| Literature DB >> 26411688 |
Jun Kunisawa1, Yuki Sugiura2, Taichi Wake3, Takahiro Nagatake4, Hidehiko Suzuki4, Risa Nagasawa5, Shiori Shikata5, Kurara Honda2, Eri Hashimoto5, Yuji Suzuki3, Mitsutoshi Setou6, Makoto Suematsu7, Hiroshi Kiyono8.
Abstract
Bioenergetic metabolism varies during cell differentiation, but details of B cell metabolism remain unclear. Here, we show the metabolic changes during B cell differentiation in the intestine, where B cells differentiate into IgA(+) plasma cells (PCs). Naive B cells in the Peyer's patches (PPs) and IgA(+) PCs in the intestinal lamina propria (iLP) both used the tricarboxylic acid (TCA) cycle, but only IgA(+) PCs underwent glycolysis. These metabolic differences reflected their dependencies on vitamin B1, an essential cofactor for the TCA cycle. Indeed, the diminished activity of the TCA cycle after dietary vitamin B1 depletion decreased the number of naive B cells in PPs without affecting IgA(+) PCs in the iLP. The maintenance of naive B cells by dietary vitamin B1 was required to induce-but not maintain-intestinal IgA responses against oral antigens. These findings reveal the diet-mediated maintenance of B cell immunometabolism in organized and diffuse intestinal tissues.Entities:
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Year: 2015 PMID: 26411688 DOI: 10.1016/j.celrep.2015.08.063
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423