{"title":"评估中枢神经系统轴突再生","authors":"","doi":"10.1126/scisignal.1362002tw205","DOIUrl":null,"url":null,"abstract":"Neurons of the central nervous system (CNS) are much less able to repair themselves after damage than are neurons of the peripheral nervous system. The causes might lie with the differences in environment and type of surrounding glia, or with the neurons themselves. Goldberg et al. (see the Perspective by McKerracher and Ellezam) have isolated retinal ganglion cells, which form part of the CNS, from the rat to study their ability to regenerate axons. RGCs isolated from embryonic rats showed a much greater capability for axon regeneration than did RGCs from early postnatal rats. The diminishing capacity for axonal regeneration correlated with developmental times at which the RGC axons would normally have reached their targets and switched from axonal growth to dendrite elaboration. The switch in growth mode was not related to intrinsic cell age but rather arose from signals from neighboring retinal cells. J. L. Goldberg, M. P. Klassen, Y. Hua, B. A. Barres, Amacrine-signaled loss of intrinsic axon growth ability by retinal ganglion cells. Science 296, 1860-1864 (2002). [Abstract] [Full Text] L. McKerracher, B. Ellezam, Putting the brakes on regeneration. Science 296, 1819-1820 (2002). [Summary] [Full Text]","PeriodicalId":21619,"journal":{"name":"Science's STKE","volume":"51 1","pages":"TW205 - tw205"},"PeriodicalIF":0.0000,"publicationDate":"2002-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Assessing CNS Axon Regeneration\",\"authors\":\"\",\"doi\":\"10.1126/scisignal.1362002tw205\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Neurons of the central nervous system (CNS) are much less able to repair themselves after damage than are neurons of the peripheral nervous system. The causes might lie with the differences in environment and type of surrounding glia, or with the neurons themselves. Goldberg et al. (see the Perspective by McKerracher and Ellezam) have isolated retinal ganglion cells, which form part of the CNS, from the rat to study their ability to regenerate axons. RGCs isolated from embryonic rats showed a much greater capability for axon regeneration than did RGCs from early postnatal rats. The diminishing capacity for axonal regeneration correlated with developmental times at which the RGC axons would normally have reached their targets and switched from axonal growth to dendrite elaboration. The switch in growth mode was not related to intrinsic cell age but rather arose from signals from neighboring retinal cells. J. L. Goldberg, M. P. Klassen, Y. Hua, B. A. Barres, Amacrine-signaled loss of intrinsic axon growth ability by retinal ganglion cells. Science 296, 1860-1864 (2002). [Abstract] [Full Text] L. McKerracher, B. Ellezam, Putting the brakes on regeneration. Science 296, 1819-1820 (2002). [Summary] [Full Text]\",\"PeriodicalId\":21619,\"journal\":{\"name\":\"Science's STKE\",\"volume\":\"51 1\",\"pages\":\"TW205 - tw205\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-06-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science's STKE\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1126/scisignal.1362002tw205\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science's STKE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1126/scisignal.1362002tw205","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
中枢神经系统(CNS)的神经元在损伤后的自我修复能力远不如周围神经系统的神经元。原因可能与环境和周围胶质细胞类型的差异有关,也可能与神经元本身有关。Goldberg等人(见McKerracher和Ellezam的观点)从大鼠身上分离出构成中枢神经系统一部分的视网膜神经节细胞,以研究它们再生轴突的能力。从胚胎大鼠中分离的RGCs比从出生后早期大鼠中分离的RGCs具有更强的轴突再生能力。轴突再生能力的减弱与发育时间有关,在发育时间内,RGC轴突通常会达到其目标,并从轴突生长转变为树突发育。生长模式的转换与细胞固有年龄无关,而是由邻近视网膜细胞的信号引起的。黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明,黄晓明。科学296,1860-1864(2002)。[摘要]L. McKerracher, B. Ellezam。科学296,1819-1820(2002)。【摘要】【全文】
Neurons of the central nervous system (CNS) are much less able to repair themselves after damage than are neurons of the peripheral nervous system. The causes might lie with the differences in environment and type of surrounding glia, or with the neurons themselves. Goldberg et al. (see the Perspective by McKerracher and Ellezam) have isolated retinal ganglion cells, which form part of the CNS, from the rat to study their ability to regenerate axons. RGCs isolated from embryonic rats showed a much greater capability for axon regeneration than did RGCs from early postnatal rats. The diminishing capacity for axonal regeneration correlated with developmental times at which the RGC axons would normally have reached their targets and switched from axonal growth to dendrite elaboration. The switch in growth mode was not related to intrinsic cell age but rather arose from signals from neighboring retinal cells. J. L. Goldberg, M. P. Klassen, Y. Hua, B. A. Barres, Amacrine-signaled loss of intrinsic axon growth ability by retinal ganglion cells. Science 296, 1860-1864 (2002). [Abstract] [Full Text] L. McKerracher, B. Ellezam, Putting the brakes on regeneration. Science 296, 1819-1820 (2002). [Summary] [Full Text]