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野生型gas3/PMP22过表达诱导的凋亡表型:其与脱髓鞘性周围神经病CMT1A的关系。

Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A.

作者信息

Fabbretti E, Edomi P, Brancolini C, Schneider C

机构信息

Laboratorio Nazionale Consorzio Interuniversitario Biotecnologie, Trieste, Italy.

出版信息

Genes Dev. 1995 Aug 1;9(15):1846-56. doi: 10.1101/gad.9.15.1846.

Abstract

Although the Gas3/PMP22 protein is expressed at highest levels in differentiated Schwann cells, its presence, albeit at lower levels, in non-neuronal tissues and in NIH-3T3 growth-arrested fibroblasts argues for a more general function of this protein that is uncoupled to myelin structure. We show that gas3/PMP22 overexpression in NIH-3T3 growing cells leads to an apoptotic-like phenotype, which is suppressed by antioxidants and characterized by typical membrane blebbing, rounding up, and chromatin condensation, but with no evidence of DNA fragmentation. REF-52 fibroblasts seem to be completely refractive to gas3/PMP22 overexpression. Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy. When gas3/PMP22 point mutations (L16P, S79C, T118M, and G150D) are similarly overexpressed in NIH-3T3 cells, the induced apoptotic-like phenotype as compared to the wild-type is significantly reduced. Both of the dominant mutations (L16P, S79C) for CMT1A behave as dominant negatives with respect to the wild type, whereas T118M, the only recessive mutant described, behaves as recessive under the same coexpression experiments. These data suggest a role for altered Schwann cell apoptosis in the pathogenesis of CMT1A.

摘要

尽管Gas3/PMP22蛋白在分化的施万细胞中表达水平最高,但其在非神经组织和处于生长停滞状态的NIH-3T3成纤维细胞中也有表达,尽管水平较低,这表明该蛋白具有更广泛的功能,与髓鞘结构无关。我们发现,在生长的NIH-3T3细胞中过表达gas3/PMP22会导致类似凋亡的表型,抗氧化剂可抑制这种表型,其特征为典型的膜泡形成、细胞变圆和染色质浓缩,但没有DNA片段化的证据。REF-52成纤维细胞似乎对gas3/PMP22过表达完全不敏感。最近,人类gas3/PMP22基因的几个点突变与1A型夏科-马里-图斯病(CMT1A)相关,CMT1A是一种常见的遗传性脱髓鞘性神经病。当gas3/PMP22点突变(L16P、S79C、T118M和G150D)在NIH-3T3细胞中同样过表达时,与野生型相比,诱导的类似凋亡的表型明显减少。CMT1A的两个显性突变(L16P、S79C)相对于野生型表现为显性负性,而唯一描述的隐性突变T118M在相同的共表达实验中表现为隐性。这些数据表明施万细胞凋亡改变在CMT1A发病机制中起作用。

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