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Mcl-1 and Bcl-x L sequestration of Bak confers differential resistance to BH3-only proteins.

机译:Bak的MCL-1和BCL-X L螯合赋予差异抗性抗性抗性蛋白质。

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摘要

The prosurvival Bcl-2 family proteins Mcl-1 and Bcl-x_(L)inhibit apoptosis by sequestering BH3-only proteins such as Bid and Bim (MODE 1) or the effector proteins Bak and Bax (MODE 2). To better understand the contributions of MODE 1 and MODE 2 in blocking cell death, and thus how to bypass resistance to cell death, we examined prescribed mixtures of Bcl-2 family proteins. In a Bim and Bak mixture, Bcl-x_(L)and Mcl-1 each sequestered not only Bim but also Bak as it became activated by Bim. In contrast, in a Bid and Bak mixture, Bcl-x_(L)preferentially sequestered Bid while Mcl-1 preferentially sequestered Bak. Notably, Bcl-x_(L)could sequester Bak in response to the BH3 mimetic ABT-737, despite this molecule targeting Bcl-x_(L). These findings highlight the importance of Bak sequestration in resistance to anti-cancer treatments, including BH3 mimetics.
机译:脱抗华Bcl-2家族蛋白质蛋白Mcl-1和Bcl-X_(L)通过螯合BH3蛋白如BID和BIM(模式1)或效应蛋白Bak和Bax(模式2)来抑制细胞凋亡。 为了更好地了解模式1和模式2在阻断细胞死亡中的贡献,因此如何绕过细胞死亡,我们检查了Bcl-2家族蛋白的规定混合物。 在BIM和Bak混合物中,Bcl-X_(L)和MCL-1各自隔离不仅是BIM,而且因为它由BIM激活而产生。 相反,在BID和Bak混合物中,Bcl-X_(L)优先被隔离,而MCL-1优先被隔离Bak。 值得注意的是,尽管该分子靶向Bcl-X_(L),但Bcl-X_(L)可以响应BH3模拟ABT-737来响应BH3模拟ABT-737。 这些发现突出了BAK封存在抗癌治疗中的重要性,包括BH3模拟物。

著录项

  • 来源
    《Cell death and differentiation》 |2018年第4期|共14页
  • 作者单位

    The Walter and Eliza Hall Institute of Medical Research Parkville VIC;

    The Walter and Eliza Hall Institute of Medical Research Parkville VIC;

    The Walter and Eliza Hall Institute of Medical Research Parkville VIC;

    Olivia Newton-John Cancer Research Institute Heidelberg VIC;

    Olivia Newton-John Cancer Research Institute Heidelberg VIC;

    The Walter and Eliza Hall Institute of Medical Research Parkville VIC;

    The Walter and Eliza Hall Institute of Medical Research Parkville VIC 3052 Australia.;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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