Differences in the inherent properties of adipose tissue-derived stem cells (ASC) may contribute to the biological specificity of the subcutaneous (Sc) and visceral (V) adipose tissue depots. In this study, three distinct subpopulations of ASC, i.e. ASCSVF, ASCBottom, and ASCCeiling, were isolated from Sc and V fat biopsies of non-obese subjects, and their gene expression and functional characteristics were investigated. Genome-wide mRNA expression profiles of ASCSVF, ASCBottom and ASCCeiling from Sc fat were significantly different as compared to their homologous subsets of V-ASCs. Furthermore, ASCSVF, ASCCeiling and ASCBottom from the same fat depot were also distinct from each other. In this respect, both principal component analysis and hierarchical clusters analysis showed that ASCCeiling and ASCSVF shared a similar pattern of closely related genes, which was highly different when compared to that of ASCBottom. However, larger variations in gene expression were found in inter-depot than in intra-depot comparisons. The analysis of connectivity of genes differently expressed in each ASC subset demonstrated that, although there was some overlap, there was also a clear distinction between each Sc-ASC and their corresponding V-ASC subsets, and among ASCSVF, ASCBottom, and ASCCeiling of Sc or V fat depots in regard to networks associated with regulation of cell cycle, cell organization and development, inflammation and metabolic responses. Finally, the release of several cytokines and growth factors in the ASC cultured medium also showed both inter- and intra-depot differences. Thus, ASCCeiling and ASCBottom can be identified as two genetically and functionally heterogeneous ASC populations in addition to the ASCSVF, with ASCBottom showing the highest degree of unmatched gene expression. On the other hand, inter-depot seem to prevail over intra-depot differences in the ASC gene expression assets and network functions, contributing to the high degree of specificity of Sc and V adipose tissue in humans.
Citation: Perrini S, Ficarella R, Picardi E, Cignarelli A, Barbaro M, Nigro P, et al. (2013) Differences in Gene Expression and Cytokine Release Profiles Highlight the Heterogeneity of Distinct Subsets of Adipose Tissue-Derived Stem Cells in the Subcutaneous and Visceral Adipose Tissue in Humans. PLoS ONE 8(3): e57892. https://doi.org/10.1371/journal.pone.0057892
Editor: Andrea Vergani, Children’s Hospital Boston, United States of America
Received: October 14, 2012; Accepted: January 28, 2013; Published: March 5, 2013
Copyright: © 2013 Perrini et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported in part by grants from the Ministero dell’Università e Ricerca (Italy), the COST Action BM0602, the Fondazione della Società Italiana di Diabetologia per la Ricerca in Diabetologia e Malattie Metaboliche (Fo.Ri.SID), and NovoNordisk to F. Giorgino. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: This study was partly funded by NovoNordisk. Francesco Giorgino is a PLOS ONE Editorial Board member. However, there are no patents, products in development or marketed products to declare. This does not alter the adherence of the authors to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
The biological diversity of adipose tissue depots has become a fundamental issue in recent years, in light of its potential impact on human health ; . It is known that visceral adipose tissue is morphologically and functionally different from subcutaneous adipose tissue ; . Depot-related variations have long been described for a variety of biological endpoints, such as signaling reactions , glucose metabolism ;  and cytokine secretion . It has been also proposed that extrinsic factors, including depot-specific blood flow, cell density, cell heterogeneity and/or innervation , could contribute to distinct gene expression patterns and metabolic profiles of adipocytes from different anatomical regions. Alternatively, variations in the inherent properties of undifferentiated fat cell progenitors may dictate the biological specificity between the two fat depots bringing about the innate characteristics of Sc and V adipose cells. This concept has been supported by the demonstration that pre-adipocytes from distinct fat depots retain specific dynamic characteristics and gene expression patterns even after 40 cell doublings . More recently, we have shown that depot-related differences in gene expression, adiponectin secretion, and insulin signaling and action were still evident when precursor cells isolated from bioptic adipose tissue fragments were differentiated in vitro . Altogether, these findings support the concept that there could be an early commitment of fat precursor stromal cells able to influence the biological responses of the resulting adipocytes, independently of extrinsic influences deriving from tissue microenvironment. However, little is known about the identity, localization, or specific characteristics of endogenous adipocyte progenitors.
Adipocyte progenitors recognizably reside in the adipose stromal-vascular fraction (SVF), a heterogeneous mixture of cells operationally defined by enzymatic dissociation of fat tissue followed by density separation from adipocytes . Initially, the stromal-derived cells were designated as «pre-adipocytes», but since 2004 the International Fat Applied Technology Society adopted the term «adipose-derived stem cells» (ASC) to define the plastic-adherent cells isolated from SVF of adipose tissue with self-renewal properties and able to regenerate adipocytes (ASCSVF) ; . Further complexity to this scenario, however, is provided by the observation that, during the procedure of fat tissue enzymatic digestion and centrifugation, two additional ASC populations can be isolated from the «fat cake» at the top of the supernatant . One ASC population is obtained from a pre-adipocyte fraction in the fat cake not previously collected together with the ASCSVF; these cells can be grown at the bottom surface of the culture flask (ASCBottom). Another ASC population develops from mature adipocytes of the fat cake adherent to the ceiling surface of the culture flask filled with growth medium (ASCCeiling). It has been suggested that ASCCeiling may derive from mature adipocytes through an asymmetric mitosis ; . In culture, ASCCeiling and ASCBottom display both cell-surface markers that are similar to those expressed by ASCSVF, including CD105, SH3, Stro-1, CD49d and CD44, and show similar potential for unlimited self-renewing proliferation and differentiation along the mesenchymal lineage to produce adipocytes, osteoblasts, and chondrocytes .
In addition to their ability to differentiate into multiple mesenchymal cell lineages, ASC actively produce paracrine factors, hormones and metabolic signals, in a distinct manner from that of differentiated fat cells. Indeed, non-fat cells and ASC are considered one of the main sources of pro-inflammatory adipokine released by the adipose tissue , with great potential for repercussions on distant target tissues and metabolic and cardiovascular regulation . Several studies have reported that ASC and adipocytes contribute roughly similarly to the overall secretion/expression of adipokines, except for adiponectin and leptin ; ; . Thus, the different production of adipokines, such as IL-6 or MCP-1, between subcutaneous and visceral adipose tissues may reflect either intrinsic properties of the resident ASC or a different ASC proportion within each fat depot ; , underlying the contribution of ASC to the biological diversity of specific adipose tissue depots.
In this study, ASCSVF, ASCBottom and ASCCeiling were isolated from abdominal subcutaneous (Sc) and visceral omental (V) adipose tissue biopsies obtained from non-obese subjects and studied through a genome-wide differential gene expression analysis followed by an in-depth bioinformatics examination. In addition, 27 cytokines were measured in the culture medium collected from each of the 6 ASC populations. By performing comparative intra-depot (i.e., ASCSVF vs. ASCCeiling vs. ASCBottom) and inter-depot (i.e., Sc-ASC vs. V-ASC) analyses, differences in transcripts data and cytokines output emerged, which allowed us to identify six ASC subsets in the Sc and V fat depots that differ among them for gene expression profiles e cell functions.
Materials and Methods
All tissue culture reagents were purchased from Life Technologies (Carlsbad, CA, US). Unless otherwise stated, all chemicals used were obtained from Sigma-Aldrich (St. Louis, MO, US). Recombinant human insulin was purchased from Roche Diagnostics (Mannheim, Germany). The thiazolinedione (TZD) compound rosiglitazone was kindly provided by GlaxoSmithKlein (Middlesex, UK). Recombinant human fibroblast growth factor 2 (FGF2) and EGF were obtained from Miltenyi Biotec (Bergisch Gladbach, Germany).
Human Donors and Adipose Tissue Biopsies
Paired Sc and V adipose tissue biopsies were obtained from 15 non-obese subjects undergoing elective open-abdominal surgery (9 men, 6 women; age 68±7 yrs; BMI 27.0±1.5 kg/m2; fasting plasma glucose 85±11 mg/dl). None of the patients had diabetes or severe systemic illness, and none were taking medications known to affect adipose tissue mass or metabolism. The protocol was approved by the Independent Ethical Committee at the Azienda Ospedaliero-Universitaria Policlinico Consorziale, Bari, Italy. All patients gave their written informed consent.
Human ASC were isolated as previously described ; , with minor modifications. Briefly, fat tissue fragments were minced and digested in medium containing 1 mg/ml collagenase, type I, with gentle shaking at 37°C for 1 h. Resulting material was filtered through 250 µm mesh, and adipocytes and free oil were separated from stromovascular components by centrifugation at 1,200 rpm for 5 min at room temperature. The floating fraction consisting of pure isolated adipocytes was placed in 25-cm2 culture flasks completely filled with DMEM/Ham’s F12 1:1 supplemented with 20% fetal bovine serum, and cells were incubated at 37°C in 5% CO2. The primary ASC grown at top and bottom of flask, respectively, were cultured for 7 days until they reached confluence (defined as passage 0), and were then split into 60-mm plates. The stromovascular pellet was resuspended in erythrocyte lysis buffer, consisting of 154 mM NH4Cl, 10 mM KHCO3, and 0.1 mM EDTA, for 5 min. The cell suspension was centrifuged at 1,200 rpm for 5 min and then resuspended in a culture medium consisting of DMEM/Ham’s F12, 10% FCS and antibiotics. This cell suspension was filtered through a 25-mm sterile nylon mesh before being plated. After a 16-h incubation for cell attachment, cells were cultured in ASC growth medium (DMEM/Ham’s F12 1:1 supplemented with 100 units/ml penicillin, 0.1 mg/ml streptomycin, 2.5% FCS, 1 ng/ml FGF2, and 10 ng/ml EGF). Except when indicated, all cells were used in the experimental procedures at passage 4.
For adipogenic differentiation, confluent ASC at passage 4 were differentiated in a chemically defined serum-free medium containing antibiotics, 2 nM triiodotyronine (T3), 100 nM human insulin, 100 nM dexamethasone, and 1 µM rosiglitazone, as previously reported ; for the first 4 days of the differentiation period, 0.5 mM of methyl-isobutylxanthine was also added. Osteogenic differentiation was induced as previously described . Differentiation into chondrocytes was induced by StemPro Chondrogenesis Differentiation Medium, according to the manufacturer’s instructions.
Histochemical Staining of Differentiated Cells
Oil-Red-O, Alizarin Red, and Alcian Blue staining, respectively, were performed as described previously ; ; , and pictures were taken on wide-field microscopes (Nikon) with a color CCD camera.
RNA Isolation and Quantitative RT-PCR (qRT-PCR)
RNA from the ASC populations was isolated by using an RNeasy kit (Qiagen, Hamburg, Germany). 250 ng of RNA were reverse-transcribed with standard reagents (Applied Biosystems). One microliter of each reverse-transcription reaction was amplified by using SYBR Green PCR master mix from Applied Biosystems, using the ABI 7500 real-time PCR system. For each gene, mRNA expression was calculated relative to 18S rRNA. Amplification of specific transcripts was confirmed by melting curve profiles at the end of each PCR. Primer sequences for each gene are given in Table S1.
Total RNA was isolated from the ASC of 5 lean subjects. The quality and integrity of total RNA (RNA Integrity Number [RIN] ≥8.0) was evaluated on an Agilent Bioanalyzer (Agilent Technologies, Waldbronn, Germany). RNA was then processed for hybridization on Human Gene 1.0 ST Array chip (Affymetrix, High Wycombe, UK), covering 28,869 well-annotated genes with 764,885 distinct probes, using standard Affymetrix protocols. Raw signal intensities of gene expression data were processed, analyzed, and linearly scaled using GeneChip Operating Software 1.1 (GCOS, Affymetrix) to a mean hybridization intensity of 500 units. For each array, GCOS output was imported as CEL files into Partek Genomic Suite (Partek GS, Partek Inc., 2008, Revision 6.3) software, and data were normalized using the RMA (Robust Multichip Averaging) algorithm. RNA hybridization intensity data obtained from the array analysis were concordant for all ASCBottom, and for 4 of the 5 ASCCeiling and ASCSVF from both Sc and V fat depot. The remaining one ASC samples were excluded from the array analysis, since their data were ambiguous or incorrect, resulting in cell-mismatched design when compared with the homologous Sc and V-ASC subsets. Similarities and differences among gene expression profiles were assessed by hierarchical clustering using Partek GS software. Statistical significance was defined as being differentially expressed with an adjusted p-value <0.01. The array data have been deposited at the Gene Expression Omnibus archive, accession number GSE37324. A further analysis to identify the biological mechanisms, pathways and functions and the most relevant overexpressed genes was performed using the Ingenuity Pathways Analysis (IPA) software and database (Ingenuity Systems, http://www.ingenuity.com). Briefly, the dataset containing gene identifiers and corresponding fold changes was uploaded into the web-delivered application, and each gene identifier was mapped to its corresponding gene object. The threshold for a significant association was determined by the p-value <0.01, becoming significant any score above 3 ; . For all analyses, Fisher’s exact test was used to calculate a p-value and to determine a score for all networks that were ranked on the probability that a collection of genes equal to or greater than the number in a network could be achieved by chance alone.
Multiplex Analysis of Cytokine Production
ASC-derived conditioned medium (CM) was obtained by incubating confluent cells in serum-free DMEM/Ham’s F12 for 16 h, after which time all CM was collected, pooled, cleared by centrifugation, frozen in dry ice, and stored at −80°C. Concentrations of various cytokines in CM were analyzed using a multiplex biometrix immunoassay from Bio-Rad, containing fluorescent dyed microspheres conjugated with a monoclonal antibody specific for the target proteins according to the manufacturer’s instructions (Bio-Plex Human Cytokine Assay; Bio-Rad, Munich, Germany). The following cytokines were assayed: IL-1β, IL-1ra, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12 (p70), IL-13, IL-15, IL-17, FGF basic, eotaxin, G-CSF, GM-CSF, IFN-γ, IP-10, MCP-1 (MCAF), MIP-1α, MIP-1β, PDGF-BB, RANTES, TNF-α, and VEGF. The amount of protein in the medium was normalized for 106 cells . The inter- and intra-assay coefficients of variation for all cytokines under investigation were less than 10%.
Data are presented as mean ± SE. Comparisons between the values were performed using a two-tailed Student’s t-test. For the comparison of multiple groups, a one-way ANOVA test followed by Fisher’s post-hoc test was applied. For all statistical analyses, the level of significance was set at a probability of p<0.05. All experiments were repeated at least 3 times. These analyses were performed using SPSS 16 (SPSS, Chicago, IL).
Phenotypic Analysis and Stem Cell Properties of ASC Populations
ASCSVF, ASCCeiling and ASCBottom isolated from the Sc and V fat depots grew as a characteristic cell monolayer in culture dishes (Fig. 1A). To identify these cells as adipocyte progenitors and to rule out potential contamination by other adipose tissue cell types, analysis by qRT-PCR for a selection of known hematopoietic, endothelial and stem cell-associated markers was carried out. The expression of the key ASC markers CD105, CD49d, and CD44 was noticeably pronounced and expressed at similar magnitude in ASCSVF, ASCCeiling and ASCBottom from both Sc and V fat depots (Fig. 1B; Table S2). The initial Sc-ASCSVF and V-ASCSVF cultures contained a subset of cells that were also positive for the endothelial and hematopoietic lineage markers CD11b, CD45, and CD31 (Fig. 2A). However, with successive passages, the expression of CD11b, CD45, and CD31 declined significantly, becoming negligible by passage 4 (p<0.001 vs. passage 0; Fig. 2A), whereas expression levels of ASC markers remained constant (p = 0.860 vs. passage 0; Fig. 2B).
A. Morphology of human ASC populations, as detected under bright field. B. Expression of specific markers measured by qRT-PCR. Cells were harvested at passage 0, and RNA was analyzed for markers of adipose-derived stem cells (CD105, CD44, CD49d), human leukocytes and macrophages (CD45, CD11b), and mature endothelial cells (CD31).+or – signs indicate the relative levels of marker expression. Results are from 5 independent adipose tissue donors.
ASCSVF were analyzed at passage 0 (P0) and at passage 4 (P4). Open bars, Sc-ASC; filled bars, V-ASC. *p<0.001 vs. P0. Results are from 5 independent adipose tissue donors.
To confirm the multipotent mesenchymal stem cell properties of the distinct ASC populations, a comparative in vitro tri-lineage differentiation assay was carried out by exposing culture-expanded ASC derived from Sc and V adipose tissue to osteogenic, chondrogenic, or adipogenic differentiation media, respectively. The qualitative histochemical evaluation of functional outcomes indicated that ASCSVF, ASCCeiling and ASCBottom from both adipose tissue depots underwent differentiation along the adipogenic (assayed by Oil-Red-staining), osteogenic (assayed by Alizarin Red staining) and chondrogenic (assayed by alcian blue staining of sections derived from 2-week-old pellet cultures) lineages, respectively (Fig. S1). The mRNA levels of fat cell-specific gene markers, including GLUT4, PPARγ2 and adiponectin, were also increased several-fold with adipocyte differentiation (p<0.001 vs. ASC), and found to be similarly expressed in the distinct ASC populations (Fig. S2). These results indicate that the differentiation process into mature adipocytes was completed in an apparently equal manner in all ASC populations.
Gene Expression Profiles of ASC Populations
To investigate the gene expression profile of ASCSVF, ASCCeiling and ASCBottom isolated from Sc and V fat depots, a genome-wide analysis was performed using an Affimetrix Human Gene 1.0 ST Array chip microarray with 764,885 probe sets representing 28,869 different annotated genes (Fig. S3). Of these, 1,019 genes were identified that differed significantly between Sc-ASC and V-ASC (Fig. 3A). These genes were identified by first testing for significant expression differences among all ASC populations using the ANOVA model implemented in Partek GS at a p-value <0.05. Then, on genes that showed a statistically significant difference, a secondary filter was applied to select those genes that varied at least 1.5-fold. Thus, of the selected 1,019 genes, 247 genes were found to be differentially expressed between Sc-ASCSVF and V-ASCSVF, 543 between Sc-ASCBottom and V-ASCBottom, and 229 between Sc-ASCCeiling and V-ASCCeiling (Fig. 3A). Of these 1,019 genes, 75 (7.4%) were found to have a conjoint differential expression in ASCSVF, ASCCeiling and ASCBottom, while 868 (85.2%) showed a differential expression unique to each ASC subset, respectively (Fig. 3A). One gene was found to have a conjoint differential expression in all three ASC populations (Fig. 3A; Table S3).
A. Genes found to be differentially expressed by comparing Sc-ASC and V-ASC subsets (inter-depot analysis). B. Genes found to be differentially expressed by comparing ASCSVF, ASCBottom, and ASCCeiling from the Sc adipose tissue (Sc intra-depot analysis). C. Genes found to be differentially expressed by comparing ASCSVF, ASCBottom, and ASCCeiling from the V adipose tissue (V intra-depot analysis). In each panel, figures for conjoint (and non-conjoint) differentially expressed genes are also indicated.
A similar analysis was conducted on the ASCSVF, ASCBottom and ASCCeiling populations within each adipose tissue depot, again selecting those genes that varied significantly and at least 1.5-fold as compared to the baseline gene expression level (Fig. 3B). In Sc-ASC populations, 256 genes were found to be differentially expressed between ASCSVF and ASCCeiling, 213 between ASCSVF and ASCBottom, and 77 between ASCBottom and ASCCeiling (Fig. 3B). Of these 546 genes, 173 (31.7%) were found to have a conjoint differential expression in ASCSVF, ASCCeiling and ASCBottom, while 194 (35.5%) showed a differential expression unique to each ASC subset, respectively (Fig. 3B). No gene was found to have a conjoint differential expression in all three Sc-ASC populations (Fig. 3B). In V-ASC populations, 267 genes were differentially expressed between ASCSVF and ASCCeiling, 574 between ASCSVF and ASCBottom, and 381 between ASCBottom and ASCCeiling (Fig. 3C). Of these 1,222 genes, 234 (19.1%) were found to have a conjoint differential expression in ASCSVF, ASCCeiling and ASCBottom, while 750 (61.4%) showed a differential expression unique to each ASC subset, respectively (Fig. 3C). In contrast to the Sc adipose tissue, 4 genes were found to have a conjoint differential expression in all three V-ASC populations (Fig. 3C; Table S3). Altogether these findings indicate that the distinct three ASC populations show larger variations in gene expression when inter-depot as compared to intra-depot analyses are carried out, and that intra-depot variations in gene expression are apparently smaller for Sc-ASC than for V-ASC subsets.
To analyze inter- and intra-depot differences in gene expression profiles further, the principal component analysis (PCA) and hierarchical clusters analysis were applied. PCA was used to demonstrate similarities and differences in the transcriptional profiles of the analyzed samples. On a PCA plot, cell types with similar expression profiles can be positioned in proximity to each other. The position of each cell sample was plotted against the PC1, PC2, and PC3 axes in a three-dimensional (3D) space (Fig. 4A). When ASCSVF, ASCBottom, and ASCCeiling from the Sc adipose tissue depot were compared with the corresponding ASC from V fat, the PCA delineated two distinct positions in the 3D space for each ASC subset (Fig. 4A). In addition, when comparisons were carried out within each fat depot, the PCA depicted three clearly separated groups, consisting of ASCSVF, ASCCeiling and ASCBottom, showing the existence of ASC populations that are clearly heterogeneous in their gene expression in both the Sc and V adipose tissues (Fig. 4B).
A. PCA comparing gene expression of Sc-ASC (blue) and V-ASC (red) subsets. B. PCA comparing gene expression of ASCSVF (red), ASCBottom (blue), and ASCCeiling (green) from Sc and V fat depots, respectively. PCA analyses were performed by Partek GS software using default settings that include a threshold to remove low background level intensities. PCA percent mapping on the top of each plot indicates the explained variability on the first coordinate.
However, a high degree of heterogeneity was found for ASCBottom, whereas ASCSVF and ASCCeiling were found to be yet distinct but more closely related (Fig. 4B). Gene expression profiles were then subjected to hierarchical clusters analysis. A more striking difference was found by comparing each ASC subset from Sc and V adipose tissue than ASC subsets within Sc or V adipose tissue depots (Fig. S4A). However, in both depots ASCSVF and ASCCeiling displayed a rather related gene expression pattern over multiple conditions, whereas ASCBottom showed a highly dissimilar pattern compared to ASCSVF and ASCCeiling (Fig. S4A).
Functional Network Analysis of Differentially Expressed Genes in the ASC Subsets
To provide an insight into the potential functional implications of the observed differences in gene expression, the transcripts whose expression varied at least 1.5-fold and that were ordered identically along both axes by hierarchical cluster analysis were placed in the context of the known interactome using the Ingenuity Pathway Analysis (IPA). The score was then determined for each network based on p-value. Scores of 3 or higher were considered significant with 99% confidence. Using these criteria and gene ontology analysis, five different highly significant networks with a score of at least 20 were identified (Table 1). As expected for data derived from adipose precursor cells, the top functions of the highly significant networks were associated with lipid and carbohydrate metabolism, cell morphology, cell cycle, cellular assembly and organization, cellular movement and embryonic and tissue development (Table 1). Although there was some overlap in functions, there was also a clear distinction between each Sc-ASC and their corresponding V-ASC subsets, and among ASCSVF, ASCBottom, and ASCCeiling of Sc or V fat depots (Table 1).
IPA also performed a canonical pathway analysis in order to associate differentially regulated genes with known specific biological pathways (Table 2). Also in this case, the top ranked upregulated canonical pathways displayed some overlaps, yet distinctions were observed both when each Sc-ASC population was compared with the corresponding V-ASCs and among ASCSVF, ASCCeiling and ASCBottom from each fat depot. The most significant pathways identified in Sc-ASC included endoplasmic reticulum stress pathway, G-protein coupled receptor signaling, and ATM signaling, while those found in V-ASC included oxidative phosphorylation, protein ubiquitination pathway, and cell cycle: G1/S checkpoint regulation. These results further underline the inter-depot and intra-depot functional heterogeneity of the human ASC.
Confirmation of Gene Expression Differences by qRT-PCR
The array analysis described above provided us with trends reflecting changes in the expression of several mRNA species in the distinct ASC subsets. To better appreciate which of these findings were reproducible by standard and more rigorous molecular testing and to what extent such analysis would provide comparable fold change values, specific candidate genes were selected for further study using qRT-PCR. Out of the 1,019 differentially expressed genes changing at least 1.5-fold (by Affimetrix analysis) in Sc-ASC compared to V-ASC, 12 genes, known to be involved in the above mentioned top ranked functional networks and canonical pathways, were selected (quantitative data from array analysis are shown in Table S4). These include HoxA5 and Tbx15 (embryonic development), FABP5 (lipid homeostasis), IL-6, IL-8, MCP-1, VEGF, and MMP3 (immune system and proinflammatory signal transduction), PI16, PITPNC1, TFPI2 and ANXA10 (cell cycle). As shown in Figure 5, all of these candidate genes were also found to be differently expressed by qRT-PCR analysis. Specifically, HoxA5 mRNA levels were more expressed in V-ASCSVF and V-ASCBottom compared to Sc-ASCSVF and Sc-ASCBottom, respectively (p<0.01), whereas Tbx15 mRNA expression was higher in Sc- than V-ASC (p<0.01). IL-8 mRNA was expressed at higher levels in V-ASCCeiling than in Sc-ASCCeiling, and VEGF and MCP-1 mRNA levels were higher in V-ASCBottom and V-ASCCeiling than in Sc-ASCBottom and Sc-ASCCeiling, respectively (p<0.01). Intra-depot differences in mRNA levels of specific genes were also found. For example, HoxA5 mRNA levels were 2.3-fold higher in V-ASCBottom compared to V-ASCSVF and V-ASCCeiling, respectively (Fig. 5; p<0.01). Tbx15, VEGF and MCP-1 mRNA levels were higher in V-ASCCeiling than in V-ASCSVF (Fig. 5; p<0.05). IL-8, IL-6 and VEGF mRNA levels were significantly higher in Sc-ASCCeiling compared to Sc-ASCSVF and Sc-ASCBottom (Fig. 5; p<0.05). mRNA levels of PITPNC1, FABP5 and PI16 were higher in Sc-ASCCeiling than in Sc-ASCSVF or Sc-ASCBottom, and TFPI2, ANXA10 and MMP3 were expressed at higher levels in V-ASCCeiling than in V-ASCSVF or V-ASCBottom, as detailed in Fig. 5 (p<0.02).
mRNA levels were analyzed by qRT-PCR, as described under Methods. Open bars, Sc-ASC; filled bars, V-ASC. All data represent mean ± SE from 9 independent adipose tissue donors. *p<0.05 vs. V-ASC; #p<0.05 vs. other ASC populations from the same adipose tissue depot (ANOVA test followed by Fisher’s post-hoc test). SVF, stromo-vascular; B, bottom; C, ceiling.
Endocrine Activity of ASC Populations
To complement the findings on the differences in gene expression patterns of the distinct ASC populations with information on their endocrine activity, the release of cytokines, chemokines, and growth factors in the conditioned medium (CM) was also measured using a multiplex detection system capable of analyzing 27 different protein factors. Of the 27 molecules specified in the array, 14 (i.e., IL-2, IL-4, IL-5 IL-7, IL-9, IL-10, IL-12, IL-13, MIP1-α, MIP1-β, PDGF-BB, FGF-basic, GM-CSF, IP-10) were found to be not released at significant levels into the CM collected after 16 h. In contrast, 13 molecules were detectable (i.e., IL-1β, IL-1ra, IL-15, IL-17, G-CSF, IFN-γ, RANTES, TNF-α, eotaxin, IL-8, MCP-1, VEGF, IL-6), and, of these, MCP-1, Eotaxin, IL-1ra, FGF-basic, IL-6, IL-8, GM-CSF, and VEGF were above 50% of the positive control in all examined samples and also significantly different in the distinct ASC subsets of both Sc and V adipose tissue. Specifically, protein levels of MCP-1, eotaxin, IL-1ra, IL-6, GM-CSF, and VEGF were significantly higher in V-ASCSVF compared to Sc-ASCSVF CM (Fig. 6; p<0.05). In addition, the protein levels of eotaxin and IL-6 were also higher in V-ASCBottom than in Sc-ASCBottom CM (Fig. 6; p<0.03). In contrast, secretion of IL-8 was significantly increased in Sc-ASCCeiling compared to V-ASCCeiling CM (Fig. 6; p<0.01). MCP-1, eotaxin, and IL-6 were secreted at higher levels in Sc-ASCCeiling than in Sc-ASCSVF and Sc-ASCBottom CM (Fig. 6; p<0.05), whereas release of IL-1ra and GM-CSF was significantly greater in Sc-ASCBottom compared to Sc-ASCSVF and Sc-ASCCeiling CM (Fig. 6; p<0.05). Finally, IL-8 was significantly increased in V-ASCSVF as compared to V-ASCBottom and V-ASCCeiling CM (Fig. 6; p<0.05). These results show that ASCSVF, ASCCeiling and ASCBottom differ from each other also in terms of their ability to release specific cytokines and growth factors in the culture medium under basal conditions.
Culture medium from Sc-ASC (open bars) and V-ASC (filled bars) subsets (106 cells) was collected after a 16-h period, and levels of specific cytokines were determined using the multiplex technique, as described under Materials and Methods. Data represent the mean ± SE of results from 9 independent adipose tissue donors. *p<0.05 vs. V; #p<0.05 vs. other ASC subsets from the same adipose tissue depot (ANOVA test followed by Fisher’s post-hoc test).
The dynamics of adipocytes turnover is considered to play a remarkable role in regulating the total fat mass. Adipocytes are continuously produced in adult human adipose tissue, and even more so in obese individuals . Furthermore, ASC originating from the SVF of adult adipose tissue are capable of reconstituting the adipocyte mass in lipodystrophy syndromes . It should be also emphasized that the ASC component represents 15% to 50% of the cells in adipose tissue and actively produces paracrine factors and hormones in a manner distinct from that of differentiated fat cells . Thus, identifying the source and inherent properties of ASC is key to understand the plasticity of adipose tissue in humans and its relation to obesity and the associated metabolic abnormalities.
Previous studies have analyzed the gene expression profiles of ASC, focusing on i.) gene expression changes during in vitro differentiation to osteogenic, chondrogenic or adipogenic lineages ; , ii.) comparative analysis of bone marrow and adipose tissue-derived mesenchymal stromal cells in in vitro adipogenic, chondrogenic or osteogenic differentiation ; , and iii.) comparative transcriptomics of human multipotent stem cells during adipogenesis and osteoblastogenesis . However, this is the first time that a quantitative large-scale gene expression analysis of ASCSVF, ASCBottom, and ASCCeiling from distinct adipose tissue depots, showing significant intra- and inter-depot heterogeneity of the ASC subsets, has been carried out.
Phenotypically, and in line with previous studies ; ; , the progenitor cells isolated from Sc and V adipose tissue were defined as mesenchymal stem cells (MSC) by a panel of surface markers, subsequent adherence to plastic surface, and their propensity to give rise to adipocytes, chondrocytes, and osteocytes (Figs. 1–2, and Figs. S1, S2, S3). All subsets of ASC isolated from both fat depots fulfilled these characteristics without showing major differences among them, at least when exposed to standard culture and differentiation conditions (Figs. 1–2, and Figs. S1, S2, S3). This indicates that, by using standardized procedures, we were able to reproducibly establish apparently homogenous Sc-ASC and V-ASC populations. However, by using gene arrays analysis, more than 1,000 mRNAs were found to be significantly different and variant more than 1.5-fold between Sc-ASC and V-ASC (Fig. 3). Furthermore, ASC populations (i.e., ASCSVF, ASCCeiling and ASCBottom) originating from the same adipose tissue depot, Sc or V, were also surprisingly distinct from each other for gene expression profiles (Fig. 3). The significant gene expression heterogeneity between Sc-ASC and V-ASC subsets and among intra-depot ASC subsets was confirmed by PCA, an unbiased method to discriminate biological differences , which showed clearly separated three-dimensional space projections of the distinct gene expression profiles (Fig. 4, A and B). The tree-like diagram, which illustrates the hierarchical relationship among genes in a dataset in which the distance from the root to a cluster indicates the similarity of the cluster , further sustained the degrees of homogeneity or more distant relationship among groups of closely related genes between Sc-ASC and V-ASC populations and among ASCSVF, ASCCeiling and ASCBottom from the same fat depot (Fig. S4, A and B). The dendrogram in Figure S4 corroborates a far more striking difference between each Sc-ASCSVF, Sc-ASCCeiling and Sc-ASCBottom and its own homologous V-ASC subset. Taking into account that ASCCeiling have been suggested to develop from an “asymmetric mitosis” of terminally differentiated adipocytes ; , it is quite surprising to find that ASCCeiling and ASCSVF shared a similar degree of closely related genes, which conversely was highly different when compared to the gene expression pattern of ASCBottom (Fig. S4B). After considering that ASCBottom derive from precursors present in the fat cake at the top of the supernatant (Fig. S3), and thus could be considered as tissue-resident adipose stem cells, it follows that these results establish, for the first time, the existence of two different tissue-resident adipose stem cells, i.e., ASCBottom and ASCSVF, characterized by an unmatched gene expression pattern within the same fat depot. In addition, the comparison of different ASC subsets by hierarchical cluster analysis demonstrated a relatively close resemblance of the profiles among all five donor samples for each subset (Fig. S4), indicating a relatively low inter-individual variation in ASC gene expression patterns.
Investigation of how the genes differently expressed by ASCSVF, ASCBottom, and ASCCeiling might interact as part of complex pathways and network functions by using the Ingenuity Pathway Analysis made it possible to reveal several and distinct functional networks between Sc-ASC and V-ASC, and among ASCSVF, ASCBottom and ASCCeiling (Tables 1 and 2). A simultaneous survey and evaluation of the top canonical pathways and associated network functions displayed that lipid and carbohydrate metabolism, cell morphology, cell cycle, cellular assembly and organization, cellular movement and embryonic and tissue development showed highly significant differences in ASC populations (Tables 1 and 2). In addition, it should be emphasized that such analyses reflect relationships of currently known genes and participation in established pathways and do not consider the potential contribution of novel genes and functions that are yet to be identified.
Confirmation of differences in network functions was also achieved by evaluating the mRNA expression of 12 genes that varied at least 1.5-fold from baseline gene expression, and are known to be involved in the above networks and up-regulated canonical pathways (Fig. 5). Interestingly, as previously observed in other studies on fat precursors and mature adipocytes, HoxA5, VEGF, IL-8 and MCP-1 mRNAs were significantly more expressed in V-ASC than in Sc-ASC ; –. In addition, these differences in gene expression were apparently independent of gender (data not shown), in spite of potential variations in the local microenvironment due to changes in sex steroids, metabolites, and possibly inflammatory cytokine levels. Thus, differences in gene expression appear to be intrinsic to each ASC population and to persist during in vitro culture, suggesting that they are cell-autonomous and largely unaffected by other (extrinsic) factors.
The overall cytokine profile of the human ASC populations was found to be comparable to that observed in mesenchymal cells derived from human bone marrow (BM-MSC) ;  and cord blood (CB-MSC) , pointing out that the cytokine secretory properties could be viewed as a common characteristic of mesenchymal stem cells, similarly to cell surface marker expression and differentiation into mesenchymal lineages. However, differences in cytokine levels in the CM from distinct ASC subsets further sustain the intrinsic gene expression diversity of each ASC population, since eight of thirteen detectable cytokines were present to a different extent (Fig. 6). These findings reveal heterogeneity in the secretory ability between Sc-ASC and V-ASC and also among ASCSVF, ASCBottom and ASCCeiling. Changes in cellular mRNA levels and protein levels in the culture medium of the individual cytokines were not always coordinated (Figs. 5 and 6), suggesting independent regulation of gene expression and protein secretion, respectively, as previously shown for adiponectin production by Sc and V adipocyte populations . Furthermore, the protein abundance of MCP-1, IL-8, IL-6, and VEGF in the CM was far higher than that of Eotaxin, IL-1ra, FGFbasic and G-CSF (i.e., in the range of 100–600 pg/ml vs. that of 1–50 pg/ml, respectively; Fig. 6), highlighting that the former set of ASC-released cytokines would more likely contribute to the overall adipose tissue cytokine output and to their circulating levels . Noteworthy, ASCCeiling from the Sc fat depot displayed higher secretion of specific cytokines (i.e., MCP-1, eotaxin, IL-8, IL-6) that regulate leukocyte recruitment and other immune responses, as compared to other Sc-ASC subsets; this feature was not observed in the ASCCeiling from the V fat depot, suggesting a potentially unique role for this Sc-ASC population in the regulation of inflammatory pathways.
In conclusion, we have analyzed the expression profiles of distinct ASC isolated from human Sc and V adipose tissue and revealed, for the first time, significant differences in the gene expression profile and related functional networks and in the cytokine release ability according to the anatomical origin of these cells. In addition, the results including the bioinformatics analysis have allowed us to identify ASCCeiling and ASCBottom as two ASC populations in addition to the ASCSVF that are characterized by an unmatched gene expression pattern. The knowledge obtained in this study provides further evidence of the heterogeneity and complexity of ASCs existing in abdominal Sc and V adipose tissue in humans.
Adipogenic, osteogenic, and chondrogenic potential of human ASC populations. ASCSVF, ASCBottom, and ASCCeiling were cultured in adipogenic, osteogenic, or chondrogenic induction media. Histochemical stainings were performed as described under Materials and Methods. Cultures are displayed at 20× magnification (representative of n = 4). A. Adipogenic differentiation. B. Osteogenic differentiation. C. Chondrogenic differentiation.
Expression of adipose tissue-specific genes in Sc and V ASC differentiated into mature adipocytes. Sc-ASC (white bars) and V-ASC (black bars) were differentiated as described under Materials and Methods. Total RNA was extracted from undifferentiated ASC and mature adipocytes, respectively, and mRNA expression levels of PPARγ, adiponectin, and GLUT4 were determined by qRT-PCR. The mRNA level was normalized for each target gene against 18S ribosomal RNA as internal control. Values are means±SE of cells from five independent donors performed in triplicate and expressed as fold-increase vs. undifferentiated ASC (p<0.001). Paired Sc-ASCs and V-ASCs were obtained from 5 non-obese individuals with normal glucose tolerance (3 men, 2 women; age 66±11 yrs; BMI 26.0±2.0 kg/m2; fasting plasma glucose 79±9 mg/dl).
Microarray workflow for whole ASC mRNA transcript analysis. A. Clinical and metabolic parameters of the donors enrolled for the microarray analysis. B. The three distinct ASC populations were cultured as described under Materials and Methods. Equal amounts of RNA were isolated from ASCSVF, ASCBottom, and ASCCeiling obtained from Sc and V adipose tissue depots of the donors, and hybridized to Affymetrix chips.
Hierarchical clusters analysis of Sc and V ASC. A. Hierarchical cluster analysis (HCL) was conducted by PartekGS software including all genes. Groupings showing differential expression were selected and inspected for downstream analyses. Hierarchical clusters analysis of Sc- and V-ASC subsets. B. Hierarchical clusters analysis of ASCSVF, ASCBottom, and ASCCeiling from Sc and V fat depots, respectively. Profiles of the transcripts were organized by hierarchical clustering. Genes were analyzed further as described in the text.
Primers used for q RT-PCR.
Threshold cycles (Ct) of qRT-PCR for markers expressed by ASCs. Cells were harvested at passage 4 and RNA was analyzed for ASC markers (CD105, CD44, CD49d), human leukocytes and macrophages (CD45, CD11b), and mature endothelial cells (CD31).
List of conjoint differentially expressed genes among ASCSVF, ASCBottom and ASCCeiling from Sc and V adipose tissue.
Quantitative array data for the selected genes assessed by q RT-PCR.
Conceived and designed the experiments: SP FG AN LL. Performed the experiments: RF EP. Analyzed the data: EP MC GP SP RF FG AN LL. Contributed reagents/materials/analysis tools: AC MB PN AP OP MDF. Wrote the paper: SP FG.
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