Suppr超能文献

Myc通过与Miz1形成复合物来调节角质形成细胞的黏附和分化。

Myc regulates keratinocyte adhesion and differentiation via complex formation with Miz1.

作者信息

Gebhardt Anneli, Frye Michaela, Herold Steffi, Benitah Salvador Aznar, Braun Kristin, Samans Birgit, Watt Fiona M, Elsässer Hans-Peter, Eilers Martin

机构信息

Institute for Cell Biology, University of Marburg, 35033 Marburg, Germany.

出版信息

J Cell Biol. 2006 Jan 2;172(1):139-49. doi: 10.1083/jcb.200506057.

Abstract

Myc plays a key role in homeostasis of the skin. We show that Miz1, which mediates Myc repression of gene expression, is expressed in the epidermal basal layer. A large percentage of genes regulated by the Myc-Miz1 complex in keratinocytes encode proteins involved in cell adhesion, and some, including the alpha6 and beta1 integrins, are directly bound by Myc and Miz1 in vivo. Using a Myc mutant deficient in Miz1 binding (MycV394D), we show that Miz1 is required for the effects of Myc on keratinocyte responsiveness to TGF-beta. Myc, but not MycV394D, decreases keratinocyte adhesion and spreading. In reconstituted epidermis, Myc induces differentiation and loss of cell polarization in a Miz1-dependent manner. In vivo, overexpression of beta1 integrins restores basal layer polarity and prevents Myc-induced premature differentiation. Our data show that regulation of cell adhesion is a major function of the Myc-Miz1 complex and suggest that it may contribute to Myc-induced exit from the epidermal stem cell compartment.

摘要

Myc在皮肤的稳态中起关键作用。我们发现,介导Myc对基因表达抑制作用的Miz1在表皮基底层表达。角质形成细胞中受Myc-Miz1复合物调控的很大一部分基因编码参与细胞黏附的蛋白质,其中一些,包括α6和β1整合素,在体内直接与Myc和Miz1结合。使用缺乏Miz1结合能力的Myc突变体(MycV394D),我们发现Miz1是Myc对角质形成细胞对转化生长因子-β反应性产生影响所必需的。Myc而非MycV394D可降低角质形成细胞的黏附与铺展。在重组表皮中,Myc以依赖Miz1的方式诱导分化和细胞极性丧失。在体内,β1整合素的过表达可恢复基底层极性并防止Myc诱导的过早分化。我们的数据表明,细胞黏附的调控是Myc-Miz1复合物的主要功能,并提示其可能有助于Myc诱导的表皮干细胞区室退出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd3/2063541/c2026d6b1054/jcb1720139f01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验