黄芪桂枝五物汤通过靶向ESR1促进骨髓间充质干细胞成骨分化。

IF 1.7 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Cytotechnology Pub Date : 2025-06-01 Epub Date: 2025-05-28 DOI:10.1007/s10616-025-00773-z
Xin Zhao, Yanping Hu, Heran Xiong, Bo Dai, Wei Liu, Meiling Chen, Fan Zhou, Chao Xiang, Song Wang
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引用次数: 0

摘要

本研究主要基于网络药理学探讨黄芪桂枝五物汤(HGWD)治疗骨关节炎(OA)的潜在机制,并通过体外实验研究黄芪桂枝五物汤是否通过上调ESR1促进骨髓间充质干细胞(BMSCs)的成骨分化。采用网络药理学分析方法分析OA治疗中与HGWD相关的核心靶基因和潜在信号通路。从大鼠体内分离骨髓间充质干细胞诱导成脂/成骨分化,分别采用油红O染色和茜素红染色进行评价。将ESR1敲低慢病毒转染到骨髓间充质干细胞中,制备不同浓度含hgwd的大鼠血清来治疗骨髓间充质干细胞。采用CCK-8法测定细胞增殖活性,为进一步实验选择最佳浓度。用含10% hgwd的血清处理细胞,并用ESR1敲低慢病毒转染细胞。通过ALP染色、ALP活性测定和茜素红染色评估成骨分化。采用qRT-PCR和Western blot检测成骨分化相关基因OCN、RUNX2、COL1A1的表达。网络药理学分析显示ESR1是HGWD治疗OA的核心靶点之一。含hgwd血清促进骨髓间充质干细胞的增殖和成骨分化能力,并增加ESR1的表达。含hgwd的血清对骨髓间充质干细胞增殖和成骨分化的促进作用在ESR1敲低的反应中得到部分修饰。综上所述,HGWD对OA的治疗作用可能是通过上调ESR1表达促进BMSCs成骨分化。补充信息:在线版本包含补充资料,可在10.1007/s10616-025-00773-z获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Huangqi Guizhi Wuwu decoction promoted the osteogenic differentiation of bone marrow mesenchymal stem cells by targeting ESR1.

This study mainly explored the potential mechanism of Huangqi Guizhi Wuwu Decoction (HGWD) in the treatment of osteoarthritis (OA) based on network pharmacology, and to investigate whether HGWD promotes osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) by upregulating ESR1 based on in vitro experiments. The core target genes and potential signaling pathways related to HGWD in OA treatment were analyzed using network pharmacology analysis. BMSCs were isolated from rats to induce for adipogenic/osteogenic differentiation, which were assessed by Oil Red O staining and Alizarin Red staining, respectively. ESR1 knockdown lentivirus was transfected into BMSCs and different concentrations of rat HGWD-containing serum was prepared to treat BMSCs. Cell proliferation activity was measured by CCK-8 assay to select the optimal concentration for further experiments. Cells were treated with 10% HGWD-containing serum and transfected with ESR1 knockdown lentivirus. Osteogenic differentiation was assessed by ALP staining, ALP activity measurement, and Alizarin Red staining. The expression of osteogenic differentiation-related genes OCN, RUNX2, and COL1A1 was detected by qRT-PCR and Western blot. Network pharmacology analysis revealed that ESR1 is one of the core targets of HGWD in OA treatment. HGWD-containing serum promoted proliferation and osteogenic differentiation ability of BMSCs, and also increased ESR1 expression. The promoting effects of HGWD-containing serum on proliferation and osteogenic differentiation were partially polished in response to ESR1 knockdown in BMSCs. Based on the collective evidence, the therapeutic effects of HGWD in OA may be achieved by promoting osteogenic differentiation of BMSCs via upregulating ESR1 expression.

Supplementary information: The online version contains supplementary material available at 10.1007/s10616-025-00773-z.

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来源期刊
Cytotechnology
Cytotechnology 生物-生物工程与应用微生物
CiteScore
4.10
自引率
0.00%
发文量
49
审稿时长
6-12 weeks
期刊介绍: The scope of the Journal includes: 1. The derivation, genetic modification and characterization of cell lines, genetic and phenotypic regulation, control of cellular metabolism, cell physiology and biochemistry related to cell function, performance and expression of cell products. 2. Cell culture techniques, substrates, environmental requirements and optimization, cloning, hybridization and molecular biology, including genomic and proteomic tools. 3. Cell culture systems, processes, reactors, scale-up, and industrial production. Descriptions of the design or construction of equipment, media or quality control procedures, that are ancillary to cellular research. 4. The application of animal/human cells in research in the field of stem cell research including maintenance of stemness, differentiation, genetics, and senescence, cancer research, research in immunology, as well as applications in tissue engineering and gene therapy. 5. The use of cell cultures as a substrate for bioassays, biomedical applications and in particular as a replacement for animal models.
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