FOXP3型
泛素
细胞生物学
免疫系统
信号转导
生物
周边公差
白细胞介素2受体
调节性T细胞
免疫耐受
T细胞
炎症
免疫学
基因
遗传学
作者
Zuojia Chen,Xiaozhu Luo,Yingru Lu,Tao Zhu,Jinhu Wang,Karin Loser,Bin Li
标识
DOI:10.1016/j.intimp.2013.01.023
摘要
Protein ubiquitination has emerged as a crucial modulator of the immune system, participating in the control of T cell differentiation, intracellular signal transduction and the induction of immune tolerance. CD4+CD25+FOXP3+ regulatory T cells are a unique subset of cells that mediate central and peripheral immune tolerance. In this review, we highlight our current understanding of the molecular mechanisms and signaling pathways that modulate protein ubiquitination in Treg cells, and how ubiquitination determines Treg cell development and function. Understanding how FOXP3 activity is regulated by ubiquitination and deubiquitination under molecular level will promote regulatory T cell therapy for treating inflammation in autoimmune disease, infection, transplantation and cancer.
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