Differential calcium requirements for growth of mouse skin epithelial and fibroblast cells.

M F Kulesz-Martin, D Fabian, J S Bertram
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引用次数: 28

Abstract

Concentration of extracellular Ca++ optimum for growth of cell types of mesodermal origin have been reported to be up to 100-fold higher than concentrations optimal for epidermal or other epithelial lining cells. In order to examine Ca++ requirements of epithelial v. fibroblastic cells derived from a common tissue source, prior to prolonged culture, freshly isolated mouse epidermal keratinocytes, hair follicle cells and dermal fibroblasts were plated at high density or at clonal density in medium ranging from 0.014 to 1.4 mM Ca++. Epithelial skin cells grew best at Ca++ levels below 0.1 mM while dermal fibroblasts grew best at a Ca++ concentration of 1.4 mM. The epithelial cell types exhibited marked morphologic changes in response to Ca++, while the fibroblasts did not. These results suggest that the variations in Ca++ response between lining epithelium and mesenchymal cells resulted from inherent differences in these cell types, but a mechanism for such differential effects has not yet been defined.

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小鼠皮肤上皮细胞和成纤维细胞生长对钙的不同需求。
据报道,中胚层来源的细胞类型生长的最佳细胞外钙离子浓度比表皮细胞或其他上皮细胞的最佳浓度高100倍。为了检验来自同一组织来源的上皮细胞和成纤维细胞对Ca++的需求,在长时间培养之前,将新鲜分离的小鼠表皮角质形成细胞、毛囊细胞和真皮成纤维细胞以高密度或克隆密度镀在0.014至1.4 mM Ca++的培养基中。在Ca++浓度低于0.1 mM时,皮肤上皮细胞生长最好,而在Ca++浓度为1.4 mM时,真皮成纤维细胞生长最好。上皮细胞类型对Ca++的反应表现出明显的形态变化,而成纤维细胞则没有。这些结果表明,衬里上皮细胞和间充质细胞之间ca2 ++反应的差异是由这些细胞类型的内在差异引起的,但这种差异效应的机制尚未明确。
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Abstracts of the joint meeting of the Cell Kinetics Society and the International Cell Cycle Society. 28-31 March 1990, St Louis, Missouri, U.S.A. Abstracts of the 16th meeting of the European Study Group for Cell Proliferation. 3-6 May 1989, Milan. Proceedings of the Cell Kinetics Society, thirteenth annual meeting. 29 March-1 April 1989, White Plains, New York, U.S.A. Bone marrow fibroblast colony-forming cells are osteogenic stem cells. Epidermal tissue homeostasis. III. Effect of hydrocortisone on cell pool size, cell birth rate and cell loss in normal toads and in toads deprived of the pars distalis of the pituitary gland.
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