| Literature DB >> 34233185 |
Yolla German1, Loan Vulliard2, Anton Kamnev3, Laurène Pfajfer1, Jakob Huemer4, Anna-Katharina Mautner3, Aude Rubio5, Artem Kalinichenko4, Kaan Boztug6, Audrey Ferrand5, Jörg Menche7, Loïc Dupré8.
Abstract
The immunological synapse is a complex structure that decodes stimulatory signals into adapted lymphocyte responses. It is a unique window to monitor lymphocyte activity because of development of systematic quantitative approaches. Here we demonstrate the applicability of high-content imaging to human T and natural killer (NK) cells and develop a pipeline for unbiased analysis of high-definition morphological profiles. Our approach reveals how distinct facets of actin cytoskeleton remodeling shape immunological synapse architecture and affect lytic granule positioning. Morphological profiling of CD8+ T cells from immunodeficient individuals allows discrimination of the roles of the ARP2/3 subunit ARPC1B and the ARP2/3 activator Wiskott-Aldrich syndrome protein (WASP) in immunological synapse assembly. Single-cell analysis further identifies uncoupling of lytic granules and F-actin radial distribution in ARPC1B-deficient lymphocytes. Our study provides a foundation for development of morphological profiling as a scalable approach to monitor primary lymphocyte responsiveness and to identify complex aspects of lymphocyte micro-architecture.Entities:
Keywords: ARPC1B deficiency; NK cells; WASP deficiency; actin cytoskeleton; cytotoxic T lymphocytes; high-content imaging; immunological synapse; lytic granules; morphological profiling
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Year: 2021 PMID: 34233185 DOI: 10.1016/j.celrep.2021.109318
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423