Run Yan , Liting Chen , Zimu Cai , Jiyao Tang , Yanlin Zhu , Yanping Li , Xuemin Wang , Yu Ruan , Qi Han
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引用次数: 0
摘要
线粒体对细胞的新陈代谢和存活至关重要,因为它们通过氧化磷酸化产生细胞的大部分 ATP,并调节细胞增殖和凋亡等关键过程。NIPSNAP 蛋白家族主要是线粒体基质蛋白。然而,NIPSNAPs(尤其是 NIPSNAP3A)的分子和细胞功能一直难以捉摸。在这里,我们证明了在 HeLa 细胞中敲除 NIPSNAP3A 可抑制其增殖和迁移,并减轻放线菌素 D(Act-D)诱导的细胞凋亡。这些发现表明,在 NIPSNAP3A 的介导下,细胞过程与线粒体功能之间存在着复杂的关系。进一步研究发现,敲除 NIPSNAP3A 不仅能通过减少 DRP1-S616 抑制线粒体分裂,还能抑制细胞凋亡中细胞色素 c 的释放。总之,我们的研究结果突显了 NIPSNAP3A 在协调细胞过程中的关键作用,这可能是通过其对线粒体动力学的影响实现的。
NIPSNAP3A regulates cellular homeostasis by modulating mitochondrial dynamics
Mitochondria are essential for cell metabolism and survival as they produce the majority of cellular ATP through oxidative phosphorylation as well as regulate critical processes such as cell proliferation and apoptosis. NIPSNAP family of proteins are predominantly mitochondrial matrix proteins. However, the molecular and cellular functions of the NIPSNAPs, particularly NIPSNAP3A, have remained elusive. Here, we demonstrated that NIPSNAP3A knockdown in HeLa cells inhibited their proliferation and migration and attenuated apoptosis induced by Actinomycin D (Act-D). These findings suggested a complex relationship between cellular processes and mitochondrial functions, mediated by NIPSNAP3A. Further investigations revealed that NIPSNAP3A knockdown not only inhibited mitochondrial fission through reduction of DRP1-S616, but also suppressed cytochrome c release in apoptosis. Collectively, our findings highlight the critical role of NIPSNAP3A in coordinating cellular processes, likely through its influence on mitochondrial dynamics.