First Author | Debuisson D | Year | 2013 |
Journal | PLoS One | Volume | 8 |
Issue | 12 | Pages | e84415 |
PubMed ID | 24386375 | Mgi Jnum | J:209842 |
Mgi Id | MGI:5568813 | Doi | 10.1371/journal.pone.0084415 |
Citation | Debuisson D, et al. (2013) Myor/ABF-1 Mrna expression marks follicular helper T cells but is dispensable for Tfh cell differentiation and function in vivo. PLoS One 8(12):e84415 |
abstractText | Follicular T helper cells (Tfh) are crucial for effective antibody responses and long term T cell-dependent humoral immunity. Although many studies are devoted to this novel T helper cell population, the molecular mechanisms governing Tfh cell differentiation have yet to be characterized. MyoR/ABF-1 is a basic helix-loop-helix transcription factor that plays a role in the differentiation of the skeletal muscle and Hodgkin lymphoma. Here we show that MyoR mRNA is progressively induced during the course of Tfh-like cell differentiation in vitro and is expressed in Tfh responding to Alum-precipitated antigens in vivo. This expression pattern suggests that MyoR could play a role in the differentiation and/or function of Tfh cells. We tested this hypothesis using MyoR-deficient mice and found this deficiency had no impact on Tfh differentiation. Hence, MyoR-deficient mice developed optimal T-dependent humoral responses to Alum-precipitated antigens. In conclusion, MyoR is a transcription factor selectively up-regulated in CD4 T cells during Tfh cell differentiation in vitro and upon response to alum-protein vaccines in vivo, but the functional significance of this up-regulation remains uncertain. |