| Literature DB >> 35143312 |
Patrick Schriek1, Alan C Ching1, Nagaraj S Moily1, Jessica Moffat1, Lynette Beattie2, Thiago M Steiner2, Laine M Hosking3, Joshua M Thurman4, V Michael Holers4, Satoshi Ishido5, Mireille H Lahoud6, Irina Caminschi6, William R Heath2, Justine D Mintern1, Jose A Villadangos1,2.
Abstract
Marginal zone (MZ) B cells produce broad-spectrum antibodies that protect against infection early in life. In some instances, antibody production requires MZ B cells to display pathogen antigens bound to major histocompatibility complex class II (MHC II) molecules to T cells. We describe the trogocytic acquisition of these molecules from conventional dendritic cells (cDCs). Complement component 3 (C3) binds to murine and human MHC II on cDCs. MZ B cells recognize C3 with complement receptor 2 (CR2) and trogocytose the MHC II-C3 complexes, which become exposed on their cell surface. The ubiquitin ligase MARCH1 limits the number of MHC II-C3 complexes displayed on cDCs to prevent their elimination through excessive trogocytosis. Capture of C3 by MHC II thus enables the transfer of cDC-like properties to MZ B cells.Entities:
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Year: 2022 PMID: 35143312 DOI: 10.1126/science.abf7470
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728