p38γ and p38δ Are Involved in T Lymphocyte Development

p38 mitogen-activated protein kinase (MAPK) signal transduction pathways are essential regulators of the immune response. Particularly, p38γ and p38δ regulate many immune cell functions such as cytokine production, migration, or T cell activation; however, their involvement in immune cell developmen...

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Published inFrontiers in immunology Vol. 9; p. 65
Main Authors Risco, Ana, Martin-Serrano, Miguel A., Barber, Domingo F., Cuenda, Ana
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.01.2018
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ISSN1664-3224
1664-3224
DOI10.3389/fimmu.2018.00065

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Summary:p38 mitogen-activated protein kinase (MAPK) signal transduction pathways are essential regulators of the immune response. Particularly, p38γ and p38δ regulate many immune cell functions such as cytokine production, migration, or T cell activation; however, their involvement in immune cell development is largely unknown. Here, we analysed the role of p38 MAPK isoforms p38γ and p38δ in T cell differentiation in the thymus and in lymph nodes, using mice deficient in p38γ, p38δ, or in both. We found that the T cell differentiation program in the thymus was affected at different stages in p38γ-, p38δ-, and p38γ/δ-deficient mice, and also peripheral T cell homaeostasis was compromised. Particularly, p38δ deletion affects different stages of early CD4 CD8 double-negative thymocyte development, whereas lack of p38γ favours thymocyte positive selection from CD4 CD8 double-positive to CD4 or CD8 single-positive cells. Our results identify unreported functions for p38γ and p38δ in T cells.
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Edited by: Hongbo Chi, St. Jude Children’s Research Hospital, United States
Reviewed by: Maria L. Toribio, Centro de Biología Molecular Severo Ochoa (CSIC), Spain; Gonghua Huang, Shanghai Jiao Tong University, China; Hongling Huang, St. Jude Children’s Research Hospital, United States
Specialty section: This article was submitted to T Cell Biology, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2018.00065