To Eat or to Die: Deciphering Selective Forms of Autophagy

被引:81
作者
Abdrakhmanov, Alibek [1 ]
Gogvadze, Vladimir [1 ,2 ]
Zhivotovsky, Boris [1 ,2 ]
机构
[1] Moscow MV Lomonosov State Univ, Fac Med, Moscow 119991, Russia
[2] Karolinska Inst, Div Toxicol, Inst Environm Med, Box 210, S-17177 Stockholm, Sweden
基金
俄罗斯科学基金会;
关键词
ENDOPLASMIC-RETICULUM; PARKINSONS-DISEASE; ULK1; COMPLEX; MITOPHAGY; PROTEIN; RECEPTOR; IRON; DEGRADATION; MUTATIONS; FERRITIN;
D O I
10.1016/j.tibs.2019.11.006
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
Autophagy is an evolutionarily conserved process whereby damaged and redundant components of the cell are degraded in structures called autophagolysosomes. Currently, three main types of autophagy are recognized: macroautophagy, microautophagy, and chaperone-mediated autophagy (CMA). However, we still know little about some specific types of autophagy that are linked to various intracellular compartments and their roles in the physiology of the whole organism and connections to various diseases. Here, we aim to shed light on the latest insights on and mechanisms of several selective forms of autophagy.
引用
收藏
页码:347 / 364
页数:18
相关论文
共 121 条
[1]   NIPSNAP1 and NIPSNAP2 Act as "Eat Me" Signals for Mitophagy [J].
Abudu, Yakubu Princely ;
Pankiv, Serhiy ;
Mathai, Benan John ;
Lystad, Aif Hakon ;
Bindesboll, Christian ;
Brenne, Hanne Britt ;
Ng, Matthew Yoke Wui ;
Thiede, Bernd ;
Yamamoto, Ai ;
Nthiga, Thaddaeus Mutugi ;
Lamark, Trond ;
Esguerra, Camila, V ;
Johansen, Terje ;
Simonsen, Anne .
DEVELOPMENTAL CELL, 2019, 49 (04) :509-+
[2]   TEX264 Is an Endoplasmic Reticulum-Resident ATG8-Interacting Protein Critical for ER Remodeling during Nutrient Stress [J].
An, Heeseon ;
Ordureau, Alban ;
Paulo, Joao A. ;
Shoemaker, Christopher J. ;
Denic, Vladimir ;
Harper, J. Wade .
MOLECULAR CELL, 2019, 74 (05) :891-+
[3]  
[Anonymous], AUTOPHAGY
[4]   NCOA4 Deficiency Impairs Systemic Iron Homeostasis [J].
Bellelli, Roberto ;
Federico, Giorgia ;
Matte', Alessandro ;
Colecchia, David ;
Iolascon, Achille ;
Chiariello, Mario ;
Santoro, Massimo ;
De Franceschi, Lucia ;
Carlomagno, Francesca .
CELL REPORTS, 2016, 14 (03) :411-421
[5]  
Bergmann TJ, 2017, MOL CELL ONCOL, V4, DOI 10.1080/23723556.2016.1264351
[6]   Ferroxidase Activity in Eukaryotic Ferritin is Controlled by Accessory-Iron-Binding Sites in the Catalytic Cavity [J].
Bernacchioni, Caterina ;
Pozzi, Cecilia ;
Di Pisa, Flavio ;
Mangani, Stefano ;
Turano, Paola .
CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (45) :16213-16219
[7]   Parkin inhibits BAK and BAX apoptotic function by distinct mechanisms during mitophagy [J].
Bernardini, Jonathan P. ;
Brouwer, Jason M. ;
Tan, Iris K. L. ;
Sandow, Jarrod J. ;
Huang, Shuai ;
Stafford, Che A. ;
Bankovacki, Aleksandra ;
Riffkin, Christopher D. ;
Wardak, Ahmad Z. ;
Czabotar, Peter E. ;
Lazarou, Michael ;
Dewson, Grant .
EMBO JOURNAL, 2019, 38 (02)
[8]   Iron storage disease: Facts, fiction and progress [J].
Beutler, Emest .
BLOOD CELLS MOLECULES AND DISEASES, 2007, 39 (02) :140-147
[9]   FKBP8 recruits LC3A to mediate Parkin-independent mitophagy [J].
Bhujabal, Zambarlal ;
Birgisdottir, Asa B. ;
Sjottem, Eva ;
Brenne, Hanne B. ;
Overvatn, Aud ;
Habisov, Sabrina ;
Kirkin, Vladimir ;
Lamark, Trond ;
Johansen, Terje .
EMBO REPORTS, 2017, 18 (06) :947-961
[10]   The LIR motif - crucial for selective autophagy [J].
Birgisdottir, Asa Birna ;
Lamark, Trond ;
Johansen, Terje .
JOURNAL OF CELL SCIENCE, 2013, 126 (15) :3237-3247