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Nonredundant Roles of IL-21 and IL-4 in the Phased Initiation of Germinal Center B Cells and Subsequent Self-Renewal Transitions.

David G GonzalezChristine M CoteJaymin R PatelColin B SmithYuqi ZhangKevin M NickersonTingting ZhangSteven M KerfootAnn M Haberman
Published in: Journal of immunology (Baltimore, Md. : 1950) (2018)
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.
Keyphrases
  • emergency department
  • cell migration
  • regulatory t cells
  • oxidative stress
  • immune response
  • dendritic cells
  • mass spectrometry
  • long non coding rna
  • cell cycle arrest