Mechanically active integrins target lytic secretion at the immune synapse to facilitate cellular cytotoxicity
Year: 2022
Type: article
Abstract: Cytotoxic lymphocytes fight pathogens and cancer by forming immune synapses with infected or transformed target cells and then secreting cytotoxic perforin and granzyme into the synaptic space, with potent and specific killing achieved by this focused delivery. The mechanisms that establish the precise location of secretory events, however, remain poorly understood. Here we use single cell biophysical measurements, micropatterning, and functional assays to demonstrate that localized mechanotransduction helps define the position of secretory events within the synapse. Ligand-bound integrins, predominantly the α L β 2 isoform LFA-1, function as spatial cues to attract lytic granules containing perforin and granzyme and induce their fusion with the plasma membrane for content release. LFA-1 is subjected to pulling forces within secretory domains, and disruption of these forces via depletion of the adaptor molecule talin abrogates cytotoxicity. We thus conclude that lymphocytes employ an integrin-dependent mechanical checkpoint to enhance their cytotoxic power and fidelity.
Source: Nature Communications
Language: English
Subfield: Immunology and Allergy
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $5,890
Awards: G1352943963, G1372984924, G145035411, G2051006376, G2114260556, G289723095, Mechanoregulation of cytotoxic lymphocyte function, G447601904, Advanced Rigidity-based Material for Enhanced Immunotherapy, Molecular imaging technologies for mechanobiology, G9000003249, G9000067677, G9000127173, G9000185667, G9000226461, Cancer Center Support Grant
OpenAlex ID: W4281611229
