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

被引:2
|
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
  • [1] Inhibition of AHNAK nucleoprotein 2 alleviates pulmonary fibrosis by downregulating the TGF-β1/Smad3 signaling pathway
    Zhu, Dongyi
    Zhang, Qian
    Li, Qinchuan
    Wang, Guangxue
    Guo, Zhongliang
    JOURNAL OF GENE MEDICINE, 2022, 24 (09):
  • [2] Ponatinib ameliorates pulmonary fibrosis by suppressing TGF-β1/Smad3 pathway
    Qu, Yubei
    Zhang, Liang
    Kang, Zechun
    Jiang, Wanglin
    Lv, Changjun
    PULMONARY PHARMACOLOGY & THERAPEUTICS, 2015, 34 : 1 - 7
  • [3] Neohesperidin inhibits TGF-β1/Smad3 signaling and alleviates bleomycin-induced pulmonary fibrosis in mice
    Guo, Jiasen
    Fang, Yinshan
    Jiang, Fangxin
    Li, Lian
    Zhou, Honggang
    Xu, Xiaojun
    Ning, Wen
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2019, 864
  • [4] Inhibition of TGF-β1/Smad3 signaling by compound 5aa: A potential treatment for idiopathic pulmonary fibrosis
    An, Baijiao
    Fang, Yanhua
    Wang, Lihan
    Nie, Wenyan
    Wang, Mengxuan
    Nie, Haoran
    Wu, Chengjun
    Wang, Ruoyu
    BIOORGANIC CHEMISTRY, 2024, 147
  • [5] Sirtuin 6 inhibits epithelial to mesenchymal transition during idiopathic pulmonary fibrosis via inactivating TGF-β1/Smad3 signaling
    Tian, Kunming
    Chen, Panpan
    Liu, Zhiping
    Si, Shutian
    Zhang, Qian
    Mou, Yong
    Han, Lianyong
    Wang, Qin
    Zhou, Xue
    ONCOTARGET, 2017, 8 (37) : 61011 - 61024
  • [6] TGF-β-Smad3 signaling in emphysema and pulmonary fibrosis: an epigenetic aberration of normal development?
    Warburton, David
    Shi, Wei
    Xu, Bing
    AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2013, 304 (02) : L83 - L85
  • [7] Knockdown of eIF3a ameliorates cardiac fibrosis by inhibiting the TGF-β1/Smad3 signaling pathway
    Li, B.
    Chen, H.
    Yang, X.
    Wang, Y.
    Qin, L.
    Chu, Y.
    CELLULAR AND MOLECULAR BIOLOGY, 2016, 62 (07) : 97 - 101
  • [8] SULF1 expression is increased and promotes fibrosis through the TGF-β1/SMAD pathway in idiopathic pulmonary fibrosis
    Tu, Meng
    Lu, Chunya
    Jia, Hongxia
    Chen, Shanshan
    Wang, Yan
    Li, Jing
    Cheng, Jiuling
    Yang, Ming
    Zhang, Guojun
    JOURNAL OF TRANSLATIONAL MEDICINE, 2024, 22 (01)
  • [9] Blueberry Juice Attenuates Pulmonary Fibrosis via Blocking the TGF-β1/Smad Signaling Pathway
    Li, Yali
    Wang, Liqun
    Zhang, Qianyu
    Tian, Li
    Gan, Cailing
    Liu, Hongyao
    Yin, Wenya
    Ye, Tinghong
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [10] Lysyl Hydroxylase Inhibition by Minoxidil Blocks Collagen Deposition and Prevents Pulmonary Fibrosis via TGF-β1/Smad3 Signaling Pathway
    Shao, Songjun
    Zhang, Xiangning
    Duan, Lingdi
    Fang, Haiyan
    Rao, Shanshan
    Liu, Weijia
    Guo, Bing
    Zhang, Xiangyan
    MEDICAL SCIENCE MONITOR, 2018, 24 : 8592 - 8601