Suppr超能文献

培养的牛主动脉内皮细胞中胞饮小泡表面密度的降低。一项定量超微结构冷冻蚀刻研究。

Reduction of pinocytotic vesicle surface density in cultured bovine aortic endothelial cells. A quantitative ultrastructural freeze-etching study.

作者信息

Bianciardi G, Berti G, Palummo N, Vatti R, Weber E, Weber G

机构信息

Institute of Pathologic Anatomy, University of Siena, Italy.

出版信息

J Submicrosc Cytol Pathol. 1988 Oct;20(4):777-82.

PMID:3224342
Abstract

The development of culture techniques for endothelium of the large vessels has stimulated many studies to understand endothelial functions in normal and pathological conditions. In this report we describe that in primary cultures the mean surface density of pinocytotic vesicles, evaluated by computerized morphometric analysis of endothelial cell plasma-membrane, dramatically decreases with respect to that of the cells immediately detached from the arterial wall (6.7 +/- 1.1 microns2 against 19.5 +/- 2.2 microns2, p less than 0.001). The results are unchanged if the cells are enzymatically or mechanically detached from the vessel wall or from the culture flask. After the first passage, the mean surface density of pinocytotic vesicles decreases further (2.5 +/- 1.3 microns2 p less than 0.01). After the 2nd and the 3rd passages, the morphometrical values of endothelial cell plasma-membrane remain low (1.5 +/- 0.2 microns2; 2.5 +/- 0.2 microns2). When endothelial cultures are employed to study pathological aspects of disease, not only the aging process but also the possible occurrence of early changes have to be taken into consideration.

摘要

大血管内皮细胞培养技术的发展推动了许多旨在了解正常和病理条件下内皮功能的研究。在本报告中,我们描述了在原代培养中,通过对内皮细胞质膜进行计算机形态计量分析评估的胞饮小泡平均表面密度,相对于刚从动脉壁分离的细胞而言显著降低(分别为6.7±1.1微米²和19.5±2.2微米²,p<0.001)。无论细胞是通过酶解法还是机械法从血管壁或培养瓶中分离,结果均无变化。首次传代后,胞饮小泡的平均表面密度进一步降低(2.5±1.3微米²,p<0.01)。在第2次和第3次传代后,内皮细胞质膜的形态计量值仍保持较低水平(1.5±0.2微米²;2.5±0.2微米²)。当利用内皮细胞培养来研究疾病的病理情况时,不仅要考虑衰老过程,还必须考虑早期变化可能的发生情况。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验