| Literature DB >> 33305952 |
Morteza Aramesh1, Simon Mergenthal2, Marcel Issler2, Birgit Plochberger3, Florian Weber3, Xiao-Hua Qin4, Robert Liska5, Georg N Duda6, Johannes B Huppa7, Jonas Ries8, Gerhard J Schütz9, Enrico Klotzsch1,2.
Abstract
When T-cells probe their environment for antigens, the bond between the T-cell receptor (TCR) and the peptide-loaded major histocompatibility complex (MHC) is put under tension, thereby influencing the antigen discrimination. Yet, the quantification of such forces in the context of T-cell signaling is technically challenging. Here, we developed a traction force microscopy platform which allows for quantifying the pulls and pushes exerted via T-cell microvilli, in both tangential and normal directions, during T-cell activation. We immobilized specific T-cell activating antibodies on the marker beads used to read out the hydrogel deformation. Microvilli targeted the functionalized beads, as confirmed by superresolution microscopy of the local actin organization. Moreover, we found that cellular components, such as actin, TCR, and CD45 reorganize upon interaction with the beads, such that actin forms a vortex-like ring structure around the beads and TCR is enriched at the bead surface, whereas CD45 is excluded from bead-microvilli contacts.Entities:
Keywords: T-cell activation; actin dynamics; microvilli; traction force microscopy
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Year: 2020 PMID: 33305952 DOI: 10.1021/acs.nanolett.0c03964
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189