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...
Saved in:
Published in | Frontiers in immunology Vol. 9; p. 65 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
29.01.2018
|
Subjects | |
Online Access | Get full text |
ISSN | 1664-3224 1664-3224 |
DOI | 10.3389/fimmu.2018.00065 |
Cover
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. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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 |