TY - JOUR
T1 - Out of the ESCPE room
T2 - Emerging roles of endosomal SNX-BARs in receptor transport and host-pathogen interaction
AU - Simonetti, Boris
AU - Daly, James L
AU - Cullen, Peter J
N1 - Funding Information:
J.L.D is supported by a Wellcome Early Career Award (225128/Z/22/Z). P.J.C. is supported by the Wellcome Trust (104568/Z/14/Z and 220260/Z/20/Z), the MRC (MR/L007363/1 and MR/P018807/1), the Lister Institute of Preventive Medicine, and the award of a Royal Society Noreen Murray Research Professorship (RSRP/R1/211004).
Publisher Copyright:
© 2023 The Authors. Traffic published by John Wiley & Sons Ltd.
PY - 2023/6
Y1 - 2023/6
N2 - Several functions of the human cell, such as sensing nutrients, cell movement and interaction with the surrounding environment, depend on a myriad of transmembrane proteins and their associated proteins and lipids (collectively termed "cargoes"). To successfully perform their tasks, cargo must be sorted and delivered to the right place, at the right time, and in the right amount. To achieve this, eukaryotic cells have evolved a highly organized sorting platform, the endosomal network. Here, a variety of specialized multiprotein complexes sort cargo into itineraries leading to either their degradation or their recycling to various organelles for further rounds of reuse. A key sorting complex is the Endosomal SNX-BAR Sorting Complex for Promoting Exit (ESCPE-1) that promotes the recycling of an array of cargos to the plasma membrane and/or the trans-Golgi network. ESCPE-1 recognizes a hydrophobic-based sorting motif in numerous cargoes and orchestrates their packaging into tubular carriers that pinch off from the endosome and travel to the target organelle. A wide range of pathogens mimic this sorting motif to hijack ESCPE-1 transport to promote their invasion and survival within infected cells. In other instances, ESCPE-1 exerts restrictive functions against pathogens by limiting their replication and infection. In this review, we discuss ESCPE-1 assembly and functions, with a particular focus on recent advances in the understanding of its role in membrane trafficking, cellular homeostasis and host-pathogen interaction.
AB - Several functions of the human cell, such as sensing nutrients, cell movement and interaction with the surrounding environment, depend on a myriad of transmembrane proteins and their associated proteins and lipids (collectively termed "cargoes"). To successfully perform their tasks, cargo must be sorted and delivered to the right place, at the right time, and in the right amount. To achieve this, eukaryotic cells have evolved a highly organized sorting platform, the endosomal network. Here, a variety of specialized multiprotein complexes sort cargo into itineraries leading to either their degradation or their recycling to various organelles for further rounds of reuse. A key sorting complex is the Endosomal SNX-BAR Sorting Complex for Promoting Exit (ESCPE-1) that promotes the recycling of an array of cargos to the plasma membrane and/or the trans-Golgi network. ESCPE-1 recognizes a hydrophobic-based sorting motif in numerous cargoes and orchestrates their packaging into tubular carriers that pinch off from the endosome and travel to the target organelle. A wide range of pathogens mimic this sorting motif to hijack ESCPE-1 transport to promote their invasion and survival within infected cells. In other instances, ESCPE-1 exerts restrictive functions against pathogens by limiting their replication and infection. In this review, we discuss ESCPE-1 assembly and functions, with a particular focus on recent advances in the understanding of its role in membrane trafficking, cellular homeostasis and host-pathogen interaction.
KW - Humans
KW - Endosomes/metabolism
KW - Carrier Proteins/metabolism
KW - Protein Transport
KW - Membrane Proteins/metabolism
KW - Host-Pathogen Interactions
KW - Sorting Nexins/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85153509866&partnerID=8YFLogxK
U2 - 10.1111/tra.12885
DO - 10.1111/tra.12885
M3 - Review article
C2 - 37089068
SN - 1398-9219
VL - 24
SP - 234
EP - 250
JO - Traffic
JF - Traffic
IS - 6
ER -