Transient assembly of F-actin on the outer mitochondrial membrane contributes to mitochondrial fission

Author:

Li Sunan11,Xu Shan11,Roelofs Brian A.11,Boyman Liron11,Lederer W. Jonathan11,Sesaki Hiromi2,Karbowski Mariusz11

Affiliation:

1. Center for Biomedical Engineering and Technology, Department of Biochemistry and Molecular Biology, and Department of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201

2. Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205

Abstract

In addition to established membrane remodeling roles in various cellular locations, actin has recently emerged as a participant in mitochondrial fission. However, the underlying mechanisms of its participation remain largely unknown. We report that transient de novo F-actin assembly on the mitochondria occurs upon induction of mitochondrial fission and F-actin accumulates on the mitochondria without forming detectable submitochondrial foci. Impairing mitochondrial division through Drp1 knockout or inhibition prolonged the time of mitochondrial accumulation of F-actin and also led to abnormal mitochondrial accumulation of the actin regulatory factors cortactin, cofilin, and Arp2/3 complexes, suggesting that disassembly of mitochondrial F-actin depends on Drp1 activity. Furthermore, down-regulation of actin regulatory proteins led to elongation of mitochondria, associated with mitochondrial accumulation of Drp1. In addition, depletion of cortactin inhibited Mfn2 down-regulation– or FCCP-induced mitochondrial fragmentation. These data indicate that the dynamic assembly and disassembly of F-actin on the mitochondria participates in Drp1-mediated mitochondrial fission.

Publisher

Rockefeller University Press

Subject

Cell Biology

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