4.3 Article

OCA-B does not act as a transcriptional coactivator in T cells

期刊

IMMUNOLOGY AND CELL BIOLOGY
卷 100, 期 5, 页码 338-351

出版社

WILEY
DOI: 10.1111/imcb.12543

关键词

B cells; germinal centers; OCA-B; Pou2af1; T cells; Tfh

资金

  1. Natural Sciences and Engineering Research Council of Canada [2019-05047]
  2. Fondation de l'Hopital Maisonneuve-Rosemont
  3. Cole Foundation
  4. Fonds de Recherche Quebec Sante

向作者/读者索取更多资源

Pou2af1 is a key coactivator in B-cell maturation, but its role in T cells is unclear. In this study, genetic disruption of Pou2af1 in T cells did not impair their cytokine production, suggesting that it does not act as a direct transcriptional coactivator in T cells. However, deletion of Pou2af1 in B cells indirectly affected Tfh differentiation, clarifying the role of OCA-B in the immune system.
Pou2af1 encodes for OCA-B, a coactivator of OCT-1/2 transcription factors, which plays a key role in B-cell maturation. The function of OCA-B has also been studied in T cells, where T cells from Pou2af1(-/-) mice have impaired functions, such as cytokine production and T follicular helper (Tfh) differentiation. Arguably, some of these T-cell phenotypes may result from impaired T-B interactions, secondary to the well-documented B-cell defects in Pou2af1(-/-) mice. Yet, Pou2af1 is actively transcribed in activated T cells, suggesting a T-cell-intrinsic role. To isolate the T-cell-intrinsic impact of Pou2af1, we generated Pou2af1(fl/fl) mice with specific genetic disruption of Pou2af1 either in all hematopoietic cells or exclusively in T cells. While we confirm that Pou2af1 is expressed in activated T cells, we surprisingly find that T-cell cytokine production is not impaired in Pou2af1-deficient T cells. Moreover, Pou2af1-sufficient and Pou2af1-deficient T cells have comparable transcriptome profiles, arguing against a T-cell-intrinsic role for Pou2af1. In line with these observations, we demonstrate that Tfh maturation is influenced by T-cell-extrinsic deletion of Pou2af1, as observed both in competitive bone marrow chimeras and in Pou2af1(fl/fl) mice with specific deletion in B cells. Overall, this study provides strong evidence that Pou2af1 does not act as a transcriptional coactivator in T cells, and conclusively demonstrates that loss of OCA-B in B cells indirectly impacts Tfh differentiation, clarifying the role of OCA-B in the immune system.

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