4.5 Article

miR-29a differentially regulates cell survival in astrocytes from cornu ammonis 1 and dentate gyrus by targeting VDAC1

期刊

MITOCHONDRION
卷 30, 期 -, 页码 248-254

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.mito.2016.08.013

关键词

Glia; MicroRNA; Brain; Glucose deprivation; Ischemia; Stroke; Hippocampus; Mitochondria

资金

  1. American Heart Association [14FTF-19970029]
  2. National Institutes of Health [R01 NS084396, R01 NS053898, R01 NS 080177]

向作者/读者索取更多资源

Neurons in the corn ammonis 1 (CM) region of the hippocampus are vulnerable to cerebral ischemia, while dentate gyrus (DG) neurons are more resistant. This effect is mediated by local astrocytes, and may reflect differences in subregional hippocampal expression of miR-29a. We investigated the role of miR-29a on survival of hippocampal astrocytes cultured selectively from CA1 and DG in response to glucose deprivation (GD). CA1 astrocytes exhibited more cell death and a greater decrease in miR-29a than DG astrocytes. A reciprocal change was observed in the mitochondrial voltage dependent cation channel-1 (VDAC1), a regulator of mitochondria and target of miR-29a. In CM astrocytes, increasing miR-29a decreased VDAC1 and improved cell survival, while knockdown of VDAC1 improved survival. Finally, the protective effect of miR-29a was eliminated by inhibition of miR-29a/VDAC1 binding. These findings suggest that the selective vulnerability of the CM to injury may be due in part to a limited miR-29a response in CA1 astrocytes, allowing a greater increase in VDAC1-mediated cellular dysfunction in CA1 astrocytes. (C) 2016 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

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