Emerging Concepts in Myeloid Cell Biology after Spinal Cord Injury (original) (raw)

• Journal List
• Neurotherapeutics
• v.8(2); 2011 Apr
• PMC3101835

Neurotherapeutics. 2011 Apr; 8(2): 252–261.

Alicia L. Hawthorne

Department of Neuroscience and Center for Brain and Spinal Cord Repair, The Ohio State University College of Medicine, 460 W. 12th Ave., 770 Biomedical Research Tower, Columbus, Ohio 43210 USA

Phillip G. Popovich

Department of Neuroscience and Center for Brain and Spinal Cord Repair, The Ohio State University College of Medicine, 460 W. 12th Ave., 770 Biomedical Research Tower, Columbus, Ohio 43210 USA

Department of Neuroscience and Center for Brain and Spinal Cord Repair, The Ohio State University College of Medicine, 460 W. 12th Ave., 770 Biomedical Research Tower, Columbus, Ohio 43210 USA

Corresponding author.

Copyright © The American Society for Experimental NeuroTherapeutics, Inc. 2011

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Summary

Traumatic spinal cord injury (SCI) affects the activation, migration, and function of microglia, neutrophils and monocyte/macrophages. Because these myeloid cells can positively and negatively affect survival of neurons and glia, they are among the most commonly studied immune cells. However, the mechanisms that regulate myeloid cell activation and recruitment after SCI have not been adequately defined. In general, the dynamics and composition of myeloid cell recruitment to the injured spinal cord are consistent between mammalian species; only the onset, duration, and magnitude of the response vary. Emerging data, mostly from rat and mouse SCI models, indicate that resident and recruited myeloid cells are derived from multiple sources, including the yolk sac during development and the bone marrow and spleen in adulthood. After SCI, a complex array of chemokines and cytokines regulate myelopoiesis and intraspinal trafficking of myeloid cells. As these cells accumulate in the injured spinal cord, the collective actions of diverse cues in the lesion environment help to create an inflammatory response marked by tremendous phenotypic and functional heterogeneity. Indeed, it is difficult to attribute specific reparative or injurious functions to one or more myeloid cells because of convergence of cell function and difficulties in using specific molecular markers to distinguish between subsets of myeloid cell populations. Here we review each of these concepts and include a discussion of future challenges that will need to be overcome to develop newer and improved immune modulatory therapies for the injured brain or spinal cord.

Electronic supplementary material

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Key Words: Monocytes, macrophages, neutrophils, microglia, cytokine, chemokine

INTRODUCTION

Spinal cord injury (SCI) elicits a robust and persistent inflammatory response. This response, involving the activation of resident microglia and the infiltration of neutrophils, monocytes, and lymphocytes, has been characterized in a number of different species including humans. The breadth and potential impact of the different components of post-SCI inflammation, including post-injury activation of peripheral immune responses, have been recently reviewed [1–5]. Therefore, this review will focus on the development, trafficking, and activation of myeloid cells after SCI and will conclude with a brief overview of possible therapeutic approaches for manipulating this distinct component of post-traumatic inflammation.

Myeloid cells in inflammation

Myeloid cells are a family of cells derived from hematopoietic progenitor cells and include monocytes, neutrophils, erythrocytes, and megakaryocytes (FIG. 1). Essentially, all leukocytes that cannot be characterized as lymphocytes are classified as myeloid cells. This review will focus on microglia, macrophages, and neutrophils because they are the main myeloid effector cells after SCI.

Updated schematic of myelopoiesis. Microglia are resident central nervous system macrophages derived from myeloid progenitors originating in the yolk sac before embryonic day 8. Adult microglia is an ontogenetically distinct population of macrophages that self renew. However, microglia may be repopulated from postnatal monocytes under certain circumstances (dashed line). Hematopoietic stem cells (HSCs) are also originally derived from the yolk sac and produce multi-lymphocyte progenitors (MLP) and common myeloid progenitors (CMP). MLPs give rise to lymphocytes (T and B) and NK cells, but also are capable of producing myeloid cells (e.g., monocytes or macrophages). CMPs, stimulated by a number of factors (see text), yield granulocyte-monocyte precursors (GMPs) and megakaryocyte-erythrocyte precursors (MEP). GMPs can be further stimulated to produce myeloid cells (e.g., neutrophils or monocytes). Monocytes differentiate into macrophages or monocyte-derived dendritic cells.

Within minutes of SCI, cells of the myeloid cell lineage become activated, creating a heterogeneous network of multifunctional cells capable of promoting injury and repair of neural tissue. Microglia are among the first myeloid cells to be set in motion, responding to changes in extracellular ions and ATP within minutes to hours post-injury [6–8]. Within the next few hours, neural and humoral signaling mechanisms elicit recruitment of cells from the circulation to the site of injury. Neutrophils arrive first, sometime between 3 to 24 h post-injury [9–11]. Monocytes arrive later, ~2 to 3 days post-injury (dpi) [11] with maximal infiltration occurring 1 to 2 weeks post-injury [9]. The dynamics and prevalence of intraspinal dendritic cells has not been well-defined, although cells expressing the dendritic cell antigen, integrin αE2 antigen, infiltrate the injured rat spinal cord 3 to 7 days post-injury [12]. Similar to dendritic cells, myeloid-derived suppressor cells (MDSCs) have received little attention after spinal cord injury (SCI); however, in mice with experimental autoimmune encephalomyelitis (i.e., the animal model for multiple sclerosis) MDSCs infiltrate the inflamed central nervous system (CNS) [13].

Normally, inflammatory cascades are self-limiting and typically resolve within a matter of days to weeks. However, within the injured spinal cord, neuroinflammatory cascades persist for extended periods of time. Activated macrophages and microglia are found in the injured spinal cord for at least 6 months in rats [9, 14], guinea pigs [15], and cats [16]. Neutrophils, although found in lesser numbers than monocytes, macrophages, and microglia, still persist for ~6 weeks post-injury in mice and ~6 months post-injury in rats [9, 17]. In injured human spinal cords, defensin-positive neutrophil infiltrates persist for ~10 days after injury, whereas activated intraspinal macrophages and microglia can be found for at least 6 months post-injury [18]. Because the lifespan of neutrophils and macrophages is ~5 days or 2 months, respectively, it is likely that chemotactic gradients specific for these myeloid cells persist indefinitely or recur periodically, allowing sustained recruitment of new cells to the injury site [19, 20].

The functional significance of resident and infiltrating myeloid cells in the injured spinal cord is controversial. Neutrophils can exacerbate hemorrhage, leading to more extensive pathology after SCI [21, 22]; however, these same cells may also trigger the onset of wound healing cascades in the injured spinal cord [23]. Similarly, microglia and macrophages can promote CNS repair (e.g., phagocytic removal of growth-inhibitory debris; stimulate neurite outgrowth) or exacerbate cell death and axonal degeneration at the site of injury [24–26]. The roles of dendritic cells and MDSCs are less well-defined. Dendritic cells may be beneficial after SCI, especially if they are prepared ex vivo and transplanted into the injury site, or if their function is augmented using exogenous growth factors/cytokines (e.g., granulocyte-macrophage colony stimulating factor [GM-CSF]) [27, 28]. MDSCs, if they are activated by SCI, could suppress deleterious autoimmune functions, including the activation of T-cells [29]. A functional role for MDSCs has not been characterized after SCI.

Damage caused by myeloid cells is not restricted to the spinal cord. Recent data show that myeloid cells activated as a result of SCI cause tissue damage in the liver and lungs [30]. Thus, activation of the immune system by SCI has long-lasting effects on the spinal cord and peripheral tissues.

Myelopoiesis and sources of intraspinal myeloid cells after injury

To fully appreciate the functional implications of myeloid cell recruitment and activation within the injured spinal cord, it is useful to know from where these cells originate and how and why they become activated. In embryos, hematopoiesis occurs in the yolk sac, then later, as the organism develops, in the liver, bone marrow, and spleen [31, 32] (FIG. 1). In classical models of hematopoiesis, a hematopoietic stem cell (HSC) gives rise to lineage-restricted precursors for lymphocytes or myeloid cells. This model has been called into question for mice because lymphocyte precursors were also found to give rise to myeloid cells [33–39]. Similarly, using human cells, recent data indicate that myeloid cell production is not limited to granulocyte-myeloid precursor cells [39, 40]. Instead, HSCs give rise to common myeloid progenitors and multi-lymphoid progenitors (FIG. 1). Monocytes and macrophages can also be derived from either granulocyte-myeloid precursor cells or multi-lymphoid progenitors, although it is not clear yet if cells derived from these distinct progenitor cell populations differ in their tissue distribution or function.

Myelopoiesis is stimulated directly or indirectly by a wide range of cytokines and growth factors, including interleukin-1 (IL-1), IL-3, IL-6, IL-7, IL-11, granulocyte-colony stimulating factor (G-CSF), granulocyte-monocyte-colony stimulating factor (GM-CSF), monocyte-colony stimulating factor (M-CSF), stem cell factor (SCF), Flt3 ligand (Flt3-L), interferon-gamma (IFN-γ), and tumor necrosis factor (TNF-α) [41–45]. When injected systemically, IL-7 increases the number of myeloid cells in the spleen and neutrophils and monocytes in the blood [41, 46, 47], presumably by increasing the mobilization of myeloid cells from sites of myelopoiesis [47, 48]. It is not known if circulating or cerebrospinal fluid levels of IL-7 increase after SCI; however, other pro-inflammatory cytokines (including IL-6 and TNF-α) do increase in SCI animals and humans [49–55].

Microglia, the resident immune cells in the CNS, and the first myeloid cells to respond to SCI, are widely believed to be derived from circulating hematopoietic precursors, mostly blood monocytes that colonize the CNS during late stages of development [56–58]. However, recent data indicate that adult microglia arise instead from extra-embryonic yolk sac myeloid precursors during embryogenesis (about embryonic day 8) [31] (FIG. 1). Accordingly, adult microglia self-replenish in the brain and spinal cord throughout life, independent of circulating monocyte precursors, presumably by a subset of radio-resistant precursors derived from the yolk sac [31, 59]. Despite the new data, the repopulation dynamics of CNS microglia will undoubtedly remain a controversial area of research. Indeed, circulating monocytes do enter the pathological CNS where they can differentiate into cells that are phenotypically and morphologically indistinguishable from resident microglia [60, 61]. Whether these former cells possess molecular and functional characteristics that are distinct from resident microglia is not known.

Neutrophils and monocytes originate from a common precursor (in bone marrow), and then travel through the blood to the site of the injury in response to CXC and CC chemokines, respectively (FIG. 2). Chemokines are produced within and outside the spinal cord. After injury to the brain or spinal cord, resident tissue macrophages in liver (Kuppfer cells [KCs]) are pivotal in regulating mobilization of leukocytes to the site of injury. KCs produce CXC ligand-10 (CXCL-10), IL-1β, CC ligand-2 (CCL-2), and macrophage inflammatory protein (MIP-1α) [62]. When KCs are depleted via systemic injection of clodronate liposomes, accumulation of neutrophils in the injured brain or spinal cord is significantly reduced [63]. This may partially explain why post-injury intravenous delivery of clodronate liposomes confers neuroprotection and promotes recovery of function after SCI [26, 64, 65].

Mechanisms of myeloid cell recruitment after spinal cord injury. (1) Injury to the spinal cord displaces pial glia, creating gaps in the glial limitans. Other astrocytes become reactive and hypertrophic. Neurons and oligodendrocytes are damaged, and microglia become reactive. Microglia, astrocytes, neurons, and oligodendrocytes synthesize and release chemokines and cytokines. (2) Chemokines and cytokines initiate chemokine synthesis in the liver. (3) Hepatic chemokines stimulate (4) myelopoiesis and the release of leukocytes from bone marrow (and maybe the spleen). (5) As they circulate, leukocytes bind to endothelia near the injury site first via selectins then (6) through stronger interactions with integrins. (7) Integrin binding allows firm attachment and margination with subsequent diapedesis through the blood-brain barrier into the perivascular space. (8) Leukocyte-derived matrix metalloproteinases (MMPs) help degrade the spinal basement membrane (9) allowing leukocytes to enter the spinal cord parenchyma.

For monocytes, emigration from the bone marrow is chemokine receptor CC receptor 2 (CCR2)-dependent [66, 67]. Recent data show that monocyte recruitment and survival also are CX3C ligand-1 (CX3CL1)/CX3C receptor-1 (CX3CR1)-dependent [68]. After infection with the intracellular bacterium Listeria monocytogenes, classical “inflammatory” Ly-6Chigh monocytes are maintained in the bone marrow of CCR2-/- mice [67]. After SCI, genetic deletion of CCR2 impairs monocyte infiltration and phagocytic uptake of degenerating myelin but does not permanently abrogate intraspinal macrophage accumulation [69]. It is likely that in the absence of CCR2+ monocytes there is compensatory proliferation of resident microglia and perhaps increased recruitment of Ly6Clow/CCR2low/CX3CR1high monocyte subsets; however, the relative contribution of different monocyte subsets to neuroinflammatory processes after SCI has not been determined (see as follows).

Although it is believed that most circulating leukocytes are derived from bone marrow, recent data indicate that the spleen may rapidly deploy a large population of monocytes into the circulation in response to ischemic injury [70] (FIG. 2). In a model of myocardial ischemia, splenectomy markedly reduced intracardiac monocyte accumulation [70]. Importantly, splenectomy did not elicit a compensatory release of CCR2+ monocytes from the bone marrow. The splenic reservoir also has been shown to be important in regulating tissue injury in a model of cerebral ischemia. Splenectomy 2 weeks prior to a middle cerebral artery occlusion was associated with a significant reduction in monocyte accumulation and lesion size in the ischemic brain [71].

The mechanisms regulating leukocyte mobilization from the spleen after injury may be numerous. After middle cerebral artery occlusion, catecholamines are released into the blood and may activate adrenergic receptors in the spleen causing the release of monocytes [72]. In the myocardial infarction model, splenic release of monocytes was impaired in angiotensin II-/- mice [70]. Whether splenic monocytes contribute to the intraspinal macrophage response elicited by traumatic SCI, in which ischemia is only one component of the pathophysiology, has not been studied.

Mechanisms regulating intraspinal accumulation of myeloid cells after SCI

After release from the bone marrow (or spleen), leukocyte transmigration from blood to spinal cord is dependent on a cadre of adhesion molecules and chemokines [73–75]. Details of the cellular and molecular characteristics of the multi-step paradigm for leukocyte–endothelial interactions at the blood-brain barrier have been published elsewhere [73–75]. A more comprehensive review of how the complex interplay between neurons and glia regulates the onset of neuroinflammatory cascades after SCI, including the recruitment of neutrophils and monocytes, can be found in recent reviews from our laboratory [3, 5]. Here we highlight newer data generated in rat and mouse models of SCI that reveal novel control mechanisms for myeloid cell entry and activation after SCI.

Within minutes to hours post-injury, intraspinal neurons and astrocytes produce IL-1β [76, 77]. Synthesis of bioactive IL-1β in neurons is dependent on the NALP1 inflammasome [76]. A similar mechanism is likely in astrocytes, microglia, and oligodendrocytes, although this has not been proven after SCI [78]. In astrocytes, the synthesis of IL-1β and chemokines (e.g., CCL2, CCL3/MIP-1α, CXCL1/KC, and CXCL2/MIP-2) is triggered via the IL-1 receptor and not by pattern recognition receptors (TLR2, TLR4) [79]. In the absence of MyD88/IL-1-receptor-dependent signaling, entry of neutrophils and to a lesser extent monocytes are reduced after SCI [79].

Myeloid cell entry into the injured spinal cord and associated changes in vascular permeability also require the induction of matrix metalloproteinases (MMPs) (see review in this issue [80] and also see Noble et al. [81] and Wells et al. [82]). In rat and human myeloid cells, CD95 ligand (CD95L)/CD95 interactions are pivotal for induction of MMP-9 and subsequent infiltration into the injured spinal cord [83]. When CD95L is deleted from myeloid cells, intraspinal inflammation is reduced and recovery of function is improved after experimental SCI [83]. Thus, chemotactic gradients at the injury site are established primarily by nonmyeloid cells, and then later, as cells begin to enter the injury site, myeloid cells amplify this response. In fact, the sequential recruitment and activation of neutrophils and monocytes is essential for amplifying and then resolving inflammatory cascades [84]. However, after SCI, cellular and molecular indices of neuroinflammation exist chronically throughout the injured spinal cord, suggesting that the resolution of inflammation is impaired. Currently, there is no explanation for this effect, and further research is needed.

Characterizing myeloid cell heterogeneity in the injured spinal cord

Spinal cord injury elicits and activates a heterogeneous population of myeloid cells (e.g., neutrophils, microglia, and monocytes) with the ability to exacerbate tissue injury and promote repair. This phenotypic and functional heterogeneity is maintained by diverse signaling cues in injured and spared tissues. For example, neuroimmune regulatory proteins present on neurons and glia regulate the phenotype and function of microglia. Neuroimmune regulatory proteins include CD47, CD22, CD95L, CD200 and CX3CL1 [5]. Loss or downregulation of these ligands causes microglia and monocyte-derived macrophages to become hyperreactive and potentially destructive [5, 85, 86]. CD200/CD200R interactions are especially intriguing because CD200R is expressed only on myeloid cells.

Intrinsic heterogeneity within the pool of resident and recruited myeloid cells results, in part, from differences in cell maturation, differentiation, and activation. A variety of antibodies are used to characterize these diverse cell subsets; however, the expression profiles of surface and cytoplasmic antigens often overlap, making it difficult to assign a definitive phenotype or function to a given cell type. For example, Ly6G/Gr-1 is widely used as specific marker for neutrophils; however, it also labels a subset of monocytes [87]. Therefore, when used as a purported neutrophil-depleting antibody, the effects of Ly6G/Gr-1-mediated cell depletion may also result from loss of monocytes. Also, granulocytic MDSCs express Ly6G and CD11b, but are distinct from monocytic MDSCs, which express CD11b and Ly6C [29]. These phenotypic distinctions are important to consider when interpreting data in which antibodies are used for depletion of circulating leukocyte subsets. For example, the Ly6G/Gr-1 antibody was used to deplete neutrophils in a mouse model of SCI [23]. The antibody was injected systemically at 2 and 24 h post-SCI, and was found to significantly reduce the number of circulating neutrophils (but not monocytes) and inflammatory cytokines, but lesion pathology and locomotor recovery were impaired in Gr-1-treated mice. From these data, one can conclude that neutrophils are important for limiting lesion pathology after SCI and should not be a target for depletion. However, future studies should also explore whether Gr-1 antibodies deplete granulocytic MDSCs. These cells have not been evaluated after SCI, but may play an important yet unappreciated role in regulating acute post-traumatic inflammation.

Flow cytometry can be used to distinguish between these closely related cell types, although one loses the ability to co-localize cells to areas of injury or repair in the spinal cord. Using flow cytometry myeloid cell subsets can be defined, based on physical properties (e.g., cell size, granularity) and expression of cell membrane or cytoplasmic antigens. For example, blood monocytes stain positive for CD11b and M-CSF receptors (CSF-1R or CD115) [88]. Neutrophils also express CD11b, but are distinguished from blood monocytes by their relative expression of CD45, Gr-1, and F4/80 [89]. Neutrophils are CD45+/Gr-1+/F4/80-, whereas monocytes are CD45+/Gr-1-/F4/80+ [89]. Relative levels of Ly6C can be used to differentiate between mature and immature monocytes/macrophages; high Ly6C levels are associated with immature or younger monocyte precursors (“inflammatory” monocytes) and low levels with a more mature cell type that has reduced migratory capacity (i.e., “resident or noninflammatory” monocytes) [88]. The relative expression of CD45 can also be used to distinguish between CNS macrophages that are derived from microglia (CD45low) and blood monocytes (CD45high) [89].

The previously described parameters are useful for broadly categorizing phenotypic and functional heterogeneity of myeloid cells at and nearby the site of injury. However, it is likely that as the lesion evolves, signaling moieties in the lesion microenvironment will also change, causing functional adaptivity in myeloid cells, especially CNS macrophages [5, 90]. Recent work from our laboratory has shown that SCI elicits a diverse macrophage response that changes as a function of time post-injury in mice. Early after injury (for at least 3 days), the lesion site is comprised of macrophages that can be defined as “classically activated” pro-inflammatory M1 cells and “alternatively activated” M2 cells. M1 cells express discrete phenotypic markers including inducible nitric oxide synthase (iNOS), CD86, and CD16/32, whereas M2 cells express CD206 and arginase I [24]. After ~7 days, the ratio of M1:M2 cells increases due to a concomitant increase in expression of M1 cell markers and a decrease in cells with an M2 phenotype. The significance of this is not clear; however, M1 macrophages are neurotoxic and promote die-back of injured CNS axons [24–26], whereas M2 macrophages seem to have no adverse effect on neurons and can promote growth of axons across inhibitory substrates that dominate sites of injury [24]. In an independent study, a subset of IL-10+ monocyte-derived macrophages was found to be anti-inflammatory and essential for tissue repair [91]. Whether CNS macrophage heterogeneity can be controlled for therapeutic gain after SCI, either through direct manipulation of myeloid cell subsets and/or the lesion environment, awaits further research.

Experimental therapies

Various pharmacological agents, toxins and antibodies have been used to deplete or functionally inactivate neutrophils, microglia, and/or monocyte-derived macrophages in pre-clinical models of SCI. A partial list of these pre-clinical therapies is summarized in Table 1. These various experiments, including the use of clodronate liposomes [64, 65], anti-CD11d antibodies [92–95], minocycline [96], silica dust [1, 97, 98], colchicine and chloroquine [98, 99], activated protein C [49], and nitrogen mustard [100, 101] have been reviewed previously [1, 5, 98] and will not be discussed further. Additionally, because 2 other review articles in this issue provide an overview of the use of MMP inhibitors for SCI [80] and provide new strategies to manipulate microglia (and macrophage) metabotropic glutamate receptors [102], we will not discuss these topics any further. Instead, we will focus on newer approaches in which blockade or infusion of select cytokines has been shown to modify the composition and phenotype of the responding myeloid cells. Additionally, the implications of recent Gr1-mediated neutrophil depletion data are described in the context of myeloid cell heterogeneity and downstream wound healing cascades.

Table 1

Pre-Clinical Manipulation of Myeloid Cells after Experimental Spinal Cord Injury

BDNF = brain-derived neurotrophic factor; GM-CSF = granulocyte-macrophage colony stimulating factor; IL = interleukin; SCI = spinal cord injury.

IL-6 is a pro-inflammatory cytokine that promotes the differentiation of monocytes into macrophages [92–95] and can also elicit monocyte recruitment [103]. When over-expressed in the injured spinal cord using genetically modified cellular vectors, excess IL-6 enhanced the endogenous neutrophil and monocyte response to SCI and exacerbated lesion pathology [104]. In mice, postinjury intraperitoneal injection of MR16-1, an antibody specific for the IL-6 receptor, profoundly affected intraspinal inflammation, lesion pathology, and functional recovery [44, 52]. Indeed, a single injection of MR16-1 reduced intraspinal inflammation and pro-inflammatory chemokine/cytokine signaling. Interestingly, MR16-1 also changed the composition of the responding myeloid cells. A single injection shifted the normal cell dynamics, resulting in a microglial-dominant reaction. At chronic times post-injury, microglial-dominant inflammation was associated with increased axonal sparing distal to and at the site of injury, and improved functional recovery. These data show that rather than deplete cells, the destructive potential of myeloid cells can be reduced (or abolished) by interfering with select acute inflammatory signaling cascades early after injury.

A similar result was achieved in SCI by blocking leukotriene B4 (LTB4) signaling. LTB4 is a lipid chemoattractant produced from membrane phospholipids as part of the arachidonic acid cascade. LTB4 binds to LTB4 receptor 1 (BLT1) on neutrophils and monocytes, enhancing their recruitment and activation at sites of inflammation [103]. After SCI, inflammatory cascades are significantly reduced in BLT1-/- mice and in SCI wild-type mice treated with the LTB4 receptor antagonist, ONO-4057 [105]. Indeed, infiltration of neutrophils and monocytes/macrophages was reduced in parallel with various myeloid-specific cytokines and chemokines, including IL-6, IL-1β, TNF-α, CXCL1, CXL2, and CCL2. These changes were associated with decreased neuronal apoptosis, enhanced conduction in axons traversing the site of injury, and improved locomotor recovery at chronic post-injury survival periods.

In contrast to blocking pro-inflammatory signaling, it may be possible to boost local concentrations of anti-inflammatory cytokines. For example, local infusions of IL-10 are neuroprotective after SCI, in part because the cytokine can antagonize pro-inflammatory signaling (e.g., NF-κB) at the site of injury [106–108]. IL-4 is another anti-inflammatory cytokine that may be important for regulating intraspinal inflammation. After SCI, neutrophils transiently produce IL-4 [109]; however, the eventual polarization of the CNS macrophage response toward a neurotoxic M1 phenotype suggests that endogenous IL-4-dependent immune regulation is inefficient. Clearly, some intrinsic immune regulation is mediated by IL-4 because injection of anti-IL-4 antibodies after SCI exacerbates pro-inflammatory signaling [109]. Blockade of endogenous IL-4 leads to an increase in CCL2 synthesis and myeloid cell influx to the injury site with a concomitant increase in lesion pathology [109]. Whether focal and sustained infusion of IL-4 could alleviate acute macrophage-mediated toxicity is under investigation. Still, caution must be exercised with cytokine therapies, especially because cytokines are pleiotropic and can have broad “off-target” effects. For example, granulocyte-macrophage colony stimulating factor is beneficial after SCI; however, its mechanism of action is difficult to pinpoint. GM-CSF exerts anti-apoptotic effects on neurons [51, 110, 111]; however, recent data indicate that GM-CSF infusion increases intraspinal brain-derived neurotrophic factor and improves locomotor recovery via mechanisms involving the activation of dendritic cells and neural stem/progenitor cells [28]. Mice treated with GM-CSF also had more brain-derived neurotrophic factor production and better locomotor recovery.

Conclusions

Spinal cord injury elicits an inflammatory response comprised of both resident and newly recruited peripheral myeloid cells. These cells can positively and negatively affect the spinal cord and tissues in the periphery. Although the bone marrow is widely believed to be the primary source of circulating myeloid cells after SCI, recent data implicate the spleen as an emergency reservoir for monocytes. Whether the spleen contributes to intraspinal inflammation has not been determined. As myeloid cells accumulate at the site of injury, their impact on spinal cord structure and function will be determined by their phenotype and the immune-modulatory signals that exist within the lesion environment. The precise nature of these signals and how they regulate macrophage phenotype and function are unknown and more research is needed to develop therapies that effectively target select myeloid cell subsets and/or factors that regulate myeloid cell differentiation and function. New studies show that it may be possible to infuse select cytokines or cytokine receptor antagonists to alter the composition and dynamics of myeloid cells. Given the early and sustained presence of myeloid cells at and nearby sites of SCI, these cells represent ideal therapeutic targets for minimizing secondary tissue injury and/or promoting repair of the injured spinal cord.

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Acknowledgment

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