Drp1-dependent mitochondrial fission via MiD49/51 is essential for apoptotic cristae remodeling

Hidenori Otera, Non Miyata, Osamu Kuge, Katsuyoshi Mihara

研究成果: ジャーナルへの寄稿学術誌査読

177 被引用数 (Scopus)

抄録

Mitochondrial fission facilitates cytochrome c release from the intracristae space into the cytoplasm during intrinsic apoptosis, although how the mitochondrial fission factor Drp1 and its mitochondrial receptors Mff, MiD49, and MiD51 are involved in this reaction remains elusive. Here, we analyzed the functional division of these receptors with their knockout (KO) cell lines. In marked contrast to Mff-KO cells, MiD49/MiD51-KO and Drp1-KO cells completely resisted cristae remodeling and cytochrome c release during apoptosis. This phenotype in MiD49/51-KO cells, but not Drp1-KO cells, was completely abolished by treatments disrupting cristae structure such as OPA1 depletion. Unexpectedly, OPA1 oligomers generally thought to resist cytochrome c release by stabilizing the cristae structure were similarly disassembled in Drp1-KO and MiD49/51-KO cells, indicating that disassembly of OPA1 oligomers is not directly linked to cristae remodeling for cytochrome c release. Together, these results indicate that Drp1-dependent mitochondrial fission through MiD49/MiD51 regulates cristae remodeling during intrinsic apoptosis.

本文言語英語
ページ(範囲)531-544
ページ数14
ジャーナルJournal of Cell Biology
212
5
DOI
出版ステータス出版済み - 2016

!!!All Science Journal Classification (ASJC) codes

  • 細胞生物学

フィンガープリント

「Drp1-dependent mitochondrial fission via MiD49/51 is essential for apoptotic cristae remodeling」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル