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胆囊上皮的单层和三维细胞培养以及活组织培养

Monolayer and three-dimensional cell culture and living tissue culture of gallbladder epithelium.

作者信息

Nakanuma Y, Katayanagi K, Kawamura Y, Yoshida K

机构信息

Second Department of Pathology, Kanazawa University School of Medicine, Japan.

出版信息

Microsc Res Tech. 1997 Oct 1;39(1):71-84. doi: 10.1002/(SICI)1097-0029(19971001)39:1<71::AID-JEMT6>3.0.CO;2-2.

Abstract

Several models for preparing and isolating human and animal gallbladder epithelial cells, including low-grade gallbladder carcinoma cells, as well as proposed systems for culturing these isolated epithelial cells are reviewed here. Several reports concerning tissue culture of the gallbladder are also reviewed. The cell culture systems are divided into monolayer cell culture on collagen-coated or uncoated culture dishes or other culture substrate and three-dimensional cell culture in collagen gel. To prepare and isolate gallbladder epithelial cells, digestion of the gallbladder mucosa, abrasion of the mucosal epithelial cells, and excision of epithelial outgrowth of mucosal explants are applied. In monolayer cell culture, most of the specific biological features of isolated and cultured cells characteristic to the gallbladder are gradually lost after several passages, though quantitative and objective analyses of the pathophysiology of cultured cells and their secretory substances can be performed. Tissue culture using explants of the gallbladder has mainly been used for physiological studies of the gallbladder, such as investigating the transport of water and electrolytes. In this tissue culture system, quantitative assessment is difficult, though the original and specific biological and histological characteristics of the gallbladder are retained. Three-dimensional collagen gel culture could be an ideal model combining monolayer cell culture and tissue culture systems, and create controllable conditions or environments when several biologically active substances, such as growth factors, proinflammatory cytokines and adhesion molecules, are added to the culture medium. Advantages and shortcomings of individual cultivation models are discussed, and selecting the culture model most appropriate to the purpose of the study will facilitate investigations of the biology and pathogenetic mechanisms of gallbladder diseases such as cholelithiasis.

摘要

本文综述了几种制备和分离人及动物胆囊上皮细胞(包括低级别胆囊癌细胞)的模型,以及一些用于培养这些分离出的上皮细胞的提议系统。同时也回顾了几篇关于胆囊组织培养的报告。细胞培养系统分为在胶原包被或未包被的培养皿或其他培养基质上的单层细胞培养,以及在胶原凝胶中的三维细胞培养。为了制备和分离胆囊上皮细胞,可采用胆囊黏膜消化法、黏膜上皮细胞刮除法以及黏膜外植体上皮生长物切除术。在单层细胞培养中,分离和培养的细胞所具有的胆囊特异性生物学特征在传代几次后会逐渐丧失,不过可以对培养细胞及其分泌物质的病理生理学进行定量和客观分析。使用胆囊外植体的组织培养主要用于胆囊的生理学研究,比如研究水和电解质的转运。在这个组织培养系统中,虽然能保留胆囊原始的特异性生物学和组织学特征,但定量评估较为困难。三维胶原凝胶培养可能是一种结合单层细胞培养和组织培养系统的理想模型,当向培养基中添加几种生物活性物质(如生长因子、促炎细胞因子和黏附分子)时,可以创造可控的条件或环境。本文讨论了各培养模型的优缺点,选择最适合研究目的的培养模型将有助于对胆结石等胆囊疾病的生物学和发病机制进行研究。

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