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Trafficking of immune cells in the central nervous system
Emma H. Wilson,1 Wolfgang Weninger,2 and Christopher A. Hunter3
1Division of Biomedical Sciences, University of California, Riverside, California, USA. 2The Centenary Institute for Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia. 3Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Address correspondence to: Emma H. Wilson, Division of Biomedical Sciences, University of California, Riverside, Riverside, California 92521, USA. Phone: 951.827.4328; Fax: 951.827.5504; E-mail: [email protected].
Find articles by Wilson, E. in: JCI | PubMed | Google Scholar
1Division of Biomedical Sciences, University of California, Riverside, California, USA. 2The Centenary Institute for Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia. 3Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Address correspondence to: Emma H. Wilson, Division of Biomedical Sciences, University of California, Riverside, Riverside, California 92521, USA. Phone: 951.827.4328; Fax: 951.827.5504; E-mail: [email protected].
Find articles by Weninger, W. in: JCI | PubMed | Google Scholar
1Division of Biomedical Sciences, University of California, Riverside, California, USA. 2The Centenary Institute for Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia. 3Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Address correspondence to: Emma H. Wilson, Division of Biomedical Sciences, University of California, Riverside, Riverside, California 92521, USA. Phone: 951.827.4328; Fax: 951.827.5504; E-mail: [email protected].
Find articles by Hunter, C. in: JCI | PubMed | Google Scholar
Published May 3, 2010 - More info
J Clin Invest. 2010;120(5):1368–1379. https://doi.org/10.1172/JCI41911.
© 2010 The American Society for Clinical Investigation
The observations of Paul Ehrlich in the late 19th century that water-soluble vital dyes injected into the peripheral circulation would stain all organs except the brain provided the first indication that the CNS was anatomically separated from the rest of the body (1). Subsequent studies by Edwin Goldmann, showing that dye injected into the spinal fluid did not stain peripheral tissues, confirmed the idea that the brain was a unique anatomical compartment (2). We now know that this feature is a consequence of the existence of the blood-brain barrier (BBB), which limits access of soluble factors to the CNS and restricts access of immune cells to this site (3–5). Combined with the lack of an obvious lymphatic system, low constitutive levels of MHC class I and II molecules, local production of suppressive factors, and, in the normal state, limited numbers of professional antigen-presenting cells, these features all reinforced the concept of the CNS as an immune-privileged site (6, 7).
The work of Peter Medawar in 1948 on graft rejection provided some of the first experimental evidence indicating that the brain might not be an immunologically pristine site (8). Those experiments demonstrated that skin transplants in the brain of naive animals did not provoke an immune response, but if animals were first exposed to graft antigens, such that immune cells in the periphery were “educated” beforehand, grafts would be rejected. It is now appreciated that these events involve the ability of a graft-specific adaptive immune response that is primed in the periphery to access the CNS and mediate rejection of the foreign tissue (9). It is also apparent that cells of the immune system have access to the three distinct anatomical compartments (i.e., cerebrospinal fluid [CSF], meninges, and parenchyma of the brain) that are relevant to the CNS under physiological circumstances and disease states. Several neurodegenerative, physical, and infectious diseases can be modeled in the mouse, allowing direct analysis of inflammatory processes in the brain (Table 1) to corroborate observations from human postmortem tissue analysis, CSF samples, and biopsies. Thus, the presence in the brain of neutrophils in the context of bacterial meningitis (10), eosinophils associated with migrating helminths (11), T cells in post-vaccinal or post-infectious CNS autoimmunity (12), and plasma cells (Mott cells) during African sleeping sickness, which is caused by Trypanosoma spp. (13), illustrate that innate and adaptive immunity are operational at this site. Indeed, immune cells are required to control certain viral, bacterial, fungal, and parasitic pathogens that affect the brain. For example, infection with the parasite Toxoplasma gondii leads to a latent infection in the CNS, and T cells are essential for its long-term control. This is illustrated by the development of toxoplasmic encephalitis in previously infected individuals that acquire defects in T cell functions (14). This can be recapitulated in experimental models in which chronically infected mice depleted of T cells develop uncontrolled parasite replication in the brain (15, 16). A similar requirement for immune cells in the CNS has been shown for the control of many pathogens, including the human polyomavirus JC virus, which causes progressive multifocal leukoencephalopathy (17); Cryptococcus spp., which can cause meningitis; and cytomegalovirus (18), which can cause encephalitis. These examples illustrate the importance of immune surveillance in the CNS.
Although the ability to recognize infections in the CNS is required to limit pathogen replication, this response is not always beneficial. The presence of the rigid bone casing of the brain makes the classic features of an inflammatory response, such as swelling and expansion, a dangerous prospect. Similarly, the development of pathology associated with meningitis and/or encephalitis can lead to reduced neuronal function and survival (19, 20). In addition, although the immune system can contribute to the successful resolution of tissue damage associated with many CNS disorders (21, 22), there is also an appreciation that inflammation in the brain may contribute to the pathogenesis of multiple neurodegenerative conditions, including Parkinson disease, Alzheimer disease, and lysosomal storage diseases (23).
This association of inflammation and adverse events may explain why the brain seems to be governed by a unique set of immunological guidelines. A clear understanding of these “rules” may inform the design of strategies to augment protective immune responses to infection while minimizing collateral damage. Similar principles would apply to tumors in the CNS and may allow for the design of rational treatments that provide better access for T cells to this relatively immune-privileged site. Conversely, in the case of autoimmune conditions of the CNS, such as MS, the ideal therapeutic strategy would ameliorate the pathological response while still allowing normal immune surveillance.
The past two decades have seen remarkable advances in understanding how cells of the immune system can access the CNS, and several recent studies have highlighted the basis for immune surveillance of this organ (24–29). More recently, the ability to directly image immune cells in the context of live tissue has been possible using multi-photon microscopy. This technique, originally used to visualize neuronal morphology in the brain (30–32), has allowed the observation of fluorescently labeled immune cell populations and their migratory and interactive behavior in primary and secondary lymphoid organs, as well as peripheral tissues, during thymic selection, priming, and activation (33, 34). Imaging of the brain presents unique challenges because the skull prevents direct access to the tissue, but brain slices and explanted tissues can be kept viable in warmed and aerated media, and partial removal or thinning of the skull in anesthetized mice can be conducted. These techniques have allowed imaging of CNS-resident cells — neurons (30, 32, 35, 36), microglia (37, 38), and astrocytes (28, 39, 40) — over the course of hours and days. In addition, imaging of inflamed brains and spinal cords has provided unprecedented insights into the behavior of immune cell populations in the CNS. In this review, we discuss these advances in the context of the trafficking and behavior of immune cells during protective and pathological immune responses in the CNS.
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Structure and routes of entry to the CNS
The presence of the BBB, which limits the entry of cells and pathogens to the brain, in addition to the lack of obvious lymphatics in the brain, indicate that there are a limited number of portals to and from the CNS. To appreciate the barriers that exist for immune cells accessing the brain, it is important to recognize that the brain has three membranes — the dura mater (outer), the arachnoid membrane (middle), and the pia mater (inner) — that enclose the parenchyma of the CNS (Figure 1). The BBB encompasses the capillaries and postcapillary venules in the brain and spinal cord and is composed of specialized endothelial cells, linked by complex tight junctions comprised of transmembrane adhesion molecules including cadherins, junctional adhesion molecules, occludin, and claudins (41, 42). This structure limits the transport of specific factors and solutes, including >98% of antibodies and small molecules, into the parenchyma, while ensuring the efflux of others (7, 43). The structure of this endothelial barrier acts to limit leukocyte trafficking directly across the BBB (44). Importantly, following injury to the CNS, the activation of endothelial cells and associated cells such as astrocytes can lead to reduced tight junction integrity and formation of transendothelial cell channels (42, 45, 46), thereby facilitating the migration of leukocytes across and through the BBB into the brain (43, 47, 48). The migration of leukocytes into the CSF is thought to occur through the choroid plexus and into the subarachnoid space (which contains the CSF), and their migration from the blood directly into the brain parenchyma occurs across the BBB via the perivascular space (Figure 1). In addition to the differences in barrier properties, the vasculature itself differs between CNS compartments, and this may influence immune cell access. Thus, the capillaries of the meninges have a simple one-layer structure, whereas the postcapillary venules of the parenchyma require cells to transition across inner and outer basement membranes (for detailed reviews of these processes see refs. 4, 7, 41, 49). In the following sections we discuss the circumstances and mechanisms facilitating access to these specific compartments.
Figure 1The structure of the brain and routes of leukocyte entry. Beneath the skull lie three membranes that enclose the parenchyma of the brain: the dura mater, the arachnoid membrane, and the pia mater. The latter two enclose the subarachnoid space. (i) Leukocytes can enter across the choroid plexus, where CSF is produced by the choroid plexus epithelium in the ventricles. CSF containing leukocytes then enters the subarachnoid space, circulates around the brain, and (ii) exits via the venous sinus to be resorbed by the blood via the arachnoid villi. (iii) Blood supply to the brain enters in the subarachnoid space over the pia mater, generating the perivascular space (or Virchow-Robin space). Main arterial branches divide into capillaries, which terminate deep within the brain, supplying the parenchyma with blood. Leukocytes can potentially enter from the blood (iii), which requires them to cross the tightly regulated vascular endothelium (i.e., the BBB: the glia limitans, the subarachnoid space, and the pia mater). Cells can adhere to the endothelium and arrest at any point during this process.
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Access to the CSF and immune surveillance
As highlighted earlier, there are numerous pathogens that invade the CNS and/or establish latent infection with the potential to cause disease. Consequently, there is a need for immune surveillance — a continuous process whereby the peripheral immune system is able to monitor the brain for signs of infection or tissue damage. This is likely distinct from the events involved in the recruitment of various immune populations to sites of ongoing infection or inflammation. In the context of immune surveillance, the compartment that has been best studied is the CSF. The choroid plexus, which is located in the ventricles of the brain (Figure 1), has secretory epithelium that produces the CSF. Unlike the BBB, the fenestrated endothelial cells of the choroid plexus lack tight junctions that would normally limit diapedesis of leukocytes. Therefore, although immune cells still have to negotiate the tight junctions of the choroid plexus epithelium, it appears that this site is specialized to allow lymphocytes more ready access to the CSF (Figure 2). Instructively, the composition of immune cells in the blood and CSF differs. Under normal circumstances, the CSF contains few innate immune cells but a much higher percentage of memory or antigen-experienced CD4+ T cells than the blood (50, 51). This observation suggests that it is these cells that are specifically involved in immune surveillance.
Figure 2Immune surveillance via the choroid plexus. The choroid plexus is composed of highly invaginated loops of capillaries and pia mater that reach into the ventricles of the brain. Cells from the blood and under the influence of chemokines undergo adhesion, rolling, and diapedesis across the fenestrated capillary endothelium and pia mater of the choroid plexus. The basement membrane and tight junctions of the choroid plexus epithelium provide a further barrier, the brain-CSF barrier. These modified epithelial cells (Kolmer cells) have bulbous microvilli that secrete the CSF. Infiltrating leukocytes migrating through these cells enter the ventricles that contain CSF and circulate around the CNS. The chemokine CCL20 is expressed on the basolateral side of the choroid plexus epithelial cells, attracting CCR6-expressing CD4+ T cells. Chemokines and their receptors demonstrated to be involved in the trafficking of immune cells into the CSF are provided in Table 2.
Activated T cells upregulate many integrins and adhesion molecules, enabling their rolling and adhesion to vessel walls. However, deciphering which of these molecules are necessary for immune surveillance is complex. Multiple integrins, chemokine receptors, and adhesion molecules expressed on circulating and CNS-resident cells have been implicated in this process (50–52). The most likely candidates are those expressed constitutively in the CNS in the absence of ongoing inflammation. These include the adhesion molecule P-selectin (51, 53); the adhesion molecules vascular cell adhesion molecule 1 (VCAM1) and intercellular adhesion molecule (ICAM1), which bind to very late antigen-4 (VLA-4, also known as α4β1 integrin) and lymphocyte function–associated-1 (LFA-1), respectively (54); and the chemokines CCL19 and CCL20 (29, 55, 56), all of which are constitutively expressed by epithelial cells of the choroid plexus (Figure 2). One recent study suggested a model in which, as part of normal immune surveillance, CD4+ T cells specific for the autoantigen myelin oligodendrocyte glycoprotein (MOG) had to express CCR6, a receptor for CCL20, for optimal access to the CSF before they could initiate experimental autoimmune encephalomyelitis (EAE) (29). However, other studies have indicated that the main contribution of CCR6 is to the priming of myelin-specific CD4+ T cells in the periphery and that CCR6 is not actually required for the ability of effector cells to access the CNS (57). Similarly, Th1 cells, which are characterized by the production of IFN-γ and are required for resistance to multiple viral, bacterial, and parasitic pathogens that affect the CNS, do not express CCR6 and can be recruited to a site of ongoing inflammation in the CNS independently of CCR6 (29). This is consistent with reports that the majority of T cells in the CSF express CXCR3, a receptor normally associated with Th1 cells (58, 59). Clearly, further studies are required to determine whether pathogen-specific (or autoantigen-specific) Th1, Th2, or Th17 and/or central memory T cells are involved in this route of immune surveillance as well as whether there are specific trafficking requirements for Tregs as a mechanism to limit inflammation (60–62).
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Migrating in the parenchyma
Adhesion molecules. Several studies that directly visualized the molecular steps that mediate the access of T cells to various compartments associated with the CNS have been performed by imaging the superficial vessels in the meninges that are associated with the spinal cord as well as pial vessels and parenchymal branches in a variety of model systems (74–78). In the context of EAE, several reports have described the initial tethering and rolling of leukocytes along the endothelium prior to firm adhesion (25, 79) and migration against the blood flow (74). Similarly, intravital microscopy studies of HSV-infected mice have demonstrated increased leukocyte rolling and adhesion in the microvasculature of the pia mater of infected mice (80), and similar neutrophil behaviors in the meninges have been identified during LCMV infection (64). These observations are consistent with the idea that inflammation in the CNS, either due to autoimmune responses or infection, leads to increased expression of adhesion molecules on endothelial cells of the BBB and choroid plexus, including members of the selectin family; cell adhesion molecules of the immunoglobulin superfamily, for example, ICAM1, VCAM1, and PECAM1; and members of the integrin family (Figure 3) (51, 53, 75, 81–83). This topic has been reviewed extensively elsewhere (41, 49, 76) and therefore is not discussed in detail here. Nevertheless, the biology of the integrin dimer VLA-4 (α4β1 integrin) and its ligand VCAM1, as well as their association with the development of MS and EAE, are particularly instructive in thinking about the need to balance immune access to the brain.
Figure 3Leukocyte trafficking across the glia limitans into the parenchyma of the brain. Activated leukocytes expressing adhesion molecules and integrins roll and attach to the vascular endothelium. Successful diapedesis requires appropriate ligation of adhesion molecules, selectins, and integrins, signaling to both the infiltrating leukocyte and the brain endothelium. Expression of CXCL12 on the basolateral surface of endothelial cells recruits CXCR4+ T cells. However, retention of cells in the perivascular space occurs in the presence of high concentrations of CXCL10. Continued migration puts cells in contact with the glia limitans, which is composed of a highly structured wall of astrocytes. Further positive migratory signals, including chemokines, from these and surrounding cells may allow leukocyte migration into the parenchyma.
Although it is controversial as to whether VCAM1 is expressed in human vasculature, the finding that blockade of VLA-4/VCAM1 interactions delayed the onset and/or decreased the severity of EAE implicated this molecule as a target for the treatment of MS (84). This led to the clinical development of a monoclonal antibody (known as natalizumab) that targets α4 integrin (a component of VLA-4); natalizumab was successfully used in clinical trials to manage this condition (85). However, a small number of patients treated with this reagent developed progressive multifocal leukoencephalopathy associated with the reactivation of latent JC polyomavirus infection (20). This observation has been paralleled by the recent withdrawal of an antibody (known as efalizumab) that blocks LFA-1, which was used for the treatment of psoriasis and also led to the reactivation of JC polyomavirus in the brain (86). Whether JC polyomavirus persists in a latent form in the CNS or these events are a consequence of reactivation of the virus in peripheral tissues and subsequent spread to the CNS is unclear (87). However, recent reports that detected the presence of JCV in normal brain tissue support the former notion (88–90). Regardless, blockade of α4 integrin has also been shown to antagonize protective immune responses to multiple pathogens in the brain, including T. gondii (28), simian immunodeficiency virus–induced AIDS encephalitis (91), and Borna virus–induced progressive encephalitis (92). Other promising strategies to block cell trafficking to the CNS (77) may encounter similar problems. Despite all of these potential complications, the number of adverse events associated with natalizumab therapy has been lower than might have been predicted from studies in experimental systems, and this therapy continues to be used for the treatment of MS. Importantly, recent studies involving the generation of bone marrow–chimeric mice in which the hematopoietic compartment lacked β1-integrin but retained α4β7 integrin signaling indicated that T cell accumulation in the CNS during EAE required α4β1-integrin but that migration of granulocytes and macrophages into the CNS was independent of β1 integrin (93). These findings highlight the potential to control the trafficking of specific immune populations and perhaps even subsets of lymphocytes into the brain.
Astrocytes and immune cell trafficking in the parenchyma. Astrocytes provide an important structural component of the BBB (94) and are thought to restrict access of immune cells to the CNS. So, after rolling along, adhering to, and finally crossing the endothelial cells of the BBB and their associated basement membrane, the migrating leukocytes reach their next barrier, the glia limitans (Figure 3). This structure surrounds the blood vessel, is composed of astrocytic foot processes, is linked to the basal membrane by the transmembrane receptor dystroglycan, and forms its own molecularly distinct basement membrane composed of laminin, fibronectin, and type IV collagen (95, 96). There are very few studies that have considered how leukocytes cross this second barrier, although several reports have provided evidence that production of MMPs by immune cells is required for cleavage of dystroglycan and the breakdown of BBB during EAE and neurocysticercosis associated with tapeworm infection (96, 97).
Reactive astrocytes are a hallmark of most inflammatory responses in the brain and this activation corresponds with increased astrocyte numbers, changes in their morphology, and upregulated expression of glial fibrillary acidic protein, an astrocyte-specific structural protein (98). The seminal studies by Fontana et al. (99), which suggested that astrocytes could present antigen to CD4+ T cells, highlighted the possible role of these glial cells in the immune response. Although the ability of astrocytes to present antigen through MHC class II remains controversial (100), the formation of synapses between astrocytes and antigen-specific CD8+ T cells in vivo is consistent with their ability to present antigen through MHC class I (101, 102). Nevertheless, reactive astrocytes are frequently associated with migrating T cells and act as a source of multiple cytokines and chemokines during inflammation (103), which may actively promote cell trafficking into and within the CNS. However, in the majority of experimental systems it has not yet been defined how these interactions affect the coordination of antimicrobial immune responses.
The possible contribution of astrocytes to immune responses within the brain has been described in several settings, including those involving the targeted overexpression of cytokines — such as TNF, IFN-α, TGF-β, IL-6, and IL-12 — by astrocytes, which leads to chronic inflammation and progressive neurodegeneration (104–108). More recent studies analyzing mice in which the ability of astrocytes to participate in immune function is compromised through the specific loss of a cytokine receptor such as gp130 or reduced NF-κB signaling, have shown that this alters the course of immune responses in the CNS (109–112). Thus, in a mouse model of spinal cord injury, astrocyte-specific inhibition of NF-κB (which is necessary for the activation of many cytokine genes) resulted in a reduction in the number of reactive astrocytes in the CNS, in lower levels of chemokines, and in reduced infiltration of T cells and macrophages (111). Consequently, this led to improved spinal cord healing. Future challenges include determining how individual cytokines, adhesion molecules, and chemokines produced by astrocytes influence the development of inflammation and the behavior of infiltrating immune cell populations.
Chemokines and migration in the parenchyma. Once cells have crossed all the membrane barriers and gained access to the parenchyma of the brain, what molecular cues guide their migration? There is an extensive list of chemokines that are either expressed constitutively or upregulated in the brain during inflammation, and infiltrating immune cells express a wide array of chemokine receptors associated with chemotaxis and/or effector function. The use of mice lacking specific chemokines or chemokine receptors and treatment with antagonists of these interactions has provided useful insights into which interactions are likely important in the brain. However, one of the frequently raised caveats is that this may not distinguish between their role in the development of immunity versus trafficking of cells to the CNS (compare conclusions of refs. 29 and 57). For example, the increased susceptibility of mice that lack CCL3 to viral infection in the brain may be due to poor activation and priming of dendritic cells rather than to a failure of T cells to traffic to and migrate within the CNS (113).
Regardless, the relevance of chemokines to immune cells in the CNS remains an area of active research and has been covered extensively in other articles (76, 114), and therefore we only provide a summary of their role in various model systems (Table 2). However, it is helpful to highlight the range of pathologies in which these molecules appear to have critical roles. The chemokine receptors CCR2 and CCR5, which are expressed on many monocytes and T cells and, despite difficulties in detecting these receptors, in MS lesions (115–117), have been implicated in CNS inflammation because blockade of their interactions leads to a reduction in inflammation in mouse models of immune-mediated demyelination (118–123). These findings are broadly consistent with the ability of chemokines to mediate their activities through chemotaxis and activation of integrins (124), but they can also have more complex effects on cell behavior. The majority of T cells found in the uninflamed CNS express CXCR3 (59), and this receptor has been implicated in cerebral malaria pathology (125, 126) and recruitment of protective CTLs during viral infection (113, 127). Furthermore, the recruitment of CXCR3+ T cells to neurons infected with West Nile virus has been attributed to the localized production of CXCL10 by the infected cells (128). However, the role of CXCR3 and one of its ligands, CXCL10, during EAE appears more complex (60). During this autoimmune condition, expression of CXCR3, rather than inducing a chemotactic response, is implicated in the retention of autoimmune cells and Tregs in the perivascular space (60). It is also implicated in the retention of antiviral CD8+ T cells during LCMV infection (129). Similarly, CXCL12, the ligand for CXCR4, is constitutively expressed in the CNS on the basolateral surface of endothelial cells and is upregulated during neuronal inflammation, and the absence of CXCR4 signaling during EAE leads to perivascular accumulation of mononuclear cells in the spinal cord (130). These studies suggest that multiple chemokines regulate access from the perivascular space to the parenchyma.
Kinetics and behavioral analysis of lymphocytes within the brain parenchyma. Related to the themes of this review, CCR7 has an important role for T cell and dendritic cell recruitment to the lymph node, where its ligands CCL19 and CCL21 provide motogenic signals required for efficient T cell and dendritic cell migration (131, 132). It has been suggested that expression of CCL19 in the uninflamed parenchyma has a role in immune surveillance by CCR7+CD4+ memory T cells (56, 133), but this expression is elevated in MS lesions (56). CCL21 is also upregulated in other models of CNS inflammation (28), and whether these chemokines also provide motogenic signals in the parenchyma of the brain is unknown. Multiphoton microscopy of the spinal cord has been used to image the behavior of encephalitogenic cells within the white and grey matter during the induction of EAE (25, 74). A recent detailed study has pinpointed three distinct phases for encephalitogenic CD4+ T cell entry into the brain: (a) arresting to leptomeningeal vessels and scanning of the luminal surface against the blood flow; (b) diapedesis and scanning of the pial membrane for antigen being presented by perivascular macrophages; and (c) successful antigen-dependent activation of T cells, triggering effector capacity and resulting in tissue invasion (74). This study challenges the notion that the choroid plexus is the major route of cell entry during EAE and solidifies data suggesting an antigen-dependent mechanism. Following activation, during the initial disease process, myelin-specific cells enter the CNS in a rapid wave and can migrate deep into the parenchyma (134). These cells could be divided into two main populations based on migratory velocities (ranging from 6–25 μm/min). After entry into the perivascular space, many of the cells displayed a restrained or stationary phenotype, suggesting that they were forming long-term contacts with resident cells. This type of arrested behavior is associated with MHC/TCR interactions, although chemokines have also been implicated in mediating cell-cell interactions (135, 136). Nevertheless, transfer of myelin-specific (encephalitogenic) CD4+ T cells led to substantially more stationary cells in the brain than did the transfer of T cells not specific for CNS proteins (25). Somewhat unexpectedly, these studies revealed that T cell migration in this microenvironment was, at the population level, random, indicating that local migration was not regulated by chemokine gradients. Thus, although the arrest of encephalitogenic CD4+ T cells was antigen specific, their migration did not seem to be directional and was more like the random motility of naive T cells found in the lymph node (25).
In contrast to EAE induced by the transfer of autoimmune T cells and intracerebral injection of LCMV, a condition with well-defined localized acute inflammatory events, mice infected with T. gondii have provided a model of chronic CNS inflammation to study the behavior of pathogen-specific CD8+ T cells (28, 137). Unlike the rapid burst of infiltration during EAE, in this experimental system, there was a continuous recruitment of antigen-specific T cells that could be observed over a prolonged period of time (1–8 weeks) (28, 137). Various migratory behaviors including clustering and homotypic T cell interactions were observed. Slowing of CD8+ T cells and clustering of antigen-specific cells were seen around actively replicating parasites but not latent cysts (137). With no correlation between the amount of antigen present and the confinement ratio (or meandering index) of cells, the pattern of motility seemed to represent a “search and destroy mission” to find infected cells, rather than directional migration in response to a chemokine gradient.
Despite extensive investigations, we still have a limited understanding of exactly how chemokines and other chemotactic factors contribute to the migratory behavior of T cells, whether in meninges, CSF, or parenchyma. Since the initial studies describing the random behavior of T cell migration in the lymph node, it has been established that cells follow chemokine-coated conduits and thus remain “directed” (138). Previously, intravital imaging of peripheral lymph nodes indicated that naive T cells migrate at speeds greater than 10 μm/min and are guided by conduits formed by follicular dendritic cells, fibroblastic reticular cells, and stromal cells expressing the fibroblast marker ERTR7 (138). ERTR7+ cells have also been detected at distinct but confined areas of the brain (such as the meninges, vasculature, and sulci) during inflammation caused by LCMV (64) and T. gondii infection (28). There is little understanding of the role that ERTR7+ stromal cells have in the CNS, but it is tempting to speculate that these cells promote trafficking or retain migratory leukocytes in these distinct compartments of the brain.
While the presence of a haptotaxic mechanism of migration (i.e., migration in response to chemokine bound to matrix molecules) has given rise to the idea of random exploration, it has not excluded the role of soluble chemokine gradients, nor has it been shown that gradients exist in an immobilized fashion on stromal networks (139). However, this has led to investigations into the existence of similar networks in non-lymphoid organs. Indeed, the ECM in the CNS may have a similar role to that of the constitutive structures in the lymph node (28, 138). Inflammation in the brain and in the periphery induces the production of ECM molecules that are known to support cell migration in the context of neural development (140, 141). A proteomics study demonstrated the production of many ECM molecules by astrocytes (142), and increased expression of collagen and laminins associated with myelin-containing macrophages is present in perivascular lesions of patients with MS (143). The use of second harmonic generation signals during multi-photon microscopy led to the visualization of a reticular network of fibers in the inflamed brain that closely associated with migrating T cells (28). These fibers were not present in the brains or spinal cord of naive mice but were upregulated during T. gondii infection and following EAE induction. This network may be the functional equivalent of the fibroblastic reticular cell network in the lymph node (138) and might not only provide structural support for migration but also display bound chemotactic signals for directional migration of lymphocytes. This model needs to be rigorously tested, but it may explain how lymphocytes can reach migratory velocities in this dense tissue that are comparable to those of naive T cells within lymph nodes.
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