MBSJ MCC Young Scientist Award 2009 REVIEW: Selective autophagy regulates various cellular functions

Genes to Cells - Tập 15 Số 9 - Trang 923-933 - 2010
Masaaki Komatsu1, Yoshinobu Ichimura1
1Protein Metabolism Project, Tokyo Metropolitan Institute of Medical Science, Setagaya‐ku, Tokyo 156‐8506, Japan

Tóm tắt

Autophagy is a self‐eating system conserved among eukaryotes, in which cellular components including organelles are entrapped into a double membrane structure called the autophagosome and then degraded by lysosomal hydrolases. In addition to its role in supplying amino acids in response to nutrient starvation, autophagy is involved in quality control to maintain cell health. Thus, inactivation of autophagy causes the formation of cytoplasmic protein inclusions, which comprise misfolded proteins and the accumulation of many degenerated organelles, resulting in liver injury, diabetes, myopathy and neurodegeneration. Furthermore, although autophagy has been considered nonselective, increasing evidence points to the selectivity of autophagy in sorting vacuolar enzymes and removal of aggregate‐prone proteins and unwanted organelles. Such selectivity allows diverse cellular regulation, similar to the ubiquitin proteasome pathway. In this review, we discuss the physiological roles of selective autophagy and their molecular mechanisms.

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Tài liệu tham khảo

10.1016/j.cmet.2008.08.009

10.1016/j.devcel.2007.12.011

10.1091/mbc.e08-03-0312

10.1091/mbc.e07-12-1257

10.1038/ncb2012

10.1038/nature02263

10.1074/jbc.C700195200

10.1146/annurev.biochem.67.1.425

10.1038/35044114

10.1074/jbc.M802182200

10.1074/jbc.M512283200

10.1016/j.cmet.2008.08.013

10.1093/emboj/19.21.5720

10.1016/j.devcel.2009.06.014

10.1073/pnas.0810611105

10.1083/jcb.151.2.263

10.1016/j.molcel.2009.01.020

10.1016/j.febslet.2010.02.017

10.1038/ncb2021

10.1038/sj.cdd.4402120

10.1038/nature04723

10.1016/j.cell.2007.10.035

10.1083/jcb.200412022

10.1038/nature03029

10.1097/00001756-200107200-00009

10.1016/S1534-5807(04)00099-1

10.1016/j.cell.2007.12.018

10.1016/j.febslet.2010.02.013

10.1016/j.febslet.2010.01.019

10.1083/jcb.200910140

10.1038/nature06639

10.1016/j.cell.2009.05.023

10.1016/j.molcel.2006.08.002

10.1038/nm1574

10.1016/j.cell.2007.05.021

10.1038/nrm2708

10.1083/jcb.200809125

10.1371/journal.pbio.1000298

10.1083/jcb.200711108

10.1111/j.1365-2443.2008.01238.x

10.1038/embor.2009.256

10.1016/j.devcel.2009.06.013

10.1074/jbc.M702824200

10.1074/jbc.C000307200

10.1016/S0896-6273(01)00569-4

10.1038/ncb1813

10.1016/j.immuni.2010.02.009

10.1016/j.bbamcr.2006.08.023

10.1038/nature07006

10.1038/emboj.2009.80

10.1073/pnas.0708818104

10.1016/S1534-5807(02)00373-8

10.1091/mbc.e08-03-0309

10.1053/jhep.2002.32674

10.1107/S0907444903011314

10.1016/S1534-5807(02)00359-3

10.4161/auto.1.2.1697

10.1074/jbc.M401461200

10.1016/0014-5793(93)80398-E

10.1126/science.1154822

10.1038/ncb1007-1102

10.1016/S0002-9440(10)64369-6

10.1016/j.cell.2008.12.022

10.4049/jimmunol.0900441