高脂肪饮食诱导的细胞外基质改变对胆囊平滑肌功能障碍的影响。

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xingguo Zhong, Feiyang Wu, Weicheng Gao, Jinlong Hu, Bing Shen, Kaiyuan Zhong, Junbin Peng, Chong Zhang, Chao Zhang
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引用次数: 0

摘要

背景:胆结石形成是一种常见的消化系统疾病,其发展机制尚不清楚。胆囊平滑肌功能障碍(GSM)可能起着至关重要的作用,特别是高脂肪饮食(HFD)。本研究旨在探讨HFD对GSM的影响,并评估其如何通过改变细胞外基质(ECM)来改变收缩性。方法:将豚鼠和C57BL/6小鼠分别饲喂HFD和普通饲料(ND)。体外实验采用豚鼠胆囊平滑肌细胞(GSMCs)原代培养。进行组织染色、rna测序、生物信息学分析、三维组织培养、实时聚合酶链反应(PCR)、Western blot、原子力显微镜和肌肉张力测量。结果:组织学证据显示HFD组胆囊肌层结构改变,ECM胶原沉积。HFD组胶原蛋白、整合素家族、基质金属蛋白酶(MMP)和磷酸肌肽3激酶(PI3K)-蛋白激酶B (PKB/Akt)信号通路表达增加。与在含有1 mg/mL I型胶原的基质上培养的GSMCs相比,2 mg/mL的基质上培养的GSMCs表现出从收缩细胞到合成细胞的表型变化。与这些发现一致,HFD组也表现出ECM僵硬增加和平滑肌收缩性降低。结论:我们的研究结果揭示了HFD改变胆囊肌ECM组成的机制,激活整合素/PI3K-Akt/MMP信号通路,从而影响GSMC表型和收缩性。这些发现增强了对胆结石形成机制的认识,并为治疗胆囊功能障碍提供了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Extracellular Matrix Changes Induced by a High-Fat Diet on Gallbladder Smooth Muscle Dysfunction.

Background: Gallstone formation is a common digestive ailment, with unclear mechanisms underlying its development. Dysfunction of the gallbladder smooth muscle (GSM) may play a crucial role, particularly with a high-fat diet (HFD). This study aimed to investigate the effects of an HFD on GSM and assess how it alters contractility through changes in the extracellular matrix (ECM).

Methods: Guinea pigs and C57BL/6 mice were fed either an HFD or normal diet (ND). Primary cultures of their (guinea pigs) gallbladder smooth muscle cells (GSMCs) were used for in vitro experiments. Histological stains, RNA-sequencing, bioinformatics analysis, three-dimensional tissue culture, real-time polymerase chain reaction (PCR), Western blot, atomic force microscopy, and muscle tension measurements were performed.

Results: Histological evidence indicated structural changes in the gallbladder muscle layer and ECM collagen deposition in the HFD group. The HFD group also showed increased expression of collagen, integrin family, and matrix metalloproteinase (MMP) and the phosphoinositide 3-kinase (PI3K)-protein kinase B (PKB/Akt) signaling pathway. Compared with GSMCs cultured on Matrigel containing 1 mg/mL of collagen I, those cultured with 2 mg/mL showed a phenotype change from contractile to synthetic cells. Consistent with these findings, the HFD group also demonstrated increased ECM stiffness and decreased smooth muscle contractility.

Conclusions: Our findings reveal a mechanism by which an HFD alters the ECM composition of the gallbladder muscle, activating the integrin/PI3K-Akt/MMP signaling pathway, thereby impacting GSMC phenotype and contractility. These insights enhance the understanding of gallstone formation mechanism and provide potential therapeutic targets to treat gallbladder dysfunction.

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