4.6 Article

AIF promotes a JNK1-mediated cadherin switch independently of respiratory chain stabilization

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 293, Issue 38, Pages 14707-14722

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.RA118.004022

Keywords

mitochondria; metabolism; oxidative stress; cancer; cell signaling; epithelial-mesenchymal transition (EMT); MAPK

Funding

  1. North Dakota State University Center for Diagnostic and Therapeutic Strategies in Pancreatic Cancer under National Institutes of Health COBRE Program [1P20GM109024]
  2. State of North Dakota Experimental Program to Stimulate Competitive Research Grant ND-EPSCoR Project [FAR0022246]
  3. Department of Defense Prostate Cancer Research Program [W81XWH-08-1-0045]
  4. American Cancer Society [RSG-09-166-01-CCG]
  5. National Institutes of Health [1R15CA206067-01]

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Apoptosis-inducing factor (AIF) is a mitochondrial flavoprotein occasionally involved in cell death that primarily regulates mitochondrial energy metabolism under normal cellular conditions. AIF catalyzes the oxidation of NADH in vitro, yet the significance of this redox activity in cells remains unclear. Here, we show that through its enzymatic activity AIF is a critical factor for oxidative stress-induced activation of the mitogen-activated protein kinases JNK1 (c-Jun N-terminal kinase), p38, and ERK (extracellular signal-regulated kinase). AIF-dependent JNK1 signaling culminates in the cadherin switch, and genetic reversal of this switch leads to apoptosis when AIF is suppressed. Notably, this widespread ability of AIF to promote JNK signaling can be uncoupled from its more limited role in respiratory chain stabilization. Thus, AIF is a transmitter of extra-mitochondrial signaling cues with important implications for human development and disease.

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