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过氧化物酶体增殖物激活受体 α 在人妊娠子宫肌层中的表达变化。

Peroxisome proliferator-activated receptor alpha expression changes in human pregnant myometrium.

机构信息

Department of Obstetrics and Gynecology, Qilu Hospital, Shandong University, Jinan, Shandong, China.

出版信息

Reprod Sci. 2013 Jun;20(6):654-60. doi: 10.1177/1933719112461187. Epub 2012 Nov 9.

Abstract

Peroxisome proliferator-activated receptor alpha (PPARα) has been demonstrated to exhibit anti-inflammatory activities that are hypothesized to play a key role in labor suppression and maintenance of uterine quiescence. The aim of this study was to identify pregnancy- and labor-associated changes in PPARα in human myometrium. For this investigation, human myometrium was obtained from premenopausal women, and the study participants were categorized into the following 4 groups: nonpregnant (NP; n = 10), preterm not in labor (PNL; n = 10, gestation range 20-35 weeks), term not in labor (TNL; n = 20, gestation range 37-41 weeks), and term in labor (TL; n = 20, gestation range 37-41 weeks). Immunohistochemistry was used to locate and confirm the expression of PPARα. Relative quantitative real-time polymerase chain reaction (PCR) and Western blotting were employed to study the expression of anti-inflammatory PPARα and proinflammatory interleukin 1β (IL-1β). Immunohistochemistry indicated that PPARα was located in the nucleus of uterine smooth muscle cells. Compared to other groups, in PNL group, the PPARα messenger RNA (mRNA) and protein increased significantly. Decreased PPARα mRNA and protein expressions in myometrium were associated with labor while IL-1β increased remarkably. There were negative correlations between PPARα and IL-1β on mRNA (r = -.765, P < .01) and protein (r = -.624, P < .01) levels analyzed using Pearson test. In conclusion, human pregnancy is associated with changes in expression of PPARα and IL-1β in myometrium. The changes observed suggest that PPARα may play a role in maintaining pregnancy or initiating labor through inhibiting the expression of IL-1β in human myometrium.

摘要

过氧化物酶体增殖物激活受体α(PPARα)已被证明具有抗炎活性,据推测其在抑制分娩和维持子宫静止方面发挥着关键作用。本研究旨在确定人子宫肌层中与妊娠和分娩相关的 PPARα变化。为此,我们从绝经前妇女中获得了人子宫肌层,并将研究参与者分为以下 4 组:非妊娠(NP;n=10)、早产未临产(PNL;n=10,妊娠周数 20-35 周)、足月未临产(TNL;n=20,妊娠周数 37-41 周)和足月临产(TL;n=20,妊娠周数 37-41 周)。免疫组织化学用于定位和确认 PPARα的表达。相对定量实时聚合酶链反应(PCR)和 Western 印迹用于研究抗炎性 PPARα和促炎性白细胞介素 1β(IL-1β)的表达。免疫组织化学表明 PPARα位于子宫平滑肌细胞核中。与其他组相比,PNL 组的 PPARα信使 RNA(mRNA)和蛋白表达显著增加。子宫肌层中 PPARα mRNA 和蛋白表达的减少与分娩有关,而 IL-1β 则显著增加。使用 Pearson 检验分析时,PPARα 和 IL-1β 在 mRNA(r=-.765,P<.01)和蛋白(r=-.624,P<.01)水平上呈负相关。总之,人妊娠与子宫肌层中 PPARα和 IL-1β表达的变化有关。观察到的变化表明,PPARα 可能通过抑制人子宫肌层中 IL-1β的表达来维持妊娠或启动分娩。

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