Mts1 protein expression in the central nervous system after injury

瓦勒氏变性 生物 小胶质细胞 下调和上调 白质 星形胶质细胞 中枢神经系统 神经科学 脊髓 小脑 神经胶质 病变 前脑 病理 解剖 细胞生物学 炎症 免疫学 医学 生物化学 放射科 磁共振成像 基因
作者
Elena N. Kozlova,Eugene Lukanidin
出处
期刊:Glia [Wiley]
卷期号:37 (4): 337-348 被引量:40
标识
DOI:10.1002/glia.10045
摘要

Abstract We recently showed that Mts1 is expressed in white matter astrocytes in the rat brain and spinal cord from the first postnatal day. Its expression level declined in the adult CNS, but its topographical localization was maintained. Only white matter astrocytes in the cerebellum did not express Mts1. After dorsal root or sciatic nerve injury, we observed a marked upregulation of Mts1 in the area of the dorsal funiculus undergoing Wallerian degeneration. Here we show that upregulation of Mts1 is a consistent feature of astrocytes in white matter undergoing Wallerian degeneration. In addition, Mts1 is upregulated in astrocytes outlining the lesion site of a penetrating injury to the forebrain, or cerebellum. Gray matter astrocytes did not express Mts1, even after direct injury. In injured brain, we consistently noted a close relationship between Mts1‐expressing astrocytes and ED1‐positive microglia/macrophages, which are known to be highly motile cells. Mts1 was expressed in the periventricular area and the rostral migratory stream, i.e., sites of ongoing neuroplasticity in adulthood, and was upregulated in these areas after injury. These data suggest that Mts1‐expressing astrocytes play a significant role in degenerative events in the mature white matter, interact with phagocytic microglia/macrophages and regulate cell migration and differentiation in areas of the adult brain with a high degree of plasticity. GLIA 37:337–348, 2002. © 2002 Wiley‐Liss, Inc.

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