Leech extract alleviates idiopathic pulmonary fibrosis by TGF-β1/Smad3 signaling pathway

被引:1
|
作者
Zhang, Yin [1 ]
Lu, Yong-Bo [1 ]
Zhu, Wei-Jie [2 ]
Gong, Xiao-Xi [1 ]
Qian, Rui [1 ]
Lu, Yi-Jing [1 ]
Li, Yu [2 ]
Yao, Wei-Feng [1 ]
Bao, Bei-Hua [1 ]
Zhang, Yi [1 ]
Zhang, Li [1 ,3 ]
Cheng, Fang -Fang [1 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resourc, Jiangsu Key Lab High Technol Res TCM Formulae, Natl & Local Collaborat Engn Ctr Chinese Med Resou, Nanjing 210023, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Med & Holist Integrat Med, Nanjing 210023, Peoples R China
[3] Nanjing Univ Chinese Med, Jiangsu Key Lab High Technol Res TCM Formulae, 138 Xianlin Rd, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Leech; The leech extract group with molecular weight greater than 10 KDa; Idiopathic pulmonary fibrosis; TGF-beta 1/Smad3 signaling pathway; Pyruvate kinase M2; TGF-BETA; PYRUVATE-KINASE; REGULATOR; BLEOMYCIN; M2;
D O I
10.1016/j.jep.2024.117737
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Leech, as a traditional Chinese medicine for the treatment of blood circulation and blood stasis, was also widely used to cure pulmonary fibrosis in China. In clinical practice, some traditional Chinese medicine preparation such as Shui Zhi Xuan Bi Hua Xian Tang and Shui Zhi Tong Luo Capsule composed of leech, could improve the clinical symptoms and pulmonary function in patients with idiopathic pulmonary fibrosis (IPF). However, the material basis of the leech in the treatment of IPF were not yet clear. Aim of the study: Screen out the components of leech that have the anti-pulmonary fibrosis effects, and further explore the therapeutic mechanism of the active components. Materials and methods: In this study, the different molecular weight components of leech extract samples were prepared using the semi-permeable membranes with different pore sizes. The therapeutic effects of the leech extract groups with molecular weight greater than 10 KDa (>10 KDa group), between 3 KDa and 10 KDa (3-10 KDa group), and less than 3 KDa (<3 KDa group) on pulmonary fibrosis were firstly investigated by cell proliferation and cytotoxicity assay (MTT), cell wound healing assay, immunofluorescence staining (IF) and Western blot (WB) assay through the TGF-beta 1-induced fibroblast cell model. Then bleomycin-induced pulmonary fibrosis (BML-induced PF) mouse model was constructed to investigate the pharmacological activities of the active component group of leech extract in vivo. Pathological changes of the mouse lung were observed by hematoxylineosin staining (H&E) and Masson's trichrome staining (Masson). The hydroxyproline (HYP) content of lung tissues was quantified by HYP detection kit. The levels of extracellular matrix-related fibronectin (FN) and collagen type I (Collagen I), pyruvate kinase M2 (PKM2) monomer and Smad7 protein were determined via WB method. PKM2 and Smad7 protein were further characterized by IF assays. Results: Using TGF-beta 1-induced HFL1 cell line as a PF cell model, the in vitro results demonstrated that the >10 KDa group could significantly inhibited the cell proliferation and migration, downregulated the expression level of cytoskeletal protein vimentin and alpha-smooth muscle actin (alpha-SMA), and reduced the deposition of FN and Collagen I. In the BML-induced PF mouse model, the >10 KDa group significantly reduced the content of HYP, downregulated the expression levels of FN and Collagen I in lung tissues, and delayed the pathological changes of lung tissue structure. The results of WB and IF assays further indicated that the >10 KDa group could up-regulate the expression level of PKM2 monomer and Smad7 protein in the cellular level, thereby delaying the progression of pulmonary fibrosis. Conclusions: Our study revealed that the >10 KDa group was the main material basis of the leech extract that inhibited pulmonary fibrosis through TGF-beta 1/Smad3 signaling pathway.
引用
收藏
页数:11
相关论文
共 50 条
  • [41] Lysine-specific demethylase-1 regulates fibroblast activation in pulmonary fibrosis via TGF-β1/Smad3 pathway
    Pan, Xiaohua
    Li, Jiahong
    Tu, Xing
    Wu, Chengfei
    Liu, He
    Luo, Yang
    Dong, Xiaoliang
    Li, Xiu
    Pan, Li-Long
    Sun, Jia
    [J]. PHARMACOLOGICAL RESEARCH, 2020, 152
  • [42] Roles of Smad3 in TGF-β signaling during carcinogenesis
    Millet, Caroline
    Zhang, Ying E.
    [J]. CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2007, 17 (04): : 281 - 293
  • [43] Inhibitory effects of astragaloside IV on silica-induced pulmonary fibrosis via inactivating TGF-β1/Smad3 signaling
    Li, Nannan
    Feng, Feifei
    Wu, Ke
    Zhang, Huanan
    Zhang, Wei
    Wang, Wei
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2019, 119
  • [44] Follistatin Attenuates Myocardial Fibrosis in Diabetic Cardiomyopathy via the TGF-β-Smad3 Pathway
    Wang, Yinhui
    Yu, Kun
    Zhao, Chengcheng
    Zhou, Ling
    Cheng, Jia
    Wang, Dao Wen
    Zhao, Chunxia
    [J]. FRONTIERS IN PHARMACOLOGY, 2021, 12
  • [45] Silica nanoparticles induce liver fibrosis via TGF-β1/Smad3 pathway in ICR mice
    Yu, Yang
    Duan, Junchao
    Li, Yang
    Li, Yanbo
    Jing, Li
    Yang, Man
    Wang, Ji
    Sun, Zhiwei
    [J]. INTERNATIONAL JOURNAL OF NANOMEDICINE, 2017, 12 : 6045 - 6057
  • [46] TGF-β/Smad3 Signaling Promotes Renal Fibrosis by Inhibiting miR-29
    Qin, Wei
    Chung, Arthur C. K.
    Huang, Xiao R.
    Meng, Xiao-Ming
    Hui, David S. C.
    Yu, Cheuk-Man
    Sung, Joseph J. Y.
    Lan, Hui Y.
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 22 (08): : 1462 - 1474
  • [47] βGemigliptin mitigates TGF-(3-induced renal fibrosis through FGF21-mediated inhibition of the TGF-β/Smad3 signaling pathway
    Byun, Jun-Kyu
    Jung, Gwon-Soo
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2024, 733
  • [49] Role and Mechanism of TGF-β1/smad3 Signal Pathways in Apoptosis in the Pathogenesis of Pulmonary Fibrosis in Mice
    Bai, Q.
    Liu, X. J.
    Qin, Z.
    Du, Y. F.
    Qian, L.
    Hao, X. Y.
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2014, 62 : S352 - S353
  • [50] Bletilla striata polysaccharide attenuated the progression of pulmonary fibrosis by inhibiting TGF-β1/Smad signaling pathway
    Wang, Siqi
    Yu, Jiabao
    Liu, Yang
    Yu, Jinjin
    Ma, Yajing
    Zhou, Lili
    Liu, Xinyao
    Liu, Lingyi
    Li, Weifeng
    Niu, Xiaofeng
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2024, 323