A novel role for MAP1 LC3 in nonautophagic cytoplasmic vacuolation death of cancer cells

R. Kar, P. K. Singha, M. A. Venkatachalam, P. Saikumar

Research output: Contribution to journalArticlepeer-review

94 Scopus citations

Abstract

Thiol reactive cyclopentenone prostaglandin, 15-deoxy-Δ 12,14-prostaglandin J 2 (15d-PGJ2), induced a novel, nonapoptotic and microtubule-associated protein 1 light chain 3 (MAP1 LC3) dependent but nonautophagic form of cell death in colon, breast and prostate cancer cell lines, characterized by extensive cytoplasmic vacuolation with dilatation of endoplasmic reticulum (ER). Disruption of sulfhydryl homeostasis, which resulted in ER stress, accumulation of ubiquitinated proteins and subsequent ER dilation, contributed to peroxisome proliferator-activated receptor γ (PPARγ)-independent cell death by 15d-PGJ2. Absence of intracellular organelles in these vacuoles, shown by electron microscopy and unique fragmentation of lamin B, suggested this form of cell death to be different from autophagy and apoptosis. Cell death induced by 15d-PGJ2 is prevented by cycloheximide and actinomycin D, suggesting a requirement of new protein synthesis for death with cytoplasmic vacuolation. Here, we report for the first time that upregulation and processing of autophagy marker LC3 is an important event in nonautophagic cytoplasmic vacuolation and cell death. Notably, knockdown of LC3 conferred significant protection against 15d-PGJ2-induced cytoplasmic vacuolation and cell death, suggesting a novel role of LC3 in a death process other than autophagy.

Original languageEnglish (US)
Pages (from-to)2556-2568
Number of pages13
JournalOncogene
Volume28
Issue number28
DOIs
StatePublished - Jul 16 2009

Keywords

  • 15d-PGJ2
  • Cell death
  • Cytoplasmic vacuolation
  • ER stress
  • LC3
  • MAPK

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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