首页> 外文期刊>General and comparative endocrinology >Expression and localization of vascular endothelial growth factor A (VEGFA) and its two receptors (VEGFR1/FLT1 and VEGFR2/FLK1/KDR) in the canine corpus luteum and utero-placental compartments during pregnancy and at normal and induced parturition
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Expression and localization of vascular endothelial growth factor A (VEGFA) and its two receptors (VEGFR1/FLT1 and VEGFR2/FLK1/KDR) in the canine corpus luteum and utero-placental compartments during pregnancy and at normal and induced parturition

机译:妊娠期以及正常分娩和人工分娩时犬黄体和子宫胎盘区室中血管内皮生长因子A(VEGFA)及其两个受体(VEGFR1 / FLT1和VEGFR2 / FLK1 / KDR)的表达和定位

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VEGFA is one of the most potent known inducers of angiogenesis. However, the function of angiogenic factors in the canine corpus luteum (CL) of pregnancy and in the pregnant uterus and placenta has not yet been elucidated. Therefore, here we investigated the expression and localization of VEGFA and its receptors (VEGFR1/FLT1 and VEGFR2/FLK1/KDR) in the canine CL and utero-placental compartments (ut-pl) throughout pregnancy until prepartum luteolysis. Antigestagen-mediated effects on expression of VEGF system in ut-pl were elucidated in mid-pregnant dogs. While displaying high individual variation, the luteal VEGFA was elevated during pre-implantation and post-implantation, followed by a decrease during mid-gestation, which was more pronounced at the mRNA level, and showed constant expression afterwards. Within the uterus, it increased following implantation and during mid-gestation in ut-pl compartments, but was downregulated at prepartum luteolysis. Luteal VEGFR1 expression resembled that of VEGFA; VEGFR2 remained unaffected throughout pregnancy. In ut-pl compartments, both receptors increased gradually towards mid-gestation; a prepartum decrease was observed for VEGFR1. Antigestagen-treatment resulted in decreased expression of ut-pl VEGFR1. In the CL, VEGFA stained in luteal cells. Uterine signals of VEGFA and its two receptors were observed in epithelial and vascular compartments, and in myometrium. In placental labyrinth, additionally, trophoblast stained positively. Luteal VEGFR1 was localized to the luteal cells and tunica media of blood vessels, whereas VEGFR2 stained only in capillary endothelial cells. The upregulation of luteal and the ut-pi VEGF system during early gestational stages supports the increased vascularization rate during this time. The diminishing effects of the prepartum endocrine milieu on VEGFA function seem to be more pronounced in the ut-pi units. (C) 2015 Elsevier Inc. All rights reserved.
机译:VEGFA是已知最有效的血管生成诱导剂之一。然而,尚未阐明妊娠的犬黄体(CL)以及妊娠的子宫和胎盘中的血管生成因子的功能。因此,在这里,我们研究了整个妊娠直至产前黄体溶解之前,在犬CL和子宫胎盘区室(ut-pl)中VEGFA及其受体(VEGFR1 / FLT1和VEGFR2 / FLK1 / KDR)的表达和定位。阐明了中孕犬对ut-pl中抗孕激素介导的VEGF系统表达的影响。尽管表现出高的个体变异性,但在植入前和植入后黄体VEGFA升高,然后在妊娠中期降低,在mRNA水平上更为明显,并在之后表现出恒定表达。在子宫内,它在ut-pl隔室中植入后和妊娠中期增加,但在产前黄体溶解时下调。黄体中VEGFR1的表达与VEGFA相似。在整个怀孕期间,VEGFR2均未受影响。在ut-pl区室中,两种受体在妊娠中期逐渐增加。观察到VEGFR1的产前减少。抗孕激素处理导致ut-pl VEGFR1的表达降低。在CL中,黄体细胞中的VEGFA染色。在上皮和血管区室以及子宫肌层中观察到VEGFA及其两个受体的子宫信号。另外,在胎盘迷宫中,滋养层染色呈阳性。黄体VEGFR1定位于黄体细胞和血管的中膜介质,而VEGFR2仅在毛细血管内皮细胞中染色。黄体和ut-pi VEGF系统在妊娠早期的上调支持这段时间内血管生成率的增加。在ut-pi单位中,产前内分泌环境对VEGFA功能的减弱作用似乎更为明显。 (C)2015 Elsevier Inc.保留所有权利。

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