학술논문

Caveolin-1 controls mitochondrial damage and ROS production by regulating fission - fusion dynamics and mitophagy
Document Type
article
Source
Subject
Biochemistry and Cell Biology
Biological Sciences
Cancer
Aetiology
2.1 Biological and endogenous factors
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Caveolin 1
Mitochondria
Mitochondrial Dynamics
Mitochondrial Proteins
Mitophagy
Reactive Oxygen Species
Cav-1
Mitochondrial dynamics
mtROS
Mitofusin 2
Dynamin-related protein 1
Medical Biochemistry and Metabolomics
Pharmacology and Pharmaceutical Sciences
Biochemistry and cell biology
Medicinal and biomolecular chemistry
Language
Abstract
As essential regulators of mitochondrial quality control, mitochondrial dynamics and mitophagy play key roles in maintenance of metabolic health and cellular homeostasis. Here we show that knockdown of the membrane-inserted scaffolding and structural protein caveolin-1 (Cav-1) and expression of tyrosine 14 phospho-defective Cav-1 mutant (Y14F), as opposed to phospho-mimicking Y14D, altered mitochondrial morphology, and increased mitochondrial matrix mixing, mitochondrial fusion and fission dynamics as well as mitophagy in MDA-MB-231 triple negative breast cancer cells. Further, we found that interaction of Cav-1 with mitochondrial fusion/fission machinery Mitofusin 2 (Mfn2) and Dynamin related protein 1 (Drp1) was enhanced by Y14D mutant indicating Cav-1 Y14 phosphorylation prevented Mfn2 and Drp1 translocation to mitochondria. Moreover, limiting mitochondrial recruitment of Mfn2 diminished formation of the PINK1/Mfn2/Parkin complex required for initiation of mitophagy resulting in accumulation of damaged mitochondria and ROS (mtROS). Thus, these studies indicate that phospho-Cav-1 may be an important switch mechanism in cancer cell survival which could lead to novel strategies for complementing cancer therapies.