Ruvbl1的靶向缺失会导致严重的表皮发育缺陷和围产期死亡率。

IF 2.4 Q1 PEDIATRICS
Claudia Dafinger, Thomas Benzing, Jörg Dötsch, Bernhard Schermer, Max C Liebau
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引用次数: 0

摘要

表皮发育是一个复杂的调控细胞增殖、分化和严格控制细胞死亡的过程,涉及多个细胞信号网络。在这里,我们首次报道了AAA+(与各种细胞活动相关的atp酶)超家族蛋白Ruvbl1与哺乳动物表皮发育的联系。角化细胞特异性Ruvbl1敲除小鼠(Ruvbl1fl/flK14:Cretg)表现出严重的表型,包括显著的结构性表皮缺陷,导致功能性皮肤屏障的丧失和围产期死亡。因此,Ruvbl1是新发现的小鼠表皮分化发育的重要参与者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality.

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality.

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality.

Epidermal development is a complex process of regulated cellular proliferation, differentiation, and tightly controlled cell death involving multiple cellular signaling networks. Here, we report a first description linking the AAA+ (ATPases associated with various cellular activities) superfamily protein Ruvbl1 to mammalian epidermal development. Keratinocyte-specific Ruvbl1 knockout mice (Ruvbl1fl/flK14:Cretg) show a severe phenotype including dramatic structural epidermal defects resulting in the loss of the functional skin barrier and perinatal death. Thus, Ruvbl1 is a newly identified essential player for the development of differentiated epidermis in mice.

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CiteScore
2.20
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