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Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance
Author(s) -
Spencer A. Freeman,
Stefan Uderhardt,
Amra Sarić,
Richard F. Collins,
Catherine M. Buckley,
Sivakami Mylvaganam,
Parastoo Boroumand,
Jonathan Plumb,
Ronald N. Germain,
Dejian Ren,
Sergio Grinstein
Publication year - 2019
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaw9544
Subject(s) - endocytic cycle , microbiology and biotechnology , endosome , endocytosis , pinocytosis , chemistry , biophysics , exocytosis , vacuole , receptor , biology , intracellular , biochemistry , membrane , cytoplasm
Ion fluxes resolve organellar volume Animal cells continuously sample the surrounding medium, a feature accentuated in immune cells. Sampling is accomplished by trapping external medium into membrane-bound vesicles or vacuoles. These structures are promptly resolved, thus avoiding accumulation of endomembranes and volume expansion. In a variety of cultured cells, Freemanet al. found that this resolution entails conversion of spherical vacuoles into thin tubules, a process that involves marked changes in surface-to-volume ratio (see the Perspective by King and Smythe). Shrinkage of membrane-bound structures is driven by ion fluxes and subsequent osmotic transfer of water. Shriveled vacuoles attract curvature-sensing proteins that promote the extension of fine tubules. Ion channels thereby control membrane remodeling, enabling receptor recycling and proper routing of cellular cargo.Science , this issue p.301 ; see also p.246

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