Centre for Reproductive Biology, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, Scotland, United Kingdom.
Fertil Steril. 2010 Oct;94(5):1601-8.e1. doi: 10.1016/j.fertnstert.2009.10.061. Epub 2010 Jan 4.
To demonstrate expression and regulation of prokineticins (PROKs) and their receptors (PROKRs) in fallopian tube (FT) from women who are not pregnant and women with ectopic pregnancy (EP).
Tissue analysis.
Large United Kingdom teaching hospital.
PATIENT(S): Women undergoing hysterectomy for benign gynecological conditions (n = 15) and surgery for EP (n = 16).
INTERVENTION(S): Quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemistry were used to determine FT PROK/PROKR messenger RNA (mRNA) expression and protein localization, respectively. The PROK/PROKR levels were measured in tubal explant cultures stimulated with estrogen (E) and progestogen.
MAIN OUTCOME MEASURE(S): Differential expression of PROK and PROKR.
RESULT(S): The FT PROK2 and PROKR1 mRNA levels were up-regulated during the P-dominant midluteal phase of the menstrual cycle. Increased PROKR1 expression was observed in tubal explant cultures treated with medroxy-progesterone acetate (MPA). The PROK and PROKR proteins were localized to the epithelium and smooth muscle layers of the FT. The PROKR1 and PROKR2 mRNA levels were lower in FT from women with EP compared with nonpregnant FT from the midluteal phase.
CONCLUSION(S): These data suggest a potential role for PROKs in FT function. The PROKs are known to affect smooth muscle contraction in the gut. Dysregulated PROK expression in FT could affect FT smooth muscle contractility and embryo-tubal transport, providing a potential cause for EP.
展示未怀孕和异位妊娠(EP)女性输卵管(FT)中促动力素(PROKs)及其受体(PROKRs)的表达和调节。
组织分析。
英国大型教学医院。
因良性妇科疾病行子宫切除术的妇女(n=15)和因 EP 而行手术的妇女(n=16)。
使用定量逆转录-聚合酶链反应(RT-PCR)和免疫组织化学分别确定 FT PROK/PROKR 信使 RNA(mRNA)表达和蛋白定位。在接受雌激素(E)和孕激素刺激的输卵管外植体培养物中测量 PROK/PROKR 水平。
PROK 和 PROKR 的差异表达。
FT PROK2 和 PROKR1 mRNA 水平在月经周期的 P 主导中期升高。在接受醋酸甲羟孕酮(MPA)处理的输卵管外植体培养物中观察到 PROKR1 表达增加。PROK 和 PROKR 蛋白定位于 FT 的上皮和平滑肌层。与非妊娠 FT 相比,EP 患者的 FT 中 PROKR1 和 PROKR2 mRNA 水平较低。
这些数据表明 PROKs 在 FT 功能中具有潜在作用。已知 PROKs 影响肠道平滑肌收缩。FT 中 PROK 表达失调可能会影响 FT 平滑肌收缩和胚胎-输卵管运输,为 EP 提供潜在原因。