Mevalonate Pathway-mediated ER Homeostasis Is Required for Haploid Stability in Human Somatic Cells.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2021-02-19 Epub Date: 2020-12-22 DOI:10.1247/csf.20055
Kan Yaguchi, Kimino Sato, Koya Yoshizawa, Daisuke Mikami, Kohei Yuyama, Yasuyuki Igarashi, Gabor Banhegyi, Eva Margittai, Ryota Uehara
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引用次数: 0

Abstract

The somatic haploidy is unstable in diplontic animals, but cellular processes determining haploid stability remain elusive. Here, we found that inhibition of mevalonate pathway by pitavastatin, a widely used cholesterol-lowering drug, drastically destabilized the haploid state in HAP1 cells. Interestingly, cholesterol supplementation did not restore haploid stability in pitavastatin-treated cells, and cholesterol inhibitor U18666A did not phenocopy haploid destabilization. These results ruled out the involvement of cholesterol in haploid stability. Besides cholesterol perturbation, pitavastatin induced endoplasmic reticulum (ER) stress, the suppression of which by a chemical chaperon significantly restored haploid stability in pitavastatin-treated cells. Our data demonstrate the involvement of the mevalonate pathway in the stability of the haploid state in human somatic cells through managing ER stress, highlighting a novel link between ploidy and ER homeostatic control.Key words: haploid, ER stress, Mevalonate pathway.

人类体细胞单倍体稳定性需要甲羟戊酸途径介导的ER平衡
体细胞单倍体在外交动物中是不稳定的,但决定单倍体稳定性的细胞过程仍然难以捉摸。在这里,我们发现吡伐他汀(一种广泛使用的降胆固醇药物)对甲羟戊酸途径的抑制,极大地破坏了HAP1细胞的单倍体状态。有趣的是,在匹伐他汀处理的细胞中,补充胆固醇并没有恢复单倍体的稳定性,胆固醇抑制剂U18666A也没有引起单倍体的失稳。这些结果排除了胆固醇对单倍体稳定性的影响。除了胆固醇扰动外,匹伐他汀还诱导内质网(ER)应激,通过化学伴侣子抑制内质网应激可显著恢复匹伐他汀处理细胞的单倍体稳定性。我们的数据表明甲羟戊酸途径通过管理内质网应激参与了人类体细胞单倍体状态的稳定性,突出了倍性和内质网稳态控制之间的新联系。关键词:单倍体,内质网应激,甲羟戊酸途径
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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