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[1]羊 丹,田婉婷,徐 菁.SDC-1调控TGF-β1/THBS1信号通路对肝纤维化进程的影响[J].国际消化病杂志,2023,06:388-393.
 YANG Dan,TIAN Wanting,XU Jing..Effect of SDC-1 regulating TGF-β1/THBS1 signaling pathway on progress of liver fibrosis[J].International Journal of Digestive Disease,2023,06:388-393.
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SDC-1调控TGF-β1/THBS1信号通路对肝纤维化进程的影响(PDF)

《国际消化病杂志》[ISSN:1673-534X/CN:31-1953/R]

期数:
2023年06期
页码:
388-393
栏目:
论著
出版日期:
2023-12-30

文章信息/Info

Title:
Effect of SDC-1 regulating TGF-β1/THBS1 signaling pathway on progress of liver fibrosis
作者:
羊 丹田婉婷徐 菁
723000 陕西汉中,三二〇一医院消化内科
Author(s):
YANG Dan TIAN Wanting XU Jing.
Department of Gastroenterology, 3201 Hospital, Hanzhong 723000, China
关键词:
慢性乙型肝炎肝纤维化多配体蛋白聚糖-1血小板反应蛋白1肝星状细胞
Keywords:
Chronic hepatitis B Liver fibrosis Syndecan-1 Thrombospondin-1 Hepatic stellate cell
分类号:
-
DOI:
10.3969/j.issn.1673-534X.2023.06.007
文献标识码:
-
摘要:
目的探究多配体蛋白聚糖-1(SDC-1)在肝纤维化进程中的作用机制。方法选择2021年4月至2023年4月于三二〇一医院住院治疗并行肝穿刺活体组织病理检查的102例慢性乙型肝炎患者作为研究对象。采集患者的空腹静脉血,采用ELISA法检测患者血清SDC-1的表达水平,并比较不同肝纤维化分期患者血清SDC-1表达水平的差异。观察经转化生长因子-β1(TGF-β1)诱导活化的LX-2细胞中SDC-1表达水平的变化,以及敲低SDC-1表达对活化的LX-2细胞中α-平滑肌肌动蛋白(α-SMA)、血小板反应蛋白1(THBS1)表达水平及细胞增殖、细胞周期的影响。结果随着肝纤维化程度逐渐加重,慢性乙型肝炎患者血清SDC-1的表达水平呈升高趋势(P<0.05)。与阴性对照(NC)组相比,TGF-β1组α-SMA、SDC-1蛋白及其mRNA的相对表达量均显著升高,细胞增殖活性显著增强,G1期细胞占比显著降低,S期和G2期细胞占比显著升高(P均<0.05)。与NC小干扰RNA(siRNA)组相比,SDC-1siRNA组α-SMA、TGF-β1、THBS1蛋白及其mRNA的相对表达量均显著降低,细胞增殖活性显著减弱,G1期细胞占比显著升高,S期和G2期细胞占比显著降低(P均<0.05)。结论敲低SDC-1表达可能通过调控TGF-β1/THBS1信号通路,抑制肝星状细胞(HSC)的活化及增殖,阻滞HSC由G1期进入S期和G2期,进而发挥抑制肝纤维化进展的作用。
Abstract:
Objective? This paper intends to explore the role of syndecan-1 (SDC-1) in the progression of liver fibrosis. Methods? From April 2021 to April 2023, a total of 102 patients with chronic hepatitis B who were hospitalized and underwent liver biopsy in the 3201 Hospital were selected as the research objects. The fasting venous blood was collected and the expression of serum SDC-1 was measured using the ELISA method. The expression of serum SDC-1 was compared among patients with different stages of liver fibrosis. The changes of SDC-1 expression in activated LX-2 cells induced by transforming growth factor-β1 (TGF-β1), and the effects of knockdown of SDC-1 on the expression of α-smooth muscle actin (α-SMA), thrombospondin 1(THBS1), cell proliferation and cell cycle in activated LX-2 cells were observed. Results? With the aggravation of liver fibrosis stages, the expression level of serum SDC-1 in patients with chronic hepatitis B increases (P<0.05). Compared with the negative control (NC) group, the relative expressions of α-SMA, SDC-1 protein and their mRNA in the TGF-β1 group are increased, the cell proliferation activity is increased, the proportion of G1 phase cells is decreased, and the proportion of S phase and G2 phase cells are increased, with statistically significant differences (P<0.05). Compared with the NC siRNA group, the relative expressions of α-SMA, TGF-β1, THBS1 protein, and their mRNA in the SDC-1 siRNA group are decreased, the cell proliferation activity is decreased, the proportion of G1 phase cells is increased, and the proportion of S phase and G2 phase cells are decreased, with statistically significant differences (P<0.05). Conclusion? Knockdown of SDC-1 expression may inhibit the activation and proliferation of hepatic stellate cells by regulating TGF-β1/THBS1 signaling pathway, and block the progression of hepatic stellate cells from entering the G1 phase to the S phase and the G2 phase, and then play a role in inhibiting the process of liver fibrosis.

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更新日期/Last Update: 1900-01-01