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.
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Acknowledgements
We thank the Koch Institute Swanson Biotechnology Center for technical support and are thankful to the Keck microscopy facility at the Whitehead Institute. This work was supported in part by the Koch Institute Support (core) Grant P30-CA14051 from the National Cancer Institute. DJI is an investigator of the Howard Hughes Medical Institute.
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Kumari, S., Irvine, D. Morphological Definition of Actin Architecture at the T Cell Immunological Synapse. J Indian Inst Sci 101, 47–50 (2021). https://doi.org/10.1007/s41745-020-00216-y
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DOI: https://doi.org/10.1007/s41745-020-00216-y