Kobielak Krzysztof, Pasolli H Amalia, Alonso Laura, Polak Lisa, Fuchs Elaine
Howard Hughes Medical Institute and Laboratory of Mammalian Cell Biology and Development, The Rockefeller University, New York, NY 10021-6399, USA.
J Cell Biol. 2003 Nov 10;163(3):609-23. doi: 10.1083/jcb.200309042.
Using conditional gene targeting in mice, we show that BMP receptor IA is essential for the differentiation of progenitor cells of the inner root sheath and hair shaft. Without BMPRIA activation, GATA-3 is down-regulated and its regulated control of IRS differentiation is compromised. In contrast, Lef1 is up-regulated, but its regulated control of hair differentiation is still blocked, and BMPRIA-null follicles fail to activate Lef1/beta-catenin-regulated genes, including keratin genes. Wnt-mediated transcriptional activation can be restored by transfecting BMPRIA-null keratinocytes with a constitutively activated beta-catenin. This places the block downstream from Lef1 expression but upstream from beta-catenin stabilization. Because mice lacking the BMP inhibitor Noggin fail to express Lef1, our findings support a model, whereby a sequential inhibition and then activation of BMPRIA is necessary to define a band of hair progenitor cells, which possess enough Lef1 and stabilized beta-catenin to activate the hair specific keratin genes and generate the hair shaft.
利用小鼠中的条件性基因靶向技术,我们发现骨形态发生蛋白受体IA(BMP receptor IA)对于内根鞘和毛干祖细胞的分化至关重要。如果没有BMPRIA的激活,GATA-3会下调,其对内根鞘分化的调控也会受到影响。相反,Lef1会上调,但其对毛发分化的调控仍然受阻,且缺乏BMPRIA的毛囊无法激活包括角蛋白基因在内的Lef1/β-连环蛋白调控的基因。通过用组成型激活的β-连环蛋白转染缺乏BMPRIA的角质形成细胞,可以恢复Wnt介导的转录激活。这表明阻断发生在Lef1表达的下游,但在β-连环蛋白稳定化的上游。由于缺乏骨形态发生蛋白抑制剂Noggin的小鼠无法表达Lef1,我们的研究结果支持一种模型,即依次抑制然后激活BMPRIA对于定义一群毛发祖细胞是必要的,这群祖细胞具有足够的Lef1和稳定的β-连环蛋白来激活毛发特异性角蛋白基因并生成毛干。