| Literature DB >> 28414328 |
Meritxell Nus1, Andrew P Sage1, Yuning Lu1, Leanne Masters1, Brian Y H Lam2, Stephen Newland1, Sandra Weller3, Dimitrios Tsiantoulas4,5, Juliette Raffort1, Damiënne Marcus1, Alison Finigan1, Lauren Kitt1, Nichola Figg1, Reinhold Schirmbeck6, Manfred Kneilling7,8, Giles S H Yeo2, Christoph J Binder4,5, José Luis de la Pompa9,10, Ziad Mallat1,11.
Abstract
Splenic marginal zone B (MZB) cells, positioned at the interface between circulating blood and lymphoid tissue, detect and respond to blood-borne antigens. Here we show that MZB cells in mice activate a homeostatic program in response to a high-cholesterol diet (HCD) and regulate both the differentiation and accumulation of T follicular helper (TFH) cells. Feeding mice an HCD resulted in upregulated MZB cell surface expression of the immunoregulatory ligand PDL1 in an ATF3-dependent manner and increased the interaction between MZB cells and pre-TFH cells, leading to PDL1-mediated suppression of TFH cell motility, alteration of TFH cell differentiation, reduced TFH abundance and suppression of the proatherogenic TFH response. Our findings reveal a previously unsuspected role for MZB cells in controlling the TFH-germinal center response to a cholesterol-rich diet and uncover a PDL1-dependent mechanism through which MZB cells use their innate immune properties to limit an exaggerated adaptive immune response.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28414328 DOI: 10.1038/nm.4315
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440