Ribose 5-phosphate isomerase inhibits LC3 processing and basal autophagy

被引:18
|
作者
Heintze, Jacob [1 ]
Costa, Joana R. [1 ]
Weber, Melanie [1 ]
Ketteler, Robin [1 ]
机构
[1] UCL, MRC Lab Mol Cell Biol, Gower St, London WC1E 6BT, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
RPIA; Autophagy; CRISPR; Cas9; Pentose phosphate pathway; shRNA; AMINO-ACID STARVATION; PENTOSE-PHOSPHATE PATHWAY; RIBOSE-5-PHOSPHATE ISOMERASE; HUMAN-LYMPHOBLASTS; LIFE-SPAN; GLUCOSE DECREASES; PROGENITOR CELLS; ACETYL-COENZYME; OVARIAN-CANCER; EXPRESSION;
D O I
10.1016/j.cellsig.2016.06.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy and cellular metabolism are tightly linked processes, but how individual metabolic enzymes regulate the process of autophagy is not well understood. This study implicates ribose-5-phosphate isomerase (RPIA), a key regulator of the pentose phosphate pathway, in the control of autophagy. We used a dual gene deletion strategy, combining shRNA-mediated knockdown studies with CRISPR/Cas9 genome editing. Knockdown of RPIA by shRNA or genomic deletion by CRISPR/Cas9 genome editing, results in an increase of ATG4B-mediated LC3 processing and in the appearance of LC3-positive autophagosomes in cells. Increased LC3 processing upon knockdown of RPIA can be reversed by treatment with the antioxidant N-acetyl cysteine. The results are consistent with a model in which RPIA suppresses autophagy and LC3 processing by modulation of redox signaling. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:1380 / 1388
页数:9
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