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p53‐mediated regulation of mitochondrial dynamics plays a pivotal role in the senescence of various normal cells as well as cancer cells
The FASEB Journal ( IF 4.4 ) Pub Date : 2021-01-12 , DOI: 10.1096/fj.202002007r
Young Yeon Kim 1, 2 , Jee-Hyun Um 1, 2 , Dong Jin Shin 1, 2, 3 , Dae Jin Jeong 1, 2, 3 , Young Bin Hong 1, 2, 3 , Jeanho Yun 1, 2, 3
Affiliation  

The tumor suppressor p53 is known as a critical mediator of many cellular processes, including cellular senescence, but its role in mitochondrial dynamics is not fully understood. We have previously shown that p53 regulates mitochondrial dynamics via the PKA-Drp1 pathway to induce cellular senescence. In this study, to further understand the role of p53-dependent regulation of mitochondrial dynamics, the effect of p53 expression on mitochondrial morphology was examined in various cancer cell lines and normal human cells. We found that p53 induced remarkable mitochondrial elongation and cellular senescence in various cancer cells regardless of their p53 status. p53 also induced mitochondrial elongation in various human primary normal cells, suggesting that p53-mediated mitochondrial elongation is a general phenomenon. Moreover, we found that p53 plays an essential role in mitochondrial elongation in H-Ras-induced cellular senescence and in the replicative senescence of normal human cells. Treatment with the MDM-2 antagonist Nutlin-3a also induced mitochondrial elongation through the PKA-Drp1 pathway in IMR90 normal human cells. Furthermore, the inhibition of PKA activity in late-passage normal cells significantly reduced both mitochondrial elongation and cellular senescence, suggesting that the p53-PKA pathway is essential for maintaining the senescence phenotype in normal cells. Together, these results further confirm the direct regulation of mitochondrial dynamics by p53 and the important role of p53-mediated mitochondrial elongation in cellular senescence.

中文翻译:

p53 介导的线粒体动力学调节在各种正常细胞和癌细胞的衰老中起关键作用

肿瘤抑制因子 p53 被认为是许多细胞过程(包括细胞衰老)的关键介质,但其在线粒体动力学中的作用尚不完全清楚。我们之前已经表明 p53 通过 PKA-Drp1 途径调节线粒体动力学以诱导细胞衰老。在这项研究中,为了进一步了解 p53 依赖性调节线粒体动力学的作用,在各种癌细胞系和正常人类细胞中检查了 p53 表达对线粒体形态的影响。我们发现 p53 在各种癌细胞中诱导显着的线粒体伸长和细胞衰老,而不管它们的 p53 状态如何。p53 还在各种人类原代正常细胞中诱导线粒体伸长,这表明 p53 介导的线粒体伸长是一种普遍现象。而且,我们发现 p53 在 H-Ras 诱导的细胞衰老和正常人类细胞的复制衰老中的线粒体伸长中起着重要作用。用 MDM-2 拮抗剂 Nutlin-3a 治疗还通过 IMR90 正常人类细胞中的 PKA-Drp1 途径诱导线粒体伸长。此外,晚期传代正常细胞中 PKA 活性的抑制显着降低了线粒体伸长和细胞衰老,表明 p53-PKA 途径对于维持正常细胞的衰老表型至关重要。总之,这些结果进一步证实了 p53 对线粒体动力学的直接调节以及 p53 介导的线粒体伸长在细胞衰老中的重要作用。
更新日期:2021-01-12
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