Volume 39 Number 2, March/April 2002
Pages 287 — 298
Cell transplantation of peripheral-myelin-forming cells to repair the injured spinal cordJeffery D. Kocsis, PhD; Yukinori Akiyama, MD, PhD; Karen L. Lankford, PhD; and Christine RadtkeDepartment of Neurology, Yale University School of Medicine, New Haven, CT, 06516, USA; Neuroscience Research Center, VA Medical Center, West Haven, CT, 06516, USAAbstract — Much excitement has been generated by recent work showing that a variety of myelin-forming cell types can elicit remyelination and facilitate axonal regeneration in animal models of demyelination and axonal transection. These cells include peripheral-myelin-forming cells, such as Schwann cells and olfactory ensheathing cells. In addition, progenitor cells derived from the subventricular zone of the brain and from bone marrow (BM) can form myelin when transplanted into demyelinated lesions in rodents. Here, we discuss recent findings that examine the remyelination potential of transplantation of peripheral-myelin-forming cells and progenitor cells derived from brain and bone marrow. Better understanding of the repair potential of these cells in animal models may offer exciting opportunities to develop cells that may be used in future clinical studies.
Key words: bone marrow, neural precursor cells, olfactory ensheathing cells, Schwann cells, spinal cord repair, transplantation.
This material is based on supported in part by Rehabilitation Research and Development Service of the Department of Veterans Affairs, the National Institutes of Health, and the National Multiple Sclerosis Society and the Myelin Project (Washington, DC).Address all correspondence and requests for reprints to Jeffery D. Kocsis, PhD, Department of Neurology, Yale University School of Medicine, Neuroscience Research Center (127A), VA Medical Center, West Haven, CT 06516; email: firstname.lastname@example.org.INTRODUCTION
Multiple sclerosis (MS) and contusive spinal cord injury both present variable amounts of axonal demyelination and transection. Currently, therapeutic approaches for both neurological disorders have limited efficacy. Recent advances in cell biology have led to the preparation of a number of cell types in culture that, upon transplantation, can remyelinate demyelinated axons and can encourage axonal regeneration. While axonal regeneration is very limited in the normal injured mammalian central nervous system (CNS), substantial axonal regeneration can occur in peripheral nerves under certain conditions. Part of this regenerative capacity of peripheral nerve has been linked to several unique properties of Schwann cells, including their production of extracellular matrix and trophic factors and their lack of growth inhibitory proteins that are present on oligodendrocytes (1). While Schwann cells normally only form myelin on peripheral nerve, they can remyelinate demyelinated axons in the CNS (2,3). Another cell type, olfactory ensheathing cell (OEC), which is located in olfactory nerves and outer layers of the olfactory bulb and normally do not form myelin, can do so when transplanted into the CNS (4,5). An interesting observation of both Schwann cells and olfactory ensheathing cells is that they can enhance axonal regeneration in the spinal cord when transplanted into axonal transection lesion sites (6-8). One practical difficulty with the potential use of either Schwann cells or olfactory ensheathing cells as an autologous cell therapy is the limitation of the number of cells that can be harvested. Recent work suggests that neural precursor cells derived from adult human subventricular zone and bone marrow (BM) cells both can form myelin when transplanted into the demyelinated spinal cord. A potential advantage of neural precursor cells is that they can be readily expanded in culture to increase cell number prior to transplantation. In the present review, we will discuss the potential of Schwann cells and olfactory ensheathing cells as cellular tools to remyelinate and to enhance axonal regeneration in the injured spinal cord, as well as the repair potential of cells derived from the adult human brain and BM, which can establish peripheral-like myelin in addition to central myelin when transplanted into the injured spinal cord.Transplantation of Schwann Cells to Remyelinate Spinal Cord
Transplantation of Schwann cells into the demyelinated rodent spinal cord results in anatomically defined myelination (2,9,10). Moreover, when anatomical repair is achieved, near normal conduction properties of the remyelinated axons ensue (3,5,11). Endogenous remyelination of CNS demyelinated axons by oligodendrocytes (12) or Schwann cells (2) results in the reestablishment of relatively normal impulse conduction in animal models of demyelination (13-15). However, endogenous remyelination is very limited in human diseases such as MS (16-18). Given the success of cell transplantation to form functional myelin in animal models, myelin-forming cell transplantation has been suggested as a potential repair strategy for demyelinated CNS axons (3,5,19,20).
Transplantation of glial cells obtained from the adult human brain failed to achieve remyelination of demyelinated rat axons in the CNS (21), while transplantation of human Schwann cells (11) and olfactory ensheathing cells (22,23) elicited remyelination of demyelinated rat axons in the CNS. Figure 1 shows low- and high-power micrographs of a rat demyelinated spinal cord 3 weeks after injection of reconstituted cryopreserved human Schwann cells. Note the relatively large number of myelinated axons with typical Schwann cell morphology, that is, large cytoplasmic and nuclear regions. Electron micrographs (not shown) reveal the presence of a basement membrane and extracellular collagen deposition (11). The conduction velocity of the axons remyelinated by the human Schwann cells was improved (see Figure 2), indicating that electrophysiological function of the remyelinated axons was restored.
Homologous or autologous tissue represents one possible source of Schwann cells for transplantation into patients with demyelinating disease. Presumably, Schwann cells are not antigenically predisposed to the immunological attack seen in MS as are oligodendrocytes. The demonstration of anatomical and electrophysiological repair of demyelinated axons by adult human Schwann cells and olfactory ensheathing cells is an important prerequisite for future consideration of these cells as candidates for autologous transplantation studies in humans.Transplantation of Olfactory Ensheathing Cells to Remyelinate Spinal Cord
OECs are unique cells that belong to the glial lineage and cannot be classified within any of the known glial populations, even though OECs belong to the glial lineage (24). OECs are an unusual population of cells, in that they share characteristics with both astrocytes in the CNS and Schwann cells in the peripheral nervous system (PNS) (24-27) and are the only glial cells known to cross the PNS-CNS transitional zone, accompanying the axons that they ensheath (28). In the normal nervous system, OECs surround or ensheath bundles of nonmyelinated axons in the olfactory nerve and do not form myelin. OECs share with Schwann cells the capability to support axonal ensheathment and regrowth (5,6,8,29-30), but they do not share the same developmental origin nor some immunocytochemical and morphological features of Schwann cells (24). The astrocyte-like characteristics of OECs include the expression of glial fibrillary acidic protein (GFAP), formation of the glial limitans at the PNS-CNS transitional zone, and end-feet at blood vessels (24,26). Although OECs and astrocytes share some phenotypic features, there are more differences than similarities between both cell types (24). They differ from each other in developmental origin, mode of association with axons, ultrastructure, and antigenic characteristics (24).
OEC tranplantation has several potential advantages to elicit remyelination within CNS compared to other glial types (4,5). First, OECs are easily cultured from the adult olfactory system in contrast to other glial cells from the mature CNS (29). Second, OECs can migrate through the adult CNS, cross the PNS-CNS transitional zone, and properly integrate within the CNS upon transplantation (29). A major obstacle to migration of myelin-forming glia in the CNS after damage is the so-called glial scar, which is predominantly formed by reactive astrocytes and microglia (31,32). OECs allow the regenerating axons to grow through known inhibitory substrates such as gliotic tissue (29), though neither CNS nor PNS axons are able to grow through this barrier (33). Thus, they might be able to navigate glial scars and remyelinate axons in the damaged CNS (29). Third, OECs are a source of neurotrophic factors, such as nerve growth factor, platelet-derived growth factor and neuropeptide Y (34-36), suggesting that trophic factor, production by OECs might enhance the survival of damaged axons. Recent work indicates that transplantation of both rodent and human (22,23) OECs can remyelinate demyelinated rat spinal cord axons (5,22,23).
The graphs in Figure 3 show dorsal column area, the demyelinating lesion area, and the number of myelinated axons in a control lesion (Figure 3a) and a lesion following transplantation of OECs at a single point in the longitudinal center of the lesion. Virtually no axons are myelinated in the control lesion, but myelinated axons can be found throughout the entire longitudinal dimension following OEC transplantation (Figure 3b). Similar results are obtained with Schwann cell transplantation where the donor cells were transfected with LacZ and identified in vivo (3). These data indicate that both OECs and Schwann cells are able to elicit relatively extensive peripheral-like myelination upon transplantation into a spinal cord demyelinating lesion. In the X-irradiation/ethidium bromide lesion model, no endogenous repair of the demyelinated lesion is observed before 6 to 8 weeks. In addition to identification of a reporter gene in some of the transplant studies, the observation of extensive remyelination at 3 weeks postlesion strongly suggests that the donor cells were responsible for the repair.
Neural Precursor Cells Derived from Adult Brain as Source of Peripheral-Myelin-Forming Cells
Multipotent neural precursor or stem cells are present in the mammalian CNS during development and in the adult brain (37-42). Neurospheres, clusters multipotent/progenitor cells, can be developed from neurogenic regions of the adult human brain (43,44). Neural precursor cells can be isolated and expanded in culture in the presence of mitogens, such as epidermal growth factor (EGF) or basic fibroblast growth factor (bFGF) (45-49). After withdrawal of the mitogens and with appropriate growth factors or substrates, these cells can differentiate into neurons or glia (43,50). When transplanted into the embryonic or neonatal CNS, both neurons (51,52) and oligodendrocytes (47,53) have been generated. These cells appear to differentiate and integrate into the host CNS because they form functional synapses (neurons) and myelinate (oligodendrocytes) axons. However, when injected into the normal adult CNS, stem cells differentiate primarily into astrocytes (54). These results indicate that environmental signals may direct the specification of cell lineage.
Multipotential neural progenitor cells derived from the fetal human brain propagate and differentiate in culture and in vivo (55-57). Progenitor cells from adult animals have been cultured from the subependymal zone (SEZ) (38,40,42,58), the subventricular zone (SVZ) (39), the hippocampus (37,41), and the spinal cord (48,59). A recent study suggested that ependymal cells may be a source of progenitor cells (58), but a GFAP-positive cell distinct from, but adjacent to, ependymal cells has been recently implicated as the primary neural progenitor cell type of the subventricular region (60). Although the precise cell type within the subventricular zone giving rise to neural precursor cells is still under investigation, it is clear that with appropriate culture and mitogen conditions, neural precursor cells can be developed and clonally expanded in culture.
While oligodendrocytes normally myelinate CNS axons, Schwann cells can remyelinate CNS axons after injury (14) and following transplantation into the demyelinated CNS (3,9). Schwann cells can be derived from single cell clones of neural crest cells (61). Mujtaba et al. have distinguished a common neural progenitor for the PNS and the CNS (59). They found that cultured neuroepithelial cells derived from embryonic rat spinal cords can differentiate into CNS precursors, giving rise to CNS neurons and glia, and into PNS precursors, which can differentiate into neural crest cells, giving rise to peripheral neurons, Schwann cells, and smooth muscle. Recently, Keirstead et al. demonstrated that immunoselected precursor cells from the neonatal rat forebrain expressing polysialyated (PSA) form of the neural cell adhesion molecule (NCAM), which mostly generates oligodendrocytes and astrocytes in vitro, can also produce peripheral myelin in vivo (62). This suggests that both peripheral and central myelin can be produced from neural precursor cells derived from the CNS.
To test the capability of neural precursor cells derived from the adult brain to differentiate into myelin-forming cells and repair the adult demyelinated CNS, we transplanted clonal neural progenitor cells derived from the adult human brain into an experimentally established glial-free zone in the dorsal columns of the rat spinal cord (44). Although these precursor cells differentiated upon mitogen withdrawal in culture into neurons and astrocytes-and to a lesser extent oligodendrocytes-when transplanted into a demyelinated glial-free zone of the adult rat spinal cord, they extensively remyelinated the axons and restored conduction velocity toward normal values (Figure 4). The majority of the myelinated axons displayed a peripheral pattern of myelination characterized by large nuclear and cytoplasmic regions of the myelin-forming cells surrounding the axons and a basement membrane. These data provide evidence that clonal neural precursor cells derived from the adult brain can elicit Schwann cells that form functional myelin when transplanted into an axon-enriched, glial-free environment of adult central white matter. Taken together these data suggest that a common neural progenitor cell for both the CNS and the PNS described for embryonic neuroepithelial cells (59) also may be present in the adult human brain. While our lesion model does not normally lead to the beginning of remyelination for 6 to 8 weeks-and we observed extensive remyelination at 3 weeks postlesion and transplantation-we cannot rule out that the cell transplantation may facilitate endogenous repair. We view this unlikely because of the nature of the lesion induction, but more efficient cell marking techniques will help resolve this issue in the future.
Bone Marrow as a Cell Source to Induce CNS Remyelination
Bone marrow stroll cells have recently been reported to differentiate into neurons and astrocytes in cell culture and into astrocytes when transplanted into normal and ischemic brain (63-65). Systemic (intravenous) application of a BM fraction into terminally X-irradiated rats results in neuronal phenotypes in brain, which were derived from the injected BM (66,67). These investigators have suggested that BM or isolated BM stromal cells, which can be harvested from a patient, may be useful for potential cell therapy approaches in neurological disease. Our preliminary work indicates that transplantation of an acutely isolated BM cell fraction (devoid of erythrocytes, platelets, and debris) into the demyelinated rat spinal cord results in relatively extensive remyelination (68). These results indicate that an acutely prepared BM cell fraction can develop a myelinating phenotype in vivo and anatomically repair demyelinated axons when injected into the spinal cord. This suggests the potential of developing an easily accessible and renewable source of autologous donor cells for cell transplantation studies in demyelinating disease.
Many of the myelinated axons induced by transplantation of BM cells are characteristic of peripheral myelin. While bone marrow-derived-peripheral-like myelinating cells have many similarities to Schwann cell myelination, a number of noted differences exist. In particular, the BM-induced remyelinating cells show larger and multilobular nuclei and larger cytoplasmic regions. In addition, while no Schwann cells were observed to engage more than one axon, some of the BM cells (2.7 percent) myelinated two to three adjacent axons. Interestingly, neural precursor cells and olfactory ensheathing cells transplanted into our lesion model show peripheral-like myelin and some of the features such as multilobular nuclei and multiple axonal myelination described here for BM cells (22,44). Given that both OECs and Schwann cells can remyelinate and encourage axonal regeneration of transected long tracts in the spinal cord, the peripheral-like differentiation of many of the BM cells may be advantageous for the development of a renewable and autologous source of cells for the treatment of spinal cord injury and demyelinating disorders.Cell Transplantation to Encourage Axonal Regeneration of Spinal Cord Tracts
Long tract axons in the mammalian spinal cord do not normally regenerate for an appreciable distance within the denervated host tract after they are transected. However, a number of experimental approaches have been reported to improve elongative regeneration of axons in the transected mammalian spinal cord. These include blockade of inhibitory proteins on glial cells and introduction of neurotrophic factor-enhanced peripheral nerve bridges (69,70). Recent attention has focused on transplants of cultured OECs into ablated corticospinal tract axons (6) and into nerve bridges in the spinal cord (7) to enhance regeneration. OECs have several unique properties that provide a rationale for their potential to enhance CNS axonal regeneration. They are specialized cells that support axons that leave the olfactory epithelium and project through the peripheral nervous system into the olfactory bulb of the CNS; they are pluripotential cells that can show Schwann cell or astrocyte-like cell properties (71,72). Interest has focused on these cells because olfactory epithelial neurons are continuously replaced and regenerate axons in the adult (72,73). It has been reasoned that the unique properties of OECs may allow them to guide and enhance regenerating CNS axons through a normally growth inhibitory environment (6,24).
OEC transplantation can enhance regeneration of transected spinal cord axons, improve forepaw reaching behavior, and remyelinate demyelinated axons in the spinal cord (4-6). Following transplantation of either OECs or Schwann cells into transected dorsal funiculus of the adult rat spinal cord, we found that the regenerating ascending sensory axons displayed stable conduction properties with regard to conduction velocity (Figure 5) and frequency-response properties (8,30). However, the conduction velocity of the regenerated axons was significantly greater than normal axons; morphological assessment of the regenerated axons indicates that they are myelinated with a peripheral pattern of myelin (Figure 6) and of a larger caliber than control axons (8). These results indicate that the regenerated spinal cord axons reconstitute electrophysiological function, an important requirement for an intervention therapy to enhance axonal regeneration after spinal cord injury, but there is a preferential regeneration of large myelinated and rapidly conducting axons. Therefore, while the number of regenerated axons induced by cell transplantation of OECs or Schwann cells is limited, a rapidly and securely conducting new information line is established which may contribute to the observed behavioral recovery of function.
Animal models of demyelination and axonal transection of the spinal cord indicate feasibility of cell transplantation as an approach to elicit at least some degree of functional recovery. One of the primary challenges to such therapies will be selecting the appropriate cell type and delivery method for the appropriate neurological condition. While oligodendrocytes normally form myelin in the CNS, the prospect of using Schwann cells to remyelinate CNS lesions in MS patients is intriguing because they can be harvesting autologously, and they may not have antigens present on oligodendrocytes that may be immunogenic. Yet the use of Schwann cells has limitations. One is that Schwann cell remyelination in the CNS does not precisely recapitulate the pattern of remyelination by oligodendroctyes. The density of axonal spacing is less with Schwann cell myelination, and one must ask what potential negative effects this could have on the system, such as a reduction in axon number. Indeed, it has been speculated that a selective force for the evolution of oligodendrocytes was to provide for maximum conduction velocity conferred by myelin deposition, with the most economic use of space. The advantage this organization achieves with oligodendrocyte myelination is a relatively compact CNS, but a disadvantage is that pathology to a single oligodendrocyte will effect a number of myelin segments. In spite of this limitation, it is reasoned that restoration of myelin and conduction in even a limited subset of axons could potentially result in significant functional recovery.
Another important concern with regard to cell transplantation therapies is the harvesting of sufficient numbers of cells for transplantation. While a number of cell types can be expanded in culture with trophic factors and mitogens, it is not clear if such expansion will alter the physiology of the cells in a way that impairs their capability to form functional myelin. Further studies to examine the myelinogenic potential of expanded cells will be required. Another concern with expanded cells is the potential risk of tumor formation. It will be absolutely essential to determine if experimental in vivo transplantation of expanded cells not only retain their capability to carry out neural repair but also do not form tumors. It is encouraging that expanded neural precursor cells derived from human subventricular zone and BM, as just reported, were able to form myelin in a rat model of demyelination and that no obvious tumor formation was observed.
Another concern is that cell-induced axonal regeneration and remyelination may not recapitulate uninjured structures but may establish new neuronal circuits and conduction channels. Such newly organized neural structures could be maladaptive and elicit neurological problems, such as inappropriate movement, pain, or paresthesae. An example of maladaptive plasticity has been well-characterized following peripheral nerve injury. A section of a peripheral nerve can result in dying back of C-fibers and A-delta fibers from the substantia gelatinosa with reoccupation of these synapses with A-beta fibers (74-77). Normally A-beta fibers are associated with nonnoxious mechanical inputs to the spinal cord and terminal in lamina III of the dorsal horn. It has been hypothesized that this aberrant regeneration of these fibers and new synapse formation may contribute to tactile allodynia, a condition that normally nonnoxious stimuli result in pain (74-77). Care must be taken to assure that new pathways and myelination elicited by interventional approaches such as cell transplantation do not result in maladaptive changes.
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