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共伴侣蛋白 Bag-1 通过与 Beclin 1 相互作用在自噬依赖性细胞存活中发挥作用。

Co-Chaperone Bag-1 Plays a Role in the Autophagy-Dependent Cell Survival through Beclin 1 Interaction.

机构信息

Molecular Biology, Genetics-Biotechnology, Graduate School of Science, Engineering and Technology, Istanbul Technical University, 34469 Istanbul, Turkey.

Department of Molecular Biology and Genetics, Istanbul Medeniyet University, 34720 Istanbul, Turkey.

出版信息

Molecules. 2021 Feb 6;26(4):854. doi: 10.3390/molecules26040854.

Abstract

Expression levels of the major mammalian autophagy regulator Beclin 1 and its interaction with Bcl-2 regulate the switch between autophagic cell survival and apoptotic cell death pathways. However, some of the regulators and the precise mechanisms of these processes still remain elusive. Bag-1 (Bcl-2 associated athanogene-1), a member of BAG family proteins, is a multifunctional pro-survival molecule that possesses critical functions in vital cellular pathways. Herein, we report the role of Bag-1 on Bcl-2/Beclin 1 crosstalk through indirectly interacting with Beclin 1. Pull-down experiments suggested a molecular interaction between Bag-1 and Beclin 1 in breast cancer cell lines. On the other hand, in vitro binding assays showed that Bag-1/Beclin 1 interaction does not occur directly but occurs through a mediator molecule. Bag-1 interaction with p-Beclin 1 (T119), indicator of early autophagy, is increased during nutrient starvation suggesting involvement of Bag-1 in the autophagic regulation. Furthermore, CRISPR/Cas9-mediated Bag-1 knock-out in MCF-7 cells hampered cell survival and proliferation and resulted in decreased levels of total LC3 under starvation. Collectively, we suggest that Bag-1 modulates cell survival/death decision through maintaining macroautophagy as a component of Beclin 1-associated complexes.

摘要

主要哺乳动物自噬调控因子 Beclin 1 的表达水平及其与 Bcl-2 的相互作用调节自噬细胞存活和凋亡细胞死亡途径之间的转换。然而,一些调节剂和这些过程的确切机制仍然难以捉摸。Bag-1(Bcl-2 相关抗凋亡基因-1)是 BAG 家族蛋白的成员,是一种多功能的促生存分子,在重要的细胞途径中具有关键功能。本文报告了 Bag-1 通过与 Beclin 1 间接相互作用对 Bcl-2/Beclin 1 串扰的作用。下拉实验表明在乳腺癌细胞系中存在 Bag-1 和 Beclin 1 之间的分子相互作用。另一方面,体外结合实验表明 Bag-1/Beclin 1 相互作用不是直接发生的,而是通过介体分子发生的。Bag-1 与 p-Beclin 1(T119)的相互作用增加,p-Beclin 1(T119)是早期自噬的标志物,在营养饥饿期间增加,表明 Bag-1 参与了自噬的调节。此外,CRISPR/Cas9 介导的 Bag-1 在 MCF-7 细胞中的敲除阻碍了细胞存活和增殖,并导致饥饿状态下总 LC3 水平降低。总之,我们认为 Bag-1 通过维持作为 Beclin 1 相关复合物一部分的巨自噬来调节细胞存活/死亡决定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdc/7914623/9207dc9e0773/molecules-26-00854-g001.jpg

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