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[一种从人气道肉芽组织中分离成纤维细胞的原代培养方法]

[A method for the primary culture of fibroblasts isolated from human airway granulation tissues].

作者信息

Chen Nan, Zhang Jie, Xu Min, Wang Yu-ling, Pei Ying-hua

机构信息

Department of Pulmonary Medicine, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2013 Apr;36(4):280-2.

Abstract

OBJECTIVE

To establish a feasible method to culture primary fibroblasts isolated from human airway granulation tissues, and therefore to provide experimental data for the investigation of the pathogenesis of benign airway stenosis.

METHODS

The granulation tissues were collected from 6 patients during routine bronchoscopy at our department of Beijing Tiantan Hospital from April to June 2011. Primary fibroblasts were obtained by culturing the explanted tissues. Cell growth was observed under inverted microscope.

RESULTS

All of these 6 primary cultures were successful. Fibroblast-like cells were observed to migrate from the tissue pieces 3 d after inoculation. After 9-11 d of culture, cells reached to 90% confluence and could be sub-cultured. After passage, the cells were still in a typical elongated spindle-shape and grew well. The cells could be sub-cultured further when they formed a monolayer.

CONCLUSION

Explant culture is a reliable method for culturing primary fibroblasts from human airway granulation tissues.

摘要

目的

建立一种可行的方法来培养从人气道肉芽组织中分离出的原代成纤维细胞,从而为研究良性气道狭窄的发病机制提供实验数据。

方法

2011年4月至6月期间,在北京天坛医院我科对6例患者进行常规支气管镜检查时收集肉芽组织。通过培养外植组织获得原代成纤维细胞。在倒置显微镜下观察细胞生长情况。

结果

这6次原代培养均成功。接种后3天观察到成纤维样细胞从组织块中迁移出来。培养9 - 11天后,细胞达到90%汇合度并可传代培养。传代后,细胞仍呈典型的细长梭形且生长良好。当细胞形成单层时可进一步传代培养。

结论

外植体培养是培养人气道肉芽组织原代成纤维细胞的可靠方法。

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