Zhang Lianjun, Yi Huanfa, Xia Xue-Pei, Zhao Yong
Transplantation Biology Research Division, State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China.
Autoimmunity. 2006 Jun;39(4):269-76. doi: 10.1080/08916930600753903.
The transforming growth factor-beta (TGF-beta) protein family is highly evolutionarily conserved and they have been implicated in many biological processes. Also, TGF-beta can exert pivotal functions in the immune system. It is widely accepted that regulatory T cells (Treg cells) play an important role in the maintenance of the immune homeostasis, but the underlying molecular mechanisms through which they can gain and/or perform suppressive functions in an active way remains to be defined. Though the engagement of TGF-beta in the Treg cells has been discounted for a period of time, an emerging body of data has established a close link between Treg cells and TGF-beta, as TGF-beta has been demonstrated to induce the expression of Foxp3, which acts as a master regulator for the development and function of Treg cells. We will, herein, focus on the crucial role of TGF-beta signaling in Treg cell biology and summarize the current studies regarding TGF-beta in the generation and function of CD4+CD25+Treg cells both in vivo and in vitro.
转化生长因子-β(TGF-β)蛋白家族在进化上高度保守,并且参与了许多生物学过程。此外,TGF-β在免疫系统中发挥关键作用。人们普遍认为调节性T细胞(Treg细胞)在维持免疫稳态中起重要作用,但其能够以主动方式获得和/或发挥抑制功能的潜在分子机制仍有待确定。尽管一段时间以来TGF-β与Treg细胞的关联被忽视,但新出现的大量数据已在Treg细胞与TGF-β之间建立了紧密联系,因为TGF-β已被证明可诱导Foxp3的表达,而Foxp3是Treg细胞发育和功能的主要调节因子。在此,我们将聚焦于TGF-β信号在Treg细胞生物学中的关键作用,并总结目前关于TGF-β在体内外CD4+CD25+Treg细胞生成和功能方面的研究。