Drozdoff V, Pledger W J
Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
J Cell Biol. 1993 Nov;123(4):909-19. doi: 10.1083/jcb.123.4.909.
In the epidermis, one of the earliest characterized events in keratinocyte differentiation is the coordinate induction of a pair of keratins specifically expressed in suprabasal cells, keratin 1 (K1) and keratin 10 (K10). Both in vivo and in vitro, extracellular calcium is necessary for several biochemical and structural changes during keratinocyte differentiation. However, it has been unclear if calcium serves as a differentiation signal in keratinocytes. In these studies, expression of suprabasal keratin mRNA and protein is used to test whether the initial differentiation of primary mouse keratinocytes in vitro is dependent on changes in the concentration of extracellular calcium. K1 mRNA was expressed at low levels in cultures of keratinocytes growing on plastic in 0.05 mM calcium but in attached cells was not further induced by increases in the concentration of extracellular calcium. Suspension of the keratinocytes into semi-solid medium induced a rapid and substantial increase in both expression of K1 mRNA and in the percentage of cells expressing suprabasal keratin proteins. The induction was unaffected by the concentration of calcium in the semi-solid medium and could not be enhanced by exposing attached cells to higher calcium before suspension. The induction of K1 mRNA could be inhibited by exposure of the keratinocytes to either EGF or fibronectin. These results suggest that commitment of mouse keratinocytes to terminal differentiation is independent of extracellular calcium and may be regulated primarily by extracellular factors other than calcium.
在表皮中,角质形成细胞分化过程中最早被明确的事件之一是一对在基底上层细胞中特异性表达的角蛋白,即角蛋白1(K1)和角蛋白10(K10)的协同诱导。在体内和体外,细胞外钙对于角质形成细胞分化过程中的多种生化和结构变化都是必需的。然而,钙是否作为角质形成细胞中的分化信号尚不清楚。在这些研究中,基底上层角蛋白mRNA和蛋白的表达被用于测试原代小鼠角质形成细胞在体外的初始分化是否依赖于细胞外钙浓度的变化。在含有0.05 mM钙的塑料培养皿中生长的角质形成细胞培养物中,K1 mRNA表达水平较低,但在贴壁细胞中,细胞外钙浓度的增加并未进一步诱导其表达。将角质形成细胞悬浮于半固体培养基中可迅速且显著地增加K1 mRNA的表达以及表达基底上层角蛋白的细胞百分比。这种诱导不受半固体培养基中钙浓度的影响,并且在悬浮前将贴壁细胞暴露于更高浓度的钙也无法增强这种诱导。将角质形成细胞暴露于表皮生长因子(EGF)或纤连蛋白中可抑制K1 mRNA的诱导。这些结果表明,小鼠角质形成细胞向终末分化的决定独立于细胞外钙,并且可能主要由除钙以外的细胞外因子调节。