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一种建立人胃上皮细胞原代培养物的方法。

A method for establishing primary cultures of human gastric epithelial cells.

作者信息

Smoot D T, Sewchand J, Young K, Desbordes B C, Allen C R, Naab T

机构信息

Division of Gastroenterology, Department of Medicine, Howard University Hospital, 2041 Georgia Avneue, N.W., Washington, DC 20060, USA.

出版信息

Methods Cell Sci. 2000;22(2-3):133-6. doi: 10.1023/a:1009846624044.

Abstract

Long-term culture of human gastric epithelial cells has been difficult, and at present no normal human gastric epithelial cell lines are readily available. As part of our experiments to study pathogenesis of H. pylori, a bacterium that infects the stomach, we developed methods to culture normal human gastric epithelial cells. Primary cultures of human gastric epithelial cells can be established from gastric biopsies taken at upper G.I. endoscopy. Enzymatically isolated gastric epithelial-like cells are present in tight colonies on culture dishes within 24 hours of placing the cells in culture. Cells isolated stain positively for cytokeratin and produce neutral mucins, indicating that they are mucin secreting epithelial cells, consistent with gastric epithelial cells. Epithelial cells can be maintained up to 4 weeks in culture with evidence of DNA synthesis up through the first week of culture.

摘要

长期培养人胃上皮细胞一直很困难,目前尚无现成的正常人胃上皮细胞系。作为我们研究幽门螺杆菌(一种感染胃部的细菌)发病机制实验的一部分,我们开发了培养正常人胃上皮细胞的方法。人胃上皮细胞的原代培养可从在上消化道内镜检查时获取的胃活检组织中建立。将细胞接种到培养基中后24小时内,酶解分离的胃上皮样细胞会紧密聚集在培养皿上。分离出的细胞细胞角蛋白染色呈阳性,并产生中性粘蛋白,表明它们是分泌粘蛋白的上皮细胞,与胃上皮细胞一致。上皮细胞在培养中可维持长达4周,在培养的第一周都有DNA合成的迹象。

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