绵羊子宫中的胃泌素释放肽(GRP):受干扰素τ和孕酮调节。

Gastrin-releasing peptide (GRP) in the ovine uterus: regulation by interferon tau and progesterone.

作者信息

Song Gwonhwa, Satterfield M Carey, Kim Jinyoung, Bazer Fuller W, Spencer Thomas E

机构信息

Center for Animal Biotechnology and Genomics, Department of Animal Science, Texas A&M University, College Station, Texas 77843, USA.

出版信息

Biol Reprod. 2008 Aug;79(2):376-86. doi: 10.1095/biolreprod.108.068403. Epub 2008 Apr 30.

Abstract

Gastrin-releasing peptide (GRP) is abundantly expressed by endometrial glands of the ovine uterus and processed into different bioactive peptides, including GRP1-27, GRP18-27, and a C-terminus, that affect cell proliferation and migration. However, little information is available concerning the hormonal regulation of endometrial GRP and expression of GRP receptors in the ovine endometrium and conceptus. These studies determined the effects of pregnancy, progesterone (P4), interferon tau (IFNT), placental lactogen (CSH1), and growth hormone (GH) on expression of GRP in the endometrium and GRP receptors (GRPR, NMBR, BRS3) in the endometrium, conceptus, and placenta. In pregnant ewes, GRP mRNA and protein were first detected predominantly in endometrial glands after Day 10 and were abundant from Days 18 through 120 of gestation. Treatment with IFNT and progesterone but not CSH1 or GH stimulated GRP expression in the endometrial glands. Western blot analyses identified proGRP in uterine luminal fluid and allantoic fluid from Day 80 unilateral pregnant ewes but not in uterine luminal fluid of either cyclic or early pregnant ewes. GRPR mRNA was very low in the Day 18 conceptus and undetectable in the endometrium and placenta; NMBR and BRS3 mRNAs were undetectable in ovine uteroplacental tissues. Collectively, the present studies validate GRP as a novel IFNT-stimulated gene in the glands of the ovine uterus, revealed that IFNT induction of GRP is dependent on P4, and found that exposure of the ovine uterus to P4 for 20 days induces GRP expression in endometrial glands.

摘要

胃泌素释放肽(GRP)在绵羊子宫的子宫内膜腺体中大量表达,并被加工成不同的生物活性肽,包括GRP1 - 27、GRP18 - 27和一个C末端,这些肽会影响细胞增殖和迁移。然而,关于绵羊子宫内膜中GRP的激素调节以及GRP受体在绵羊子宫内膜和孕体中的表达,目前所知甚少。这些研究确定了妊娠、孕酮(P4)、干扰素τ(IFNT)、胎盘催乳素(CSH1)和生长激素(GH)对子宫内膜中GRP表达以及子宫内膜、孕体和胎盘中GRP受体(GRPR、NMBR、BRS3)表达的影响。在怀孕母羊中,GRP mRNA和蛋白在第10天后首次主要在子宫内膜腺体中被检测到,并且在妊娠第18天至120天含量丰富。用IFNT和孕酮处理可刺激子宫内膜腺体中GRP的表达,但CSH1或GH处理则无此作用。蛋白质印迹分析在第80天单侧怀孕母羊的子宫腔液和尿囊液中鉴定出了前GRP,但在发情周期母羊或怀孕早期母羊的子宫腔液中未检测到。GRPR mRNA在第18天的孕体中含量极低,在子宫内膜和胎盘中无法检测到;NMBR和BRS3 mRNA在绵羊子宫胎盘组织中无法检测到。总体而言,本研究证实GRP是绵羊子宫腺体中一种新的IFNT刺激基因,揭示了IFNT诱导GRP依赖于P4,并发现绵羊子宫暴露于P4 20天可诱导子宫内膜腺体中GRP的表达。

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