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CIITA promoter i CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments

机译:CIITA启动子i CARD缺陷小鼠在髓样和淋巴区室表达功能性MHC II类基因

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摘要

Three distinct promoters control the master regulator of major histocompatibility complex (MHC) class II expression, class II transactivator (CIITA), in a cell type-specific manner. Promoter I (pI) CIITA, expressed primarily by dendritic cells (DCs) and macrophages, expresses a unique isoform that contains a caspase-recruitment domain (CARD). The activity and function of this isoform are not understood, but are believed to enhance the function of CIITA in antigen-presenting cells. To determine whether isoform I of CIITA has specific functions, CIITA mutant mice were created in which isoform I was replaced with isoform III sequences. Mice in which pI and the CARD-encoding exon were deleted were also created. No defect in the formation of CD4 T cells, the ability to respond to a model antigen or bacterial or viral challenge was observed in mice lacking CIITA isoform I. Although CIITA and MHC-II expression was decreased in splenic DCs, pI knockout animals expressed CIITA from downstream promoters, suggesting that control of pI activity is mediated by unknown distal elements that could act at pIII, the B-cell promoter. Thus, no critical function is linked to the CARD domain of CIITA isoform I with respect to basic immune system development, function and challenge.
机译:三个不同的启动子以细胞类型特异性方式控制主要组织相容性复合体(MHC)II类表达,II类反式激活因子(CIITA)的主调节剂。启动子I(pI)CIITA主要由树突状细胞(DC)和巨噬细胞表达,表达一种独特的亚型,该亚型包含胱天蛋白酶招募结构域(CARD)。该亚型的活性和功能尚不清楚,但据信可增强CIITA在抗原呈递细胞中的功能。为了确定CIITA的同工型I是否具有特定功能,创建了CIITA突变小鼠,其中同工型I被同工型III序列取代。还创建了其中删除了pI和CARD编码外显子的小鼠。在缺乏CIITA亚型I的小鼠中未观察到CD4 T细胞形成缺陷,对模型抗原或细菌或病毒攻击的反应能力。尽管脾脏DC中CIITA和MHC-II表达降低,但pI基因敲除动物表达CIITA从下游启动子,提示pI活性的控制是由可能作用于pIII的未知远端元件B细胞启动子介导的。因此,就基本的免疫系统发育,功能和挑战而言,没有关键功能与CIITA亚型I的CARD域相连。

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