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在无血清培养基中培养、传代和分化表皮角质形成细胞。

Cultivation, serial transfer, and differentiation of epidermal keratinocytes in serum-free medium.

作者信息

Castro-Muñozledo F, Hernández-Quintero M, Marsch-Moreno M, Kuri-Harcuch W

机构信息

Department of Cell Biology, Centro de Investigación y de Estudios Avanzados del IPN, Mexico City, Mexico.

出版信息

Biochem Biophys Res Commun. 1997 Jul 9;236(1):167-72. doi: 10.1006/bbrc.1997.6924.

Abstract

We describe serum-free culture conditions for human epidermal keratinocytes using lethally treated 3T3 cells as feeder layers and normal Ca++ concentrations (1.2 mM), in a DMEM/F12-Ham nutrient mixture supplemented with several additives, and 10 mg/ml bovine serum albumin instead of animal serum. Keratinocytes were serially grown to 15-18 cell generations (4 subcultivations) and formed a stratified squamous epithelium that could be detached as a graftable epithelial sheet. EGF and TGF alpha significantly increased keratinocyte proliferation under these conditions; EGF reduced the expression of keratin K1, which is specific for stratified and terminally differentiated epidermal keratinocytes. In contrast with previous reports, the serum-free medium we describe here supports serial growth and normal differentiation of human epidermal keratinocytes, and the formation of graftable stratified epithelia; it also supports the assay of a variety of cytokines or compounds that modulate epidermal keratinocyte proliferation and differentiation.

摘要

我们描述了一种用于人表皮角质形成细胞的无血清培养条件,使用经过致死处理的3T3细胞作为饲养层,在正常钙离子浓度(1.2 mM)下,于添加了多种添加剂的DMEM/F12-Ham营养混合物中培养,并使用10 mg/ml牛血清白蛋白替代动物血清。角质形成细胞连续传代培养至15 - 18代(4次传代培养),形成了可作为可移植上皮片分离的复层鳞状上皮。在这些条件下,表皮生长因子(EGF)和转化生长因子α(TGFα)显著增加角质形成细胞的增殖;EGF降低了角质形成细胞特异性的、用于复层和终末分化表皮角质形成细胞的角蛋白K1的表达。与先前的报道不同,我们在此描述的无血清培养基支持人表皮角质形成细胞的连续生长和正常分化,以及可移植复层上皮的形成;它还支持对多种调节表皮角质形成细胞增殖和分化的细胞因子或化合物进行检测。

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