Nakamura Morihiko, Nakagawa Mai, Watanabe Jun
Department of Cooperative Medical Research, Collaboration Center, Shimane University , Izumo , Japan.
Immunol Invest. 2015;44(1):1-12. doi: 10.3109/08820139.2014.909454. Epub 2014 Sep 2.
Monoclonal non-specific suppressor factor β (MNSFβ) is a ubiquitously expressed member of the ubiquitin-like family that is involved in various biological functions. Previous studies have demonstrated that MNSFβ covalently binds to intracellular pro-apoptotic protein Bcl-G and regulates apoptosis in macrophages. In this study, we demonstrate that MNSFβ negatively regulates T cell function. In murine T-helper type 2 clone, D10.G4.1 (D10) cells transfected with MNSFβ cDNA, CD3/CD28-induced ERK1/2 phosphorylation leading to IL-4 production was significantly inhibited. The formation of MNSFβ-Bcl-G complex was induced by the CD3/CD28 stimulation. Co-transfection with MNSFβ and Bcl-G greatly enhanced CD3/CD28-induced apoptosis in D10 cells. Similarly, co-over-expression of MNSFβ and Bcl-G caused a marked enhancement of apoptosis in purified splenic T cells. Interestingly, this MNSFβ adduct was also induced in T cells derived from DO11.10 mice stimulated with antigen. Collectively, CD3/CD28-inducible MNSFβ-Bcl-G complex may be involved in the regulation of T cell function and survival.
单克隆非特异性抑制因子β(MNSFβ)是泛素样家族中一种广泛表达的成员,参与多种生物学功能。先前的研究表明,MNSFβ与细胞内促凋亡蛋白Bcl-G共价结合,并调节巨噬细胞中的细胞凋亡。在本研究中,我们证明MNSFβ负向调节T细胞功能。在转染了MNSFβ cDNA的小鼠2型辅助性T细胞克隆D10.G4.1(D10)细胞中,CD3/CD28诱导的导致IL-4产生的ERK1/2磷酸化被显著抑制。CD3/CD28刺激诱导了MNSFβ-Bcl-G复合物的形成。MNSFβ和Bcl-G共转染极大地增强了CD3/CD28诱导的Dl0细胞凋亡。同样,MNSFβ和Bcl-G的共过表达导致纯化的脾T细胞凋亡显著增强。有趣的是,在用抗原刺激的DO11.10小鼠来源的T细胞中也诱导了这种MNSFβ加合物。总体而言,CD3/CD28诱导的MNSFβ-Bcl-G复合物可能参与T细胞功能和存活的调节。