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Original Research

Sequential Matrix Metalloproteinase-1 Expression Triggered by Infiltrating Monocytic Lineage Cells Modulates Pathophysiological Aspects of Human Nonalcoholic Steatohepatitis

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Pages 1-13 | Published online: 21 Jul 2020

References

  • Younossi ZM, Loomba R, Rinella ME, et al. Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Hepatology. 2018;68:361–371. doi:10.1002/hep.29724
  • Okazaki I, Noro T, Tsutsui N, et al. Fibrogenesis and carcinogenesis in nonalcoholic steatohepatitis (NASH): involvement of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinase (TIMPs). Cancers. 2014;6:1220–1255. doi:10.3390/cancers6031220
  • Okazaki I, Ninomiya Y, Friedman SL, Tanikawa K, eds, Extracellular Matrix and the Liver. Approach to Gene Therapy. London, New York: Academic Press, Amsterdam, Boston; 2003:1–467.
  • Okazaki I, Nabeshima K. Introduction: MMPs, ADAMs/ADAMTSs research products to achieve big dream. Anticancer Agents Med Chem. 2012;12:688–706. doi:10.2174/187152012802650200
  • Okazaki I, Maruyama K. Collagenase activity in experimental hepatic fibrosis. Nature. 1974;252:49–50. doi:10.1038/252049a0
  • Watanabe T, Niioka M, Hozawa S, et al. Gene expression of interstitial collagenase in both progressive and recovery phase of rat liver fibrosis induced by carbon tetrachloride. J Hepatol. 2000;33:224–235. doi:10.1016/S0168-8278(00)80363-3
  • Watanabe T, Niioka M, Ishikawa A, et al. Dynamic change of cells expressing MMP-2 mRNA and MT1-MMP mRNA in the recovery from liver fibrosis in the rat. J Hepatol. 2001;35:465–473. doi:10.1016/S0168-8278(01)00177-5
  • Higashiyama R, Inagaki Y, Hong YY, et al. Bone marrow-derived cells express matrix metalloproteinases and contribute to regression of liver fibrosis in mice. Hepatology. 2007;45:213–222. doi:10.1002/hep.21477
  • Endo H, Niioka M, Sugioka Y, et al. Matrix metalloproteinase-13 promotes recovery from experimental liver cirrhosis in rats. Pathobiology. 2011;78:239–252. doi:10.1159/000328841
  • Yokomori H, Inagaki Y, Ando W, et al. Spatiotemporal expression of metalloproteinase-1 in progression of nonalcoholic steatohepatitis. J Mod Hum Pathol. 2016;1:11–20. doi:10.14312/2397-6845.2016-3
  • Yokomori H, Ando W, Oda M, Inagaki Y, Okazaki I. Hepatic progenitor cell expansion in early-stage nonalcoholic steatohepatitis: evidence from immunohistochemistry and immunoelectron microscopy of matrix metalloproteinase-1. Med Mol Morphol. 2017;50:238–242. doi:10.1007/.s00795-017-0162-y
  • Ando W, Yokomori H, Tsutsui N, et al. Serum matrix metalloproteinase-1 represents disease activity as opposed to fibrosis in patients with histologically proven nonalcoholic steatohepatitis. Clin Mol Hepatol. 2018;24:61–76. doi:10.3350/cmh.2017.0030
  • Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of nonalcoholic fatty liver disease: practice guidance from the American association for the study of liver diseases. Hepatology. 2018;67:328–357. doi:10.1002/hep.29367
  • Younossi ZM, Loomba R, Anstee QM, et al. Diagnostic modalities for nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, and associated fibrosis. Hepatology. 2018;68:349–360. doi:10.1002/hep.29721
  • American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2011;34:S62-S69. doi:10.2337/dc11-S062
  • The Japanese Task Force Committee for Diagnosis Criteria of Metabolic Syndrome. Definition and diagnosis criteria of metabolic syndrome. J Jap Inter Med Ass. 2005;94:794–809.
  • Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA. 2001;285:2486–2497. doi:10.1001/jama.285.19.2486
  • Morini S, Carotti S, Carpino G, et al. GFAP expression in the liver as an early marker of stellate cells activation. It J Anat Embryol. 2005;110:193–2007.
  • Yang L, Jung Y, Omenetti A, et al. Fate-mapping evidence that hepatic stellate cells are epithelial progenitors in adult mouse livers. Stem Cells. 2008;26:2104–2113. doi:10.1634/stemcells.2008-0115
  • Shibata S, Iseda T, Mitsuhashi T, et al. Large-area fluorescence and electron microscopic correlative imaging with multibeam scanning electron microscopy. Front Neural Circuits. 2019;13:29. doi:10.3389/fncir2019.00029
  • Sugioka Y, Watanabe T, Inagaki Y, et al. c-JUN NH2-terminal kinase pathway is involved in constitutive matrix metalloproteinase-1 expression in a hepatocellular carcinoma-derived cell line. Int J Cancer. 2004;109:867–874. doi:10.1002/ijc.20095
  • Yanagawa T, Sumiyoshi H, Higashi K, et al. Identification of a novel bone marrow cell-derived accelerator of fibrotic liver regeneration through mobilization of hepatic progenitor cells in mice. Stem Cells. 2019;37:89–101. doi:10.1002/stem.2916
  • Heissig B, Hattori K, Dias S, et al. Recruitment of stem and progenitor cells from the bone marrow niche requires MMP-9 mediated release of kit-ligand. Cell. 2002;109:625–637. doi:10.1016/s0092-8674(02)00754-7
  • Bihari C, Anand L, Rooge S, et al. Bone marrow stem cells and their niche components are adversely affected in advanced cirrhosis of the liver. Hepatology. 2016;64:1273–1288. doi:10.1002/hep.28754
  • Boulter L, Govaere O, Bird TG, et al. Macrophage derived Wnt opposes Notch signaling to specify hepatic progenitor cell fate in chronic liver disease. Nat Med. 2012;18:572–579. doi:10.1038/nm.2667
  • Pollard JW. Tropic macrophages in development and disease. Nat Rev Immunol. 2009;9:259–270. doi:10.1038/nri2528
  • Saunders WB, Bayless KJ, Davis GE. MMP-1 activation by serine proteases and MMP-10 induces human capillary tubular network collapse and regression in 3D collagen matrices. J Cell Sci. 2005;118(Pt 10):2325–2340. doi:10.1242/jcs.02360
  • Iimuro Y, Nishio T, Morimoto T, et al. Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat. Gastroenterology. 2003;124:445–458. doi:10.1053/gast.2003.50063
  • Siller-Lόpez F, Sandoval A, Salgado S, et al. Treatment with human metalloproteinase-8 gene delivery ameliorates experimental rat liver cirrhosis. Gastroenterology. 2004;126:1122–1133. doi:10.1053/j.gastro.2003.12.045
  • Zeisberg M, Yang C, Martino M, et al. Fibroblasts derive from hepatocytes in liver fibrosis via epithelial to mesenchymal transition. J Biol Chem. 2007;282(32):23337–23347. doi:10.1074/jbc.M700194200
  • Syn W-K, Jung Y, Omenetti A, et al. Hedgehog-mediated epithelial-to-mesenchymal transition and fibrogenic repair in non-alcoholic fatty liver disease. Gastroenterology. 2009;137:1478–1488. doi:10.1053/j.gastro.2009.06.051
  • Zhao Y-L, Zhu R-T, Sun Y-L. Epithelial-mesenchymal transition in liver fibrosis (Review). Biomed Rep. 2016;4:269–274. doi:10.3892/br.2016.578
  • Huber MA, Kraut N, Beug H. Molecular requirements for epithelial-mesenchymal transition during tumor progression. Curr Opin Cell Biol. 2005;17:548–558. doi:10.1016/j.ceb.2005.08.001
  • Giannelli G, Koudelkova P, Dituri F, Mikulits W. Role of epithelial to mesenchymal transition in hepatocellular carcinoma. J Hepatol. 2016;65:798–808. doi:10.1016/j.jhep.2016.05.007
  • Okazaki I, Wada N, Nakano M, et al. Difference in gene expression for matrix metalloproteinase-1 between early and advanced hepatocellular carcinomas. Hepatology. 1997;25:580–584. doi:10.1002/hep.510250315
  • Kessenbrock K, Plaks V, Werb Z. Matrix metalloproteinases: regulators of the tumor microenvironment. Cell. 2010;141:52–67. doi:10.1016/j.cell.2010.03.015
  • Ma F, Zhang L, Li M, Zhang Y, Zhang J, Guo B. Mir-361-5p inhibits glycolytic metabolism, proliferation and invasion of breast cancer by targeting FGFR1 and MMP-1. J Exp Clin Cancer Res. 2017;36:158. doi:10.1186/s13046-017-0630-1
  • Ma H, Cai H, Zhang Y, et al. Membrane palmitoylated protein 3 promotes hepatocellular carcinoma cell migration and invasion via up-regulating matrix metalloproteinase 1. Cancer Lett. 2014;344:74–81. doi:10.1016/j.canlet.2013.10.017
  • Kim E, Kim D, Lee J-S, et al. Capicua suppresses hepatocellular carcinoma progression by controlling the ETV4-MMP-1 axis. Hepatology. 2018;67:2287–2301. doi:10.1002/hep.29738
  • Sauter W, Rosenberger A, Beckmann L, et al. Matrix metalloproteinase 1 (MMP-1) is associated with early-onset lung cancer. Cancer Epidemiol Biomarkers Prev. 2008;17:1127–1135. doi:10.1158/1055-9965.EPI-07-2840
  • Saito R, Miki Y, Ishida N, et al. The significance of MMP-1 in EGFR-TKI-resistant lung adenocarcinoma: potential for therapeutic targeting. Int J Mol Sci. 2018;19:609. doi:10.3390/ijms.19020609
  • Lee Y-S, Kim S-Y, Ko E, et al. Exosomes derived from palmitic acid-treated hepatocytes induce fibrotic activation of hepatic stellate cells. Sci Rep. 2017;7:3710. doi:10.1038/s41598-017-03389-2
  • Hohenester S, Christiansen S, Nagel J, et al. Lifestyle intervention for morbid obesity: effects on liver steatosis, inflammation and fibrosis. Am J Physiol Gastrointest Liver Physiol. 2018;315:G329-G338. doi:10.1152/ajpgi.00044.2018
  • Balbin M, Fueyo A, Knauper V, et al. Identification and enzymatic characterization of two diverging murine counterparts of human interstitial collagenase (MMP-1) expressed at sites of embryo implantation. J Biol Chem. 2001;276:10253–10262. doi:10.1074/jbc.M009586200
  • Nevzorova YA, Boyer-Diaz Z, Cubero FJ, Gracia-Sancho J. Animal models for liver disease - a practical approach for translational research. J Hepatol. 2020. doi:10.1016/j.jhep.2020.04.011
  • Ouchi R, Togo S, Kimura M, et al. Modeling steatohepatitis in humans with pluripotent stem cell-derived organoids. Cell Metab. 2019;30:374–384.e6. doi:10.1016/j.cmet.2019.05.007
  • Kim K-H, Jung J-Y, Son ED, Shin DW, Noh M, Lee TR. miR-526b targets 3ʹUTR of MMP-1 mRNA. Exp Mol Med. 2015;47:e178. doi:10.38/emm.2015.52
  • Li W-D, Zhou D-M, Sun -L-L, et al. LncRNA WTAPP1 promotes migration and angiogenesis of endothelial progenitor cells via MMP-1 through microRNA 3,120 and AKT/P13K/autophagy pathways. Stem Cells. 2018. doi:10.1002/stem.2904