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在晶状体纤维细胞终末分化过程中,丝裂原活化蛋白激酶/应激活化蛋白激酶-哺乳动物雷帕霉素靶蛋白复合物1(MAPK/JNK-MTORC1)信号通路的抑制会通过自噬导致细胞器和细胞核过早丢失。

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

作者信息

Basu Subhasree, Rajakaruna Suren, Reyes Beverly, Van Bockstaele Elisabeth, Menko A Sue

机构信息

Department of Pathology, Anatomy and Cell Biology; Thomas Jefferson University; Philadelphia, PA USA.

Department of Neuroscience; Farber Institute for Neuroscience; Thomas Jefferson University; Philadelphia, PA USA.

出版信息

Autophagy. 2014 Jul;10(7):1193-211. doi: 10.4161/auto.28768. Epub 2014 May 9.

DOI:10.4161/auto.28768
PMID:24813396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4203547/
Abstract

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, BECN1/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.

摘要

尽管自噬途径对于发育过程至关重要,但在分化背景下,关于调节自噬的起始信号仍存在许多问题。为了解决这些问题,我们研究了眼晶状体,因为细胞核和细胞器的程序性清除以精确调控的时空方式发生,以形成无细胞器区(OFZ),这是视力敏锐度所必需的特征。在此,我们报告我们的发现,即MAPK/JNK的失活通过其对MTORC1的调节诱导自噬以形成OFZ,其中MAPK/JNK信号传导对于MTOR激活和RPTOR/RAPTOR磷酸化均是必需的。在存在MAPK/JNK或MTOR抑制剂的情况下,包括ULK1、BECN1/Beclin 1和MAP1LC3B2/LC3B-II在内的自噬途径蛋白被上调,诱导细胞器的自噬性丢失以形成OFZ。这些结果表明,MAPK/JNK是MTORC1信号传导的正调节因子,其发育调控的失活为晶状体功能所需的细胞核和细胞器的协同自噬清除提供了诱导信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/69e67a4fa83a/auto-10-1193-g10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/90e435c8200a/auto-10-1193-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/b88320e6022e/auto-10-1193-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/215c5b2dcca8/auto-10-1193-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/275344d6e19b/auto-10-1193-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/a25288dcd80e/auto-10-1193-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/1460087b8be3/auto-10-1193-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/6c2913c61d91/auto-10-1193-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/5a252732802d/auto-10-1193-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/8619ee992d4a/auto-10-1193-g9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/69e67a4fa83a/auto-10-1193-g10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/90e435c8200a/auto-10-1193-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/b88320e6022e/auto-10-1193-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/215c5b2dcca8/auto-10-1193-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/275344d6e19b/auto-10-1193-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/a25288dcd80e/auto-10-1193-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/1460087b8be3/auto-10-1193-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/6c2913c61d91/auto-10-1193-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/5a252732802d/auto-10-1193-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/8619ee992d4a/auto-10-1193-g9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/4203547/69e67a4fa83a/auto-10-1193-g10.jpg

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