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      Roles of ES Cell-Derived Gliogenic Neural Stem/Progenitor Cells in Functional Recovery after Spinal Cord Injury

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          Abstract

          Transplantation of neural stem/progenitor cells (NS/PCs) following the sub-acute phase of spinal cord injury (SCI) has been shown to promote functional recovery in rodent models. However, the types of cells most effective for treating SCI have not been clarified. Taking advantage of our recently established neurosphere-based culture system of ES cell-derived NS/PCs, in which primary neurospheres (PNS) and passaged secondary neurospheres (SNS) exhibit neurogenic and gliogenic potentials, respectively, here we examined the distinct effects of transplanting neurogenic and gliogenic NS/PCs on the functional recovery of a mouse model of SCI. ES cell-derived PNS and SNS transplanted 9 days after contusive injury at the Th10 level exhibited neurogenic and gliogenic differentiation tendencies, respectively, similar to those seen in vitro. Interestingly, transplantation of the gliogenic SNS, but not the neurogenic PNS, promoted axonal growth, remyelination, and angiogenesis, and resulted in significant locomotor functional recovery after SCI. These findings suggest that gliogenic NS/PCs are effective for promoting the recovery from SCI, and provide essential insight into the mechanisms through which cellular transplantation leads to functional improvement after SCI.

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          Most cited references36

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          Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain.

          Reactive gliosis is the universal reaction to brain injury, but the precise origin and subsequent fate of the glial cells reacting to injury are unknown. Astrocytes react to injury by hypertrophy and up-regulation of the glial-fibrillary acidic protein (GFAP). Whereas mature astrocytes do not normally divide, a subpopulation of the reactive GFAP(+) cells does so, prompting the question of whether the proliferating GFAP(+) cells arise from endogenous glial progenitors or from mature astrocytes that start to proliferate in response to brain injury. Here we show by genetic fate mapping and cell type-specific viral targeting that quiescent astrocytes start to proliferate after stab wound injury and contribute to the reactive gliosis and proliferating GFAP(+) cells. These proliferating astrocytes remain within their lineage in vivo, while a more favorable environment in vitro revealed their multipotency and capacity for self-renewal. Conversely, progenitors present in the adult mouse cerebral cortex labeled by NG2 or the receptor for the platelet-derived growth factor (PDGFRalpha) did not form neurospheres after (or before) brain injury. Taken together, the first fate-mapping analysis of astrocytes in the adult mouse cerebral cortex shows that some astrocytes acquire stem cell properties after injury and hence may provide a promising cell type to initiate repair after brain injury.
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            HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells.

            Embryonal stem (ES) cell lines, established in culture from peri-implantation mouse blastocysts, can colonize both the somatic and germ-cell lineages of chimaeric mice following injection into host blastocysts. Recently, ES cells with multiple integrations of retroviral sequences have been used to introduce these sequences into the germ-line of chimaeric mice, demonstrating an alternative to the microinjection of fertilized eggs for the production of transgenic mice. However, the properties of ES cells raise a unique possibility: that of using the techniques of somatic cell genetics to select cells with genetic modifications such as recessive mutations, and of introducing these mutations into the mouse germ line. Here we report the realization of this possibility by the selection in vitro of variant ES cells deficient in hypoxanthine guanine phosphoribosyl transferase (HPRT; EC 2.4.2.8), their use to produce germline chimaeras resulting in female offspring heterozygous for HPRT-deficiency, and the generation of HPRT-deficient preimplantation embryos from these females. In human males, HPRT deficiency causes Lesch-Nyhan syndrome, which is characterized by mental retardation and self-mutilation.
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              Human neural stem cells differentiate and promote locomotor recovery in spinal cord-injured mice.

              We report that prospectively isolated, human CNS stem cells grown as neurospheres (hCNS-SCns) survive, migrate, and express differentiation markers for neurons and oligodendrocytes after long-term engraftment in spinal cord-injured NOD-scid mice. hCNS-SCns engraftment was associated with locomotor recovery, an observation that was abolished by selective ablation of engrafted cells by diphtheria toxin. Remyelination by hCNS-SCns was found in both the spinal cord injury NOD-scid model and myelin-deficient shiverer mice. Moreover, electron microscopic evidence consistent with synapse formation between hCNS-SCns and mouse host neurons was observed. Glial fibrillary acidic protein-positive astrocytic differentiation was rare, and hCNS-SCns did not appear to contribute to the scar. These data suggest that hCNS-SCns may possess therapeutic potential for CNS injury and disease.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2009
                6 November 2009
                : 4
                : 11
                : e7706
                Affiliations
                [1 ]Department of Physiology, Keio University School of Medicine, Tokyo, Japan
                [2 ]Department of Orthopedic Surgery, Keio University School of Medicine, Tokyo, Japan
                [3 ]Department of Orthopedic Surgery, Hirosaki University Graduate School of Medicine, Hirosaki, Japan
                [4 ]Department of Neurology, Graduate School of Medicine, Nagoya University, Nagoya, Japan
                [5 ]Kanrinmaru Project, Keio University School of Medicine, Tokyo, Japan
                [6 ]Department of Rehabilitation Medicine, Keio University School of Medicine, Tokyo, Japan
                [7 ]Department of Research Super Star Program Stem Cell Unit, Graduate School of Medical Science, Kyusyu University, Fukuoka, Japan
                Chiba University Center for Forensic Mental Health, Japan
                Author notes

                Conceived and designed the experiments: GK YO YT MN HO. Performed the experiments: GK YO JY NN KK MM OT KF HK SS. Analyzed the data: GK MN. Contributed reagents/materials/analysis tools: GK YO SO SS YM ST MN HO. Wrote the paper: GK YO HK MN HO.

                Article
                09-PONE-RA-12322R1
                10.1371/journal.pone.0007706
                2768792
                19893739
                f9c41e5f-77ad-4247-8288-8b13f7788a46
                Kumagai et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 18 August 2009
                : 9 October 2009
                Page count
                Pages: 13
                Categories
                Research Article
                Cell Biology/Neuronal and Glial Cell Biology
                Neuroscience/Neurobiology of Disease and Regeneration
                Neuroscience/Neuronal and Glial Cell Biology
                Neurological Disorders/Spinal Disorders

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                Uncategorized

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