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原癌基因bcl-2可选择性地挽救依赖神经营养因子的神经元免于凋亡。

The proto-oncogene bcl-2 can selectively rescue neurotrophic factor-dependent neurons from apoptosis.

作者信息

Allsopp T E, Wyatt S, Paterson H F, Davies A M

机构信息

School of Biological and Medical Sciences, St. Andrews, Fife, Scotland.

出版信息

Cell. 1993 Apr 23;73(2):295-307. doi: 10.1016/0092-8674(93)90230-n.

Abstract

Apoptosis plays an important role in regulating cell numbers in a wide variety of tissues during development. The product of the bcl-2 gene inhibits apoptosis in certain cells of the myeloid and lymphoid lineages and is expressed in many cells that have an extended life span. To assess the role of bcl-2 in neuronal apoptosis, we microinjected a bcl-2 expression vector into neurotrophic factor-deprived embryonic neurons. Sensory neurons that depend for survival on one or more members of the nerve growth factor family of neurotrophic factors (nerve growth factor, brain-derived neurotrophic factor, and neurotrophin-3) were rescued by bcl-2, whereas ciliary neurotrophic factor (CNTF)-dependent ciliary neurons were not. Sensory neurons, however, became refractory to bcl-2 after exposure to CNTF. These findings indicate that at least two death pathways operate in neurons that are distinguished by their susceptibility to bcl-2. Neurons may die by either pathway, depending on the factors to which they have been exposed.

摘要

在发育过程中,细胞凋亡在调节多种组织中的细胞数量方面发挥着重要作用。bcl - 2基因的产物可抑制髓系和淋巴系某些细胞中的细胞凋亡,并在许多寿命延长的细胞中表达。为了评估bcl - 2在神经元细胞凋亡中的作用,我们将bcl - 2表达载体显微注射到缺乏神经营养因子的胚胎神经元中。依赖神经生长因子家族(神经生长因子、脑源性神经营养因子和神经营养素 - 3)中一种或多种成员存活的感觉神经元可被bcl - 2拯救,而依赖睫状神经营养因子(CNTF)的睫状神经元则不能。然而,感觉神经元在暴露于CNTF后对bcl - 2变得不敏感。这些发现表明,至少有两条死亡途径在神经元中起作用,它们对bcl - 2的敏感性不同。神经元可能通过任何一条途径死亡,这取决于它们所接触的因子。

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