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类SKINT1基因在类人猿中失活,但并非在所有灵长类物种中都如此:对树突状表皮T细胞起源的启示。

The SKINT1-like gene is inactivated in hominoids but not in all primate species: implications for the origin of dendritic epidermal T cells.

作者信息

Mohamed Rania Hassan, Sutoh Yoichi, Itoh Yasushi, Otsuka Noriyuki, Miyatake Yukiko, Ogasawara Kazumasa, Kasahara Masanori

机构信息

Department of Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

Department of Pathology, Shiga University of Medical Science, Otsu, Japan.

出版信息

PLoS One. 2015 Apr 1;10(4):e0123258. doi: 10.1371/journal.pone.0123258. eCollection 2015.

Abstract

Dendritic epidermal T cells, which express an invariant Vγ5Vδ1 T-cell receptor and account for 95% of all resident T cells in the mouse epidermis, play a critical role in skin immune surveillance. These γδ T cells are generated by positive selection in the fetal thymus, after which they migrate to the skin. The development of dendritic epidermal T cells is critically dependent on the Skint1 gene expressed specifically in keratinocytes and thymic epithelial cells, suggesting an indispensable role for Skint1 in the selection machinery for specific intraepithelial lymphocytes. Phylogenetically, rodents have functional SKINT1 molecules, but humans and chimpanzees have a SKINT1-like (SKINT1L) gene with multiple inactivating mutations. In the present study, we analyzed SKINT1L sequences in representative primate species and found that all hominoid species have a common inactivating mutation, but that Old World monkeys such as olive baboons, green monkeys, cynomolgus macaques and rhesus macaques have apparently functional SKINT1L sequences, indicating that SKINT1L was inactivated in a common ancestor of hominoids. Interestingly, the epidermis of cynomolgus macaques contained a population of dendritic-shaped γδ T cells expressing a semi-invariant Vγ10/Vδ1 T-cell receptor. However, this population of macaque T cells differed from rodent dendritic epidermal T cells in that their Vγ10/Vδ1 T-cell receptors displayed junctional diversity and expression of Vγ10 was not epidermis-specific. Therefore, macaques do not appear to have rodent-type dendritic epidermal T cells despite having apparently functional SKINT1L. Comprehensive bioinformatics analysis indicates that SKINT1L emerged in an ancestor of placental mammals but was inactivated or lost multiple times in mammalian evolution and that Skint1 arose by gene duplication in a rodent lineage, suggesting that authentic dendritic epidermal T cells are presumably unique to rodents.

摘要

树突状表皮T细胞表达恒定的Vγ5Vδ1 T细胞受体,占小鼠表皮中所有驻留T细胞的95%,在皮肤免疫监视中起关键作用。这些γδ T细胞在胎儿胸腺中通过阳性选择产生,之后迁移至皮肤。树突状表皮T细胞的发育严重依赖于角质形成细胞和胸腺上皮细胞中特异性表达的Skint1基因,这表明Skint1在特定上皮内淋巴细胞的选择机制中具有不可或缺的作用。从系统发育角度来看,啮齿动物具有功能性的SKINT1分子,但人类和黑猩猩具有一个带有多个失活突变的类SKINT1(SKINT1L)基因。在本研究中,我们分析了代表性灵长类物种中的SKINT1L序列,发现所有类人猿物种都有一个共同的失活突变,但诸如橄榄狒狒、绿猴、食蟹猴和恒河猴等旧世界猴具有明显功能性的SKINT1L序列,这表明SKINT1L在类人猿的共同祖先中失活。有趣的是,食蟹猴的表皮含有一群表达半恒定Vγ10/Vδ1 T细胞受体的树突状γδ T细胞。然而,这群猕猴T细胞与啮齿动物的树突状表皮T细胞不同,因为它们的Vγ10/Vδ1 T细胞受体表现出连接多样性,且Vγ10的表达并非表皮特异性。因此,尽管猕猴具有明显功能性的SKINT1L,但它们似乎没有啮齿动物型的树突状表皮T细胞。综合生物信息学分析表明,SKINT1L出现在胎盘哺乳动物的祖先中,但在哺乳动物进化过程中多次失活或丢失,而Skint1是通过啮齿动物谱系中的基因复制产生的,这表明真正的树突状表皮T细胞可能是啮齿动物所特有的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fab/4382165/38e6730dd91c/pone.0123258.g001.jpg

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