Suppr超能文献

肝星状细胞中的可诱导型鞘氨醇激酶 1 增强肝纤维化。

An inducible sphingosine kinase 1 in hepatic stellate cells potentiates liver fibrosis.

机构信息

MRC-OSTRC, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Chosun University, Gwangju 61452, South Korea.

MRC-OSTRC, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Chosun University, Gwangju 61452, South Korea; Department of Biomedical Science, College of Natural Science, Chosun University, Gwangju 61452, Republic of Korea; Institute of Well-Aging Medicare & Chosun University G-LAMP Project Group, Chosun University, Gwangju 61452, Republic of Korea.

出版信息

Biochem Pharmacol. 2024 Nov;229:116520. doi: 10.1016/j.bcp.2024.116520. Epub 2024 Sep 3.

Abstract

Hepatic stellate cells (HSCs) play a role in hepatic fibrosis and sphingosine kinase (SphK) is involved in biological processes. As studies on the regulatory mechanisms and functions of SphK in HSCs during liver fibrosis are currently limited, this study aimed to elucidate the regulatory mechanism and connected pathways of SphK upon HSC activation. The expression of SphK1 was higher in HSCs than in hepatocytes, and upregulated in activated primary HSCs. SphK1 was also increased in liver homogenates of carbon tetrachloride-treated or bile duct ligated mice and in transforming growth factor-β (TGF-β)-treated LX-2 cells. TGF-β-mediated SphK1 induction was due to Smad3 signaling in LX-2 cells. SphK1 modulation altered the expression of liver fibrogenesis-related genes. This SphK1-mediated profibrogenic effect was dependent on SphK1/sphingosine-1-phosphate/sphingosine-1-phosphate receptor signaling through ERK. Epigallocatechin gallate blocked TGF-β-induced SphK1 expression and hepatic fibrogenesis by attenuating Smad and MAPK activation. SphK1 induced by TGF-β facilitates HSC activation and liver fibrogenesis, which is reversed by epigallocatechin gallate. Accordingly, SphK1 and related signal transduction may be utilized to treat liver fibrosis.

摘要

肝星状细胞(HSCs)在肝纤维化中起作用,并且鞘氨醇激酶(SphK)参与了生物过程。由于目前对肝纤维化过程中 SphK 在 HSCs 中的调节机制和功能的研究有限,本研究旨在阐明 SphK 在 HSCs 激活时的调节机制和相关途径。SphK1 在 HSCs 中的表达高于肝细胞,在激活的原代 HSCs 中上调。四氯化碳处理或胆管结扎小鼠的肝匀浆以及转化生长因子-β(TGF-β)处理的 LX-2 细胞中 SphK1 也增加。TGF-β 介导的 SphK1 诱导归因于 LX-2 细胞中的 Smad3 信号。SphK1 调节改变了与肝纤维化相关基因的表达。这种 SphK1 介导的促纤维化作用依赖于 SphK1/鞘氨醇-1-磷酸/鞘氨醇-1-磷酸受体信号通过 ERK。表没食子儿茶素没食子酸酯通过减弱 Smad 和 MAPK 激活来阻断 TGF-β诱导的 SphK1 表达和肝纤维化。TGF-β诱导的 SphK1 促进 HSC 激活和肝纤维化,表没食子儿茶素没食子酸酯可逆转这种作用。因此,SphK1 及其相关信号转导可用于治疗肝纤维化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验