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大黄蛰虫丸通过miR-29b-2-5p/己糖激酶2介导的糖酵解途径改善肺纤维化。

Dahuang Zhechong Pill Improves Pulmonary Fibrosis through miR-29b-2-5p/HK2 Mediated Glycolysis Pathway.

作者信息

He Xiao-Yan, Liang Jing-Tao, Xiao Jing-Yi, Li Xin, Zhang Xiao-Bo, Chen Da-Yi, Wu Li-Juan

机构信息

College of Public Health, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.

Department of Neurology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China.

出版信息

Chin J Integr Med. 2024 Sep 5. doi: 10.1007/s11655-024-3765-x.

Abstract

OBJECTIVE

To explore the preventive and therapeutic effects of Dahuang Zhechong Pill (DZP) on pulmonary fibrosis and the underlying mechanisms.

METHODS

The first key rate-limiting enzyme hexokinase 2 (HK2) of glycolysis was silenced and over-expressed through small interfering RNA and lentivirus using lung fibroblast MRC-5 cell line, respectively. The cell viability, migration, invasion and proliferation were detected by cell counting kit-8, wound healing assay, transwell assay, and flow cytometry. The mRNA and protein expression levels of HK2 were detected by RT-PCR and Western blotting, respectively. The contents of glucose, adenosine triphosphate (ATP) and lactate in MRC-5 cells were determined by enzyme-linked immunosorbnent assay (ELISA). Then, the relationship between miR-29b-2-5p and HK2 was explored by luciferase reporter gene assay. Pulmonary fibrosis cell model was induced by transforming growth factor-β 1 (TGF-β 1) in MRC-5 cells, and the medicated serum of DZP (DMS) was prepared in rats. MRC-5 cells were divided into control, TGF-β 1, TGF-β 1+10% DMS, TGF-β 1+10% DMS+miR-29b-2-5p inhibitor, TGF-β 1+10% DMS+inhibitor negative control, TGF-β 1+10% DMS+miR-29b-2-5p mimic and TGF-β 1+10% DMS+mimic negative control groups. After miR-29b-2-5p mimics and inhibitors were transfected into MRC-5 cells, all groups except control and model group were treated with DMS. The effect of DMS on MRC-5 cells were detected using aforementioned methods and immunofluorescence. Similarly, the contents of glucose, ATP and lactate in each group were measured by ELISA.

RESULTS

The mRNA and protein expressions of HK2 in MRC-5 cells were successfully silenced and overexpressed through si-HK2-3 and lentiviral transfection, respectively. After silencing HK2, the mRNA and protein expressions of HK2 were significantly decreased (P<0.01), and the concentrations of glucose, ATP and lactate were also significantly decreased (P<0.05). The proliferation, migration and invasion of MRC-5 cells were significantly declined (P<0.05 or P<0.01), while the apoptosis of MRC-5 cells was significantly increased (P<0.01). After overexpressing HK2, the mRNA and protein expressions of HK2 were significantly increased (P<0.05), and the concentrations of glucose, ATP and lactate were also significantly increased (P<0.05 or P<0.01). The proliferation, migration and invasion of MRC-5 cells were significantly increased (P<0.05 or P<0.01), while the apoptosis of MRC-5 cells was significantly decreased (P<0.05). The relative luciferase activity of 3'UTR-WT+hsa-miR-29b-2-5p transfected with HK2 was significantly decreased (P<0.01). After miR-29b-2-5p mimic and inhibitor were transfected into the MRC-5 cells, DMS intervention could significantly reduce the concentration of glucose, ATP and lactate, and the mRNA and proteins expressions of HK2, phosphofructokinase and pyruvate kinase isoform M2 (P<0.05 or P<0.01). The proliferation, migration and invasion of MRC-5 cells were alleviated (P<0.05 or P<0.01), and the deposition of fibronectin, α-smooth muscle actin, and collagen I were significantly decreased (P<0.05 or P<0.01).

CONCLUSIONS

Glycolysis is closely related to pulmonary fibrosis. DZP reduced glycolysis and inhibited fibroblasts' excessive differentiation and abnormal collagen deposition through the miR-29b-2-5p/HK2 pathway, which played a role in delaying the process of pulmonary fibrosis.

摘要

目的

探讨大黄蛰虫丸(DZP)对肺纤维化的防治作用及其潜在机制。

方法

分别采用小干扰RNA和慢病毒,在肺成纤维细胞MRC-5细胞系中沉默和过表达糖酵解的首个关键限速酶己糖激酶2(HK2)。通过细胞计数试剂盒-8、伤口愈合试验、Transwell试验和流式细胞术检测细胞活力、迁移、侵袭和增殖。分别用RT-PCR和Western印迹法检测HK2的mRNA和蛋白表达水平。采用酶联免疫吸附测定(ELISA)法测定MRC-5细胞中葡萄糖、三磷酸腺苷(ATP)和乳酸的含量。然后,通过荧光素酶报告基因试验探讨miR-29b-2-5p与HK2之间的关系。用转化生长因子-β1(TGF-β1)诱导MRC-5细胞建立肺纤维化细胞模型,并制备大鼠含药血清(DMS)。将MRC-5细胞分为对照组、TGF-β1组、TGF-β1+10% DMS组、TGF-β1+10% DMS+miR-29b-2-5p抑制剂组、TGF-β1+10% DMS+抑制剂阴性对照组、TGF-β1+10% DMS+miR-29b-2-5p模拟物组和TGF-β1+10% DMS+模拟物阴性对照组。将miR-29b-2-5p模拟物和抑制剂转染到MRC-5细胞后除对照组和模型组外,其余各组均用DMS处理。采用上述方法和免疫荧光法检测DMS对MRC-5细胞的作用。同样,用ELISA法测定各组葡萄糖、ATP和乳酸的含量。

结果

通过si-HK2-3和慢病毒转染分别成功沉默和过表达了MRC-5细胞中HK2的mRNA和蛋白表达。沉默HK2后,HK2的mRNA和蛋白表达显著降低(P<0.01),葡萄糖、ATP和乳酸的浓度也显著降低(P<0.05)。MRC-5细胞的增殖、迁移和侵袭显著下降(P<0.05或P<0.01),而MRC-5细胞的凋亡显著增加(P<0.01)。过表达HK2后,HK2的mRNA和蛋白表达显著增加(P<0.05),葡萄糖、ATP和乳酸的浓度也显著增加(P<0.05或P<0.01)。MRC-5细胞的增殖、迁移和侵袭显著增加(P<0.05或P<0.01),而MRC-5细胞的凋亡显著减少(P<0.05)。转染HK2的3'UTR-WT+hsa-miR-29b-2-5p的相对荧光素酶活性显著降低(P<0.01)。将miR-29b-2-5p模拟物和抑制剂转染到MRC-5细胞后,DMS干预可显著降低葡萄糖、ATP和乳酸的浓度以及HK2、磷酸果糖激酶和丙酮酸激酶同工酶M2的mRNA和蛋白表达(P<0.05或P<0.01)。MRC-5细胞的增殖、迁移和侵袭得到缓解(P<0.05或P<0.01),纤连蛋白、α-平滑肌肌动蛋白和I型胶原的沉积显著减少(P<0.05或P<0.01)。

结论

糖酵解与肺纤维化密切相关。DZP通过miR-29b-2-5p/HK2途径降低糖酵解,抑制成纤维细胞过度分化和异常胶原沉积,在延缓肺纤维化进程中发挥作用。

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