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Metabolic changes during B cell differentiation for the production of intestinal IgA antibody

期刊

CELLULAR AND MOLECULAR LIFE SCIENCES
卷 74, 期 8, 页码 1503-1509

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-016-2414-8

关键词

B cell; Immunometabolism; IgA antibody; Lipid; Commensal bacteria; Glycolysis; TCA cycle; Vitamin B1; Mucosal vaccine; Signaling

资金

  1. MEXT/JSPS KAKENHI [26293111, 16H01373, 15H05790]
  2. Ministry of Health, Labour and Welfare (MHLW)
  3. Research on Development of New Drugs
  4. Japan Agency for Medical Research and Development (AMED)
  5. Science and Technology Research Promotion Program for Agriculture, Forestry, Fisheries, and Food Industry
  6. Astellas Foundation for Research on Metabolic Disorders
  7. Terumo Foundation for Life Sciences and Arts and Suzuken Memorial Foundation
  8. Grants-in-Aid for Scientific Research [15H05790, 16H01373, 26293111] Funding Source: KAKEN

向作者/读者索取更多资源

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.

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