MiR-155 promotes T follicular helper cell accumulation during chronic, low-grade inflammation.
Ontology highlight
ABSTRACT: Chronic inflammation is a contributing factor to most life-shortening human diseases. However, the molecular and cellular mechanisms that sustain chronic inflammatory responses remain poorly understood, making it difficult to treat this deleterious condition. Using a mouse model of age-dependent inflammation that results from a deficiency in miR-146a, we demonstrate that miR-155 contributed to the progressive inflammatory disease that emerged as Mir146a(-/-) mice grew older. Upon analyzing lymphocytes from inflamed versus healthy middle-aged mice, we found elevated numbers of T follicular helper (Tfh) cells, germinal center (GC) B cells, and autoantibodies, all occurring in a miR-155-dependent manner. Further, Cd4-cre Mir155(fl/fl) mice were generated and demonstrated that miR-155 function
SUBMITTER: Hu R
PROVIDER: S-EPMC4657560 | biostudies-literature | 2014 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA