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人角质形成细胞在体外的生长与分化:一项免疫组织化学与流式细胞术联合研究

The growth and differentiation of human keratinocytes in vitro: a combined immunohistochemical and flow cytometric study.

作者信息

van Erp P E, de Jongh G J, Boezeman J B, Schalkwijk J

机构信息

Department of Dermatology, University Hospital Nijmegen, The Netherlands.

出版信息

Arch Dermatol Res. 1994;286(2):115-22. doi: 10.1007/BF00370737.

Abstract

In this study we performed a cell kinetic characterization of the growth and differentiation of human keratinocytes. Using a combination of immunohistochemical and flow cytometric techniques it was possible to obtain a detailed description of these processes. The proliferative activity of the cell cultures was analysed with flow cytometric techniques, measuring relative DNA content, iododeoxyuridine incorporation and the expression of the antigen recognized by Ki-67. In addition to a standard monolayer culture technique, cells were maintained in suspension. Under these conditions these cells were not capable of dividing, started to lose their nuclei, and the expression of differentiation-related proteins such as involucrin and filaggrin was induced, suggesting that the cells changed towards a differentiated phenotype. Binding of the antibody Ks8.12, recognizing keratins 13 and 16, occurred under all culture conditions, independent of cell density, and also in suspension, suggesting that it is a marker for abnormal differentiation rather than for hyperproliferation.

摘要

在本研究中,我们对人角质形成细胞的生长和分化进行了细胞动力学特征分析。通过结合免疫组织化学和流式细胞术技术,得以详细描述这些过程。运用流式细胞术技术分析细胞培养物的增殖活性,测量相对DNA含量、碘脱氧尿苷掺入量以及Ki-67识别的抗原表达。除了标准的单层培养技术外,细胞还维持在悬浮状态。在这些条件下,这些细胞无法分裂,开始失去细胞核,并诱导了与分化相关的蛋白质如兜甲蛋白和细丝聚集蛋白的表达,这表明细胞向分化表型转变。识别角蛋白13和16的抗体Ks8.12的结合在所有培养条件下均会发生,与细胞密度无关,在悬浮状态下也会发生,这表明它是异常分化而非过度增殖的标志物。

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