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Origin, organization, dynamics, and function of actin and actomyosin networks at the t cell immunological synapse
NHLBI, Cell Biol & Physiol Ctr, NIH, Bethesda, MD 20892 USA.
NHLBI, Cell Biol & Physiol Ctr, NIH, Bethesda, MD 20892 USA.
NHLBI, Cell Biol & Physiol Ctr, NIH, Bethesda, MD 20892 USA.ORCID iD: 0000-0003-1921-6015
NHLBI, Cell Biol & Physiol Ctr, NIH, Bethesda, MD 20892 USA.
2019 (English)In: Annual Review of Immunology, ISSN 0732-0582, E-ISSN 1545-3278, Vol. 37, p. 201-224Article in journal (Refereed) Published
Abstract [en]

The engagement of a T cell with an antigen-presenting cell (APC) or activating surface results in the formation within the T cell of several distinct actin and actomyosin networks. These networks reside largely within a narrow zone immediately under the T cell's plasma membrane at its site of contact with the APC or activating surface, i.e., at the immunological synapse. Here we review the origin, organization, dynamics, and function of these synapse-associated actin and actomyosin networks. Importantly, recent insights into the nature of these actin-based cytoskeletal structures were made possible in several cases by advances in light microscopy.

Place, publisher, year, edition, pages
Annual Reviews , 2019. Vol. 37, p. 201-224
Keywords [en]
T cell, actin, formin, immunological synapse, lytic granule, myosin
National Category
Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)
Identifiers
URN: urn:nbn:se:kth:diva-352195DOI: 10.1146/annurev-immunol-042718-041341ISI: 000482702900009PubMedID: 30576253Scopus ID: 2-s2.0-85065018188OAI: oai:DiVA.org:kth-352195DiVA, id: diva2:1892052
Note

QC 20240904

Available from: 2024-08-25 Created: 2024-08-25 Last updated: 2024-09-04Bibliographically approved

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Saeed, Mezida

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