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mTORC1 and mTORC2 regulate skin morphogenesis and epidermal barrier formation

机译:mTORC1和mTORC2调节皮肤形态发生和表皮屏障形成

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Mammalian target of rapamycin (mTOR), a regulator of growth in many tissues, mediates its activity through two multiprotein complexes, mTORC1 or mTORC2. The role of mTOR signalling in skin morphogenesis and epidermal development is unknown. Here we identify mTOR as an essential regulator in skin morphogenesis by epidermis-specific deletion of Mtor in mice (mTOREKO). mTOREKO mutants are viable, but die shortly after birth due to deficits primarily during the early epidermal differentiation programme and lack of a protective barrier development. Epidermis-specific loss of Raptor , which encodes an essential component of mTORC1, confers the same skin phenotype as seen in mTOREKO mutants. In contrast, newborns with an epidermal deficiency of Rictor , an essential component of mTORC2, survive despite a hypoplastic epidermis and disruption in late stage terminal differentiation. These findings highlight a fundamental role for mTOR in epidermal morphogenesis that is regulated by distinct functions for mTORC1 and mTORC2.
机译:雷帕霉素的哺乳动物靶标(mTOR)是许多组织中的生长调节剂,它通过两种多蛋白复合物mTORC1或mTORC2介导其活性。 mTOR信号在皮肤形态发生和表皮发育中的作用尚不清楚。在这里,我们确定了mTOR是小鼠表皮特异性Mtor(mTOR EKO )的缺失,它是皮肤形态发生中必不可少的调节剂。 mTOR EKO 突变体是可行的,但由于主要在表皮分化早期阶段的缺陷和缺乏保护性屏障的形成而在出生后不久就死亡。编码mTORC1必需成分的Raptor的表皮特异性缺失赋予了与mTOR EKO 突变体相同的皮肤表型。相反,尽管表皮发育不良和晚期终末分化受到破坏,但具有Rictor(mTORC2的重要组成部分)的表皮缺陷的新生儿仍能生存。这些发现强调了mTOR在表皮形态发生中的基本作用,该作用由mTORC1和mTORC2的独特功能调节。

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