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GTSF-2:一种适用于多种正常及转化哺乳动物细胞的新型通用细胞培养基。

GTSF-2: a new, versatile cell culture medium for diverse normal and transformed mammalian cells.

作者信息

Lelkes P I, Ramos E, Nikolaychik V V, Wankowski D M, Unsworth B R, Goodwin T J

机构信息

Department of Medicine, University of Wisconsin Medical School, Milwaukee 53201, USA.

出版信息

In Vitro Cell Dev Biol Anim. 1997 May;33(5):344-51. doi: 10.1007/s11626-997-0004-7.

Abstract

The aim of this study was to test the versatility of a new basal cell culture medium, GTSF-2. In addition to traditional growth-factors, GTSF-2 contains a blend of three sugars (glucose, galactose, and fructose) at their physiological levels. For these studies, we isolated normal endothelial cells from human, bovine, and rat large blood vessels and microvessels. In addition, GTSF-2 was also tested as a replacement for high-glucose-containing medium for PC12 pheochromocytoma cells and for other, transformed cell lines. The cell growth characteristics were assessed with a novel cell viability and proliferation assay, which is based on the bioreduction of the fluorescent dye, Alamar Blue. After appropriate calibration, the Alamar Blue assay was found to be equivalent to established cell proliferation assays. Alamar Blue offers the advantage that cell proliferation can be measured in the same wells over an extended period of time. For some of the cell types (e.g., endothelial cells isolated from the bovine aorta, the rat adrenal medulla, or the transformed cells), proliferation in unmodified GTSF-2 was equivalent to that in the original culture media. For others cell types (e.g., human umbilical vein endothelial cells and PC12 cells), GTSF-2 proved to be a superior growth medium, when supplemented with simple additives, such as endothelial cell growth supplement (bFGF) or horse serum. Our results suggest that GTSF-2 is a versatile basal medium that will be useful for studying organ-specific differentiation in heterotypic coculture studies.

摘要

本研究的目的是测试一种新型基础细胞培养基GTSF-2的通用性。除了传统的生长因子外,GTSF-2还含有生理水平的三种糖类(葡萄糖、半乳糖和果糖)的混合物。在这些研究中,我们从人、牛和大鼠的大血管及微血管中分离出正常内皮细胞。此外,GTSF-2还被测试作为PC12嗜铬细胞瘤细胞和其他转化细胞系的含高糖培养基的替代品。使用一种基于荧光染料Alamar Blue生物还原的新型细胞活力和增殖测定法评估细胞生长特性。经过适当校准后,发现Alamar Blue测定法与已建立的细胞增殖测定法相当。Alamar Blue的优点是可以在同一孔中长时间测量细胞增殖。对于某些细胞类型(例如从牛主动脉、大鼠肾上腺髓质分离的内皮细胞或转化细胞),未修饰的GTSF-2中的增殖与原始培养基中的增殖相当。对于其他细胞类型(例如人脐静脉内皮细胞和PC12细胞),当添加简单添加剂(如内皮细胞生长补充剂(bFGF)或马血清)时,GTSF-2被证明是一种优质的生长培养基。我们的结果表明,GTSF-2是一种通用的基础培养基,将有助于在异型共培养研究中研究器官特异性分化。

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