Towards a molecular understanding of endosomal trafficking by Retromer and Retriever

被引:127
作者
Chen, Kai-En [1 ]
Healy, Michael D. [1 ]
Collins, Brett M. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4072, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
C16orf62; CCC; CCDC22; CCDC93; Commander; COMMD; DSCR3; endosome; Retriever; Retromer; sorting nexin; Vps26; Vps29; Vps35; WASH complex; WASH COMPLEX; CARGO-RECOGNITION; MULTIPROTEIN COMPLEX; RETROGRADE TRANSPORT; PROTEIN TRAFFICKING; ALZHEIMERS-DISEASE; MAMMALIAN RETROMER; HUMAN INTERACTOME; SORTING RECEPTOR; HOMOLOGY DOMAIN;
D O I
10.1111/tra.12649
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endosomes are dynamic intracellular compartments that control the sorting of a constant stream of different transmembrane cargos either for ESCRT-mediated degradation or for egress and recycling to compartments such as the Golgi and the plasma membrane. The recycling of cargos occurs within tubulovesicular membrane domains and is facilitated by peripheral membrane protein machineries that control both membrane remodelling and selection of specific transmembrane cargos. One of the primary sorting machineries is the Retromer complex, which controls the recycling of a large array of different cargo molecules in cooperation with various sorting nexin (SNX) adaptor proteins. Recently a Retromer-like complex was also identified that controls plasma membrane recycling of cargos including integrins and lipoprotein receptors. Termed "Retriever," this complex uses a different SNX family member SNX17 for cargo recognition, and cooperates with the COMMD/CCDC93/CCDC22 (CCC) complex to form a larger assembly called "Commander" to mediate endosomal trafficking. In this review we focus on recent advances that have begun to provide a molecular understanding of these two distantly related transport machineries.
引用
收藏
页码:465 / 478
页数:14
相关论文
共 50 条
  • [1] Endosomal Trafficking: Retromer and Retriever Are Relatives in Recycling
    Gershlick, David C.
    Lucas, Maria
    CURRENT BIOLOGY, 2017, 27 (22) : R1233 - R1236
  • [2] Endosomal receptor trafficking: Retromer and beyond
    Wang, Jing
    Fedoseienko, Alina
    Chen, Baoyu
    Burstein, Ezra
    Jia, Da
    Billadeau, Daniel D.
    TRAFFIC, 2018, 19 (08) : 578 - 590
  • [3] Retromer's Role in Endosomal Trafficking and Impaired Function in Neurodegenerative Diseases
    Follett, Jordan
    Bugarcic, Andrea
    Collins, Brett M.
    Teasdale, Rohan D.
    CURRENT PROTEIN & PEPTIDE SCIENCE, 2017, 18 (07) : 687 - 701
  • [4] Retriever is a multiprotein complex for retromer-independent endosomal cargo recycling
    McNally, Kerrie E.
    Faulkner, Rebecca
    Steinberg, Florian
    Gallon, Matthew
    Ghai, Rajesh
    Pim, David
    Langton, Paul
    Pearson, Neil
    Danson, Chris M.
    Naegele, Heike
    Morris, Lindsey L.
    Singla, Amika
    Overlee, Brittany L.
    Heesom, Kate J.
    Sessions, Richard
    Banks, Lawrence
    Collins, Brett M.
    Berger, Imre
    Billadeau, Daniel D.
    Burstein, Ezra
    Cullen, Peter J.
    NATURE CELL BIOLOGY, 2017, 19 (10) : 1214 - +
  • [5] Endosomal Retrieval of Cargo: Retromer Is Not Alone
    McNally, Kerrie E.
    Cullen, Peter J.
    TRENDS IN CELL BIOLOGY, 2018, 28 (10) : 807 - 822
  • [6] Retromer-Mediated Protein Sorting and Vesicular Trafficking
    Liu, Jia-Jia
    JOURNAL OF GENETICS AND GENOMICS, 2016, 43 (04) : 165 - 177
  • [7] Endosomal sorting and trafficking, the retromer complex and neurodegeneration
    Vagnozzi, Alana N.
    Pratico, Domenico
    MOLECULAR PSYCHIATRY, 2019, 24 (06) : 857 - 868
  • [8] Navigating the Controversies of Retromer-Mediated Endosomal Protein Sorting
    Tu, Yingfeng
    Seaman, Matthew N. J.
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
  • [9] Recognising the signals for endosomal trafficking
    Weeratunga, Saroja
    Paul, Blessy
    Collins, Brett M.
    CURRENT OPINION IN CELL BIOLOGY, 2020, 65 : 17 - 27
  • [10] The retromer complex - endosomal protein recycling and beyond
    Seaman, Matthew N. J.
    JOURNAL OF CELL SCIENCE, 2012, 125 (20) : 4693 - 4702