间质细胞
生物
永生化细胞系
蜕膜化
细胞培养
内科学
内分泌学
细胞生物学
体细胞
癌症研究
遗传学
医学
基因
作者
Graciela Krikun,Gil Mor,Ayesha B. Alvero,Seth Guller,Frederick Schatz,Eva Sapi,Md Mizanur Rahman,Rebeca Caze,Mazin Β. Qumsiyeh,Charles J. Lockwood
出处
期刊:Endocrinology
[Oxford University Press]
日期:2004-01-20
卷期号:145 (5): 2291-2296
被引量:269
摘要
Obtaining primary human endometrial stromal cells (HESCs) for in vitro studies is limited by the scarcity of adequate human material and the inability to passage these cells in culture for long periods. Immortalization of these cells would greatly facilitate studies; however, the process of immortalization often results in abnormal karyotypes and aberrant functional characteristics. To meet this need, we have introduced telomerase into cultured HESCs to prevent the normal shortening of telomeres observed in adult somatic cells during mitosis. We have now developed and analyzed a newly immortalized HESC line that contains no clonal chromosomal structural or numerical abnormalities. In addition, when compared with the primary unpassaged parent cells, the new cell line displayed similar biochemical endpoints after treatment with ovarian steroids. Classical decidualization response to estradiol plus medroxyprogesterone acetate were seen in both morphologically, and progestin was seen to induce or regulate the expression of IGF binding protein-1, fibronectin, prolactin, tissue factor, plasminogen activator inhibitor-1, and Fas/Fas ligand. In summary, an immortalized HESC line has been developed that is karyotypically, morphologically, and phenotypically similar to the primary parent cells, and it is a powerful and consistent resource for in vitro work.
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