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人食管上皮细胞在原代外植体和连续培养中的生长特性

Growth characteristics of human esophageal epithelial cells in primary explant and serial culture.

作者信息

Zboralske F F, Karasek M A

出版信息

In Vitro. 1984 Feb;20(2):109-18. doi: 10.1007/BF02626651.

Abstract

Growth characteristics of human esophageal epithelial cells have been determined in primary explant and serial culture. Normal human esophagus was obtained from donor patients in a heart/lung transplantation program; tissue obtained at autopsy (6 to 22 h after death) was not viable. When mucosal specimens (1.5 mm2) were explanted on a plastic surface and attached with a plasma clot, 35% of explants detached from the surface within 48 h. The addition of epsilon amino caproic acid (EACA) to the culture medium increased explant attachment to 93% (P less than 0.001). Outgrowth kinetics were similar in both the presence and absence of EACA. No advantage of human serum over nonhuman sera was observed in primary culture. Esophageal epithelium could be frozen in 10% dimethyl sulfoxide without affecting growth kinetics. Addition of dexamethasone (DEX) significantly altered esophageal cell morphology in primary culture and increased viability on serial culture. Studies of pH revealed an optimum at pH 7.4 with significantly decreased growth occurring at 6.8 and no growth at 6.2. Esophageal cells in primary explant cultures could be released by trypsin and passaged two additional times with an eightfold increase in total number. An increased rate of attachment and multiplication was observed for cells plated on a collagen substrate compared to plastic. The addition of EACA and DEX to the culture media and the subculture on a collagen substrate provide a method for the isolation and serial cultivation of human esophageal cells from biopsy-sized specimens of normal esophageal epithelium.

摘要

已在原代外植体和连续培养中确定了人食管上皮细胞的生长特性。正常人类食管取自心肺移植项目中的供体患者;尸检(死亡后6至22小时)获得的组织没有活力。当将黏膜标本(1.5平方毫米)接种到塑料表面并用血浆凝块附着时,35%的外植体在48小时内从表面脱落。向培养基中添加ε-氨基己酸(EACA)可使外植体附着率提高到93%(P小于0.001)。无论有无EACA,生长动力学相似。在原代培养中未观察到人类血清相对于非人类血清的优势。食管上皮细胞可在10%二甲基亚砜中冷冻,而不影响生长动力学。添加地塞米松(DEX)可显著改变原代培养中食管细胞的形态,并提高连续培养中的活力。pH研究表明,最适pH为7.4,在pH 6.8时生长显著下降,在pH 6.2时无生长。原代外植体培养中的食管细胞可用胰蛋白酶释放,并再传代两次,总数增加八倍。与塑料相比,接种在胶原底物上的细胞附着和增殖速率增加。向培养基中添加EACA和DEX以及在胶原底物上进行传代培养,为从正常食管上皮活检大小的标本中分离和连续培养人食管细胞提供了一种方法。

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