磷酸化
生物
细胞生物学
效应器
磷酸酶
调节器
蛋白质磷酸化
蛋白磷酸酶2
细胞
MAPK/ERK通路
双特异性磷酸酶
激酶
蛋白激酶A
信号转导
生物化学
基因
作者
Fei Sun,Tiantian Yue,Chunliang Yang,Faxi Wang,Jia‐Hui Luo,Shan-Jie Rong,Meng Zhang,Yanchao Guo,Fei Xiong,Cong‐Yi Wang
标识
DOI:10.1016/j.intimp.2021.107906
摘要
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.
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