RETRACTED: Tissue-specific autophagy alterations and increased tumorigenesis in mice deficient in Atg4C/Autophagin-3 (Retracted article. See vol. 294, pg. 1435, 2019)

被引:322
作者
Marino, Guillermo
Salvador-Montoliu, Natalia
Fueyo, Antonio
Knecht, Erwin
Mizushima, Noboru
Lopez-Otin, Carlos [1 ]
机构
[1] Univ Oviedo, Inst Univ Oncol, Fac Med, Dept Bioquim & Biol Mol, E-33006 Oviedo, Spain
[2] Univ Oviedo, Inst Univ Oncol, Dept Biol Funct, E-33006 Oviedo, Spain
[3] Ctr Invest Prinipe Felipe, Lab Biol Celular, E-46013 Valencia, Spain
[4] Tokyo Metropolitan Inst Med Sci, Dept Bioregulat & Metab, Tokyo 1138613, Japan
[5] Tokyo Med & Dent Univ, Dept Physiol & Cell Biol, Tokyo 1138519, Japan
[6] Japan Sci & Technol Agcy, SORST, Kawguchi 3320012, Japan
关键词
D O I
10.1074/jbc.M701194200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atg4C/autophagin-3 is a member of a family of cysteine proteinases proposed to be involved in the processing and delipidation of the mammalian orthologues of yeast Atg8, an essential component of an ubiquitin-like modification system required for execution of autophagy. To date, the in vivo role of the different members of this family of proteinases remains unclear. To gain further insights into the functional relevance of Atg4 orthologues, we have generated mutant mice deficient in Atg4C/autophagin-3. These mice are viable and fertile and do not display any obvious abnormalities, indicating that they are able to develop the autophagic response required during the early neonatal period. However, Atg4C(-/-)-starved mice show a decreased autophagic activity in the diaphragm as assessed by immunoblotting studies and by fluorescence microscopic analysis of samples from Atg4C(-/-) GFP-LC3 transgenic mice. In addition, animals deficient in Atg4C show an increased susceptibility to develop fibrosarcomas induced by chemical carcinogens. Based on these results, we propose that Atg4C is not essential for autophagy development under normal conditions but is required for a proper autophagic response under stressful conditions such as prolonged starvation. We also propose that this enzyme could play an in vivo role in events associated with tumor progression.
引用
收藏
页码:18573 / 18583
页数:11
相关论文
共 66 条
[1]   Loss of collagenase-2 confers increased skin tumor susceptibility to male mice [J].
Balbín, M ;
Fueyo, A ;
Tester, AM ;
Pendás, AM ;
Pitiot, AS ;
Astudillo, A ;
Overall, CM ;
Shapiro, SD ;
López-Otín, C .
NATURE GENETICS, 2003, 35 (03) :252-257
[2]   Oncogenic kinase signalling [J].
Blume-Jensen, P ;
Hunter, T .
NATURE, 2001, 411 (6835) :355-365
[3]   Inhibition of mammalian target of rapamycin or apoptotic pathway induces autophagy and radiosensitizes PTEN null prostate cancer cells [J].
Cao, Carolyn ;
Subhawong, Ty ;
Albert, Jeffrey M. ;
Kim, Kwang Woon ;
Geng, Ling ;
Sekhar, Konjeti R. ;
Gi, Young Jin ;
Lu, Bo .
CANCER RESEARCH, 2006, 66 (20) :10040-10047
[4]   GABAA receptor associated proteins:: a key factor regulating GABAA receptor function [J].
Chen, Zi-Wei ;
Olsen, Richard W. .
JOURNAL OF NEUROCHEMISTRY, 2007, 100 (02) :279-294
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   DRAM, a p53-induced modulator of autophagy, is critical for apoptosis [J].
Crighton, Diane ;
Wilkinson, Simon ;
O'Prey, Jim ;
Syed, Nelofer ;
Smith, Paul ;
Harrison, Paul R. ;
Gasco, Milena ;
Garrone, Ornella ;
Crook, Tim ;
Ryan, Kevin M. .
CELL, 2006, 126 (01) :121-134
[7]   Autophagy: Many paths to the same end [J].
Cuervo, AM .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 263 (01) :55-72
[8]   Behavioral, neurochemical, and electrophysiological characterization of a genetic mouse model of depression [J].
El Yacoubi, M ;
Bouali, S ;
Popa, D ;
Naudon, L ;
Leroux-Nicollet, I ;
Hamon, M ;
Costentin, J ;
Adrien, J ;
Vaugeois, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :6227-6232
[9]   Conductance of recombinant GABAA channels is increased in cells co-expressing GABAA receptor-associated protein [J].
Everitt, AB ;
Luu, T ;
Cromer, B ;
Tierney, ML ;
Birnir, B ;
Olsen, RW ;
Gage, PW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (21) :21701-21706
[10]   The coordinate regulation of the p53 and rnTOR pathways in cells [J].
Feng, ZH ;
Zhang, H ;
Levine, AJ ;
Jin, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (23) :8204-8209