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在位和异位子宫内膜中的血管内皮生长因子信使核糖核酸

Vascular endothelial growth factor mRNA in eutopic and ectopic endometrium.

作者信息

Kressin P, Wolber E M, Wodrich H, Meyhöfer-Malik A, Buchweitz O, Diedrich K, Malik E

机构信息

Department of Obstetrics and Gynecology, Medical University of Lübeck, Lübeck, Germany.

出版信息

Fertil Steril. 2001 Dec;76(6):1220-4. doi: 10.1016/s0015-0282(01)02898-9.

DOI:10.1016/s0015-0282(01)02898-9
PMID:11730754
Abstract

OBJECTIVE

To evaluate changes in expression levels of vascular endothelial growth factor (VEGF) mRNA in human endometrial explants in a chicken chorioallantoic membrane model of endometriosis.

DESIGN

Experimental prospective study.

SETTING

University hospital.

PATIENT(S): Endometrial biopsy samples were obtained from healthy, ovulating women undergoing elective surgery.

INTERVENTION(S): Endometrial fragments were placed on the chicken chorioallantoic membrane and removed for analysis after 0, 24, 48, and 72 hours.

MAIN OUTCOME MEASURE(S): Expression of different VEGF mRNA splice variants was tested. Expression of VEGF(165) mRNA was assessed by using competitive polymerase chain reaction and normalized to expression of the housekeeping gene human glyceraldehyde 3-phosphate dehydrogenase (GAPDH) mRNA.

RESULT(S): After 0, 24, 48, and 72 hours of incubation, all grafts expressed VEGF(121), VEGF(145), VEGF(165), and VEGF(189) mRNA. Expression of VEGF(165) mRNA increased up to 10-fold at 24 to 72 hours compared with precultivation values.

CONCLUSION(S): Levels of VEGF(165) mRNA in endometrial grafts increase after implantation on chicken chorioallantoic membrane. Hypoxic induction of VEGF mRNA expression in endometrial cell cultures has been reported previously. Induction of VEGF expression might indicate relative hypoxia of the specimen due to insufficient vascularization. Expression of VEGF may assist in vascularization of endometrial explants after retrograde menstruation.

摘要

目的

在子宫内膜异位症的鸡绒毛尿囊膜模型中评估人子宫内膜外植体中血管内皮生长因子(VEGF)mRNA表达水平的变化。

设计

实验性前瞻性研究。

地点

大学医院。

患者

子宫内膜活检样本取自接受择期手术的健康、有排卵的女性。

干预措施

将子宫内膜碎片置于鸡绒毛尿囊膜上,在0、24、48和72小时后取出进行分析。

主要观察指标

检测不同VEGF mRNA剪接变体的表达。通过竞争性聚合酶链反应评估VEGF(165) mRNA的表达,并将其标准化为管家基因人甘油醛-3-磷酸脱氢酶(GAPDH)mRNA的表达。

结果

在孵育0、24、48和72小时后,所有移植物均表达VEGF(121)、VEGF(145)、VEGF(165)和VEGF(189) mRNA。与预培养值相比,VEGF(165) mRNA的表达在24至72小时增加了10倍。

结论

子宫内膜移植物在植入鸡绒毛尿囊膜后,VEGF(165) mRNA水平升高。此前已有报道在子宫内膜细胞培养中低氧诱导VEGF mRNA表达。VEGF表达的诱导可能表明由于血管化不足,标本存在相对缺氧。VEGF的表达可能有助于逆行月经后子宫内膜外植体的血管化。

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Vascular endothelial growth factor mRNA in eutopic and ectopic endometrium.在位和异位子宫内膜中的血管内皮生长因子信使核糖核酸
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