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Cutting Edge: Myosin 18A Is a Novel Checkpoint Regulator in B Cell Differentiation and Antibody-Mediated Immunity.
Cheung, Michael B; Enyindah-Asonye, Gospel; Matsui, Ken; Kosik, Ivan; Dvorina, Nina; Baldwin, William M; Yewdell, Jonathan W; Gupta, Neetu.
Affiliation
  • Cheung MB; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and.
  • Enyindah-Asonye G; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and.
  • Matsui K; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and.
  • Kosik I; Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
  • Dvorina N; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and.
  • Baldwin WM; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and.
  • Yewdell JW; Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
  • Gupta N; Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH; and guptan@ccf.org.
J Immunol ; 206(11): 2521-2526, 2021 06 01.
Article in En | MEDLINE | ID: mdl-34001658
ABSTRACT
We investigated the function of the newly discovered myosin family protein myosin 18A (Myo18A) in Ab-mediated immunity by generating B cell-conditional Myo18A-deficient mice. Myo18A deficiency led to expansion of bone marrow progenitor B cells and mature B cells in secondary lymphoid organs. Myo18A-deficient mice displayed serum IgM hyperglobulinemia and increased splenic IgM-secreting cells, with older mice switching to IgG1 hyperglobulinemia and autoantibody development. Immunization of Myo18A-deficient mice with inactivated influenza virus led to development of more potent neutralizing Abs against the major Ag hemagglutinin, associated with persistent accumulation of Ag-specific germinal center B cells and more Ag-specific bone marrow plasma cells. In vitro stimulation with TLR7 and BCR ligands revealed a greater ability of Myo18A-deficient B cells to differentiate into Ab-secreting cells, associated with higher AID and Blimp-1 expression. Overall, our study demonstrates that Myo18A is a novel negative regulator of B cell homeostasis, differentiation, and humoral immunity.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: B-Lymphocytes / Myosins / Immunity, Humoral / Antibodies, Monoclonal Limits: Animals Language: En Journal: J Immunol Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: B-Lymphocytes / Myosins / Immunity, Humoral / Antibodies, Monoclonal Limits: Animals Language: En Journal: J Immunol Year: 2021 Type: Article