| Literature DB >> 31442401 |
Motoyoshi Nagai1, Ryotaro Noguchi1, Daisuke Takahashi2, Takayuki Morikawa3, Kouhei Koshida2, Seiga Komiyama2, Narumi Ishihara2, Takahiro Yamada2, Yuki I Kawamura4, Kisara Muroi2, Kouya Hattori2, Nobuhide Kobayashi2, Yumiko Fujimura2, Masato Hirota2, Ryohtaroh Matsumoto2, Ryo Aoki5, Miwa Tamura-Nakano6, Machiko Sugiyama7, Tomoya Katakai8, Shintaro Sato9, Keiyo Takubo3, Taeko Dohi1, Koji Hase10.
Abstract
Nutritional status potentially influences immune responses; however, how nutritional signals regulate cellular dynamics and functionality remains obscure. Herein, we report that temporary fasting drastically reduces the number of lymphocytes by ∼50% in Peyer's patches (PPs), the inductive site of the gut immune response. Subsequent refeeding seemingly restored the number of lymphocytes, but whose cellular composition was conspicuously altered. A large portion of germinal center and IgA+ B cells were lost via apoptosis during fasting. Meanwhile, naive B cells migrated from PPs to the bone marrow during fasting and then back to PPs during refeeding when stromal cells sensed nutritional signals and upregulated CXCL13 expression to recruit naive B cells. Furthermore, temporal fasting before oral immunization with ovalbumin abolished the induction of antigen-specific IgA, failed to induce oral tolerance, and eventually exacerbated food antigen-induced diarrhea. Thus, nutritional signals are critical in maintaining gut immune homeostasis.Entities:
Keywords: B cell; CXCL13; IgA; Immunometabolism; Peyer's patch; bone marrow; fasting; mTOR signaling; mucosal immunity; nutritional signals; stroma cell
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Year: 2019 PMID: 31442401 DOI: 10.1016/j.cell.2019.07.047
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582