Literature DB >> 30024280

Artificial MicroRNA-Mediated Tgfbr2 and Pdgfrb Co-Silencing Ameliorates Carbon Tetrachloride-Induced Hepatic Fibrosis in Mice.

Yan Jiang1, Yuanyuan Zhao1, Fuchu He1,2, Haijian Wang1.   

Abstract

Hepatic stellate cells (HSCs) are the primary cell type responsible for liver fibrogenesis. Transforming growth factor beta 1 (TGF-β1) and platelet-derived growth factor (PDGF) are key profibrotic cytokines that regulate HSC activation and proliferation with functional convergence. Dual RNA interference against their receptors may achieve therapeutic effects. A novel RNAi strategy based on HSC-specific GFAP promoter-driven and lentiviral-expressed artificial microRNAs (amiRNAs) was devised that consists of an microRNA-30a backbone and effective shRNAs against mouse Pdgfrβ and Tgfbr2. Then, its antifibrotic efficacy was tested in primary and cultured HSCs and in mice affected with carbon tetrachloride-induced hepatic fibrosis. The study shows that amiRNA-mediated Pdgfrβ and Tgfbr2 co-silencing inhibits HSC activation and proliferation. After recombinant lentiviral particles were delivered into the liver via tail-vein injection, therapeutic amiRNAs were preferentially expressed in HSCs and efficiently co-knocked down in situ Tgfbr2 and Pdgfrβ expression, which correlates with downregulated expression of target or effector genes of their signaling, which include Pai-1, P70S6K, and D-cyclins. amiRNA-based HSC-specific co-silencing of Tgfbr2 and Pdgfrβ significantly suppressed hepatic expression of fibrotic markers α-Sma and Col1a1, extracellular matrix regulators Mmps and Timp1, and phenotypically ameliorated liver fibrosis, as indicated by reductions in serum alanine aminotransferase activity, collagen deposition, and α-Sma-positive staining. The findings provide proof of concept for the use of amiRNA-mediated co-silencing of two profibrogenic pathways in liver fibrosis treatment and highlight the therapeutic potential of concatenated amiRNAs for gene therapy.

Entities:  

Keywords:  artificial microRNA; hepatic stellate cells; liver fibrosis

Mesh:

Substances:

Year:  2018        PMID: 30024280     DOI: 10.1089/hum.2018.047

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  5 in total

1.  Histone H3K27 methyltransferase EZH2 and demethylase JMJD3 regulate hepatic stellate cells activation and liver fibrosis.

Authors:  Yan Jiang; Chan Xiang; Fan Zhong; Yang Zhang; Liyan Wang; Yuanyuan Zhao; Jiucun Wang; Chen Ding; Li Jin; Fuchu He; Haijian Wang
Journal:  Theranostics       Date:  2021-01-01       Impact factor: 11.556

2.  The Effects of Naringenin on miRNA-mRNA Profiles in HepaRG Cells.

Authors:  Weiyang Fan; Rui Shi; Minyi Guan; Pan Chen; Hao Wu; Weiwei Su; Yonggang Wang; Peibo Li
Journal:  Int J Mol Sci       Date:  2021-02-25       Impact factor: 5.923

3.  Autophagy-Related Activation of Hepatic Stellate Cells Reduces Cellular miR-29a by Promoting Its Vesicular Secretion.

Authors:  Xiaojie Yu; Natalia Elfimova; Marion Müller; Daniel Bachurski; Ulrike Koitzsch; Uta Drebber; Esther Mahabir; Hinrich P Hansen; Scott L Friedman; Sabine Klein; Hans Peter Dienes; Marianna Hösel; Reinhard Buettner; Jonel Trebicka; Vangelis Kondylis; Inge Mannaerts; Margarete Odenthal
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2022-02-24

Review 4.  Targeting fibrosis, mechanisms and cilinical trials.

Authors:  Manyu Zhao; Liqun Wang; Mengzhu Wang; Shijie Zhou; Ying Lu; Huijie Cui; Alexandra C Racanelli; Ling Zhang; Tinghong Ye; Bisen Ding; Ben Zhang; Jinliang Yang; Yuqin Yao
Journal:  Signal Transduct Target Ther       Date:  2022-06-30

5.  Strategy to enhance transgene expression in proximity of amyloid plaques in a mouse model of Alzheimer's disease.

Authors:  Danielle Weber-Adrian; Rikke Hahn Kofoed; Josephine Wing Yee Chan; Joseph Silburt; Zeinab Noroozian; Sebastian Kügler; Kullervo Hynynen; Isabelle Aubert
Journal:  Theranostics       Date:  2019-10-18       Impact factor: 11.556

  5 in total

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