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DOI | 10.1126/science.aaw9544 |
Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance | |
Freeman S.A.; Uderhardt S.; Saric A.; Collins R.F.; Buckley C.M.; Mylvaganam S.; Boroumand P.; Plumb J.; Germain R.N.; Ren D.; Grinstein S. | |
发表日期 | 2020 |
ISSN | 0036-8075 |
起始页码 | 301 |
结束页码 | 305 |
卷号 | 367期号:6475 |
英文摘要 | Despite ongoing (macro)pinocytosis of extracellular fluid, the volume of the endocytic pathway remains unchanged. To investigate the underlying mechanism, we used high-resolution video imaging to analyze the fate of macropinosomes formed by macrophages in vitro and in situ. Na+, the primary cationic osmolyte internalized, exited endocytic vacuoles via two-pore channels, accompanied by parallel efflux of Cl− and osmotically coupled water. The resulting shrinkage caused crenation of the membrane, which fostered recruitment of curvature-sensing proteins. These proteins stabilized tubules and promoted their elongation, driving vacuolar remodeling, receptor recycling, and resolution of the organelles. Failure to resolve internalized fluid impairs the tissue surveillance activity of resident macrophages. Thus, osmotically driven increases in the surface-to-volume ratio of endomembranes promote traffic between compartments and help to ensure tissue homeostasis. © 2020 American Association for the Advancement of Science. All rights reserved. |
关键词 | cation channelchemokine receptor CCR2chloridecolony stimulating factor 1epidermal growth factorepidermal growth factor receptorlipidsialoadhesinsodium iontetrandrinetwo pore channelunclassified drugcalcium channellipidMcoln1 protein, mousesodiumTPCN1 protein, mouseTPCN2 protein, mousetransient receptor potential channelcationhomeostasisimmune systemproteinrecyclinganimal experimentArticlebone marrow derived macrophagecell vacuolecell volumechannel gatingchloride transportconcentration (parameter)controlled studyendocytosisextracellular fluidextracellular spacehomeostasishumanhuman cellhuman tissueimmunosurveillancein vitro studyinternalizationion currentknockout mousemacropinocytosismousenonhumanpriority journalprotein stabilityRNA interferencesodium transporttonoplastanimalcell organelleendosomegeneticsimmunologyion transportmacrophagemetabolismosmosisphysiologypinocytosisAnimalsCalcium ChannelsEndosomesImmunologic SurveillanceIon TransportLipidsMacrophagesMiceMice, KnockoutOrganellesOsmosisPinocytosisSodiumTransient Receptor Potential ChannelsVacuoles |
语种 | 英语 |
来源机构 | Science |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/133773 |
推荐引用方式 GB/T 7714 | Freeman S.A.,Uderhardt S.,Saric A.,et al. Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance[J]. Science,2020,367(6475). |
APA | Freeman S.A..,Uderhardt S..,Saric A..,Collins R.F..,Buckley C.M..,...&Grinstein S..(2020).Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance.,367(6475). |
MLA | Freeman S.A.,et al."Lipid-gated monovalent ion fluxes regulate endocytic traffic and support immune surveillance".367.6475(2020). |
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