Loss of macroautophagy promotes or prevents fibroblast apoptosis depending on the death stimulus

Yongjun Wang, Rajat Singh, Ashish C. Massey, Saul S. Kane, Susmita Kaushik, Taneisha Grant, Youqing Xiang, Ana Maria Cuervo, Mark J. Czaja

Research output: Contribution to journalArticle

112 Citations (Scopus)

Abstract

Macroautophagy has been implicated as a mechanism of cell death. However, the relationship between this degradative pathway and cell death is unclear as macroautophagy has been shown recently to protect against apoptosis. To better define the interplay between these two critical cellular processes, we determined whether inhibition of macroautophagy could have both pro-apoptotic and anti-apoptotic effects in the same cell. Embryonic fibroblasts from mice with a knock-out of the essential macroautophagy gene atg5 were treated with activators of the extrinsic and intrinsic death pathways. Loss of macroautophagy sensitized these cells to caspase-dependent apoptosis from the death receptor ligands Fas and tumor necrosis factor-α (TNF-α). Atg5-/- mouse embryonic fibroblasts had increased activation of the mitochondrial death pathway in response to Fas/TNF-α in concert with decreased ATP levels. Fas/TNF-α treatment failed to up-regulate macroautophagy, and in fact, decreased activity at late time points. In contrast to their sensitization to Fas/TNF-α, Atg5-/- cells were resistant to death from menadione and UV light. In the absence of macroautophagy, an up-regulation of chaperone-mediated autophagy induced resistance to these stressors. These results demonstrate that inhibition of macroautophagy can promote or prevent apoptosis in the same cell and that the response is governed by the nature of the death stimulus and compensatory changes in other forms of autophagy. Experimental findings that an inhibition of macroautophagy blocks apoptosis do not prove that autophagy mediates cell death as this effect may result from the protective up-regulation of other autophagic pathways such as chaperone-mediated autophagy.

Original languageEnglish (US)
Pages (from-to)4766-4777
Number of pages12
JournalJournal of Biological Chemistry
Volume283
Issue number8
DOIs
StatePublished - Feb 22 2008

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Autophagy
Fibroblasts
Cell death
Tumor Necrosis Factor-alpha
Apoptosis
Vitamin K 3
Death Domain Receptors
Fas Ligand Protein
Caspases
Ultraviolet radiation
Genes
Adenosine Triphosphate
Chemical activation
Cell Death
Up-Regulation
Essential Genes
Ultraviolet Rays

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Loss of macroautophagy promotes or prevents fibroblast apoptosis depending on the death stimulus. / Wang, Yongjun; Singh, Rajat; Massey, Ashish C.; Kane, Saul S.; Kaushik, Susmita; Grant, Taneisha; Xiang, Youqing; Cuervo, Ana Maria; Czaja, Mark J.

In: Journal of Biological Chemistry, Vol. 283, No. 8, 22.02.2008, p. 4766-4777.

Research output: Contribution to journalArticle

Wang, Yongjun ; Singh, Rajat ; Massey, Ashish C. ; Kane, Saul S. ; Kaushik, Susmita ; Grant, Taneisha ; Xiang, Youqing ; Cuervo, Ana Maria ; Czaja, Mark J. / Loss of macroautophagy promotes or prevents fibroblast apoptosis depending on the death stimulus. In: Journal of Biological Chemistry. 2008 ; Vol. 283, No. 8. pp. 4766-4777.
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