| Literature DB >> 34294890 |
Nagaja Capitani1, Anna Onnis2, Francesca Finetti2, Chiara Cassioli2, Alessandro Plebani3, Jlenia Brunetti4, Arianna Troilo5, Sofia D'Elios6, Manuela Baronio3, Luisa Gazzurelli3, Chiara Della Bella5, Daniel D Billadeau7, Mario Milco D'Elios5, Vassilios Lougaris3, Cosima T Baldari8.
Abstract
Ciliogenesis proteins orchestrate vesicular trafficking pathways that regulate immune synapse (IS) assembly in the non-ciliated T-cells. We hypothesized that ciliogenesis-related genes might be disease candidates for common variable immunodeficiency with impaired T-cell function (T-CVID). We identified a heterozygous, predicted pathogenic variant in the ciliogenesis protein CCDC28B present with increased frequency in a large CVID cohort. We show that CCDC28B participates in IS assembly by regulating polarized T-cell antigen receptor (TCR) recycling. This involves the CCDC28B-dependent, FAM21-mediated recruitment of the actin regulator WASH to retromer at early endosomes to promote actin polymerization. The CVID-associated CCDC28BR25W variant failed to interact with FAM21, leading to impaired synaptic TCR recycling. CVID T cells carrying the ccdc28b 211 C > T allele displayed IS defects mapping to this pathway that were corrected by overexpression of the wild-type allele. These results identify a new disease gene in T-CVID and pinpoint CCDC28B as a new player in IS assembly.Entities:
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Year: 2021 PMID: 34294890 PMCID: PMC8738737 DOI: 10.1038/s41418-021-00837-5
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 12.067