反刍动物干扰素-tau的内分泌作用。

T R Hansen, L K Henkes, R L Ashley, R C Bott, A Q Antoniazzi, H Han
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引用次数: 52

摘要

绵羊妊娠期释放干扰素-tau (IFNT),阻止子宫内膜雌激素受体(ESR1)的上调,从而阻止催产素受体(OXTR)的上调,从而破坏响应催产素的前列腺素f2 - α (PGF)的搏动释放。IFNT通过对子宫内膜的旁分泌作用,在母体识别妊娠期间保护黄体(CL)。怀孕还会诱导外周血单核细胞(PBMCs)中的IFN刺激基因(ISGs),这被解释为反刍动物外周血中“提示”的抗病毒和免疫细胞反应。IFNT最近被证明从子宫中以200微克(2 × 10(7) U)/24小时的量通过子宫静脉释放,并在母体识别怀孕期间诱导CL中的isg。从第10天到第17天,将重组羊IFNT(重组羊IFNT)送入子宫-卵巢丛上游的子宫静脉,维持血清黄体酮浓度,并将正常的16-17天的发情周期延长至32天以上。从这些研究中可以得出结论,IFNT释放到子宫静脉并启动外周抗病毒反应,以保护妊娠免受母体病毒感染。它也可能通过诱导黄体对PGF的抵抗,使CL的长期生存和妊娠的维持而具有内分泌作用。
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Endocrine actions of interferon-tau in ruminants.

The ovine conceptus releases interferon-tau (IFNT), which prevents upregulation of the endometrial estrogen receptor (ESR1) and, consequently, oxytocin receptor (OXTR), thereby disrupting pulsatile release of prostaglandin F2alpha (PGF) in response to oxytocin. IFNT, through paracrine action on the endometrium, protects the corpus luteum (CL) during maternal recognition of pregnancy. Pregnancy also induces IFN stimulated genes (ISGs) in peripheral blood mononuclear cells (PBMCs), which is interpreted to reflect a "prompted" antiviral and immune cell response peripherally in ruminants. IFNT was recently demonstrated to be released from the uterus in amounts of 200 microg (2 x 10(7) U)/24 h via the uterine vein and to induce ISGs in the CL during maternal recognition of pregnancy. Delivery of recombinant ovine (ro) IFNT into the uterine vein in a location that is upstream of the utero-ovarian plexus from Day 10 to 17 maintained serum progesterone concentrations and extended normal 16-17 d estrous cycles to beyond 32 d. It is concluded from these studies that IFNT is released into the uterine vein and initiates a peripheral antiviral response to protect pregnancy from maternal viral infection. It also may have endocrine action through inducing luteal resistance to PGF and longer-term survival of the CL and maintenance of pregnancy.

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Development of the pig placenta. Conceptus-uterus interactions in pigs: endometrial gene expression in response to estrogens and interferons from conceptuses. Temporal candidate gene expression patterns in the sow placenta during early gestation and the effect of maternal L-arginine supplementation. Genetic selection for lifetime reproductive performance. Global protein profiling of porcine cumulus cells in response to native oocyte secreted factors in vitro.
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