ID1和CEBPA协调表皮祖细胞分化

C. G. Kantzer, Wei Yang, David Grommisch, K. V. Patil, Kylie Hin-Man Mak, Maria Genander
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引用次数: 1

摘要

在发育过程中协调表皮分化的调控回路仍未完全了解。在这里,我们报道了转录调节因子ID1在基底表皮祖细胞中富集,并发现ID1的表达在分化过程中减少。在子宫内沉默Id1会损害祖细胞的增殖,导致目标祖细胞过早分层,并使分化的角质形成细胞保留祖细胞的标记和特征。转录谱分析表明,ID1通过介导基底膜的粘附而抑制棘层分化。共免疫沉淀显示ID1与I类bHLH家族的转录调节因子结合。我们在表皮分层过程中将bHLH Tcf3、Tcf4和Tcf12定位于表皮祖细胞,并确定Tcf3是id1介导的表皮增殖的下游效应因子。最后,我们确定了CEBPA(一种已知的表皮分化介质)与Id1之间的串扰,并证明CEBPA可以拮抗bmp诱导的Id1激活。我们的研究表明,ID1是表皮发育的关键协调者,在祖细胞增殖和分化之间发挥平衡作用,并揭示了CEBPA和ID1之间的功能串扰如何协调表皮谱系的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ID1 and CEBPA coordinate epidermal progenitor cell differentiation
The regulatory circuits that coordinate epidermal differentiation during development are still not fully understood. Here we report that the transcriptional regulator ID1 is enriched in basal epidermal progenitor cells and find ID1 expression to be diminished upon differentiation. In utero silencing of Id1 impairs progenitor cell proliferation, leads to precocious delamination of targeted progenitor cells and enables differentiated keratinocytes to retain progenitor markers and characteristics. Transcriptional profiling suggests ID1 acts by mediating adhesion to the basement membrane while inhibiting spinous layer differentiation. Co-immunoprecipitation reveals ID1 binding to transcriptional regulators of the class I bHLH family. We localize bHLH Tcf3, Tcf4 and Tcf12 to epidermal progenitor cells during epidermal stratification and established TCF3 as a downstream effector of ID1-mediated epidermal proliferation. Finally, we identify crosstalk between CEBPA, a known mediator of epidermal differentiation, and Id1 and demonstrate that CEBPA antagonizes BMP-induced activation of Id1. Our work establishes ID1 as a key coordinator of epidermal development, acting to balance progenitor proliferation with differentiation and unveils how functional crosstalk between CEBPA and Id1 orchestrates epidermal lineage progression.
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