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Epidermal terminal differentiation depends on B lymphocyte-induced maturation protein-1

机译:表皮末端分化取决于B淋巴细胞诱导的成熟蛋白-1

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摘要

The cornified layer is a compacted lattice of lipid-embedded cor-neocytes that provides an organism's barrier to the external environment. Cornification is the final differentiative step for epidermal keratinocytes and involves dramatic cell condensation before death. Using conditional gene deletion in mice, we identified the transcriptional repressor Blimp-1 (B lymphocyte-induced maturation protein-1) as an important regulator of keratinocyte transition from the granular to the cornified layer. More than 250 genes are misregulated in conditional knockout epidermis, including those encoding transcription factors, signal transduction components, proteinases, and enzymes involved in lipid metabolism. Steady-state mRNA and ChIP analyses of a subset of these genes provide evidence that nfat5, fos, prdm1, and dusp16 are novel direct targets of Blimp-1. Identifying nfat5 as a target of Blimp-1 repression indicates that cornification involves suppression of normal osmotic regulation in granular cells. Consistently, conditional knockout mice have delayed barrier formation as embryos, enlarged granular layer cells and corneocytes, and a morphologically abnormal cornified layer. These studies provide insight into cornification, identifying transcriptional regulatory circuitry and indicating the importance of blocking osmotic homeostasis.
机译:角质层是嵌入脂质的新细胞的紧密晶格,它为生物体提供了对外部环境的屏障。角质化是表皮角质形成细胞的最后分化步骤,涉及死亡前细胞的剧烈凝结。使用小鼠中的条件基因缺失,我们确定了转录阻抑物Blimp-1(B淋巴细胞诱导的成熟蛋白-1)是角质形成细胞从颗粒层过渡到角质层的重要调节剂。有条件的敲除表皮中有250多个基因被错误调节,包括编码转录因子,信号转导成分,蛋白酶和参与脂质代谢的酶的基因。这些基因的一个子集的稳态mRNA和ChIP分析提供了证据,证明nfat5,fos,prdm1和dusp16是Blimp-1的新型直接靶标。将nfat5鉴定为Blimp-1抑制的靶标,表明角质化涉及抑制颗粒细胞中正常的渗透调节。一致地,条件性基因敲除小鼠的胚胎,较大的颗粒层细胞和角质细胞以及形态异常的角质层的屏障形成延迟。这些研究提供了有关角质形成的见解,确定了转录调控电路,并表明了阻止渗透稳态的重要性。

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