Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.1301766110
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dc.titlePlasma membrane tension orchestrates membrane trafficking, cytoskeletal remodeling, and biochemical signaling during phagocytosis
dc.contributor.authorMasters, T.A.
dc.contributor.authorPontes, B.
dc.contributor.authorViasnoff, V.
dc.contributor.authorLi, Y.
dc.contributor.authorGauthier, N.C.
dc.date.accessioned2016-09-06T05:44:37Z
dc.date.available2016-09-06T05:44:37Z
dc.date.issued2013-07-16
dc.identifier.citationMasters, T.A., Pontes, B., Viasnoff, V., Li, Y., Gauthier, N.C. (2013-07-16). Plasma membrane tension orchestrates membrane trafficking, cytoskeletal remodeling, and biochemical signaling during phagocytosis. Proceedings of the National Academy of Sciences of the United States of America 110 (29) : 11875-11880. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.1301766110
dc.identifier.issn00278424
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/126674
dc.description.abstractPhagocytes clear the body of undesirable particles such as infectious agents and debris. To extend pseudopods over the surface of targeted particles during engulfment, cells must change shape through extensive membrane and cytoskeleton remodeling. We observed that pseudopod extension occurred in two phases. In the first phase, pseudopods extended rapidly, with actin polymerization pushing the plasma membrane forward. The second phase occurred once the membrane area from preexisting reservoirs was depleted, leading to increased membrane tension. Increased tension directly altered the small Rho GTPase Rac1, 3'-phosphoinositide, and cytoskeletal organization. Furthermore, it activated exocytosis of vesicles containing GPI-Anchored proteins, increasing membrane area and phagocytosis efficiency for large particles. We thus propose that, during phagocytosis, membrane remodeling, cytoskeletal organization, and biochemical signaling are orchestrated by the mechanical signal of membrane tension. These results put a simple mechanical signal at the heart of understanding immunological responses.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1073/pnas.1301766110
dc.sourceScopus
dc.subjectFrustrated phagocytosis
dc.subjectImmunology
dc.subjectPhagocytic cell
dc.subjectRho GTPases
dc.subjectTraffic
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1073/pnas.1301766110
dc.description.sourcetitleProceedings of the National Academy of Sciences of the United States of America
dc.description.volume110
dc.description.issue29
dc.description.page11875-11880
dc.description.codenPNASA
dc.identifier.isiut000322086100054
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