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dc.contributor.authorKumari, Sudha
dc.contributor.authorIrvine, Darrell J
dc.date.accessioned2021-11-24T16:47:15Z
dc.date.available2021-09-20T17:41:26Z
dc.date.available2021-11-24T16:47:15Z
dc.date.issued2021-01
dc.identifier.urihttps://hdl.handle.net/1721.1/132015.2
dc.description.abstractT lymphocytes (T cells) are the major mediators of adaptive immune response. They detect pathogens primarily via the interaction of their T cell receptor (TCR) with the cognate pathogen-derived peptide displayed in the context of MHC on the infected cell. A critical step in T cell activation is the formation of immunological synapse, a specialized cell–cell conjugate interface between the T cell and infected cell, where massive TCR-induced actin remodeling and polymerization take place. Dynamic actin polymerization at the immunological synapse is essential for T cell activation and subsequently, immune response.en_US
dc.publisherSpringer Indiaen_US
dc.relation.isversionofhttps://doi.org/10.1007/s41745-020-00216-yen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceSpringer Indiaen_US
dc.titleMorphological Definition of Actin Architecture at the T Cell Immunological Synapseen_US
dc.typeArticleen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-02-25T04:47:41Z
dc.language.rfc3066en
dc.rights.holderIndian Institute of Science
dspace.embargo.termsY
dspace.date.submission2021-02-25T04:47:41Z
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusPublication Information Neededen_US


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