| Literature DB >> 34198238 |
Fei Sun1, Tian-Tian Yue1, Chun-Liang Yang1, Fa-Xi Wang1, Jia-Hui Luo1, Shan-Jie Rong1, Meng Zhang2, Yanchao Guo2, Fei Xiong3, Cong-Yi Wang4.
Abstract
The functional state of T cells is diverse and under dynamic control for adapting to the changes of microenvironment. Reversible protein phosphorylation represents an important post-translational modification that not only involves in the immediate early response of T cells, but also affects their functionality in the long run. Perturbation of global phosphorylation profile and/or phosphorylation of specific signaling nodes result in aberrant T cell activity. Dual specific phosphatases (DUSPs), which target MAPKs and beyond, have increasingly been emerged as a versatile regulator in T cell biology. Herein in this mini review, we sought to summarize and discuss the impact of DUSP proteins on the regulation of effector T cell activity, T cell polarization, regulatory T cell development and T cell senescence/exhaustion. Given the distinctive engagement of each DUSP member under various disease settings such as chronic infection, autoimmune disorders, cancer and age-related diseases, DUSP proteins likely hold the promise to become a druggable target other than the existing therapeutics that are predominantly by manipulating protein kinase activity.Entities:
Keywords: DUSPs; Effector T cell; Regulatory T cell; T cell senescence/exhaustion
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Year: 2021 PMID: 34198238 DOI: 10.1016/j.intimp.2021.107906
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932