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在不同细胞外基质替代物“上方”和“内部”培养的增生性大鼠胆管上皮细胞的生化特性

Biochemical characteristics of hyperplastic rat bile ductular epithelial cells cultured "on top" and "inside" different extracellular matrix substitutes.

作者信息

Mathis G A, Walls S A, Sirica A E

机构信息

Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

出版信息

Cancer Res. 1988 Nov 1;48(21):6145-53.

PMID:2901908
Abstract

An essentially pure population of bile ductular epithelial cells isolated from bile duct-ligated rats was placed in primary culture by plating the cells either "on top" of or "inside" different extracellular matrix substitutes, including basement membrane Matrigel, type I collagen gel, and agarose gel. Plating efficiencies of greater than 60% were obtained when the cells were seeded in the presence of 1.0% fetal calf serum on top of Matrigel and collagen gel, but there was very little if any cell attachment to the agarose surface. In contrast, the cells could be maintained equally well and at very similar densities when they were cultured inside the various gel substances, including agarose. Regardless of substratum condition, bile ductular cells at 10 days in primary culture expressed specific activities of the marker enzymes gamma-glutamyl transpeptidase and leucine aminopeptidase which were significantly higher than those shown by freshly isolated cells. On the other hand, alkaline phosphatase activity of the cells became undetectable by day 3 of culture when they were cultured on top of either Matrigel or collagen gel but was retained at approximately 50% of its original level in cells cultured for 10 days within Matrigel or agarose gel. Treatments with dexamethasone or hydrocortisone (i.e., 10(-6) M) inhibited the increase in gamma-glutamyl transpeptidase activity of the cultured cells but did not affect the other enzyme changes. Subcultures of the bile ductular epithelial cells were developed by passing the cells in the presence of 10% fetal calf serum on surfaces coated with either type I collagen or Matrigel. In either case, cells subjected to at least 4-6 passages (up to 100 days of culture) were still characterized by a high gamma-glutamyl transpeptidase activity. Preliminary results obtained with cells plated at very low density within Matrigel also indicated the development of cell growths that appeared to be organized in the form of distinct acinar-like structures.

摘要

从胆管结扎大鼠分离得到的基本纯净的胆管上皮细胞群体,通过将细胞接种在不同的细胞外基质替代物“之上”或“之内”进行原代培养,这些替代物包括基底膜基质胶、I型胶原凝胶和琼脂糖凝胶。当细胞在含有1.0%胎牛血清的情况下接种在基质胶和胶原凝胶之上时,接种效率超过60%,但细胞在琼脂糖表面几乎没有附着。相比之下,当细胞在包括琼脂糖在内的各种凝胶物质中培养时,它们能够以相同的良好状态和非常相似的密度维持生长。无论基质条件如何,原代培养10天的胆管细胞中,标记酶γ-谷氨酰转肽酶和亮氨酸氨肽酶的比活性显著高于新鲜分离的细胞。另一方面,当细胞在基质胶或胶原凝胶上培养时,培养第3天细胞的碱性磷酸酶活性就检测不到了,但在基质胶或琼脂糖凝胶中培养10天的细胞中,该活性保留在其原始水平的约50%。用10(-6)M地塞米松或氢化可的松处理可抑制培养细胞γ-谷氨酰转肽酶活性的增加,但不影响其他酶的变化。胆管上皮细胞的传代培养是在含有10%胎牛血清的情况下,将细胞接种在涂有I型胶原或基质胶的表面进行的。在这两种情况下,至少经过4 - 6次传代(长达100天培养)的细胞仍具有较高的γ-谷氨酰转肽酶活性。在基质胶中以非常低密度接种细胞获得的初步结果也表明,细胞生长形成了似乎以独特的腺泡样结构形式组织的生长物。

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