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在补充有人子宫血管生成因子的无血清培养基中分离和培养人蜕膜毛细血管内皮细胞。

Isolation and culture of human decidual capillary endothelial cells in serum-free medium supplemented with human uterine angiogenic factor.

作者信息

Lindenbaum E S, Langer N, Beach D

机构信息

Morphology Research Unit, Faculty of Medicine, Technion IIT, Haifa, Israel.

出版信息

Acta Anat (Basel). 1991;140(3):273-9. doi: 10.1159/000147068.

Abstract

Human decidual capillary endothelial (HDCE) cells, obtained from decidual fragments of legally induced first-trimester terminations of pregnancies, were cultured in a serum-free medium supplemented with human uterine angiogenic factor (HUAF). The method of isolating the cells from the decidual tissue is described. Identification of the decidual endothelial cells was based on light- and electron-microscopic observations as well as on antifactor VIII immunoperoxidase-staining technique. The HDCE cell culture in the serum-free medium lasted for 25 weeks through eight subcultures. The cells frozen in glycerin yielded 80% viability after thawing. Electron-microscopic observations of the monolayer demonstrated Weibel-Palade bodies, desmosomes and tight junctions. HUAF is mitogenic to HDCE at 10-100 ng/ml. The dependency of HDCE cells grown in culture on HUAF may explain in part the mechanism involved in the dynamic vascular expansion occurring during gestation.

摘要

从合法人工终止妊娠的孕早期蜕膜组织碎片中获取人蜕膜毛细血管内皮(HDCE)细胞,将其培养于添加人子宫血管生成因子(HUAF)的无血清培养基中。文中描述了从蜕膜组织中分离细胞的方法。蜕膜内皮细胞的鉴定基于光镜和电镜观察以及抗因子VIII免疫过氧化物酶染色技术。在无血清培养基中进行的HDCE细胞培养持续了25周,传代八次。冻存于甘油中的细胞解冻后存活率达80%。单层细胞的电镜观察显示有魏-帕小体、桥粒和紧密连接。HUAF在10 - 100 ng/ml时对HDCE有促有丝分裂作用。培养的HDCE细胞对HUAF的依赖性可能部分解释了妊娠期间发生的动态血管扩张所涉及的机制。

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