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细胞培养中表皮角质形成细胞的分化:角质包膜的形成。

Differentiation of the epidermal keratinocyte in cell culture: formation of the cornified envelope.

作者信息

Sun T T, Green H

出版信息

Cell. 1976 Dec;9(4 Pt 1):511-21. doi: 10.1016/0092-8674(76)90033-7.

DOI:10.1016/0092-8674(76)90033-7
PMID:1009573
Abstract

Human epidermal keratinocytes grow from single cells into stratified colonies. Cells in the upper layers of the colonies lose their ability to divide and begin terminal differentiation. In this process, there develops a cornified cell envelope that remains insoluble after heating in solutions of sodium dodecylsulfate and beta-mercaptoethanol. The insolubility of the cornified envelope depends upon proteins, since after treatment with proteolytic enzymes, the envelope becomes soluble in the detergent. Cells with cornified envelopes can be identified under the light microscope either in living colonies or following fixation and silver nitrate staining. Keratinocytes of the basal layer move in a characteristic way, but cornified cells do not move at all and form an immobile upper layer in the colonies. Keratinocytes disaggregated from growing colonies are of differing size and density, and can be separated on isopycnic gradients of Ficoll. The DNA-synthesizing cells are small (mean diameter 14 mum). The nonmultiplying cells are large and have a protein content proportionate to their size. Their final diameter may exceed 30 microns (volume increase greater than 10 fold). Cornified envelopes are found in some of the large cells but in none of the small. In growing colonies, usually 5-10% of the cells have cornified envelopes. The fraction is reduced in colonies growing in the presence of epidermal growth factor. Strain XB, an established keratinocyte line of mouse teratomal origin, also forms cornified envelopes, but the kinetics of the process are different, indicating that the program of terminal differentiation is not initiated at corresponding times in the two cell types.

摘要

人表皮角质形成细胞从单细胞生长为分层的集落。集落上层的细胞失去分裂能力并开始终末分化。在此过程中,会形成一种角质化细胞包膜,在十二烷基硫酸钠和β-巯基乙醇溶液中加热后仍不溶解。角质化包膜的不溶性取决于蛋白质,因为用蛋白水解酶处理后,包膜可溶于去污剂。带有角质化包膜的细胞在活的集落中或固定及硝酸银染色后,可在光学显微镜下识别。基底层的角质形成细胞以一种特征性方式移动,但角质化细胞根本不移动,在集落中形成一个固定的上层。从生长中的集落中解离的角质形成细胞大小和密度不同,可通过菲可(Ficoll)等密度梯度分离。进行DNA合成的细胞较小(平均直径14μm)。不增殖的细胞较大,其蛋白质含量与其大小成比例。它们的最终直径可能超过30μm(体积增加超过10倍)。在一些大细胞中发现有角质化包膜,但小细胞中没有。在生长中的集落中,通常5% - 10%的细胞有角质化包膜。在表皮生长因子存在下生长的集落中,这一比例会降低。XB株是一种已建立的源自小鼠畸胎瘤的角质形成细胞系,也形成角质化包膜,但该过程的动力学不同,表明两种细胞类型在相应时间并未启动终末分化程序。

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