- Open Access
Developmental stage of oligodendrocytes determines their response to activated microglia in vitro
© Miller et al; licensee BioMed Central Ltd. 2007
- Received: 10 August 2007
- Accepted: 26 November 2007
- Published: 26 November 2007
Oligodendrocyte progenitor cells (OPCs) and mature oligodendrocytes are both lost in central nervous system injury and disease. Activated microglia may play a role in OPC and oligodendrocyte loss or replacement, but it is not clear how the responses of OPCs and oligodendrocytes to activated microglia differ.
OPCs and microglia were isolated from rat cortex. OPCs were induced to differentiate into oligodendrocytes with thyroid hormone in defined medium. For selected experiments, microglia were added to OPC or oligodendrocyte cultures. Lipopolysaccharide was used to activate microglia and microglial activation was confirmed by TNFα ELISA. Cell survival was assessed with immunocytochemistry and cell counts. OPC proliferation and oligodendrocyte apoptosis were also assessed.
OPCs and oligodendrocytes displayed phenotypes representative of immature and mature oligodendrocytes, respectively. Activated microglia reduced OPC survival, but increased survival and reduced apoptosis of mature oligodendrocytes. Activated microglia also underwent cell death themselves.
Activated microglia may have divergent effects on OPCs and mature oligodendrocytes, reducing OPC survival and increasing mature oligodendrocyte survival. This may be of importance because activated microglia are present in several disease states where both OPCs and mature oligodendrocytes are also reacting to injury. Activated microglia may simultaneously have deleterious and helpful effects on different cells after central nervous system injury.
- Spinal Cord Injury
- Microglial Activation
- Mature Oligodendrocyte
- Spastic Cerebral Palsy
- Periventricular Leukomalacia
Oligodendrocytes develop from a bipotential progenitor cell, often referred to as an oligodendrocyte progenitor cell (OPC), or oligodendrocyte – type 2 astrocyte cell (O2A), as it can differentiate into either an oligodendrocyte or astrocyte in vitro . Though more prevalent in the immature CNS, OPCs persist in the CNS of mature animals and humans [2, 3], and have been shown to respond to CNS injury by proliferating and possibly taking the place of mature oligodendrocytes that are lost during injury or disease [4–6].
Both OPCs and oligodendrocytes die in a variety of CNS diseases. In periventricular leukomalacia (PVL), OPCs are lost as a consequence of hypoxia, ischemia, or intrauterine infection . This loss of OPCs, and the resulting failure to replace mature oligodendrocytes, is thought to be the pathologic cause of spastic cerebral palsy . Mature oligodendrocytes are lost in multiple sclerosis (MS), the most common disease of the adult CNS, affecting over 250,000 people living in the US . Oligodendrocytes and OPCs also die after CNS trauma, such as brain and spinal cord injury [10, 11] and it has been shown that oligodendrocyte apoptosis in experimental spinal cord injury peaks over a week after the initial insult [12, 13]. This delayed oligodendrocyte death may reduce the effectiveness of neural conduction in the spared axons that often exist after spinal cord injury.
CNS inflammation occurs in both disease and trauma, and is mediated in part by microglia, the resident immune cells of the CNS. Microglia originate from bone marrow and migrate into the CNS during early stages of development . Microglia display graded levels of activation in the CNS, from resting, highly ramified microglia, to phagocytic macrophages . Microglia react quickly in response to CNS injury or disease , migrating into an injury site  and secreting a wide array of molecules that can be toxic to OPCs and oligodendrocytes, including tumor necrosis factor-α (TNFα) [18–20], glutamate , and free radicals . Activated microglia contribute to OPC and oligodendrocyte death in models of PVL and MS [23–25]. Furthermore, molecules that induce oligodendrocyte death can also lead to microglial activation, such as glutamate [26, 27] and proinflammatory cytokines .
In vitro, microglia are capable of inducing OPC death even without the two cell populations being in direct contact . However, in vivo microglia have been observed in close proximity to dying oligodendrocytes after spinal cord injury . This proximity after injury suggests a mechanism by which microglia may influence oligodendrocyte and OPC survival, as it has been shown in vitro that microglia in contact with oligodendrocytes can induce oligodendrocyte death via membrane-bound TNFα which is more potent than soluble TNFα . Additionally, any soluble factors secreted by microglia could have a higher effective concentration if secreted into a small space between cells.
There is also evidence that microglia may play a protective or helpful role in the injured CNS [31, 32]. In vitro, microglia can be recruited by soluble factors released by stressed oligodendrocytes, and support oligodendrocyte survival via insulin-like growth factor 2 [33, 34]. Additionally, cytokines produced by microglia may aid in repair after injury, as mice lacking TNFα undergo delayed remyelination . Even the observations of Shuman and colleagues , that activated microglia are found in contact with apoptotic oligodendrocytes after spinal cord injury, raises the question of whether microglia destroy oligodendrocytes that would otherwise survive after injury, or are simply phagocytosing oligodendrocytes already destroyed by other toxins in the damaged CNS. Some data suggest that microglia play a dual role in CNS injury, exacerbating damage in some instances or at some times, and promoting repair or regeneration at others [36, 37]. Shuman and colleagues  also reported that microglia undergo apoptosis after spinal cord injury. It has been demonstrated that certain types of toxin-induced microglial activation can result in microglial death both in vitro and in vivo [38, 39] and microglial death has also been described in concert with microglial activation in other in vivo injury paradigms .
All procedures were approved by The Ohio State University Institutional Laboratory Animal Care and Use Committee. All reagents were purchased from Sigma (St. Louis, MO) unless otherwise noted. OPCs and oligodendrocytes were isolated by a protocol similar to that described by McCarthy and de Vellis  with some modifications. Postnatal day 2 Long Evans rat pups were sacrificed by rapid decapitation and the cortices were removed and placed in media containing 7.1 mg/ml NaCl, 0.36 mg/ml KCl, 0.166 mg/ml KH2PO4, 2.57 mg/ml d-Glucose, 2.4 mg/ml NaHCO3, 0.01 mg/ml phenol red, 0.9 mg/ml BSA Fraction V, and 0.33 mg/ml MgSO4, (hereafter referred to as "dissection media") and minced. The tissue was resuspended with 10 mls of dissection media with 0.280 μg/ml trypsin and shaken on an orbital shaker at 200 rpm for 20 minutes, at 37°C. Next, 10 mls of dissection media with 1.28 μg/ml DNAse and 83.2 μg/ml soy bean trypsin inhibitor was added and the mixture was briefly shaken and centrifuged at 690 rcf for 5 minutes. The pellet was then resuspended in 3 ml of dissection media with 80 μg/ml DNAse and 520 μg/ml soy bean trypsin inhibitor and triturated to a single cell suspension. Cells were resuspended in DMEM (Invitrogen, Carlsbad, CA) with 10% fetal bovine serum containing 292 μg/ml L-glutamine, 1 mM sodium pyruvate (Invitrogen) and 0.04 mg/ml gentamicin (Invitrogen) at a volume of approximately 5 ml per brain. The suspension was then plated into uncoated T-75 flasks at 10 mls per flask. Flasks were kept in an incubator at 37°C and 5% CO2. Media was replaced after 24 hours and every 4–6 days thereafter.
Cells were allowed to proliferate until confluent, corresponding to day 9–13 post-dissection. At this time, the mixed cortical cultures consisted of a layer of astrocytes adherent to the bottom of the flasks, with OPCs and microglia growing on top of the astrocytes. Before isolating pure OPCs, the numbers of microglia in the flasks were reduced by placing sealed flasks on an orbital shaker at 200 rpm for 2 hours. After shaking, the supernatant was replaced with fresh media and flasks were returned to the incubator for 2 hours. After equilibration, flasks were shaken overnight to detach OPCs from the microglia-depleted population. At the completion of the overnight shake, floating cells were resuspended in 4 ml of serum-free DMEM Sato with either thyroid hormone (as we have described previously, ) in order to induce maturation of OPCs to oligodendrocytes, or 10 ng/ml PDGF and 10 ng/ml bFGF in order to maintain cells as OPCs. In order to remove any microglia that were not removed during the 2 hour shake, the cell suspension was plated onto a sterile petri dish with a radius of 2.5 mm and returned to the incubator for 45 minutes where both OPCs and microglia adhered to the petri dish. Petri dishes were then gently rinsed with culture media in order to remove OPCs, but leave the more tightly adherent microglia behind. The resulting cell suspension was adjusted to a density of 20,000 cells per ml and plated onto poly-L-lysine coated 12 mm glass coverslips in 4-well plates, with 500 ul of cell suspension added per well. These OPC/oligodendrocyte cultures were >95% pure with <5% microglia as verified by immunocytochemistry.
Addition of microglia to oligodendrocyte cultures and experimental timeline
In selected experiments, microglia were added to OPCs or oligodendrocytes exactly one day after OPCs/oligodendrocytes were isolated from flasks containing mixed glial cultures. LPS treatments took place exactly 2 days after OPC/oligodendrocyte plating, and fixation took place exactly 3 days after OPC/oligodendrocyte plating. Microglia were harvested from flasks derived from the same primary dissections as the OPCs or oligodendrocytes with which they were combined. To remove microglia from flasks without removing OPCs, T75 flasks were tapped on the lab bench and the supernatant removed. Microglia were resuspended in the same medium as the OPCs or oligodendrocytes with which they were combined. When plated alone, the resuspended cells were shown to be > 95% pure microglia. Microglia were plated onto pre-existing OPC or oligodendrocyte cultures at a ratio of 1:1 by initially resuspending microglia at twice the desired concentration, removing 250 μl of media from the OPC or oligodendrocyte cultures and adding 250 μl of microglia suspension to OPC or oligodendrocyte cultures. The 1:1 ratio of microglia to oligodendrocyte lineage cells was chosen to be close to that observed in counts of microglia:oligodendrocyte ratios in the rat dorsal column (~2:3, data not shown).
Immunocytochemistry and cell counts
At the conclusion of all experiments, cells were fixed with 2% formaldehyde prepared from paraformaldehyde. All primary antibodies were purchased from Chemicon (Temecula, CA) unless otherwise noted. All secondary antibodies were purchased from Molecular Probes (Carlsbad, CA). Antibodies were diluted in Hank's Balanced Salt Solution with 5% donor calf serum and coverslips were rinsed twice between all antibody applications. For NG2 labeling, cells were first permeabilized with 0.1% Triton for 10 minutes, and then incubated with anti-NG2 antibody at a concentration of 1:400 for 1.5 hours, followed by goat anti-rabbit Alexa 594 at 1:100 for 1 hour. For A2B5 labeling, cells were incubated with an antibody to A2B5 conjugated to Alexa 488 (Chemicon) at 1:100 for 1.5 hours. For GalC labeling, cells were incubated with an antibody to GalC at 1:400 for 1 hour followed by goat anti-mouse Alexa 488 at 1:200 for 1 hour. For MBP labeling, cells were first permeabilized with 0.1% Triton for 10 minutes and incubated with an antibody against MBP at 1:200 for 1 hour followed by goat anti-rabbit Alexa 488 at 1:100 for 1 hour. For IB4 labeling, which was completed following staining for OPC/oligodendrocyte markers, cells were incubated with Alexa 594-conjugated IB4 (Molecular Probes) at 1:100 for 30 minutes in a solution of HBSS with 1 mM calcium and no serum. For all experiments, cells were incubated with 10 μg/ml Hoechst for 5 minutes and mounted on glass slides with Immu-Mount (Thermo, Pittsburgh, PA) after antibody application.
Cell counts were conducted by an experimenter who was blind to experimental conditions, using a Zeiss Axioplan 2 microscope (Carl Zeiss, Thornwood, NY). Counts were conducted using the 40× objective. Continuous, non-overlapping fields were assessed across the entire coverslip diameter and every cell whose cell body was within the eyepiece reticle was assessed. For experiments involving OPCs or oligodendrocytes, the control condition was defined as OPCs or oligodendrocytes alone with no microglia or LPS added. For mature oligodendrocytes, both live and dead cells were visible, with live cells having intact nuclei and cell bodies, and dead cells having absent or fragmented nuclei and fragmented cell bodies. Counts of both live and dead oligodendrocytes were performed and values are expressed as percent cell death. Actual cell counts rather than biochemical assays of cell death were used to allow discrimination of microglial and oligodendrocyte/OPC cell death in the combined culture studies. Previous work in our laboratory has shown that morphology-based live/dead counts of oligodendrocyte lineage cells correlate well with lactate dehydrogenase (LDH) assay-based cell death estimates (data not shown). Live OPCs were defined as A2B5 positive cells with two or more intact processes and intact nuclei. It was not possible to reliably quantify dead OPCs, as dead OPC cell bodies were often absent and it could not be determined how many OPCs were represented by debris, composed of OPC processes, left behind after fixation and staining. Therefore, for OPCs, values were expressed as live cells counted relative to control. For microglia, live cells were visible as IB4 stained cells with intact nuclei, and values were expressed relative to those under conditions in which microglia, but not LPS, were added to OPC/oligodendrocyte cultures.
A commercially available caspase assay (FLICA, Immunochemistry Technologies, Bloomington, Minnesota) that utilizes a fluorescently-tagged poly caspase inhibitor was utilized in accordance with the manufacturer's recommendations. The use of this assay has been described previously by Grabarek and colleagues . Caspase positive oligodendrocytes were defined as cells with fragmented nuclei that also labeled brightly with the caspase indicator, so that the cell body and processes were visible to confirm oligodendrocyte morphology. Cells counts were performed as described above, and caspase activation was expressed as percent of control.
A TNFα ELISA was used to verify that the selected dose of LPS activated microglia under different media conditions. TNFα concentrations were determined using a double sandwich ELISA following R&D Systems' (Minneapolis, MN) recommended protocol. Briefly, 96 well plates were coated with 4 μg/ml of capture antibody (R&D Systems) in PBS pH 7.4 overnight. Nonspecific binding was blocked with PBS containing 1% bovine serum albumin (BSA) for one hour. Experimental samples and known standards were diluted 1:2 in PBS with 0.05% Tween and 0.1% BSA and added to the capture antibody for 2 hours at room temperature. 100 μl per well of biotinylated anti-rat TNFα antibody (R&D Systems) at a concentration of 400 ng/ml was added for 2 hours at room temperature followed by streptavidin horseradish peroxidase conjugate at 1:4000 for 20 minutes. 100 μl per well of K-Blue Max substrate (Neogen, Randolph, WI) was added and allowed to develop in the dark for 20 minutes. The reaction was stopped by the addition of 1 M H2SO4. Plates were read using a Genios plate reader (Tecan, Switzerland) at 490 nm.
Cell proliferation assay
A BrdU incorporation assay, similar to that employed by Kondo and Raff  was used to assess OPC and oligodendrocyte proliferation. Cells were exposed to 20 uM BrdU for six hours prior to fixation, and then fixed in 2% formaldehyde as previously described. Cells were post-fixed in 100% methanol for 10 minutes at -20°C, followed by DNA denaturation with 2 M hydrochloric acid for 30 minutes. Acid was then neutralized with 0.1 M sodium borate at pH of 8.5 for 10 minutes. Cells were then permeabilized with 0.1% Triton for 10 minutes and incubated with primary antibody against BrdU (hybridoma monoclonal antibody developed by Stephen J. Kaufman, Developmental Studies Hybridoma Bank, The University of Iowa, Department of Biological Sciences, Iowa City, IA) at 1:5 for 1 hour followed by goat anti-mouse secondary antibody conjugated to Alexa 594 at 1:100 for 1 hour. This staining was done in combination with A2B5 labeling for OPCs and followed by Hoechst labeling of nuclei. BrdU labeling was evaluated by examining five random fields per coverslip and the percentage of OPCs or oligodendrocytes incorporating BrdU was compared to that of the control condition. All BrdU, cell survival, and caspase experiments were replicated using cells from at least two different primary cultures, and all "n" values refer to individual coverslips on which experiments were carried out. OPC/oligodendrocyte survival, BrdU and caspase experiments were analyzed via factorial ANOVA. Additionally, a one way ANOVA with Tukey's post-hoc test was conducted to determine what groups differed from OPCs or oligodendrocytes alone. All error bars represent ± SEM. Significance was set at p < 0.05.
LDH assay for assessment of microglia death
A commercially available LDH assay kit (Roche, Indianapolis, IN) was used to quantify LDH release in experiments with microglia grown alone. In 3 independent replications, microglia were isolated as described above, and plated at concentrations varying from 50,000 to 150,000 cells/ml into a 96 well plate coated with poly-L-lysine. 24 hours after plating, 10 ng/ml LPS was administered for 24 hours and LDH release was assayed according to the manufacturer's instructions. For positive controls, microglia were treated with 1% triton for 10 minutes prior to LDH release quantification. Cell death was measured as [experimental value - negative control]/[positive control - negative control]. LDH release by microglia treated in the two conditions was compared using Student's T-test.
OPCs cultured with bFGF and PDGF express markers of both immature and mature oligodendrocyte lineage cells
LPS-activated microglia release TNFα
A preliminary experiment was conducted to determine the response of microglia to varying doses of LPS. Microglia were exposed to 1 ng/ml, 10 ng/ml and 100 ng/ml of TNFα for 24 hours. This resulted in increasing production of TNFα (Fig. 1). There was no detectable TNFα production by OPCs or mature oligodendrocytes alone treated with LPS or microglia cultures that were not treated with LPS (data not shown). We chose 10 ng/ml LPS for use in further experiments, as this dose has been shown by others to induce microglia-mediated OPC death  and was in the middle of our range of LPS doses that induced TNFα production. In microglia isolated for use in OPC/oligodendrocyte survival experiments, there was no significant effect of media composition (OPC versus oligodendrocyte media) on TNFα production by microglia (data not shown).
LPS-activated microglia reduce OPC survival
Effects of activated microglia on proliferation of OPCs
Oligodendrocytes cultured with thyroid hormone only express markers of mature oligodendrocytes
Both "resting" and LPS-activated microglia reduce cell death of mature oligodendrocytes
Thyroid hormone has been shown to inhibit oligodendrocyte proliferation . As expected, no oligodendrocytes in the control condition incorporated BrdU, and neither microglia nor LPS alone or in combination induced BrdU incorporation into oligodendrocytes (data not shown). This verifies that microglia mediated protection of oligodendrocytes was due to increased oligodendrocyte survival and not cell division.
To exclude a possible influence of thyroid hormone on the pro-survival effect of microglia, the experiment was repeated with thyroid hormone-containing media being replaced with thyroid hormone-free media on day 1 in vitro (at the same time microglia were added to oligodendrocytes). Under these conditions, the significant protective effect of microglia was retained (p = 0.043, factorial ANOVA, data not shown).
Microglia reduce apoptosis of mature oligodendrocytes
Microglia undergo cell death in response to LPS activation
To determine if activation-induced microglia death was due to the presence of OPCs or oligodendrocytes in culture with microglia, an experiment was conducted with microglia cultured alone. As in the previous experiment, microglia survival in both media compositions was significantly reduced in response to activation with 10 ng/ml LPS (data not shown). Thus, microglial cell death in response to LPS-activation was not due to the presence of OPCs or oligodendrocytes in culture. To confirm that lower numbers of microglia counted were due to microglial death and not simply detachment from coverslips before fixation, a LDH assay was used to assess microglial cell death in response to LPS in the aforementioned media compositions. 10 ng/ml LPS induced significant LDH release from microglia as compared to controls in both media compositions (data not shown). Therefore, lower microglia counts represent cell death and not simply detachment of microglia from the culture substrate.
Here we demonstrate that the maturation state of oligodendrocyte lineage cells has a profound effect on their response to microglia and microglial activation. While reducing the survival of OPCs, LPS-activated microglia increase the survival of mature oligodendrocytes. It is especially significant that in both cases, activated microglia were able to reverse the baseline state of oligodendrocyte lineage cells: normally proliferating OPCs were lost as a consequence of microglia activation, and mature oligodendrocytes that are normally undergoing apoptosis are rescued by activated microglia. A recent study has shown that as OPCs mature to oligodendrocytes a wide range of genes are differentially transcribed . It is important to appreciate that even though OPCs are able to differentiate into mature oligodendrocytes in a matter of days both in vitro  and in vivo , these two cell types have very different properties and functional capabilities. Our data support the growing appreciation of the differences between these cells, showing that OPCs and mature oligodendrocytes could undergo divergent fates in an environment where activated microglia are present.
Several previous studies have shown that LPS-activated microglia are toxic to OPCs both in vitro and in vivo [23, 24, 48] and that this effect is mediated in part by oxidative stress . Our studies indicate that mature oligodendrocytes benefit from the presence of microglia, and presumably resist the deleterious effects that activated microglia exert on OPCs. This is consistent with other studies showing oligodendrocytes to be more resistant than OPCs to a wide variety of insults, including TNFα , interferon gamma , excitotoxicity [54, 55], radiation injury , and free radical mediated injury . Many changes that occur in oligodendrocytes as they mature could promote resistance to injury, including a decrease in ionotropic glutamate receptor expression , an increase in metabotropic glutamate receptor expression , changes in pro- or anti-apoptotic gene expression , or increased antioxidant enzymes . It is possible that mature oligodendrocytes in our study resisted microglia-mediated injury due to increased glutathione stores compared to OPCs, as reported by Fragoso and colleagues , which would render them less susceptible to microglia-mediated oxidative injury.
Though our data show that microglia only induced a trend toward increased OPC proliferation (Fig. 4), a previous report has shown that media from activated microglia have the ability to increase OPC proliferation . The difference between this study and ours may lie in the different preparations used. While Filipovic and Zecevic  showed that microglia secrete factors that can induce OPC proliferation, this does not exclude the possibility that other microglia-derived factors can induce OPC cell death as well. If OPC death is induced by short-acting substances such as free radicals, and OPC proliferation is induced by more stable proteins, it is possible that conditioned medium from activated microglia, as used by Filipovic and Zecevic , would be more likely to isolate the proliferative effects of activated microglia. This is in contrast to our preparation where microglia and OPCs were in culture together and all substances produced by microglia had direct and immediate access to OPCs.
Understanding the physiologic differences between mature and immature oligodendrocytes may lead to therapeutic strategies for preserving OPCs vulnerable to loss in periventricular leukomalacia, or for preserving OPCs that proliferate after CNS injury. It has been shown previously that OPCs proliferate after SCI . However, the net effect of SCI is to reduce oligodendrocyte numbers, at least in the long tracts damaged by the lesion . Recent data from our laboratory suggest that some OPCs that proliferate after spinal cord injury die by apoptosis after the population initially expands (unpublished data). It is possible that proliferating OPCs in vivo, as in our in vitro study, are unable to withstand toxins produced by activated microglia after spinal cord injury. This OPC proliferation followed by apoptosis may represent a failed attempt at remyelination after spinal cord injury due to OPCs' intrinsic vulnerability to inflammation.
Though no previous study to our knowledge has directly compared the effects of activated microglia on different stages of oligodendrocyte lineage cells, some studies have previously examined microglia-mediated oligodendrocyte survival. Pro-survival factors secreted by microglia, such as insulin-like growth factor-2, may protect oligodendrocytes from TNFα and other molecules produced by activated microglia . However, microglia have been shown to reverse their phenotype from protective to toxic for oligodendrocytes after activation with interferon-gamma . The fact that in our experiments, LPS-activation did not change the anti-apoptotic effect of microglia, shows that increased activation does not always cause microglia to lose their protective effects. Additionally, recent data show that activated microglia can induce or hinder OPC proliferation depending on the cytokine profile used to activate microglia . Recently, different pro-inflammatory substances that activate microglia have been shown to have different effects on demyelination and OPC proliferation in vivo . In the injured CNS, multiple inflammatory cytokines are produced  and the combination of cytokines and other molecules that induce inflammation may change over time, potentially resulting in a dynamic microglia phenotype after injury. Further studies should be directed toward ascertaining how microglial activation changes over time and in response to different stimuli.
Microglia activated with LPS have been previously shown to undergo cell death in a dose-responsive manner . As with microglia-mediated OPC death, microglial "autocrine" death can be mediated by free radicals . LPS exposure can induce caspase activation in microglia , but LPS can also cause microglia to be more likely to undergo necrotic cell death under some conditions . In our experiments, we did not observe caspase activation in microglia. This may be because microglial apoptosis occurred early after LPS addition, or that microglial cell death was primarily necrotic in nature. It is also possible that microglia detached from the growth substrate prior to undergoing cell death, as microglia fragments were rarely observed, unlike OPCs and oligodendrocytes. Regardless of the nature of microglial cell death, it is important to note that the pro-survival effect of microglia on oligodendrocytes was preserved even as microglia numbers were markedly reduced due to LPS activation. It is possible that sufficient microglia-derived survival factors for oligodendrocytes were produced before microglia were lost due to LPS activation. Alternately, the pro-survival effects of microglia may only require a small number of microglia, and the microglia that persist in the presence of LPS-activation may be sufficient to support oligodendrocyte survival. In either case, the ability of a reduced population of microglia to maintain their pro-survival effect on oligodendrocytes demonstrates that microglial activation is not necessarily harmful to all CNS cells. Microglial cell death also occurs during neuroinflammation and after injury in vivo [13, 71] and may be a form of autoregulation to limit the microglial response to injury and reduce damage to other CNS cells.
In conclusion, we demonstrate that activated microglia decrease survival of OPCs but that microglia, whether or not they have been stimulated with LPS, reduce apoptosis and increase survival of mature oligodendrocytes in vitro. The effects of activated microglia on OPC and oligodendrocyte viability are present even as microglia themselves undergo cell death due to activation, indicating that the effects of microglia on OPC and oligodendrocyte survival may not require a stable population of microglia. A further understanding of the mechanisms behind OPCs' and oligodendrocytes' differential response to microglia may aid in the development of therapies for several CNS diseases where microglial activation and OPC and oligodendrocyte death occur together.
The authors thank Rochelle Deibert, Crystal Forrider and Yvette Nout for assistance with animal care and Dana McTigue for discussing BrdU immunochemistry. This study was funded by NIH F30 NS053185-01A1 to BAM, NS38079, NS31193, and the C.H. Neilsen Foundation.
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