Abstract:
:The intestinal tract is constantly exposed to various stimuli. Group 3 innate lymphoid cells (ILC3s) reside in lymphoid organs and in the intestinal tract and are required for immunity to enteric bacterial infection. However, the mechanisms that regulate the ILC3s in vivo remain incompletely defined. Here, we show that GPR183, a chemotactic receptor expressed on murine and human ILC3s, regulates ILC3 migration toward its ligand 7α,25-dihydroxycholesterol (7α,25-OHC) in vitro, and GPR183 deficiency in vivo leads to a disorganized distribution of ILC3s in mesenteric lymph nodes and decreased ILC3 accumulation in the intestine. GPR183 functions intrinsically in ILC3s, and GPR183-deficient mice are more susceptible to enteric bacterial infection. Together, these results reveal a role for the GPR183-7α,25-OHC pathway in regulating the accumulation, distribution, and anti-microbial and tissue-protective functions of ILC3s and define a critical role for this pathway in promoting innate immunity to enteric bacterial infection.
journal_name
Cell Repjournal_title
Cell reportsauthors
Chu C,Moriyama S,Li Z,Zhou L,Flamar AL,Klose CSN,Moeller JB,Putzel GG,Withers DR,Sonnenberg GF,Artis Ddoi
10.1016/j.celrep.2018.05.099subject
Has Abstractpub_date
2018-06-26 00:00:00pages
3750-3758issue
13issn
2211-1247pii
S2211-1247(18)30895-7journal_volume
23pub_type
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