) astrocyte generation in vanishing white matter leukodystrophy. Nat Med 11: 277–283.
- 8. Nagai M, Re DB, Nagata T, Chalazonitis A, Jessell TM, et al. (2007) Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons. Nat Neurosci 10: 615–622.
- 9. Ouyang YB, Voloboueva LA, Xu LJ, Giffard RG (2007) Selective dysfunction of hippocampal CA1 astrocytes contributes to delayed neuronal damage after transient forebrain ischemia. J Neurosci 27: 4253–4260.
- 10. Seifert G, Carmignoto G, Steinhauser C (2009) Astrocyte dysfunction in epilepsy. Brain Res Rev.
- 11. Bradford J, Shin JY, Roberts M, Wang CE, Li XJ, et al. (2009) Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptoms. Proc Natl Acad Sci U S A 106: 22480–22485.
- 12. Xu L, Zeng LH, Wong M (2009) Impaired astrocytic gap junction coupling and potassium buffering in a mouse model of tuberous sclerosis complex. Neurobiol Dis 34: 291–299.
- 13. Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW (2009) Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. J Neurosci 29: 5051–5061.
- 14. Davies JE, Huang C, Proschel C, Noble M, Mayer-Proschel M, et al. (2006) Astrocytes derived from glial-restricted precursors promote spinal cord repair. J Biol 5: 7.
- 15. Weible MW 2nd, Chan-Ling T (2007) Phenotypic characterization of neural stem cells from human fetal spinal cord: synergistic effect of LIF and BMP4 to generate astrocytes. Glia 55: 1156–1168.
- 16. Oberheim NA, Takano T, Han X, He W, Lin JH, et al. (2009) Uniquely hominid features of adult human astrocytes. J Neurosci 29: 3276–3287.
- 17. Bignami A, Eng LF, Dahl D, Uyeda CT (1972) Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. Brain Res 43: 429–435.
- 18. Gomori E, Pal J, Abraham H, Vajda Z, Sulyok E, et al. (2006) Fetal development of membrane water channel proteins aquaporin-1 and aquaporin-4 in the human brain. Int J Dev Neurosci 24: 295–305.
- 19. Haglid KG, Hamberger A, Hansson HA, Hyden H, Persson L, et al. (1976) Cellular and subcellular distribution of the S-100 protein in rabbit and rat central nervous system. J Neurosci Res 2: 175–191.
- 20. Ludwin SK, Kosek JC, Eng LF (1976) The topographical distribution of S-100 and GFA proteins in the adult rat brain: an immunohistochemical study using horseradish peroxidase-labelled antibodies. J Comp Neurol 165: 197–207.
- 21. Rash JE, Yasumura T, Hudson CS, Agre P, Nielsen S (1998) Direct immunogold labeling of aquaporin-4 in square arrays of astrocyte and ependymocyte plasma membranes in rat brain and spinal cord. Proc Natl Acad Sci U S A 95: 11981–11986.
- 22. Brunet JF, Grollimund L, Chatton JY, Lengacher S, Magistretti PJ, et al. (2004) Early acquisition of typical metabolic features upon differentiation of mouse neural stem cells into astrocytes. Glia 46: 8–17.
- 23. Ochalski PA, Frankenstein UN, Hertzberg EL, Nagy JI (1997) Connexin-43 in rat spinal cord: localization in astrocytes and identification of heterotypic astro-oligodendrocytic gap junctions. Neuroscience 76: 931–945.
- 24. Lee SW, Kim WJ, Choi YK, Song HS, Son MJ, et al. (2003) SSeCKS regulates angiogenesis and tight junction formation in blood-brain barrier. Nat Med 9: 900–906.
- 25. Rothstein JD, Martin L, Levey AI, Dykes-Hoberg M, Jin L, et al. (1994) Localization of neuronal and glial glutamate transporters. Neuron 13: 713–725.
- 26. Cassiani-Ingoni R, Coksaygan T, Xue H, Reichert-Scrivner SA, Wiendl H, et al. (2006) Cytoplasmic translocation of Olig2 in adult glial progenitors marks the generation of reactive astrocytes following autoimmune inflammation. Exp Neurol 201: 349–358.
- 27. Chen Y, Miles DK, Hoang T, Shi J, Hurlock E, et al. (2008) The basic helix-loop-helix transcription factor olig2 is critical for reactive astrocyte proliferation after cortical injury. J Neurosci 28: 10983–10989.
- 28. Jones LL, Yamaguchi Y, Stallcup WB, Tuszynski MH (2002) NG2 is a major chondroitin sulfate proteoglycan produced after spinal cord injury and is expressed by macrophages and oligodendrocyte progenitors. J Neurosci 22: 2792–2803.
- 29. Massey JM, Amps J, Viapiano MS, Matthews RT, Wagoner MR, et al. (2008) Increased chondroitin sulfate proteoglycan expression in denervated brainstem targets following spinal cord injury creates a barrier to axonal regeneration overcome by chondroitinase ABC and neurotrophin-3. Exp Neurol 209: 426–445.
- 30. Zhao JW, Raha-Chowdhury R, Fawcett JW, Watts C (2009) Astrocytes and oligodendrocytes can be generated from NG2+ progenitors after acute brain injury: intracellular localization of oligodendrocyte transcription factor 2 is associated with their fate choice. Eur J Neurosci 29: 1853–1869.
- 31. Tang X, Davies JE, Davies SJ (2003) Changes in distribution, cell associations, and protein expression levels of NG2, neurocan, phosphacan, brevican, versican V2, and tenascin-C during acute to chronic maturation of spinal cord scar tissue. J Neurosci Res 71: 427–444.
- 32. Muir GD, Whishaw IQ (2000) Red nucleus lesions impair overground locomotion in rats: a kinetic analysis. Eur J Neurosci 12: 1113–1122.
- 33. Schucht P, Raineteau O, Schwab ME, Fouad K (2002) Anatomical correlates of locomotor recovery following dorsal and ventral lesions of the rat spinal cord. Exp Neurol 176: 143–153.
- 34. Huang WL, George KJ, Ibba V, Liu MC, Averill S, et al. (2007) The characteristics of neuronal injury in a static compression model of spinal cord injury in adult rats. Eur J Neurosci 25: 362–372.
- 35. Antal M, Sholomenko GN, Moschovakis AK, Storm-Mathisen J, Heizmann CW, et al. (1992) The termination pattern and postsynaptic targets of rubrospinal fibers in the rat spinal cord: a light and electron microscopic study. J Comp Neurol 325: 22–37.
- 36. Casale EJ, Light AR, Rustioni A (1988) Direct projection of the corticospinal tract to the superficial laminae of the spinal cord in the rat. J Comp Neurol 278: 275–286.
- 37. Holstege JC, Kuypers HG (1987) Brainstem projections to spinal motoneurons: an update. Neuroscience 23: 809–821.
- 38. Jones SL, Light AR (1990) Termination patterns of serotoninergic medullary raphespinal fibers in the rat lumbar spinal cord: an anterograde immunohistochemical study. J Comp Neurol 297: 267–282.
- 39. Grant G, Koerber , R H (2004) Spinal Cord Cytoarchitecture; Paxinos G, editor. San Diego, CA: Elsevier Academic Press.
- 40. Gumpel M, Lachapelle F, Gansmuller A, Baulac M, Baron van Evercooren A, et al. (1987) Transplantation of human embryonic oligodendrocytes into shiverer brain. Ann N Y Acad Sci 495: 71–85.
- 41. Cloutier F, Siegenthaler MM, Nistor G, Keirstead HS (2006) Transplantation of human embryonic stem cell-derived oligodendrocyte progenitors into rat spinal cord injuries does not cause harm. Regen Med 1: 469–479.
- 42. Izrael M, Zhang P, Kaufman R, Shinder V, Ella R, et al. (2007) Human oligodendrocytes derived from embryonic stem cells: Effect of noggin on phenotypic differentiation in vitro and on myelination in vivo. Mol Cell Neurosci 34: 310–323.
- 43. Keirstead HS, Nistor G, Bernal G, Totoiu M, Cloutier F, et al. (2005) Human embryonic stem cell-derived oligodendrocyte progenitor cell transplants remyelinate and restore locomotion after spinal cord injury. J Neurosci 25: 4694–4705.
- 44. Kerr CL, Letzen BS, Hill CM, Agrawal G, Thakor NV, et al. Efficient differentiation of human embryonic stem cells into oligodendrocyte progenitors for application in a rat contusion model of spinal cord injury. Int J Neurosci 120: 305–313.
- 45. Nistor GI, Totoiu MO, Haque N, Carpenter MK, Keirstead HS (2005) Human embryonic stem cells differentiate into oligodendrocytes in high purity and myelinate after spinal cord transplantation. Glia 49: 385–396.
- 46. Sharp J, Frame J, Siegenthaler M, Nistor G, Keirstead HSHuman embryonic stem cell-derived oligodendrocyte progenitor cell transplants improve recovery after cervical spinal cord injury. Stem Cells 28: 152–163.
- 47. Windrem MS, Nunes MC, Rashbaum WK, Schwartz TH, Goodman RA, et al. (2004) Fetal and adult human oligodendrocyte progenitor cell isolates myelinate the congenitally dysmyelinated brain. Nat Med 10: 93–97.
- 48. Windrem MS, Schanz SJ, Guo M, Tian GF, Washco V, et al. (2008) Neonatal chimerization with human glial progenitor cells can both remyelinate and rescue the otherwise lethally hypomyelinated shiverer mouse. Cell Stem Cell 2: 553–565.
- 49. Smith GM, Silver J (1988) Transplantation of immature and mature astrocytes and their effect on scar formation in the lesioned central nervous system. Prog Brain Res 78: 353–361.
- 50. Kliot M, Smith GM, Siegal JD, Silver J (1990) Astrocyte-polymer implants promote regeneration of dorsal root fibers into the adult mammalian spinal cord. Exp Neurol 109: 57–69.
- 51. Wunderlich G, Stichel CC, Schroeder WO, Muller HW (1994) Transplants of immature astrocytes promote axonal regeneration in the adult rat brain. Glia 10: 49–58.
- 52. Wang JJ, Chuah MI, Yew DT, Leung PC, Tsang DS (1995) Effects of astrocyte implantation into the hemisected adult rat spinal cord. Neuroscience 65: 973–981.
- 53. Joosten EA, Veldhuis WB, Hamers FP (2004) Collagen containing neonatal astrocytes stimulates regrowth of injured fibers and promotes modest locomotor recovery after spinal cord injury. J Neurosci Res 77: 127–142.
- 54. Archer DR, Cuddon PA, Lipsitz D, Duncan ID (1997) Myelination of the canine central nervous system by glial cell transplantation: a model for repair of human myelin disease. Nat Med 3: 54–59.
- 55. Warrington AE, Barbarese E, Pfeiffer SE (1993) Differential myelinogenic capacity of specific developmental stages of the oligodendrocyte lineage upon transplantation into hypomyelinating hosts. J Neurosci Res 34: 1–13.
- 56. Lepore AC, Rauck B, Dejea C, Pardo AC, Rao MS, et al. (2008) Focal transplantation-based astrocyte replacement is neuroprotective in a model of motor neuron disease. Nat Neurosci 11: 1294–1301.
- 57. Davies JE, Proschel C, Zhang N, Noble M, Mayer-Proschel M, et al. (2008) Transplanted astrocytes derived from BMP- or CNTF-treated glial-restricted precursors have opposite effects on recovery and allodynia after spinal cord injury. J Biol 7: 24.
- 58. Maeda S, Kawamoto A, Yatani Y, Shirakawa H, Nakagawa T, et al. (2008) Gene transfer of GLT-1, a glial glutamate transporter, into the spinal cord by recombinant adenovirus attenuates inflammatory and neuropathic pain in rats. Mol Pain 4: 65.
- 59. Nakase T, Fushiki S, Sohl G, Theis M, Willecke K, et al. (2003) Neuroprotective role of astrocytic gap junctions in ischemic stroke. Cell Commun Adhes 10: 413–417.
- 60. O'Carroll SJ, Alkadhi M, Nicholson LF, Green CR (2008) Connexin 43 mimetic peptides reduce swelling, astrogliosis, and neuronal cell death after spinal cord injury. Cell Commun Adhes 15: 27–42.
- 61. Rothstein JD, Dykes-Hoberg M, Pardo CA, Bristol LA, Jin L, et al. (1996) Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron 16: 675–686.
- 62. Dietrich J, Noble M, Mayer-Proschel M (2002) Characterization of A2B5+ glial precursor cells from cryopreserved human fetal brain progenitor cells. Glia 40: 65–77.
- 63. Barami K, Grever WE, Diaz FG, Lyman WD (2001) An efficient method for the culturing and generation of neurons and astrocytes from second trimester human central nervous system tissue. Neurol Res 23: 321–326.
- 64. Rao MS, Noble M, Mayer-Proschel M (1998) A tripotential glial precursor cell is present in the developing spinal cord. Proc Natl Acad Sci U S A 95: 3996–4001.
- 65. Li Z, Dong T, Proschel C, Noble M (2007) Chemically diverse toxicants converge on Fyn and c-Cbl to disrupt precursor cell function. PLoS Biol 5: e35.
- 66. Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25: 402–408.