dc.contributor.author | Kumari, Sudha | |
dc.contributor.author | Irvine, Darrell J | |
dc.date.accessioned | 2021-11-24T16:47:15Z | |
dc.date.available | 2021-09-20T17:41:26Z | |
dc.date.available | 2021-11-24T16:47:15Z | |
dc.date.issued | 2021-01 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/132015.2 | |
dc.description.abstract | T 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.publisher | Springer India | en_US |
dc.relation.isversionof | https://doi.org/10.1007/s41745-020-00216-y | en_US |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
dc.source | Springer India | en_US |
dc.title | Morphological Definition of Actin Architecture at the T Cell Immunological Synapse | en_US |
dc.type | Article | en_US |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2021-02-25T04:47:41Z | |
dc.language.rfc3066 | en | |
dc.rights.holder | Indian Institute of Science | |
dspace.embargo.terms | Y | |
dspace.date.submission | 2021-02-25T04:47:41Z | |
mit.license | OPEN_ACCESS_POLICY | |
mit.metadata.status | Publication Information Needed | en_US |