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保护性热休克因子 1 的促死亡信号:NOXA 的上调导致热敏细胞凋亡。

Pro-death signaling of cytoprotective heat shock factor 1: upregulation of NOXA leading to apoptosis in heat-sensitive cells.

机构信息

Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Wybrzeże Armii Krajowej 15, 44-102, Gliwice, Poland.

Department of Data Science and Engineering, The Silesian University of Technology, Akademicka 16, 44-100, Gliwice, Poland.

出版信息

Cell Death Differ. 2020 Jul;27(7):2280-2292. doi: 10.1038/s41418-020-0501-8. Epub 2020 Jan 29.

Abstract

Heat shock can induce either cytoprotective mechanisms or cell death. We found that in certain human and mouse cells, including spermatocytes, activated heat shock factor 1 (HSF1) binds to sequences located in the intron(s) of the PMAIP1 (NOXA) gene and upregulates its expression which induces apoptosis. Such a mode of PMAIP1 activation is not dependent on p53. Therefore, HSF1 not only can activate the expression of genes encoding cytoprotective heat shock proteins, which prevents apoptosis, but it can also positively regulate the proapoptotic PMAIP1 gene, which facilitates cell death. This could be the primary cause of hyperthermia-induced elimination of heat-sensitive cells, yet other pro-death mechanisms might also be involved.

摘要

热休克可以诱导细胞保护机制或细胞死亡。我们发现,在某些人类和小鼠细胞中,包括精母细胞,激活的热休克因子 1(HSF1)与位于 PMAIP1(NOXA)基因内含子中的序列结合,并上调其表达,从而诱导细胞凋亡。这种 PMAIP1 激活方式不依赖于 p53。因此,HSF1 不仅可以激活编码细胞保护热休克蛋白的基因的表达,防止细胞凋亡,还可以正向调节促凋亡的 PMAIP1 基因,促进细胞死亡。这可能是高热诱导热敏细胞消除的主要原因,但也可能涉及其他促死亡机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d9/7308270/c2bf13d44b83/41418_2020_501_Fig1_HTML.jpg

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