Pillai S, Bikle D D
Department of Medicine, University of California, San Francisco 94143.
J Cell Physiol. 1991 Jan;146(1):94-100. doi: 10.1002/jcp.1041460113.
Extracellular calcium (Cao) and the steroid hormone 1,25(OH)2D, induce the differentiation of human epidermal cells in culture. Recent studies suggest that increases in intracellular free calcium (Cai) levels may be an initial signal that triggers keratinocyte differentiation. In the present study, we evaluated cornified envelope formation, the terminal event during keratinocyte differentiation, and correlated it with changes in the Cai levels during differentiation of keratinocytes in culture induced by Cao or 1,25(OH)2D. Keratinocytes were grown in different Cao concentrations (0.1 or 1.2 mM) or in the presence of 1,25(OH)2D (10(-11) to 10(-7) M), and the Cai levels were measured using the fluorescent probe Indo-1. Our results suggest that the induction of cornified envelope formation is associated with an increase in Cai level during calcium-induced differentiation. Cao and the calcium ionophore ionomycin acutely increased Cai and cornified envelope formation. In contrast, the effect of 1,25(OH)2D on increasing Cai levels and stimulating cornified envelope formation was long-term, requiring days of treatment with 1,25(OH)2D. Our data are consistent with other recent studies and support the hypothesis that Cao regulates keratinocyte differentiation primarily by acutely increasing their Cai levels. The role of calcium in the mechanism of action of 1,25(OH)2D on keratinocyte differentiation is less clear. The increase in Cai of keratinocytes during 1,25(OH)2D induced differentiation may be essential for or subsequent to its prodifferentiation effects.
细胞外钙(Caₒ)和类固醇激素1,25(OH)₂D可诱导培养的人表皮细胞分化。最近的研究表明,细胞内游离钙(Caᵢ)水平的升高可能是触发角质形成细胞分化的初始信号。在本研究中,我们评估了角质化包膜的形成,这是角质形成细胞分化的终末事件,并将其与培养的角质形成细胞在Caₒ或1,25(OH)₂D诱导分化过程中Caᵢ水平的变化相关联。角质形成细胞在不同的Caₒ浓度(0.1或1.2 mM)下或在1,25(OH)₂D(10⁻¹¹至10⁻⁷ M)存在的情况下生长,并使用荧光探针Indo-1测量Caᵢ水平。我们的结果表明,在钙诱导的分化过程中,角质化包膜形成的诱导与Caᵢ水平的升高相关。Caₒ和钙离子载体离子霉素可急性增加Caᵢ和角质化包膜的形成。相比之下,1,25(OH)₂D增加Caᵢ水平和刺激角质化包膜形成的作用是长期的,需要用1,25(OH)₂D处理数天。我们的数据与最近的其他研究一致,并支持以下假设:Caₒ主要通过急性增加角质形成细胞的Caᵢ水平来调节其分化。钙在1,25(OH)₂D对角质形成细胞分化的作用机制中的作用尚不清楚。在1,25(OH)₂D诱导的分化过程中角质形成细胞Caᵢ的增加可能对其促分化作用至关重要或在其之后发生。