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海蟾蜍精是子痫前期中Gadd45a应激信号的上游调节因子。

Marinobufagenin is an upstream modulator of Gadd45a stress signaling in preeclampsia.

作者信息

Uddin Mohammad N, Horvat Darijana, Demorrow Sharon, Agunanne Enoch, Puschett Jules B

机构信息

Division of Nephrology and Hypertension, Department of Medicine, Texas A&M Health Science Center College of Medicine and Scott & White Memorial Hospital, Temple, TX 76508, USA.

出版信息

Biochim Biophys Acta. 2011 Jan;1812(1):49-58. doi: 10.1016/j.bbadis.2010.09.006. Epub 2010 Sep 17.

Abstract

Preeclampsia (PE) is a hypertensive disorder of pregnancy, in which marinobufagenin (MBG), a circulating cardiotonic steroid, is increased. The Gadd45a stress sensor protein is an upstream modulator of the pathophysiological changes observed in PE. However, the effects of MBG on Gadd45a stress signaling remain unknown. We examined the expression of Gadd45a, the sFlt-1 receptor, and p38, as well as caspase 3 and 8 activities in placental samples from four groups of rats. These were: normal pregnant (NP, n=8); pregnant rats which received weekly injections of desoxycorticosterone acetate and 0.9% saline as their drinking water (PDS, n=9); normal pregnant rats injected with MBG (NPM, n=8); and PDS rats injected with resibufogenin (RBG), an in vivo antagonist of MBG (PDSR, n=8). Utilizing human cytotrophoblast (CTB) cells, we examined the effect of MBG on these stress signaling proteins in vitro. Placental Gadd45a expression, caspase 3 and 8 activities, sFlt-1 concentrations, and sFlt-1 receptor expression were significantly higher in PDS and NPM compared to NP and PDSR rats. Gadd45a protein was significantly upregulated in the CTB cells when MBG was present in concentrations ≥1nM. Treatment with MBG (≥1nM) also significantly arrested cell cycle progression and activated the expression of the Gadd45a-mediated stress signaling proteins. Inhibition of Gadd45a through RNAi-mediation attenuated MBG-induced CTB cell stress signaling. In conclusion, MBG is involved in the alteration in Gadd45a stress signaling both in vivo and in vitro and RBG prevents these changes when administered in vivo.

摘要

子痫前期(PE)是一种妊娠期高血压疾病,其中循环强心甾体类物质海蟾蜍精(MBG)水平升高。Gadd45a应激感应蛋白是PE中观察到的病理生理变化的上游调节因子。然而,MBG对Gadd45a应激信号的影响尚不清楚。我们检测了四组大鼠胎盘样本中Gadd45a、可溶性血管内皮生长因子受体-1(sFlt-1)受体、p38以及半胱天冬酶3和8的活性表达。这四组分别为:正常妊娠组(NP,n = 8);每周注射醋酸脱氧皮质酮并饮用0.9%盐水的妊娠大鼠组(PDS,n = 9);注射MBG的正常妊娠大鼠组(NPM,n = 8);以及注射蟾毒配基(RBG,MBG的体内拮抗剂)的PDS大鼠组(PDSR,n = 8)。利用人细胞滋养层(CTB)细胞,我们在体外检测了MBG对这些应激信号蛋白的影响。与NP和PDSR大鼠相比,PDS和NPM大鼠的胎盘Gadd45a表达、半胱天冬酶3和8活性、sFlt-1浓度以及sFlt-1受体表达显著更高。当MBG浓度≥1nM时,CTB细胞中的Gadd45a蛋白显著上调。用MBG(≥1nM)处理也显著阻止了细胞周期进程并激活了Gadd45a介导的应激信号蛋白的表达。通过RNA干扰介导抑制Gadd45a可减弱MBG诱导的CTB细胞应激信号。总之,MBG在体内和体外均参与了Gadd45a应激信号的改变,并且RBG在体内给药时可预防这些变化。

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