| Literature DB >> 27838744 |
Jun Kunisawa1,2,3,4.
Abstract
To sustain the bio-energetic demands of growth, proliferation, and effector functions, the metabolism of immune cells changes dramatically in response to immunologic stimuli. In this review, I focus on B cell metabolism, especially regarding the production of intestinal IgA antibody. Accumulating evidence has implicated not only host-derived factors (e.g., cytokines) but also gut environmental factors, including the possible involvement of commensal bacteria and diet, in the control of B cell metabolism during intestinal IgA antibody production. These findings yield new insights into the regulation of immunosurveillance and homeostasis in the gut.Keywords: B cell; Commensal bacteria; Glycolysis; IgA antibody; Immunometabolism; Lipid; Mucosal vaccine; Signaling; TCA cycle; Vitamin B1
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Year: 2016 PMID: 27838744 DOI: 10.1007/s00018-016-2414-8
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261