Ohmura-Hoshino Mari, Matsuki Yohei, Mito-Yoshida Mari, Goto Eiji, Aoki-Kawasumi Masami, Nakayama Manabu, Ohara Osamu, Ishido Satoshi
Laboratory for Infectious Immunity, RIKENResearch Center for Allergy and Immunology, Tsurumi-ku, Yokohama, Kanagawa, Japan.
J Immunol. 2009 Dec 1;183(11):6893-7. doi: 10.4049/jimmunol.0902178. Epub 2009 Nov 16.
MARCH-I (membrane-associated RING-CH I) has been suggested as a physiological E3 ubiquitin ligase for both MHC class II (MHC II) and B7-2. In this study, we show that MARCH-I-mediated MHC II ubiquitination is necessary for the maintenance of conventional dendritic cell (cDC) functions in the steady state. MARCH-I-deficient cDCs accumulated MHC II and B7-2 and exhibited low Ag-presenting ability for exogenous Ags and low cytokine-producing ability upon stimulation in vivo. Importantly, MHC II, but not B7-2, was required for impaired cDC function induced by loss of MARCH-I in vivo. Moreover, MHC II knockin mice whose MHC II was not ubiquitinated showed dysfunction of cDC similar to that of MARCH-I knockout mice. These results suggest that the accumulation of MHC II resulting from loss of ubiquitination caused cDC abnormality; therefore, MARCH-I may function as a housekeeper of cDC in the steady state.
MARCH-I(膜相关RING-CH结构域蛋白1)被认为是主要组织相容性复合体II类分子(MHC II)和B7-2的生理性E3泛素连接酶。在本研究中,我们发现MARCH-I介导的MHC II泛素化对于维持稳态下常规树突状细胞(cDC)的功能是必需的。MARCH-I缺陷的cDC积累了MHC II和B7-2,并且在体内受到刺激时对外源性抗原的抗原呈递能力较低,细胞因子产生能力也较低。重要的是,体内MARCH-I缺失诱导的cDC功能受损需要MHC II,但不需要B7-2。此外,MHC II不被泛素化的MHC II基因敲入小鼠表现出与MARCH-I基因敲除小鼠类似的cDC功能障碍。这些结果表明,泛素化缺失导致的MHC II积累引起了cDC异常;因此,MARCH-I可能在稳态下作为cDC的管家蛋白发挥作用。