Kalma Yael, Granot Irit, Gnainsky Yulia, Or Yuval, Czernobilsky Bernard, Dekel Nava, Barash Amihai
Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Fertil Steril. 2009 Apr;91(4):1042-9, 1049.e1-9. doi: 10.1016/j.fertnstert.2008.01.043. Epub 2008 Mar 19.
To explore the possibility that endometrial injury modulates the expression of specific genes that may increase uterine receptivity.
Controlled clinical study.
Clinical IVF unit and academic research center.
PATIENT(S): IVF patients with 28- to 30-day menstrual cycles.
INTERVENTION(S): Endometrial biopsies from two groups of patients were collected on days 20-21 of their spontaneous menstrual cycle. The experimental, but not the control, group underwent biopsies on days 11-13 and 21-24 of their preceding cycle.
MAIN OUTCOME MEASURE(S): Global endometrial gene expression and specific analysis of uroplakin Ib (UPIb) mRNA level throughout the menstrual cycle.
RESULT(S): Local injury modulated the expression of a wide variety of genes. One of the prominently up-regulated genes was the bladder transmembranal protein, UPIb, whose expression by the endometrium is shown here for the first time. Endometrial UPIb mRNA increases after biopsy in the same cycle wct 2with an additional elevation in the following cycle. Immunohistochemical analysis localized the UPIb protein to the glandular-epithelial cells. Genes encoding other membrane proteins such as adipose differentiation-related protein and mucin 1, transmembrane, were also up-regulated.
CONCLUSION(S): The biopsy-induced increase in the expression of UPIb and other genes encoding membrane proteins supports the possible importance of the membrane structure and stability during implantation. The specific role of UPIb in uterine receptivity should be elucidated.
探讨子宫内膜损伤调节特定基因表达从而可能增加子宫容受性的可能性。
对照临床研究。
临床体外受精单位和学术研究中心。
月经周期为28至30天的体外受精患者。
在两组患者自然月经周期的第20 - 21天采集子宫内膜活检样本。试验组在前一周期的第11 - 13天和第21 - 24天进行活检,而对照组不进行。
整个月经周期中子宫内膜基因的整体表达以及尿血小板溶素Ib(UPIb)mRNA水平的特异性分析。
局部损伤调节了多种基因的表达。其中一个显著上调的基因是膀胱跨膜蛋白UPIb,其在子宫内膜中的表达在此首次展示。在活检后的同一周期,子宫内膜UPIb mRNA增加,在下一周期进一步升高。免疫组织化学分析将UPIb蛋白定位在腺上皮细胞。编码其他膜蛋白的基因,如脂肪分化相关蛋白和跨膜黏蛋白1,也上调。
活检诱导的UPIb和其他编码膜蛋白的基因表达增加支持了植入过程中膜结构和稳定性可能具有的重要性。UPIb在子宫容受性中的具体作用有待阐明。