Deaglio Silvia, Dwyer Karen M, Gao Wenda, Friedman David, Usheva Anny, Erat Anna, Chen Jiang-Fan, Enjyoji Keiichii, Linden Joel, Oukka Mohamed, Kuchroo Vijay K, Strom Terry B, Robson Simon C
Department of Medicine, Harvard Medical School, Transplantation Research Center, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
J Exp Med. 2007 Jun 11;204(6):1257-65. doi: 10.1084/jem.20062512. Epub 2007 May 14.
The study of T regulatory cells (T reg cells) has been limited by the lack of specific surface markers and an inability to define mechanisms of suppression. We show that the expression of CD39/ENTPD1 in concert with CD73/ecto-5'-nucleotidase distinguishes CD4(+)/CD25(+)/Foxp3(+) T reg cells from other T cells. These ectoenzymes generate pericellular adenosine from extracellular nucleotides. The coordinated expression of CD39/CD73 on T reg cells and the adenosine A2A receptor on activated T effector cells generates immunosuppressive loops, indicating roles in the inhibitory function of T reg cells. Consequently, T reg cells from Cd39-null mice show impaired suppressive properties in vitro and fail to block allograft rejection in vivo. We conclude that CD39 and CD73 are surface markers of T reg cells that impart a specific biochemical signature characterized by adenosine generation that has functional relevance for cellular immunoregulation.
调节性T细胞(Treg细胞)的研究一直受到缺乏特异性表面标志物以及无法明确抑制机制的限制。我们发现,CD39/ENTPD1与CD73/胞外5'-核苷酸酶协同表达,可将CD4(+)/CD25(+)/Foxp3(+) Treg细胞与其他T细胞区分开来。这些胞外酶可从细胞外核苷酸生成细胞周围的腺苷。Treg细胞上CD39/CD73与活化的效应T细胞上的腺苷A2A受体的协同表达产生免疫抑制环,表明其在Treg细胞抑制功能中的作用。因此,来自Cd39基因敲除小鼠的Treg细胞在体外表现出抑制特性受损,并且在体内无法阻止同种异体移植排斥反应。我们得出结论,CD39和CD73是Treg细胞的表面标志物,它们赋予了一种特定的生化特征,其特点是生成腺苷,这对细胞免疫调节具有功能相关性。