| Literature DB >> 30446568 |
David G Gonzalez1,2, Christine M Cote1, Jaymin R Patel3, Colin B Smith4, Yuqi Zhang5, Kevin M Nickerson6, Tingting Zhang1, Steven M Kerfoot7, Ann M Haberman8,9.
Abstract
We examined the unique contributions of the cytokines IL-21 and IL-4 on germinal center (GC) B cell initiation and subsequent maturation in a murine model system. Similar to other reports, we found T follicular helper cell expression of IL-21 begins prior to T follicular helper cell migration into the B cell follicle and precedes that of IL-4. Consistent with this timing, IL-21 signaling has a greater influence on the perifollicular pre-GC B cell transition to the intrafollicular stage. Notably, Bcl6hi B cells can form in the combined absence of IL-21R- and STAT6-derived signals; however, these nascent GC B cells cease to proliferate and are more prone to apoptosis. When B cells lack either IL-21R or STAT6, aberrant GCs form atypical centroblasts and centrocytes that differ in their phenotypic maturation and costimulatory molecule expression. Thus, IL-4 and IL-21 play nonredundant roles in the phased progression of GC B cell development that can initiate in the combined absence of these cytokine signals.Entities:
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Year: 2018 PMID: 30446568 PMCID: PMC6289626 DOI: 10.4049/jimmunol.1500497
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422