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少突胶质细胞谱系中的细胞死亡与细胞存活调控

Cell death and control of cell survival in the oligodendrocyte lineage.

作者信息

Barres B A, Hart I K, Coles H S, Burne J F, Voyvodic J T, Richardson W D, Raff M C

机构信息

Medical Research Council Developmental Neurobiology Programme, University College, London, England.

出版信息

Cell. 1992 Jul 10;70(1):31-46. doi: 10.1016/0092-8674(92)90531-g.

Abstract

Dead cells are observed in many developing animal tissues, but the causes of these normal cell deaths are mostly unknown. We show that about 50% of oligodendrocytes normally die in the developing rat optic nerve, apparently as a result of a competition for limiting amounts of survival signals. Both platelet-derived growth factor and insulin-like growth factors are survival factors for newly formed oligodendrocytes and their precursors in culture. Increasing platelet-derived growth factor in the developing optic nerve decreases normal oligodendrocyte death by up to 90% and doubles the number of oligodendrocytes in 4 days. These results suggest that a requirement for survival signals is more general than previously thought and that some normal cell deaths in nonneural tissues may also reflect competition for survival factors.

摘要

在许多发育中的动物组织中都观察到了死亡细胞,但这些正常细胞死亡的原因大多未知。我们发现,在发育中的大鼠视神经中,约50%的少突胶质细胞会正常死亡,这显然是由于对有限数量生存信号的竞争所致。血小板衍生生长因子和胰岛素样生长因子都是培养中新形成的少突胶质细胞及其前体细胞的生存因子。在发育中的视神经中增加血小板衍生生长因子可使正常少突胶质细胞死亡减少多达90%,并在4天内使少突胶质细胞数量增加一倍。这些结果表明,对生存信号的需求比以前认为的更为普遍,并且非神经组织中的一些正常细胞死亡也可能反映了对生存因子的竞争。

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