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NIPSNAP3A regulates cellular homeostasis by modulating mitochondrial dynamics.
- Source :
-
Gene [Gene] 2025 Jan 15; Vol. 933, pp. 148976. Date of Electronic Publication: 2024 Oct 01. - Publication Year :
- 2025
-
Abstract
- 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.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Humans
HeLa Cells
Mitochondrial Proteins genetics
Mitochondrial Proteins metabolism
Cell Movement genetics
Cytochromes c metabolism
Cytochromes c genetics
Dynamins metabolism
Dynamins genetics
Gene Knockdown Techniques
Dactinomycin pharmacology
Mitochondrial Dynamics
Apoptosis genetics
Cell Proliferation
Homeostasis
Mitochondria metabolism
Mitochondria genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0038
- Volume :
- 933
- Database :
- MEDLINE
- Journal :
- Gene
- Publication Type :
- Academic Journal
- Accession number :
- 39362349
- Full Text :
- https://doi.org/10.1016/j.gene.2024.148976