Suppression of MAPK/JNK-MTORC1 signaling leads to premature loss of organelles and nuclei by autophagy during terminal differentiation of lens fiber cells

被引:106
作者
Basu, Subhasree [1 ]
Rajakaruna, Suren [1 ]
Reyes, Beverly [2 ]
Van Bockstaele, Elisabeth [2 ]
Menko, A. Sue [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Farber Inst Neurosci, Dept Neurosci, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
autophagy; mechanistic target of rapamycin; MAPK/JNK (mitogen-activated protein kinase/c-Jun N-terminal kinase); RAPTOR; organelles; signal transduction; cell development; cell maturation; lens; organelle-free zone formation; ENDOPLASMIC-RETICULUM; MAMMALIAN TARGET; JNK1-MEDIATED PHOSPHORYLATION; ALPHA-6; INTEGRIN; COMPLEX; PROTEIN; RAPTOR; DEGRADATION; INHIBITION; INDUCTION;
D O I
10.4161/auto.28768
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although autophagic pathways are essential to developmental processes, many questions still remain regarding the initiation signals that regulate autophagy in the context of differentiation. To address these questions we studied the ocular lens, as the programmed elimination of nuclei and organelles occurs in a precisely regulated spatiotemporal manner to form the organelle-free zone (OFZ), a characteristic essential for vision acuity. Here, we report our discovery that inactivation of MAPK/JNK induces autophagy for formation of the OFZ through its regulation of MTORC1, where MAPK/ JNK signaling is required for both MTOR activation and RPTOR/RAPTOR phosphorylation. Autophagy pathway proteins including ULK1, BEC N1/Beclin 1, and MAP1LC3B2/LC3B-II were upregulated in the presence of inhibitors to either MAPK/ JNK or MTOR, inducing autophagic loss of organelles to form the OFZ. These results reveal that MAPK/JNK is a positive regulator of MTORC1 signaling and its developmentally regulated inactivation provides an inducing signal for the coordinated autophagic removal of nuclei and organelles required for lens function.
引用
收藏
页码:1193 / 1211
页数:19
相关论文
共 95 条
[1]   58K, a microtubule-binding golgi protein, is a formiminotransferase cyclodeaminase [J].
Bashour, AM ;
Bloom, GS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (31) :19612-19617
[2]   Lens organelle degradation [J].
Bassnett, S .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (01) :1-6
[3]  
BASSNETT S, 1995, INVEST OPHTH VIS SCI, V36, P1793
[4]   On the mechanism of organelle degradation in the vertebrate lens [J].
Bassnett, Steven .
EXPERIMENTAL EYE RESEARCH, 2009, 88 (02) :133-139
[5]   Insulin-like Growth Factor Receptor-1 and Nuclear Factor κB Are Crucial Survival Signals That Regulate Caspase-3-mediated Lens Epithelial Cell Differentiation Initiation [J].
Basu, Subhasree ;
Rajakaruna, Suren ;
Menko, A. Sue .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (11) :8384-8397
[6]   SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase [J].
Bennett, BL ;
Sasaki, DT ;
Murray, BW ;
O'Leary, EC ;
Sakata, ST ;
Xu, WM ;
Leisten, JC ;
Motiwala, A ;
Pierce, S ;
Satoh, Y ;
Bhagwat, SS ;
Manning, AM ;
Anderson, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13681-13686
[7]   Chondrocyte autophagy is stimulated by HIF-1 dependent AMPK activation and mTOR suppression [J].
Bohensky, Jolene ;
Leshinsky, Serge ;
Srinivas, Vickram ;
Shapiro, Irving M. .
PEDIATRIC NEPHROLOGY, 2010, 25 (04) :633-642
[8]  
Brennan LA, 2012, MOL VIS, V18, P1773
[9]   A novel image-based cytometry method for autophagy detection in living cells [J].
Chan, Leo Li-Ying ;
Shen, Dee ;
Wilkinson, Alisha R. ;
Patton, Wayne ;
Lai, Ning ;
Chan, Eric ;
Kuksin, Dmitry ;
Lin, Bo ;
Qiu, Jean .
AUTOPHAGY, 2012, 8 (09) :1371-1382
[10]   Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts [J].
Chen, Jianjun ;
Ma, Zhiwei ;
Jiao, Xiaodong ;
Fariss, Robert ;
Kantorow, Wanda Lee ;
Kantorow, Marc ;
Pras, Eran ;
Frydman, Moshe ;
Pras, Elon ;
Riazuddin, Sheikh ;
Riazuddin, S. Amer ;
Hejtmancik, J. Fielding .
AMERICAN JOURNAL OF HUMAN GENETICS, 2011, 88 (06) :827-838