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首页> 外文期刊>Placenta >Effect of nuclear factor-kappa B inhibitors and peroxisome proliferator-activated receptor-gamma ligands on PTHrP release from human fetal membranes.
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Effect of nuclear factor-kappa B inhibitors and peroxisome proliferator-activated receptor-gamma ligands on PTHrP release from human fetal membranes.

机译:核因子-κB抑制剂和过氧化物酶体增殖物激活的受体-γ配体对人胎膜上PTHrP释放的影响。

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Parathyroid hormone-related protein (PTHrP) has been implicated in many processes during normal and pathological pregnancies. In the human fetal membranes, PTHrP exhibits cytokine-like actions. We have recently shown that inhibitors of the nuclear factor-kappa B (NF-kappaB) and activators of the peroxisome proliferator-activated receptor (PPAR)-gamma signalling pathways down-regulate cytokine release from human gestational tissues. Therefore, the aim of this study was to determine whether NF-kappaB and PPAR-gamma also regulate PTHrP release from human fetal membranes. Human amnion and choriodecidua explants were incubated in the absence (control) or presence of two known NF-kappaB inhibitors (1, 5 and 10 mM sulphasalazine (SASP) or 5, 10 and 15 mM N-acetyl-cysteine (NAC)), and two PPAR-gamma ligands (15 and 30 microM 15-deoxy-Delta(12,14)-PGJ(2) (15d-PGJ(2)) or 15 and 30 microM troglitazone), under basal conditions. After 18 h incubation, the tissues were collected and NF-kappaB p65 DNA binding activity in nuclear extracts was assessed by ELISA, and the incubation medium was collected and the release of PTHrP was quantified by RIA. Treatment of amnion and choriodecidual tissues with SASP concentrations greater than 5 mM, 15 mM NAC, 30 microM 15d-PGJ(2) and 30 microM troglitazone significantly reduced the release of PTHrP (p < 0.05). This study demonstrates that PTHrP release from human fetal membranes is regulated by inhibitors of NF-kappaB, and ligands of PPAR-gamma.
机译:正常妊娠和病理妊娠期间,甲状旁腺激素相关蛋白(PTHrP)已涉及许多过程。在人胎膜中,PTHrP表现出类似细胞因子的作用。我们最近发现,核因子-κB(NF-kappaB)抑制剂和过氧化物酶体增殖物激活受体(PPAR)-γ信号通路的激活剂下调了人类妊娠组织中细胞因子的释放。因此,本研究的目的是确定NF-κB和PPAR-γ是否也调节人胎膜中PTHrP的释放。在不存在(对照)或存在两种已知的NF-κB抑制剂(1、5和10 mM柳氮磺吡啶(SASP)或5、10和15 mM N-乙酰半胱氨酸(NAC))的情况下,孵育人羊膜和绒毛膜外植体,和两个PPAR-γ配体(15和30 microM 15-脱氧-Delta(12,14)-PGJ(2)(15d-PGJ(2))或15和30 microM曲格列酮),在基础条件下。温育18小时后,收集组织并通过ELISA评估核提取物中的NF-κBp65 DNA结合活性,并收集温育培养基并通过RIA定量PTHrP的释放。 SASP浓度大于5 mM,15 mM NAC,30 microM 15d-PGJ(2)和30 microM曲格列酮治疗羊膜和绒毛膜蜕膜组织可显着降低PTHrP的释放(p <0.05)。这项研究表明,从人胎膜释放的PTHrP受NF-κB抑制剂和PPAR-γ配体的调节。

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