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瘦素对人子宫肌层炎症体外模型中脂多糖诱导的重构的影响。

Effects of leptin on lipopolysaccharide-induced remodeling in an in vitro model of human myometrial inflammation.

机构信息

Institut National de la Santé Et de la Recherche Médicale (INSERM), U866, Lipides, Nutrition, Cancer, Dijon, France.

出版信息

Biol Reprod. 2013 Feb 21;88(2):45. doi: 10.1095/biolreprod.112.104844. Print 2013 Feb.

Abstract

Reorganization of myometrial extracellular matrix (ECM) is essential for the uterus to achieve powerful synchronous contractions during labor. Remodeling of the ECM has been implicated in membrane rupture and cervical ripening. Because maternal obesity is associated with both delivery disorders and elevated circulating leptin levels, this study aimed to assess the ability of leptin to interfere with lipopolysaccharide (LPS)-induced myometrial ECM remodeling. Myometrial biopsy samples were obtained from women undergoing cesarean delivery before labor onset. Myometrial explants were incubated for 48 h with LPS and leptin. LPS challenge was associated with a marked decrease in collagen content and in heat shock protein (HSP) 47 expression, reflecting a disruption in collagen synthesis and an increase in matrix metalloproteinase (MMP) 2 and MMP9 activity and in MMP2, MMP9, and MMP13 expression. Leptin prevented an LPS-induced decrease in myometrial collagen content in a concentration-dependent manner. This effect was associated with an increase in HSP47 expression and a decrease in MMP2 and MMP9 activity and expression. These results show that leptin prevents LPS-induced myometrial remodeling through collagen synthesis stimulation and inhibition of MMP2 and MMP9. Our study strengthens the hypothesis that leptin plays a role in the development of obesity-related delivery disorders.

摘要

子宫肌层细胞外基质(ECM)的重组对于子宫在分娩时实现有力的同步收缩至关重要。ECM 的重塑与胎膜破裂和宫颈成熟有关。由于母体肥胖与分娩障碍和循环瘦素水平升高有关,因此本研究旨在评估瘦素干扰脂多糖(LPS)诱导的子宫肌层 ECM 重塑的能力。在分娩前,通过剖宫产术从女性中获得子宫肌活检样本。用 LPS 和瘦素孵育子宫肌外植体 48 小时。LPS 刺激与胶原蛋白含量和热休克蛋白(HSP)47 表达明显减少有关,这反映了胶原合成的破坏以及基质金属蛋白酶(MMP)2 和 MMP9 活性以及 MMP2、MMP9 和 MMP13 表达的增加。瘦素以浓度依赖的方式阻止 LPS 诱导的子宫肌胶原蛋白含量减少。这种作用与 HSP47 表达增加以及 MMP2 和 MMP9 活性和表达减少有关。这些结果表明,瘦素通过刺激胶原蛋白合成和抑制 MMP2 和 MMP9 来防止 LPS 诱导的子宫肌重塑。我们的研究加强了这样一种假设,即瘦素在肥胖相关分娩障碍的发展中起作用。

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