Severe sepsis and septic shock are major causes of morbidity and mortality worldwide. In experimental sepsis there is prominent apoptosis of various cell types, and genetic manipulation of death and survival pathways has been shown to modulate organ injury and survival.
We investigated the effect of extracellular administration of two anti-apoptotic members of the BCL2 (B-cell lymphoma 2) family of intracellular regulators of cell death in a murine model of sepsis induced by cecal ligation and puncture (CLP). We show that intraperitoneal injection of picomole range doses of recombinant human (rh) BCL2 or rhBCL2A1 protein markedly improved survival as assessed by surrogate markers of death. Treatment with rhBCL2 or rhBCL2A1 protein significantly reduced the number of apoptotic cells in the intestine and heart following CLP, and this was accompanied by increased expression of endogenous mouse BCL2 protein. Further, mice treated with rhBCL2A1 protein showed an increase in the total number of neutrophils in the peritoneum following CLP with reduced neutrophil apoptosis. Finally, although neither BCL2 nor BCL2A1 are a direct TLR2 ligand, TLR2-null mice were not protected by rhBCL2A1 protein, indicating that TLR2 signaling was required for the protective activity of extracellularly adminsitered BCL2A1 protein in vivo.
Citation: Iwata A, de Claro RA, Morgan-Stevenson VL, Tupper JC, Schwartz BR, Liu L, et al. (2011) Extracellular Administration of BCL2 Protein Reduces Apoptosis and Improves Survival in a Murine Model of Sepsis. PLoS ONE 6(2): e14729. https://doi.org/10.1371/journal.pone.0014729
Editor: Lisa F. P. Ng, Singapore Immunology Network, Singapore
Received: May 25, 2010; Accepted: January 31, 2011; Published: February 24, 2011
Copyright: © 2011 Iwata 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: National Institutes of Health grants GM042686 (RKW, JMH) and GM071398 (JMH) supported this work. The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The University of Washington holds intellectual property related to the use of BCL2 proteins as therapeutic agents in diseases associated with cell death and inflammation. AI, VM-S, JCT, JMH, and RKW are employees of the University of Washington and inventors on patent applications submitted by the University of Washington related to this intellectual property. The authors confirm their adherence to all the PLoS ONE policies on sharing data and materials.
Severe sepsis and its major complications of multiple organ dysfunction and shock are major causes of morbidity and mortality worldwide. Although there have been substantial improvements in antimicrobial therapy and supportive critical care, severe sepsis remains the leading cause of death among hospitalized patients in non-coronary intensive care units. Unfortunately, decades of clinical trials with a variety of drug candidates have largely failed to reduce mortality , . Consequently, there is an urgent need to understand better the pathophysiology of severe sepsis and identify new therapeutic targets.
One of the hallmarks of experimental sepsis is increased apoptosis of a number of cell types. Although apoptosis of immune cells has been investigated most extensively , , there is also apoptosis of other cell types , including endothelial cells , , neutrophils , hepatocytes , cardiomyocytes , and intestinal epithelial cells . Moreover, genetic manipulation of cell death and survival pathways has marked effects in murine models of sepsis (e.g., ). These observations suggest that pharmacological inhibition of apoptosis by blocking cell death pathways or promoting cell survival pathways could provide a new therapeutic approach to sepsis in man .
BCL2 and BCL2A1 (A1, Bfl-1) are both anti-apoptotic members of the larger BCL2 family of intracellular proteins. Transgenic over-expression of BCL2 in T-cells and B-cells , intestinal epithelium  and myeloid cells  all resulted in a decrease in apoptosis in those cell types and improved survival in septic mice. Thus, increased intracellular BCL2 in multiple lineages is able to confer protection in experimental sepsis.
There is growing evidence that some proteins with well-defined intracellular functions can exert new activities when released extracellularly, engaging the innate immune system to act as danger signals to promote host defense or repair, i.e., alarmins  or danger-associated molecular patterns (DAMPs) , many of which are hydrophobic molecules . For example, high mobility group box 1 (HMGB1) is a nucleoprotein that is released extracellularly when cells undergo necrosis or, in some cell types, by a non-canonical secretory pathway. High levels of HMGB1 accumulate in animals  and humans with severe sepsis , . Administration of antibodies against HMGB1 results in increased survival and protection against organ damage in septic animals . However, even for this prototypic DAMP the mechanism(s) by which it acts in vivo remains uncertain as highly purified HMGB1 lacks significant activity in vitro -. Recently, we reported that the intracellular BCL2 and BCL2A1 proteins and peptides derived from them that contain the BH4-domain function as cytoprotective DAMPs, conferring tissue protection when administered extracellularly . At very low, cytokine-like doses extracellular administration of rhBCL2 or rhBCL2A1 protein or peptides containing the BH4 domain of BCL2 or BCL2A1 reduced apoptosis and tissue damage in stringent murine models of hind limb and myocardial ischemia-reperfusion injury. Further, in preliminary studies rhBCL2A1 protein also reduced hypertrophy and fibrosis in pressure overload-induced heart failure . Here, we show that extracellular administration of rhBCL2 or rhBCL2A1 protein also provides striking protection in experimental sepsis induced by CLP, and that this protective effect is associated with marked reduction of apoptosis in heart, intestine, and peritoneal neutrophils. These studies extend the range of experimental models of tissue and organ injury in which BCL2 BH4-domain proteins exert a protective effect, further highlighting their novel and potent extracellular activity.
Treatment with extracellular rhBCL2A1 or rhBCL2 protein improves survival after CLP
Mice were subjected to CLP and followed for 7 days as described in Methods. An assessment table was used as a surrogate marker for death and the animals euthanized according to approved criteria. In the initial experiments, mice were treated with 1 µg (∼40 picomoles) of rhBCL2A1 or saline vehicle at 18 hours prior to CLP and then every 12 hours for 3 consecutive days for a total of eight doses. Treatment with the BH4-domain protein, rhBCL2A1, was protective (Fig. 1A), whereas treatment with the BH3-domain protein, rhBim, was not (Fig. 1B). In separate experiments, rhBCL2A1 and rhBCL2 were compared directly with other recombinant proteins, which had been prepared similarly in E. coli and were also his-tagged. Treatment with the anti-apoptotic BH4-domain BCL2 proteins conferred a significant increase in survival, compared with treatment with the control recombinant proteins, rhUbiquitin (Fig. 1C) or rhBim (Fig. 1D). Consequently, rhBim was used as control in most experiments.
Mice were subjected to CLP and followed for 7 days. An assessment table was used as a surrogate marker for death and the animals euthanized according to approved criteria. (A) Mice were treated by i.p. injection of 1 µg rhBCL2A1 or saline 18 hours prior to CLP and then every 12 hours for 3 consecutive days. Treatment with rhBCL2A1 conferred significant protection compared to saline. *p = 0.012. (B) Mice were treated by i.p. injection of 1 µg rhBim or saline 18 hours prior to CLP and then every 12 hours for 3 consecutive days. Treatment with rhBim did not improve survival compared to saline. (C) Mice were treated by i.p. injection of 1 µg rhBCL2 or 0.5 µg of rhUbiquitin at 18 hours prior to CLP, at time of CLP, and then every 12 hours for 3 consecutive days. Treatment with rhBCL2 conferred significant protection compared to rhUbiquitin *p = 0.003. (D) Mice were treated by i.p. injection of 1 µg rhBCL2A1 or rhBim at 18 hours prior to CLP and then every 12 hours for 3 consecutive days. Treatment with rhBCL2A1 conferred significant protection compared to rhBim. *p = 0.005.
Treatment with extracellular rhBCL2 or rhBCL2A1 reduces apoptosis after CLP
As compared to mice treated with rhBim (Fig. 2A, C), treatment with rhBCL2 (Fig. 2B, D) reduced the number of TUNEL-positive cells detected at 24 hours after CLP in the heart by 76% (Fig. 2G) and in the intestine by 58% (Fig. 2H). Likewise, treatment with rhBCL2A1 significantly reduced the number of TUNEL-positive cells in the heart (Fig. 2I) and the intestine (Fig. 2F, J). Furthermore, mice treated with rhBCL2 protein had a significant reduction in cleaved caspase-3 expression following CLP in the heart (Fig. 3B, F) and intestine (Fig. 3D, E) compared to mice treated with rhBim (Fig. 3A, C, E, F). Taken together, these data indicate that treatment with rhBCL2 or rhBCL2A1 protein reduces sepsis-induced apoptosis in multiple target organs.
Animals were treated with a single i.p. injection of 1 µg rhBim or rhBCL2 or rhBCL2A1 at 18 hours prior to CLP. Tissues were removed and processed at 24 hours following CLP. In the photomicrograph (A-F) TUNEL-positive cells are labeled with FITC (green) and nuclei are labeled with DAPI (blue). Panels A and B shows myocardium from mice treated with rhBim (A) or rhBCL2 (B). Panels C-F show intestinal villi from mice treated of rhBim (C, E), rhBCL2 (D) or rhBCL2A1 (F). The graph shows quantitation of TUNEL-staining in cardiomyocytes (G, I) or intestine (H, J) following treatment with rhBim or rhBCL2 (G, H) or rhBCL2A1 (I, J). The number of TUNEL-positive cells in mice treated with rhBim was significantly greater than in mice treated with rhBCL2 or rhBCL2A1. *p<0.05.
Mice were treated with a single i.p. injection of 1 µg rhBim (A, C) or 1 µg rhBCL2 (B, D) at 18 hours prior to CLP. Heart (A, B) or intestine (C, D) was stained for cleaved caspase with 3, 3′-diaminobenzidine (brown). Nuclei were stained with hematoxylin (purple). Original magnification is 400×. Panels E and F show quantitation of cleaved caspase-3 expression in myocardium (E) and intestinal villi (F) in mice treated with rhBim compared to those treated with rhBCL2. *p<0.05.
Endogenous mouse BCL2 protein is up-regulated in the hearts and intestine of rhBCL2A1-treated mice
We next determined whether treatment with rhBCL2A1 altered expression of endogenous BCL2. Using an anti-mouse BCL2 antibody that does not cross-react with human BCL2, we found that mice treated with rhBCL2A1 (Fig. 4B, D) showed increased expression of endogenous mouse BCL2 protein in both the heart muscle and intestine, as compared to mice that were untreated or treated with rhBim (Fig. 4A, C). We confirmed the up-regulation of endogenous mouse BCL2 protein using flow cytometry analysis. Cardiomyocytes from mice treated with rhBCL2A1 showed an increase in endogenous BCL2 expression 24 hours after CLP (Fig. 4E, F). Taken together, these data suggest that protection may be conferred in some tissues by up-regulation of endogenous BCL2 in the stressed tissue.
Mice were treated with a single i.p. injection of 1 µg rhBim (A, C) or rhBCL2A1 (B, D) at 18 hours prior to CLP. Heart (A, B) and intestine (C, D) were examined at 24 hours following CLP. Endogenous mouse BCL2 protein was detected by immuno-staining with rabbit anti-mouse BCL2 antibody detected with 3, 3′-diaminobenzidine (brown) and the nuclei were stained with hematoxylin (purple). Representative FACS analysis of endogenous BCL2 expression in cardiomyocytes from mice treated as above with rhBim (E) or rhBCL2A1 (F). Green line represents isotype control and red line represents anti-mouse BCL2 antibody.
Cell populations and cytokines in peritoneum and peripheral blood
Peripheral blood leukocyte counts were analyzed following CLP. Mice were treated with a single i.p. injection of 1 µg rhBCL2A1 or 1 µg of rhBim at 18 hours prior to CLP. Animals were euthanized at 24 hours following CLP and whole blood was analyzed. Peripheral blood leukocyte counts and neutrophil counts were similar in rhBCL2-treated and rhBim-treated animals (total leukocytes were 2.184×106 +/− 0.3336 SEM in rhBim-treated and 1.993×106 +/− 0.4202 SEM in rhBCL2A1-treated; total neutrophils were 0.8356×106 +/− 0.8356 SEM in rhBim-treated and 0.7789×106 +/− 0.1221 SEM in rhBCL2A1-treated).
In separate experiments, leukocyte populations in peritoneal lavage were evaluated. Mice received rhBim, rhBCL2A1, or no treatment followed 18 hours later by CLP. Additionally, some mice received either rhBim or rhBCL2A1, but did not have CLP. In those animals not subjected to CLP, there was no significant accumulation of total leukocytes or neutrophils in animals treated with rhBCL2A1 (Fig. 5 A, B). In contrast, in animals subjected to CLP there was a significant increase in the total number of leukocytes in the peritoneal lavage fluid in mice treated with rhBCL2A1 as compared to the other treatment groups (Fig. 5A). This increase in total cells was due specifically to an increase in neutrophils in the peritoneal lavage fluid (Fig. 5B). We did not observe any changes in circulating neutrophil counts, and G-CSF levels in peritoneal fluid and G-CSF mRNA expression in spleen (Fig. S1) were similar in the rhBCL2A1-treated mice compared to rhBim-treated mice following CLP, making it less likely that the increase in peritoneal neutrophils following CLP was due solely to increased production. However, annexin V-staining of peritoneal cells showed that there were more viable neutrophils in the peritoneal lavage of rhBCL2A1-treated animals following CLP (Fig. 5C), consistent with a reduction in apoptosis.
Mice were treated once by i.p. injection with 1 µg of rhBCL2A1 or rhBim at 18 hours prior to CLP. Peritoneal lavage fluid was collected at 24 hours following CLP. Panels A and B show the total number of leukocytes and neutrophils (PMNs) in lavage fluid. Mice treated with rhBCL2A1 showed an increase in peritoneal PMNs following CLP as compared to mice that did not receive CLP or mice that were treated with rhBim. Panel C shows the viability of peritoneal neutrophils at 24 hours following CLP as assessed by staining with annexin V and 7-amino-actinomycin D. Treatment with rhBCL2 significantly increased the number of viable neutrophils compared to treatment with saline or rhBCL2A1. *p<0.01.
We determined the generation of reactive oxygen species by peritoneal neutrophils as determined by flow cytometry using dihydrorhodamine-123 to detect intracellular ROS. At 24 hours post-CLP there was no difference in ROS generation by unstimulated neutrophils between saline-treated mice and rhBCL2A1-treated mice (mean channel fluorescence: 8.07±4.5 in saline versus 7.06±2.2 in rhBCL2A1; means±SD of 3 mice). Similarly, there was no difference between saline-treated and rhBCL2A1-treated following stimulation by phorbol myristate acetate (mean channel fluorescence: 17.4±4.1 in saline versus 25.7±9.0 in rhBCL2A1; means±SD of 3 mice).
We also assayed the levels of 20 different cytokines, chemokines, or growth factors in the peritoneal lavage fluid. Despite the marked improvement in survival with treatment with BCL2A1, there were no significant differences between levels in rhBCL2A1- and rhBim-treated animals (Table S1).
Protection by rhBCL2A1 requires TLR2 signaling
Although rhBCL2 and rhBCL2A1 are not direct TLR2 agonists or antagonists in vitro , we recently demonstrated that protection against ischemia-reperfusion injury of hind limb by rhBCL2A1 required TLR2 and signaling in vivo as evidenced by lack of protection in TLR2-null or MyD88-null mice . Consistent with these results in ischemia-reperfusion injury, treatment with rhBCL2A1 did not protect TLR2-null mice following CLP (Fig. 6).
C57BL/6 or TLR2-null mice were subjected to CLP and followed for 7 days. An assessment table was used as a surrogate marker for death, and the animals were euthanized according to approved criteria. Animals were treated by i.p. injection of saline or 1 µg rhBCL2A1 at 18 hours prior to CLP, at the time of CLP, and then every 12 hours for the 3 consecutive days. There was no significant difference in survival between the treatment groups.
There is compelling experimental evidence that apoptosis is a major contributor to the multiple organ dysfunction in experimental sepsis . Among the genes related to apoptosis, BCL2 and family members are the most extensively investigated [reviewed in ]. In multiple studies transgenic mice over-expressing BCL2 in various target cells have decreased apoptosis and improved survival in sepsis , , , . In a recent study we showed that extracellular administration of rhBCL2 or rhBCL2A1 protein provided protection in murine models of hind limb and cardiac ischemia . In the present study, we demonstrate that exogenous administration of rhBCL2 or rhBCL2A1 protein reduces apoptosis in heart, intestine, and peritoneal neutrophils and improves survival following CLP-induced sepsis. We previously showed that BCL2 is released extracellularly with cell necrosis in vitro . In this regard, it is notable that Hotchkiss et al  reported that administration of necrotic cells improved survival in CLP-induced sepsis. Further, since BCL2 and BCL2A1 are expressed on the plasma membrane in some cells , , it is also possible that BH4-domain proteins are shed during activation or apoptosis as occurs with other plasma membrane proteins. Notably, soluble BCL2 has been detected in extracellular fluids in a variety of clinical conditions -. Thus, BCL2 and BCL2A1 join a growing list of alarmins or DAMPs that modulate the response of the innate immune system to tissue injury , . However, in contrast to many other alarmins or DAMPs, BCL2 and BCL2A1 do not appear to elicit a pro-inflammatory response in unstressed animals, either in vitro  or in vivo. Indeed, we analyzed 69 serum proteins following intravenous administration of BCL2A1 protein and found no significant changes from baseline (Table S2).
In preliminary experiments we sought to determine whether treatment following induction of CLP might still be protective. As shown in Fig. S2, treatment at 24 hours after CLP was not effective. However, it is important to note that this is a highly lethal model of sepsis with many animals succumbing within the first 24–48 hours. Consequently, it is likely that many of the animals are already not salvageable by 24 hours. To definitively address the question as to whether post-treatment would be effective would require establishing a less stringent model of sepsis in which the early mortality was not as marked.
Animals treated with rhBCL2- or rhBCL2A1 exhibited reduced numbers of TUNEL-positive cells as well as decreased caspase-3 expression in cardiomyocytes and intestinal cells following CLP, suggesting that improved survival may be due, at least in part, to a reduction of apoptosis in multiple organs. Interestingly, the decreased apoptosis in the rhBCL2A1-treated animals was associated with increased expression of endogenous mouse BCL2 protein in heart and intestinal cells as determined by both immuno-cytochemistry and flow cytometry. Also, there was a significant increase in the total number of neutrophils in the peritoneal lavage fluid from mice receiving rhBCL2A1 followed by CLP, which was likely due to a reduction in neutrophil apoptosis as evidenced by decreased annexin-V staining. This early increase in neutrophils at the site of infection might serve to contain the infection, consequently improving survival. Since murine neutrophils express BCL2A1 but not BCL2, it sees likely that protection by BCL2 or BCL2A1 protein involves up-regulation of other cytoprotective genes (or down-regulation of pro-apoptotic genes).
The endoplasmic reticulum (ER) stress pathway or unfolded protein response (UPR) is one potential target for extracellular BCL2 or BCL2A1 protein . Sepsis  and I/R  have both been shown to activate the ER stress response and modulation of the response reduces apoptosis in these models. In previous studies we showed that the BH4-domains of BCL2, BCL2A1, and BCL-Xl were protective . Extracellular BCL2 or BCL2A1 protein (via the BH4 domain) could regulate the ER stress response by binding to and signaling through a receptor such as a cell surface Bax inhibitor-1 (BI-1) family member - or membrane voltage–dependent anion channel (VDAC) . BCL2 or BCL2A1 protein could internalize and bind to ER BI-1 or 1,4,5-inositol trisphosphate receptor (I3PR)  to suppress an ER stress. BCL2A1 binding to VDAC may also impact ER-triggered mitochondrial membrane permeabilization . In preliminary studies, we have observed uptake of extracellularly administered rhBCL2 protein by neutrophils in vivo (Fig. S3, A, B) and by cells in vitro (Fig. S3, C-F). Further, we have also demonstrated binding of a biotinylated-BH4-BCL2 peptide to cells in vitro (Fig. S4). Future studies should identify the plasma membrane or intracellular target(s) of the extracellularly administered BCL2 proteins.
As previously reported for ischemia-reperfusion injury , we found that administration of rhBCL2A1 failed to protect TLR2-null mice from sepsis-induced mortality, indicating that there is a requisite role for TLR2 signaling for the protective effect in vivo. However, neither rhBCL2 nor rhBCL2A1 is a direct TLR2 ligand as assessed by IL-8 production in HEK cells transfected with TLR2/6 or by activation of NF-κB in the THP1 macrophage cell line . Also, the response of THP1 macrophage cells to several TLR2 and TLR4 ligands was unaffected by pretreatment with rhBCL2A1 . As discussed previously , there are several potential explanations for the discrepancy between the in vivo dependence on TLR2 signaling and the lack of direct TLR signaling in vitro results with respect to TLR2. First, there may be an intermediate effector cell(s) in vivo that elaborates an endogenous TLR2 ligand(s) in response to stimulation by rhBCL2A1 or rhBCL2. Second, BCL2 or BCL2A1 may require a co-factor for activity in vivo as has been described for the prototypic DAMP, HMGB1, which lacks significant activity in vitro when it is highly purified -, but acquires activity upon binding to other TLR ligands  or cytokines . Third, since TLR2 heterodimerizes with TLR1 and TLR6 and TLR2 signaling is modulated by several non-TLR receptors -, it is possible that signaling in response to rhBCL2 or rhBCL2A1 protein involves a co-receptor and that co-operative signaling by this receptor and TLR2 is responsible for cytoprotection in vivo. Fourth, A1 may prime cells for a TLR2 response to oxidized lipoproteins produced during ischemia . Significantly, TLR2 signaling has recently been shown to suppress the ER stress response .
In summary, we report that extracellular administration of rhBCL2 or rhBCL2A1 protein provides substantial protection in CLP-induced sepsis in mice. Although the precise cellular and molecular pathways involved in the extracellular activity of BCL2 and BCL2A1 remain to be elucidated, the protective effect is associated with a reduction in apoptosis in the intestine and heart, increased expression of endogenous BCL2 in epithelial cells and cardiomyocytes, and increased neutrophil accumulation in peritoneum. Given that the BCL2 BH4-domain proteins themselves do not appear to elicit a pro-inflammatory response (Table S2), as is observed with many other DAMPs, it is possible that extracellular administration of rhBCL2 or rhBCL2A1 protein may offer a new approach to therapy of sepsis.
Materials and Methods
All protocols were approved by the Animal Care and Use Committee of the University of Washington (IACUC #2234-10, 08/05/2009) and complied with the NIH guidelines for care and use of animals. Mice were maintained at the University of Washington, Department of Comparative Medicine facility. C57BL/6 mice were obtained from Charles River Breeding Laboratory (Wilmington, MA). TLR2-null on C57BL/6 background were bred in the animal facility at the University of Washington. Breeding pairs were a gift of Dr. S. Akira (Osaka, Japan).
rhBCL2, rhUbiquitin, rhBim, and rhBCL2A1 were purchased from R&D Systems (Minneapolis, MN). rhBCL2 protein consisted of amino acids 1-212 (accession number P10415) of human BCL2 with the carboxyl terminus replaced with a ten histidine tag. rhBCL2A1 protein consisted of amino acids 1-152 of human BCL2-related protein BCL2A1 (accession number NP004040) missing the carboxyl terminal hydrophobic domain, which was replaced with a six histidine tag. rhUbiquitn consisted of amino acids 1-76 (accession number CAA28495.1) containing the amino acids ATVID followed by a 10 histidine tag at its amino terminal. rhBim consisted of amino acids 2-120 (accession number AAC39594) of human Bim long with a deleted carboxyl terminal transmembrane domain replaced with a six histidine tag. Purity of the proteins was >95% for the recombinant proteins as determined by SDS-PAGE and visualized by silver stain per manufacturer (R&D Systems). In addition, endotoxin concentration in the recombinant proteins was less than 0.15 EU/mg protein (R&D systems).
Cecal ligation and puncture
Mice were anesthetized with halothane, an abdominal midline incision made and the cecum was gently removed and ligated below the ileocecal valve without obstruction of the ileum or colon. The cecum was then subjected to a single ‘through and through’ perforation with a 20-gauge needle and a small amount of cecal contents gently expressed through the needle wound. The bowel was carefully returned to its original position, and then the abdominal incision was closed in layers with 4-0 sutures.
Survival after CLP
Mice were followed for up to 7 days after CLP. Each animal was scored using an assessment form that evaluated each animal's health as described by Morton and Griffiths , and the animal was euthanized if it exceeded a predetermined score indicative of irreversible sepsis. All animals received 0.5 mg of imipenem in 1.0 ml of 5% dextrose in water 2 hours after CLP. Additional doses of 0.5 mg/mouse of imipenem in 1.0 ml of 5% dextrose in water were given twice a day for 4 days. Mice were treated with rhBCL2A1, rhBCL2, rhBim or rhUbiquitin as indicated.
Mice were sacrificed 24 hours after CLP, and their heart and entire intestine were removed. The intestine was opened along the length of its cephalocaudal axis and washed in 4% neutral-buffered formalin to removed lumenal contents. The tissue was rolled from the proximal to the distal end and fixed with 10% neutral-buffered formalin. Paraffin-embedded sections from heart and intestine were examined for DNA strand breaks by TUNEL (In Situ Cell Death Kit, Roche Molecular Biochemicals) as described by the manufacturer.
Tissue sections were pre-treated by boiling in citrate buffer (pH 6.0) in a microwave oven. Immunocytochemistry was accomplished using rabbit anti-mouse BCL2 polyclonal antibody (Upstate, Waltham, MA), or an antibody recognizing active caspase-3 (Cell Signaling, Beverly, MA) using a Vectastain ABC elite kit (Vector Labs, Burlingame, CA), and 3, 3′-diaminobenzidine (Vector Labs) as a chromagenic substrate with hematoxylin counterstaining.
Quantitation of Images
Images were acquired using a Nikon Labphot microscope with Nikon Plan Fluor 20 Ph3DL (numerical aperture: 0.75) objective (Nikon Instruments, Inc, NY) and Spot v.3.5.9 (Diagnostic Instruments Sterling Heights, MI) digital imaging system. The images from the tissue stained for mBCL2 were opened in Photoshop (Adobe Systems Inc. San Jose, CA), and staining intensity was determined by luminosity of the image with no alteration to the original image.
Leukocytes and cytokines in peritoneal lavage fluid and peripheral blood
Peritoneal lavage fluid was collected from mice 24 hours after CLP as described previously . The total number of cells and percent of subpopulations in peritoneal lavage fluid were also determined as previously described . The concentration of cytokines in the peritoneal lavage fluid was determined using a mouse cytokine twenty-plex according to manufacturer's protocol (Invitrogen, Multiplex Kit #LMC0006). The numbers of various cell populations in whole blood were determined using a HEMAVET 950 (Drew Scientific Inc., Dallas, TX).
Assessment of neutrophil viability in peritoneal lavage fluid
Peritoneal neurtophils were collected by lavage, and contaminating fecal debris was removed by filtering through 100 µm filters. Cells were washed with PBS-1%FBS and resuspended in PBS-1%FBS for determination of cell counts. Cell viability was assessed using annexin V apoptosis detection kit (BD Biosciences, San Jose, CA) containing annexin V-PE and. 2×105 cells in 100 µl of binding buffer were incubated with 2 µl of annexin V-PE and 2 µl of 7-amino-actinomycin D for 15 min at 25 °C in the dark. Flow cytometry analysis was performed on a BD FACScan. Live cells were defined as staining negatively for both annexin V and 7-amino-actinomycin D. Flow cytometry data was analyzed with CellQuest software (BD Biosciences). Data are presented as percentage of live cells in each treatment group.
We prepared single cell suspensions of cardiomyocytes from hearts harvested 24 hours after CLP as follows. Mice received an injection of heparin (5000 U/kg, ip.) 10 minutes prior to euthansia by exsanguination by cardiac puncture under anesthesia. The animal's chest was opened, heart exposed, and the aorta cannulated with a 24-guage angio-catheter. The heart was perfused with 3 ml of perfusion buffer (AfCS Procedure Protocol PP00000125), followed by perfusion with a digestion buffer (collagenase type II, 75 U/mL, trypsin, 0.14 mg/ml, CaCl2, 1.5 in perfusion buffer) for 20 minutes at 0.5 ml/min. The hearts were placed into a petri dish containing the digestion buffer and manually cut into small pieces. The tissues were transferred to 15 ml tubes in stop buffer (10% BCS, 12.5 µM CaCl2 in perfusion buffer) and further dissociated by triturating using a Pasteur pipette. The samples were centrifuged, the supernatant removed and transferred to a 60 mm petri dish. Calcium was adjusted to a final calcium concentration of 1 mM by adding CaCl2. A single cell suspension was prepared by passing the samples through a 40 mm mesh filter. Cells were fixed (BD Cytofix Buffer) for 30 minutes at 4 °C, washed and incubated overnight with the primary antibody to mouse BCL2 or isotype control (BD Pharmingen 556537) at 4 °C. The following day, the cells were washed, resuspended in FACS buffer, and analyzed by FACScan.
Determination of Reactive Oygen Species generation
Three ml of peritoneal fluid were obtained from each mouse at 24 hours post-CLP. Leukocytes were obtained by centrifugation and lysis of red cells. Equal numbers of leukocytes were loaded with 5 µM DHR123 (Molecular Probes, Eugene, OR) and washed. Cells were resuspended in RPMI medium containing 2% serum. After a15 min incubation at 37 °C with or without 100 ng/ml phorbol myristate acetate (PMA) (Sigma-Aldrich, ST. Louis, MO), cells were removed to ice and fixed with formaldehyde (Polysciences, Inc., Warrington, PA). Flow cytometry data were acquired on a FACScan (Becton-Dickinson, San Jose, CA) and analyzed using CELLQuest software (BD).
The data are presented as the means ± standard error of the mean. Statistical analysis was performed using the two-tailed t-test (GraphPad Prism). Survival curves were analyzed by logrank test (GraphPad Prism). Differences associated with a value of p<0.05 were considered statistically significant.
Treatment with rhBCL2A1 does not alter cytokine, chemokine, or growth factor levels in peritoneal lavage fluid following CLP.
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Plasma analytes after injection of rhBCL2A1 in rats
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G-CSF levels in spleen and peritoneal fluid following CLP. Mice were treated with 1 µg of rhBCL2A1 or saline on the day prior to and at time of CLP. Spleen and peritoneal lavage fluid were collected at 24 hrs after CLP. G-CSF expression levels were determined in spleen by RT-PCR using primer probes and 7900HT system from Applied Biosystems. Mouse G-CSF protein was determined in the peritoneal fluids using a single analyte ELISA kit (SABiosciences Corporation, Frederick, MD) according to the manufacturer's instructions. *p = 0.049 by unpaired t-test.
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Treatment with rhBCLA1 at 24 hours following CLP. Animals were subjected to CLP with no pretreatment. At 24 hours after CLP mice were given 10 µg rhBCLA1 by i.p. injection or saline vehicle control and then treated with 1 µg rhBCL2A1 or saline every twice daily for next 3 days for a total of seven doses.
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Uptake of rhBCL2 by rodent cells in vivo and in vitro. In vivo: A rat was treated with 20 µg of rhBCL2 protein given by i.p. injection and at one hour after treatment peripheral blood was collected and leukocytes were isolated following lysis of red cells. Immuno-staining for hBCL2 was performed using an anti-hBCL2 antibody (BD Pharmingen #554231), which does not cross-react with the rodent protein. (A) A preparation of peripheral blood rat leukocytes is shown in low magnification with nuclei counter-stained with DAPI (blue). (B) ∼5% of rat neutrophils showed immuno-staining for hBCL2 protein as shown in the confocal microscopic image (original magnification: ×600). In vitro: JAWSII dendritic cells were incubated with medium containing 2 µg/ml hBCL2 protein for 4 (D) or 24 hours (E, F). In (C) cells were incubated with isotype-control antibody. (D) After four hours incubation prominent immuno-staining for hBCL2 was observed in cytoplasm (original magnification ×400). (E, F) After 24 hours incubation, immuno-staining for hBCL2 was still observed but was not as prominent as at 4 hours. (original magnification: E, ×100; F, ×400).
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Binding of BH4-BCL2 peptide to cell surface in vitro. The binding of biotinylated-BH4-BCL2 peptide (SynPep, Dublin CA), scrambled biotinylated-sBH4-BCL2 peptide, and biotinylated-BH3-Bax peptide to JAWS2 dendritic cells grown in (A) suspension or (B) adherent was assessed after incubation for 30 minutes at 4C. Binding was determined by subsequent binding of phycoerythrin-strepavidin and flow cytometry.
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Conceived and designed the experiments: RKW JMH. Performed the experiments: AI RAdC VLMS JCT BRS LL XZ KJ. Analyzed the data: AI RAdC JCT BRS LL XZ KJ RKW JMH. Wrote the paper: AI RKW JMH.
- 1. Rice TW, Bernard GR (2005) Therapeutic intervention and targets for sepsis. Annu Rev Med 56: 225–248.
- 2. Houston G, Cuthbertson BH (2009) Activated protein C for the treatment of severe sepsis. Clin Microbiol Infect 15: 319–324.
- 3. Hotchkiss RS, Osmon SB, Chang KC, Wagner TH, Coopersmith CM, et al. (2005) Accelerated lymphocyte death in sepsis occurs by both the death receptor and mitochondrial pathways. J Immunol 174: 5110–5118.
- 4. Wesche DE, Lomas-Neira JL, Perl M, Chung CS, Ayala A (2005) Leukocyte apoptosis and its significance in sepsis and shock. J Leukoc Biol 78: 325–337.
- 5. Ayala A, Perl M, Venet F, Lomas-Neira J, Swan R, et al. (2008) Apoptosis in sepsis: mechanisms, clinical impact and potential therapeutic targets. Curr Pharm Des 14: 1853–1859.
- 6. Hotchkiss RS, Tinsley KW, Swanson PE, Karl IE (2002) Endothelial cell apoptosis in sepsis. Crit Care Med 30: S225–228.
- 7. Mzayek F, Ylostalo J, Krogstad DJ (2008) Apoptosis of endothelial cells in bacterial sepsis and severe Plasmodium falciparum malaria: do we know enough to consider clinical trials? Crit Care Med 36: 2690–2692.
- 8. Fialkow L, Fochesatto Filho L, Bozzetti MC, Milani AR, Rodrigues Filho EM, et al. (2006) Neutrophil apoptosis: a marker of disease severity in sepsis and sepsis-induced acute respiratory distress syndrome. Crit Care 10: R155.
- 9. Baier PK, Baumgartner U, Wolff-Vorbeck G, Hempel S, Hopt UT (2006) Hepatocyte proliferation and apoptosis in rat liver after liver injury. Hepatogastroenterology 53: 747–752.
- 10. Buerke U, Carter JM, Schlitt A, Russ M, Schmidt H, et al. (2008) Apoptosis contributes to septic cardiomyopathy and is improved by simvastatin therapy. Shock 29: 497–503.
- 11. Vyas D, Robertson CM, Stromberg PE, Martin JR, Dunne WM, et al. (2007) Epithelial apoptosis in mechanistically distinct methods of injury in the murine small intestine. Histol Histopathol 22: 623–630.
- 12. Chang KC, Unsinger J, Davis CG, Schwulst SJ, Muenzer JT, et al. (2007) Multiple triggers of cell death in sepsis: death receptor and mitochondrial-mediated apoptosis. FASEB J 21: 708–719.
- 13. Hotchkiss RS, Swanson PE, Knudson CM, Chang KC, Cobb JP, et al. (1999) Overexpression of Bcl-2 in transgenic mice decreases apoptosis and improves survival in sepsis. J Immunol 162: 4148–4156.
- 14. Coopersmith CM, Chang KC, Swanson PE, Tinsley KW, Stromberg PE, et al. (2002) Overexpression of Bcl-2 in the intestinal epithelium improves survival in septic mice. Crit Care Med 30: 195–201.
- 15. Iwata A, Stevenson VM, Minard A, Tasch M, Tupper J, et al. (2003) Over-expression of Bcl-2 provides protection in septic mice by a trans effect. J Immunol 171: 3136–3141.
- 16. Bianchi ME (2007) DAMPs, PAMPs and alarmins: all we need to know about danger. J Leukoc Biol 81: 1–5.
- 17. Kono H, Rock KL (2008) How dying cells alert the immune system to danger. Nat Rev Immunol 8: 279–289.
- 18. Seong SY, Matzinger P (2004) Hydrophobicity: an ancient damage-associated molecular pattern that initiates innate immune responses. Nat Rev Immunol 4: 469–478.
- 19. Hagiwara S, Iwasaka H, Hasegawa A, Asai N, Noguchi T (2008) High-dose intravenous immunoglobulin G improves systemic inflammation in a rat model of CLP-induced sepsis. Intensive Care Med 34: 1812–1819.
- 20. Hatada T, Wada H, Nobori T, Okabayashi K, Maruyama K, et al. (2005) Plasma concentrations and importance of High Mobility Group Box protein in the prognosis of organ failure in patients with disseminated intravascular coagulation. Thromb Haemost 94: 975–979.
- 21. Sunden-Cullberg J, Norrby-Teglund A, Rouhiainen A, Rauvala H, Herman G, et al. (2005) Persistent elevation of high mobility group box-1 protein (HMGB1) in patients with severe sepsis and septic shock. Crit Care Med 33: 564–573.
- 22. Qin S, Wang H, Yuan R, Li H, Ochani M, et al. (2006) Role of HMGB1 in apoptosis-mediated sepsis lethality. J Exp Med 203: 1637–1642.
- 23. Rouhiainen A, Tumova S, Valmu L, Kalkkinen N, Rauvala H (2007) Pivotal advance: analysis of proinflammatory activity of highly purified eukaryotic recombinant HMGB1 (amphoterin). J Leukoc Biol 81: 49–58.
- 24. Sha Y, Zmijewski J, Xu Z, Abraham E (2008) HMGB1 develops enhanced proinflammatory activity by binding to cytokines. J Immunol 180: 2531–2537.
- 25. Hreggvidsdottir HS, Ostberg T, Wahamaa H, Schierbeck H, Aveberger AC, et al. (2009) The alarmin HMGB1 acts in synergy with endogenous and exogenous danger signals to promote inflammation. J Leukoc Biol 86: 655–662.
- 26. Iwata A, Morgan-Stevenson V, Schwartz B, Liu L, Tupper J, et al. (2010) Extracellular BCL2 Proteins Are Danger-Associated Molecular Patterns That Reduce Tissue Damage in Murine Models of Ischemia-Reperfusion Injury. PLoS One 5: e9103.
- 27. Reed JC (2008) Bcl-2-family proteins and hematologic malignancies: history and future prospects. Blood 111: 3322–3330.
- 28. Hotchkiss RS, Tinsley KW, Swanson PE, Chang KC, Cobb JP, et al. (1999) Prevention of lymphocyte cell death in sepsis improves survival in mice. Proc Natl Acad Sci U S A 96: 14541–14546.
- 29. Oberholzer C, Oberholzer A, Bahjat FR, Minter RM, Tannahill CL, et al. (2001) Targeted adenovirus-induced expression of IL-10 decreases thymic apoptosis and improves survival in murine sepsis. Proc Natl Acad Sci U S A 98: 11503–11508.
- 30. Hotchkiss RS, Chang KC, Grayson MH, Tinsley KW, Dunne BS, et al. (2003) Adoptive transfer of apoptotic splenocytes worsens survival, whereas adoptive transfer of necrotic splenocytes improves survival in sepsis. Proc Natl Acad Sci U S A 100: 6724–6729.
- 31. Walsh M, Lutz RJ, Cotter TG, O'Connor R (2002) Erythrocyte survival is promoted by plasma and suppressed by a Bak-derived BH3 peptide that interacts with membrane-associated Bcl-X(L). Blood 99: 3439–3448.
- 32. McCarthy BA, Boyle E, Wang XP, Guzowski D, Paul S, et al. (2008) Surface expression of Bcl-2 in chronic lymphocytic leukemia and other B-cell leukemias and lymphomas without a breakpoint t(14;18). Mol Med 14: 618–627.
- 33. Sakai T, Inoue A, Koh CS, Osame M (1999) Serum levels of apoptosis-related molecules in patients with multiple sclerosis and human T-lymphotropic virus Type I-associated myelopathy. J Interferon Cytokine Res 19: 999–1004.
- 34. Fathi NA, Hussein MR, Hassan HI, Mosad E, Galal H, et al. (2006) Glomerular expression and elevated serum Bcl-2 and Fas proteins in lupus nephritis: preliminary findings. Clin Exp Immunol 146: 339–343.
- 35. Osman HG, Gabr OM, Lotfy S, Gabr S (2007) Serum levels of bcl-2 and cellular oxidative stress in patients with viral hepatitis. Indian J Med Microbiol 25: 323–329.
- 36. Protopsaltis J, Kokkoris S, Nikolopoulos G, Spyropoulou P, Katsaros T, et al. (2007) Correlation between increased serum sFas levels and microalbuminuria in type 1 diabetic patients. Med Princ Pract 16: 222–225.
- 37. Clark RS, Kochanek PM, Adelson PD, Bell MJ, Carcillo JA, et al. (2000) Increases in bcl-2 protein in cerebrospinal fluid and evidence for programmed cell death in infants and children after severe traumatic brain injury. J Pediatr 137: 197–204.
- 38. Kim I, Xu W, Reed JC (2008) Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities. Nat Rev Drug Discov 7: 1013–1030.
- 39. Woo CW, Cui D, Arellano J, Dorweiler B, Harding H, et al. (2009) Adaptive suppression of the ATF4-CHOP branch of the unfolded protein response by toll-like receptor signalling. Nat Cell Biol 11: 1473–1480.
- 40. Bailly-Maitre B, Fondevila C, Kaldas F, Droin N, Luciano F, et al. (2006) Cytoprotective gene bi-1 is required for intrinsic protection from endoplasmic reticulum stress and ischemia-reperfusion injury. Proc Natl Acad Sci U S A 103: 2809–2814.
- 41. Reimers K, Choi CY, Bucan V, Vogt PM (2007) The growth-hormone inducible transmembrane protein (Ghitm) belongs to the Bax inhibitory protein-like family. Int J Biol Sci 3: 471–476.
- 42. Ahn T, Yun CH, Kim HR, Chae HJ (2010) Cardiolipin, phosphatidylserine, and BH4 domain of Bcl-2 family regulate Ca2+/H+ antiporter activity of human Bax inhibitor-1. Cell Calcium 47: 387–396.
- 43. Akanda N, Tofighi R, Brask J, Tamm C, Elinder F, et al. (2008) Voltage-dependent anion channels (VDAC) in the plasma membrane play a critical role in apoptosis in differentiated hippocampal neurons but not in neural stem cells. Cell Cycle 7: 3225–3234.
- 44. Rong YP, Bultynck G, Aromolaran AS, Zhong F, Parys JB, et al. (2009) The BH4 domain of Bcl-2 inhibits ER calcium release and apoptosis by binding the regulatory and coupling domain of the IP3 receptor. Proc Natl Acad Sci U S A 106: 14397–14402.
- 45. Deniaud A, Sharaf el dein O, Maillier E, Poncet D, Kroemer G, et al. (2008) Endoplasmic reticulum stress induces calcium-dependent permeability transition, mitochondrial outer membrane permeabilization and apoptosis. Oncogene 27: 285–299.
- 46. Soong G, Reddy B, Sokol S, Adamo R, Prince A (2004) TLR2 is mobilized into an apical lipid raft receptor complex to signal infection in airway epithelial cells. J Clin Invest 113: 1482–1489.
- 47. Brown GD (2006) Dectin-1: a signalling non-TLR pattern-recognition receptor. Nat Rev Immunol 6: 33–43.
- 48. Hajishengallis G, Wang M, Liang S, Triantafilou M, Triantafilou K (2008) Pathogen induction of CXCR4/TLR2 cross-talk impairs host defense function. Proc Natl Acad Sci U S A 105: 13532–13537.
- 49. West XZ, Malinin NL, Merkulova AA, Tischenko M, Kerr BA, et al. (2010) Oxidative stress induces angiogenesis by activating TLR2 with novel endogenous ligands. Nature 467: 972–976.
- 50. Martinon F, Chen X, Lee AH, Glimcher LH (2010) TLR activation of the transcription factor XBP1 regulates innate immune responses in macrophages. Nat Immunol 11: 411–418.
- 51. Morton DB, Griffiths PH (1985) Guidelines on the recognition of pain, distress and discomfort in experimental animals and an hypothesis for assessment. Vet Rec 116: 431–436.