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Autophagy promotes T-cell survival through degradation of proteins of the cell death machinery

  • J. R. Kovacs
  • , C. Li
  • , Q. Yang
  • , G. Li
  • , I. G. Garcia
  • , S. Ju
  • , D. G. Roodman
  • , J. J. Windle
  • , X. Zhang
  • , B. Lu
  • University of Pittsburgh
  • Guangdong Medical College
  • Soochow University
  • Virginia Commonwealth University

Research output: Contribution to journal › Article › peer-review

204 Scopus citations

Abstract

Autophagy is implicated in regulating cell death in activated T cells, but the underlying mechanism is unclear. Here, we show that inhibition of autophagy via Beclin 1 gene deletion in T cells leads to rampant apoptosis in these cells upon TCR stimulation. Beclin 1-deficient mice fail to mount autoreactive T-cell responses and are resistant to experimental autoimmune encephalomyelitis. Compared with Th17 cells, Th1 cells are much more susceptible to cell death upon Beclin 1 deletion. Cell death proteins are highly increased in Beclin 1-deficient T cells and inhibition of caspases and genetic deletion of Bim reverse apoptosis. In addition, p62/sequestosome 1 binds to caspase-8 but does not control levels of procaspase-8 or other cell death-related proteins. These results establish a direct role of autophagy in inhibiting the programmed cell death through degradation of apoptosis proteins in activated T cells.

Original languageEnglish
Pages (from-to)144-152
Number of pages9
JournalCell Death and Differentiation
Volume19
Issue number1
DOIs
StatePublished - Jan 2012

Keywords

  • Beclin 1
  • T cell
  • Th1 cell
  • apoptosis
  • autophagy
  • caspase

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