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Uterine artery leptin receptors during the ovarian cycle and pregnancy regulate angiogenesis in ovine uterine artery endothelial cells

机译:卵巢周期和妊娠期间子宫动脉瘦素受体调节绵羊子宫动脉内皮细胞的血管生成

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摘要

Leptin regulates body weight, reproductive functions, blood pressure, endothelial function, and fetoplacental angiogenesis. Compared to the luteal phase, the follicular phase and pregnancy are physiological states of elevated estrogen, angiogenesis, and uterine blood flow (UBF). Little is known concerning regulation of uterine artery (UA) angiogenesis by leptin and its receptors. We hypothesized that (1) ex vivo expression of leptin receptors (LEPR) in UA endothelium (UAendo) and UA vascular smooth muscle (UAvsm) is elevated in pregnant versus nonpregnant (Luteal and Follicular) sheep; (2) in vitro leptin treatments differentially modulate mitogenesis in uterine artery endothelial cells from pregnant (P-UAECs) more than in nonpregnant (NP-UAECs) ewes; and (3) LEPR are upregulated in P-UAECs versus NP-UAECs in association with leptin activation of phospho-STAT3 signaling. Local UA adaptations were evaluated using a unilateral pregnant sheep model where prebreeding uterine horn isolation (nongravid) restricted gravidity to one horn. Immunolocalization revealed LEPR in UAendo and UAvsm from pregnant and nonpregnant sheep. Contrary to our hypothesis, western analysis revealed that follicular UAendo and UAvsm LEPR were greater than luteal, nongravid, gravid, and control pregnant. Compared to pregnant groups, LEPR were elevated in renal artery endothelium of follicular and luteal sheep. Leptin treatment significantly increased mitogenesis in follicular phase NP-UAECs and P-UAECs, but not luteal phase NP-UAECs. Although UAEC expression of LEPR was similar between groups, leptin treatment only activated phospho-STAT3 in follicular NP-UAECs and P-UAECs. Thus, leptin may play an angiogenic role particularly in preparation for the increased UBF during the periovulatory period and subsequently to meet the demands of the growing fetus.
机译:瘦素调节体重,生殖功能,血压,内皮功能和胎儿胎盘血管生成。与黄体期相比,卵泡期和妊娠是雌激素升高,血管生成和子宫血流(UBF)升高的生理状态。关于瘦素及其受体对子宫动脉(UA)血管生成的调控知之甚少。我们假设(1)妊娠绵羊和未妊娠绵羊(黄体和滤泡)的瘦素受体(LEPR)在UA内皮(UAendo)和UA血管平滑肌(UAvsm)中的体外表达升高; (2)瘦素的体外治疗比未怀孕(NP-UAECs)的母羊对子宫动脉内皮细胞的促有丝分裂的调节作用更大。 (3)与瘦素激活磷酸STAT3信号有关,P-UAECs和NP-UAECs中的PRPR上调。使用单侧怀孕绵羊模型评估局部UA适应性,其中预繁殖子宫角隔离(非重力)将妊娠限制在一个角上。免疫定位显示孕妇和非孕妇羊的UAendo和UAvsm中都有LEPR。与我们的假设相反,西方分析显示,卵泡UAendo和UAvsm LEPR大于黄体,非妊娠,妊娠和对照妊娠。与妊娠组相比,卵泡和黄体绵羊的肾动脉内皮中的LEPR升高。瘦素治疗可显着增加卵泡期NP-UAEC和P-UAEC中的有丝分裂,但不影响黄体期NP-UAEC。尽管各组之间LEPR的UAEC表达相似,但瘦素治疗仅激活了卵泡NP-UAEC和P-UAEC中的磷酸化STAT3。因此,瘦素可能在血管生成过程中起着血管生成作用,特别是在准备好在排卵期UBF增加并随后满足胎儿生长的需求方面。

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