Abstract
Liver disease, regardless of etiology, shares a similar natural history of disease progress and is common worldwide. This spectrum of diseases progresses from simple steatosis (fat accumulation), to inflammation, and eventually to fibrosis and cirrhosis. Hepatic fibrosis is primarily characterized by robust accumulation of collagen ECM that leads to organ dysfunction and decompensation. The role of the ECM in early stages of chronic liver disease is less well-understood, but recent studies have demonstrated that a number of changes in the hepatic ECM in early-stage liver disease may also contribute to disease progression. The purpose of this review is to summarize the established and proposed changes to the hepatic extracellular matrix (ECM) that may contribute to inflammation during earlier stages of disease development, and to discuss potential mechanisms by which these changes may mediate the progression of the disease.
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Allen AM, Shah VH, Therneau TM, Venkatesh SK, Mounajjed T, Larson JJ, Mara KC, Schulte PJ, Kellogg TA, Kendrick ML, McKenzie TJ, Greiner SM, Li J, Glaser KJ, Wells ML, Chen J, Ehman RL, Yin M (2018) The role of three-dimensional magnetic resonance elastography in the diagnosis of nonalcoholic steatohepatitis in obese patients undergoing bariatric surgery. Hepatology. https://doi.org/10.1002/hep.30483
Altamirano J, Bataller R (2011) Alcoholic liver disease: pathogenesis and new targets for therapy. Nat Rev Gastroenterol Hepatol 8(9):491–501. https://doi.org/10.1038/nrgastro.2011.134
Ankney JA, Muneer A, Chen X (2018) Relative and absolute quantitation in mass spectrometry-based proteomics. Annu Rev Anal Chem (Palo Alto, Calif) 11(1):49–77. https://doi.org/10.1146/annurev-anchem-061516-045357
Arteel GE, Naba A (2020) The liver matrisome, looking beyond collagens. JHEP Rep. https://doi.org/10.1016/j.jhepr.2020.100115
Beier JI, Arteel GE (2012) Alcoholic liver disease and the potential role of plasminogen activator inhibitor-1 and fibrin metabolism. Exp Biol Med (Maywood) 237(1):1–9. https://doi.org/10.1258/ebm.2011.011255
Beier JI, Luyendyk JP, Guo L, von Montfort C, Staunton DE, Arteel GE (2009) Fibrin accumulation plays a critical role in the sensitization to lipopolysaccharide-induced liver injury caused by ethanol in mice. Hepatology 49(5):1545–1553. https://doi.org/10.1002/hep.22847
Benyon RC, Arthur MJ (2001) Extracellular matrix degradation and the role of hepatic stellate cells. Semin Liver Dis 21(3):373–384. https://doi.org/10.1055/s-2001-17552
Bonnans C, Chou J, Werb Z (2014) Remodelling the extracellular matrix in development and disease. Nat Rev Mol Cell Biol 15(12):786–801. https://doi.org/10.1038/nrm3904
Brix K, McInnes J, Al-Hashimi A, Rehders M, Tamhane T, Haugen MH (2015) Proteolysis mediated by cysteine cathepsins and legumain-recent advances and cell biological challenges. Protoplasma 252(3):755–774. https://doi.org/10.1007/s00709-014-0730-0
Byass P (2014) The global burden of liver disease: a challenge for methods and for public health. BMC Med 12:159. https://doi.org/10.1186/s12916-014-0159-5
Calabro SR, Maczurek AE, Morgan AJ, Tu T, Wen VW, Yee C, Mridha A, Lee M, d’Avigdor W, Locarnini SA, McCaughan GW, Warner FJ, McLennan SV, Shackel NA (2014) Hepatocyte produced matrix metalloproteinases are regulated by CD147 in liver fibrogenesis. PLoS One 9(7):e90571. https://doi.org/10.1371/journal.pone.0090571
Canedo-Dorantes L, Canedo-Ayala M (2019) Skin acute wound healing: a comprehensive review. Int J Inflamm 2019:3706315. https://doi.org/10.1155/2019/3706315
Cassiman D, Libbrecht L, Desmet V, Denef C, Roskams T (2002) Hepatic stellate cell/myofibroblast subpopulations in fibrotic human and rat livers. J Hepatol 36(2):200–209. https://doi.org/10.1016/s0168-8278(01)00260-4
Coco B, Oliveri F, Maina AM, Ciccorossi P, Sacco R, Colombatto P, Bonino F, Brunetto MR (2007) Transient elastography: a new surrogate marker of liver fibrosis influenced by major changes of transaminases. J Viral Hepat 14(5):360–369. https://doi.org/10.1111/j.1365-2893.2006.00811.x
Cox J, Mann M (2011) Quantitative, high-resolution proteomics for data-driven systems biology. Annu Rev Biochem 80:273–299. https://doi.org/10.1146/annurev-biochem-061308-093216
Crosby HA, Lalor PF, Ross E, Newsome PN, Adams DH (2009) Adhesion of human haematopoietic (CD34(+)) stem cells to. Human liver compartments is integrin and CD44 dependent and modulated by CXCR3 and CXCR4. J Hepatol 51(4):734–749. https://doi.org/10.1016/j.jhep.2009.06.021
de Castro Bras LE, Ramirez TA, DeLeon-Pennell KY, Chiao YA, Ma Y, Dai Q, Halade GV, Hakala K, Weintraub ST, Lindsey ML (2013) Texas 3-step decellularization protocol: looking at the cardiac extracellular matrix. J Proteome 86:43–52. https://doi.org/10.1016/j.jprot.2013.05.004
Didangelos A, Yin X, Mandal K, Saje A, Smith A, Xu Q, Jahangiri M, Mayr M (2011) Extracellular matrix composition and remodeling in human abdominal aortic aneurysms: a proteomics approach. MCP 10(8):M111 008128. https://doi.org/10.1074/mcp.M111.008128
Dolin CE, Arteel GE (2020) The matrisome, inflammation and liver disease. Semin Liver Dis 40:180–188. https://doi.org/10.1055/s-0039-3402516
Dong X, Liu J, Xu Y, Cao H (2019) Role of macrophages in experimental liver injury and repair in mice. Exp Ther Med 17(5):3835–3847. https://doi.org/10.3892/etm.2019.7450
Duarte S, Baber J, Fujii T, Coito AJ (2015) Matrix metalloproteinases in liver injury, repair and fibrosis. Matrix Biol 44-46:147–156. https://doi.org/10.1016/j.matbio.2015.01.004
Dubail J, Apte SS (2015) Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics. Matrix Biol 44-46:24–37. https://doi.org/10.1016/j.matbio.2015.03.001
Edwards DR, Handsley MM, Pennington CJ (2008) The ADAM metalloproteinases. Mol Asp Med 29(5):258–289. https://doi.org/10.1016/j.mam.2008.08.001
Federman S, Miller LM, Sagi I (2002) Following matrix metalloproteinases activity near the cell boundary by infrared micro-spectroscopy. Matrix Biol 21(7):567–577
Forbes SJ, Newsome PN (2016) Liver regeneration - mechanisms and models to clinical application. Nat Rev Gastroenterol Hepatol 13(8):473–485. https://doi.org/10.1038/nrgastro.2016.97
Fox-Robichaud A, Kubes P (2000) Molecular mechanisms of tumor necrosis factor alpha-stimulated leukocyte recruitment into the murine hepatic circulation. Hepatology 31(5):1123–1127. https://doi.org/10.1053/he.2000.6961
Franitza S, Hershkoviz R, Kam N, Lichtenstein N, Vaday GG, Alon R, Lider O (2000) TNF-alpha associated with extracellular matrix fibronectin provides a stop signal for chemotactically migrating T cells. J Immunol 165(5):2738–2747. https://doi.org/10.4049/jimmunol.165.5.2738
Friedman SL (2010) Extracellular Matrix. In: Dufour JF, Clavien PA (eds) Signaling pathways in liver diseases. Springer, Berlin, pp 93–104. https://doi.org/10.1007/978-3-642-00150-5_6
Ganesan M, Poluektova LY, Kharbanda KK, Osna NA (2018) Liver as a target of human immunodeficiency virus infection. World J Gastroenterol 24(42):4728–4737. https://doi.org/10.3748/wjg.v24.i42.4728
Gao B, Ahmad MF, Nagy LE, Tsukamoto H (2019) Inflammatory pathways in alcoholic steatohepatitis. J Hepatol 70(2):249–259. https://doi.org/10.1016/j.jhep.2018.10.023
Gay NJ, Gangloff M (2007) Structure and function of toll receptors and their ligands. Annu Rev Biochem 76:141–165. https://doi.org/10.1146/annurev.biochem.76.060305.151318
Gilbert TW, Sellaro TL, Badylak SF (2006) Decellularization of tissues and organs. Biomaterials 27(19):3675–3683. https://doi.org/10.1016/j.biomaterials.2006.02.014
Gillis SE, Nagy LE (1997) Deposition of cellular fibronectin increases before stellate cell activation in rat liver during ethanol feeding. Alcohol Clin Exp Res 21(5):857–861
Godfrey HP (1990) T cell fibronectin: an unexpected inflammatory lymphokine. Lymphokine Res 9(3):435–447
Gressner AM, Bachem MG (1990) Cellular sources of noncollagenous matrix proteins: role of fat-storing cells in fibrogenesis. Semin Liver Dis 10(1):30–46. https://doi.org/10.1055/s-2008-1040455
Gressner OA, Weiskirchen R, Gressner AM (2007) Evolving concepts of liver fibrogenesis provide new diagnostic and therapeutic options. Comp Hepatol 6:7. https://doi.org/10.1186/1476-5926-6-7
Grgurevic I, Bozin T, Madir A (2017) Hepatitis C is now curable, but what happens with cirrhosis and portal hypertension afterwards? Clin Exp Hepatol 3(4):181–186. https://doi.org/10.5114/ceh.2017.71491
Griffiths MR, Keir S, Burt AD (1991) Basement membrane proteins in the space of Disse: a reappraisal. J Clin Pathol 44(8):646–648. https://doi.org/10.1136/jcp.44.8.646
Hajarizadeh B, Grebely J, Dore GJ (2013) Epidemiology and natural history of HCV infection. Nat Rev Gastroenterol Hepatol 10(9):553–562. https://doi.org/10.1038/nrgastro.2013.107
Hamada T, Fondevila C, Busuttil RW, Coito AJ (2008) Metalloproteinase-9 deficiency protects against hepatic ischemia/reperfusion injury. Hepatology 47(1):186–198. https://doi.org/10.1002/hep.21922
Hamidi H, Ivaska J (2018) Every step of the way: integrins in cancer progression and metastasis. Nat Rev Cancer 18(9):533–548. https://doi.org/10.1038/s41568-018-0038-z
Harburger DS, Calderwood DA (2009) Integrin signalling at a glance. J Cell Sci 122(Pt 2):159–163. https://doi.org/10.1242/jcs.018093
Harvey A, Montezano AC, Lopes RA, Rios F, Touyz RM (2016) Vascular fibrosis in aging and hypertension: molecular mechanisms and clinical implications. Can J Cardiol 32(5):659–668. https://doi.org/10.1016/j.cjca.2016.02.070
Hensley MK, Deng JC (2018) Acute on chronic liver failure and immune dysfunction: a mimic of sepsis. Semin Respir Crit Care Med 39(5):588–597. https://doi.org/10.1055/s-0038-1672201
Heydtmann M, Lalor PF, Eksteen JA, Hubscher SG, Briskin M, Adams DH (2005) CXC chemokine ligand 16 promotes integrin-mediated adhesion of liver-infiltrating lymphocytes to cholangiocytes and hepatocytes within the inflamed human liver. J Immunol 174(2):1055–1062. https://doi.org/10.4049/jimmunol.174.2.1055
Hobeika L, Barati MT, Caster DJ, McLeish KR, Merchant ML (2017) Characterization of glomerular extracellular matrix by proteomic analysis of laser-captured microdissected glomeruli. Kidney Int 91(2):501–511. https://doi.org/10.1016/j.kint.2016.09.044
Hodivala-Dilke KM, Reynolds AR, Reynolds LE (2003) Integrins in angiogenesis: multitalented molecules in a balancing act. Cell Tissue Res 314(1):131–144. https://doi.org/10.1007/s00441-003-0774-5
Hsu JJ, Lim J, Tintut Y, Demer LL (2016) Cell-matrix mechanics and pattern formation in inflammatory cardiovascular calcification. Heart 102(21):1710–1715. https://doi.org/10.1136/heartjnl-2016-309667
Huijberts MS, Schaper NC, Schalkwijk CG (2008) Advanced glycation end products and diabetic foot disease. Diabetes Metab Res Rev 24(Suppl 1):S19–S24. https://doi.org/10.1002/dmrr.861
Humphries JD, Byron A, Humphries MJ (2006) Integrin ligands at a glance. J Cell Sci 119(19):3901–3903. https://doi.org/10.1242/jcs.03098
Hyldig K, Riis S, Pennisi CP, Zachar V, Fink T (2017) Implications of extracellular matrix production by adipose tissue-derived stem cells for development of wound healing therapies. Int J Mol Sci 18(6). https://doi.org/10.3390/ijms18061167
Hynes RO (2009) The extracellular matrix: not just pretty fibrils. Science 326(5957):1216–1219
Hynes RO, Naba A (2012) Overview of the matrisome—an inventory of extracellular matrix constituents and functions. Cold Spring Harb Perspect Biol 4(1):a004903. https://doi.org/10.1101/cshperspect.a004903
Iredale JP, Benyon RC, Pickering J, McCullen M, Northrop M, Pawley S, Hovell C, Arthur MJ (1998) Mechanisms of spontaneous resolution of rat liver fibrosis. Hepatic stellate cell apoptosis and reduced hepatic expression of metalloproteinase inhibitors. J Clin Invest 102(3):538–549. https://doi.org/10.1172/jci1018
Issa R, Zhou X, Constandinou CM, Fallowfield J, Millward-Sadler H, Gaca MD, Sands E, Suliman I, Trim N, Knorr A, Arthur MJ, Benyon RC, Iredale JP (2004) Spontaneous recovery from micronodular cirrhosis: evidence for incomplete resolution associated with matrix cross-linking. Gastroenterology 126(7):1795–1808. https://doi.org/10.1053/j.gastro.2004.03.009
Ivaska J, Heino J (2011) Cooperation between integrins and growth factor receptors in signaling and endocytosis. Annu Rev Cell Dev Biol 27:291–320. https://doi.org/10.1146/annurev-cellbio-092910-154017
Iwamoto DV, Calderwood DA (2015) Regulation of integrin-mediated adhesions. Curr Opin Cell Biol 36:41–47. https://doi.org/10.1016/j.ceb.2015.06.009
Julich D, Cobb G, Melo AM, McMillen P, Lawton AK, Mochrie SG, Rhoades E, Holley SA (2015) Cross-scale integrin regulation organizes ECM and tissue topology. Dev Cell 34(1):33–44. https://doi.org/10.1016/j.devcel.2015.05.005
Kagan HM (2000) Intra- and extracellular enzymes of collagen biosynthesis as biological and chemical targets in the control of fibrosis. Acta Trop 77(1):147–152
Karki P, Birukova AA (2018) Substrate stiffness-dependent exacerbation of endothelial permeability and inflammation: mechanisms and potential implications in ALI and PH (2017 Grover conference series). Pulm Circ 8(2). https://doi.org/10.1177/2045894018773044
Karlmark KR, Weiskirchen R, Zimmermann HW, Gassler N, Ginhoux F, Weber C, Merad M, Luedde T, Trautwein C, Tacke F (2009) Hepatic recruitment of the inflammatory Gr1+ monocyte subset upon liver injury promotes hepatic fibrosis. Hepatology 50(1):261–274. https://doi.org/10.1002/hep.22950
Karsdal MA, Manon-Jensen T, Genovese F, Kristensen JH, Nielsen MJ, Sand JM, Hansen NU, Bay-Jensen AC, Bager CL, Krag A, Blanchard A, Krarup H, Leeming DJ, Schuppan D (2015) Novel insights into the function and dynamics of extracellular matrix in liver fibrosis. Am J Physiol Gastrointest Liver Physiol 308(10):G807–G830. https://doi.org/10.1152/ajpgi.00447.2014
Kirpich IA, Marsano LS, McClain CJ (2015) Gut-liver axis, nutrition, and non-alcoholic fatty liver disease. Clin Biochem 48(13–14):923–930. https://doi.org/10.1016/j.clinbiochem.2015.06.023
Kisseleva T, Brenner DA (2006) Hepatic stellate cells and the reversal of fibrosis. J Gastroenterol Hepatol 21(Suppl 3):S84–S87. https://doi.org/10.1111/j.1440-1746.2006.04584.x
Klaas M, Kangur T, Viil J, Maemets-Allas K, Minajeva A, Vadi K, Antsov M, Lapidus N, Jarvekulg M, Jaks V (2016) The alterations in the extracellular matrix composition guide the repair of damaged liver tissue. Sci Rep 6:27398. https://doi.org/10.1038/srep27398
Lee WY, Kubes P (2008) Leukocyte adhesion in the liver: distinct adhesion paradigm from other organs. J Hepatol 48(3):504–512. https://doi.org/10.1016/j.jhep.2007.12.005
Lee-Montiel FT, George SM, Gough AH, Sharma AD, Wu J, DeBiasio R, Vernetti LA, Taylor DL (2017) Control of oxygen tension recapitulates zone-specific functions in human liver microphysiology systems. Exp Biol Med (Maywood) 242(16):1617–1632. https://doi.org/10.1177/1535370217703978
Ley K, Laudanna C, Cybulsky MI, Nourshargh S (2007) Getting to the site of inflammation: the leukocyte adhesion cascade updated. Nat Rev Immunol 7(9):678–689. https://doi.org/10.1038/nri2156
Li B, Selmi C, Tang R, Gershwin ME, Ma X (2018) The microbiome and autoimmunity: a paradigm from the gut-liver axis. Cell Mol Immunol 15(6):595–609. https://doi.org/10.1038/cmi.2018.7
Libanio D, Marinho RT (2017) Impact of hepatitis C oral therapy in portal hypertension. World J Gastroenterol 23(26):4669–4674. https://doi.org/10.3748/wjg.v23.i26.4669
Lieber CS, Jones DP, Decarli LM (1965) Effects of prolonged ethanol intake: production of fatty liver despite adequate diets. J Clin Invest 44:1009–1021. https://doi.org/10.1172/JCI105200
Lipowsky HH (2018) Role of the glycocalyx as a barrier to leukocyte-endothelium adhesion. Adv Exp Med Biol 1097:51–68. https://doi.org/10.1007/978-3-319-96445-4_3
Liu SB, Ikenaga N, Peng ZW, Sverdlov DY, Greenstein A, Smith V, Schuppan D, Popov Y (2016) Lysyl oxidase activity contributes to collagen stabilization during liver fibrosis progression and limits spontaneous fibrosis reversal in mice. FASEB J 30(4):1599–1609. https://doi.org/10.1096/fj.14-268425
Lorenz L, Axnick J, Buschmann T, Henning C, Urner S, Fang S, Nurmi H, Eichhorst N, Holtmeier R, Bodis K, Hwang JH, Mussig K, Eberhard D, Stypmann J, Kuss O, Roden M, Alitalo K, Haussinger D, Lammert E (2018) Mechanosensing by beta1 integrin induces angiocrine signals for liver growth and survival. Nature 562(7725):128–132. https://doi.org/10.1038/s41586-018-0522-3
Luedde T, Kaplowitz N, Schwabe RF (2014) Cell death and cell death responses in liver disease: mechanisms and clinical relevance. Gastroenterology 147(4):765–783. https://doi.org/10.1053/j.gastro.2014.07.018
Lumelsky N, O’Hayre M, Chander P, Shum L, Somerman MJ (2018) Autotherapies: enhancing endogenous healing and regeneration. Trends Mol Med 24(11):919–930. https://doi.org/10.1016/j.molmed.2018.08.004
Mak KM, Png CY, Lee DJ (2016) Type V collagen in health, disease, and fibrosis. Anat Rec (Hoboken) 299(5):613–629. https://doi.org/10.1002/ar.23330
Mammoto A, Mammoto T, Kanapathipillai M, Wing Yung C, Jiang E, Jiang A, Lofgren K, Gee EP, Ingber DE (2013) Control of lung vascular permeability and endotoxin-induced pulmonary oedema by changes in extracellular matrix mechanics. Nat Commun 4:1759. https://doi.org/10.1038/ncomms2774
Martinez-Hernandez A, Amenta PS (1993) The hepatic extracellular matrix. I. Components and distribution in normal liver. Virchows Arch A Pathol Anat Histopathol 423(1):1–11
Martinez-Hernandez A, Amenta PS (1995) The extracellular matrix in hepatic regeneration. FASEB J 9(14):1401–1410. https://doi.org/10.1096/fasebj.9.14.7589981
Massey VL (2014) Extracellular matrix proteins and the liver-lung axis in disease. Electronic theses and dissertations. Paper 1752. https://doi.org/10.18297/etd/1752
Massey VL, Dolin CE, Poole LG, Hudson SV, Siow DL, Brock GN, Merchant ML, Wilkey DW, Arteel GE (2017) The hepatic “matrisome” responds dynamically to injury: characterization of transitional changes to the extracellular matrix in mice. Hepatology 65(3):969–982. https://doi.org/10.1002/hep.28918
McClelland R, Wauthier E, Uronis J, Reid L (2008) Gradients in the liver’s extracellular matrix chemistry from periportal to pericentral zones: influence on human hepatic progenitors. Tissue Eng A 14(1):59–70. https://doi.org/10.1089/ten.a.2007.0058
McDonald B, Kubes P (2015) Interactions between CD44 and Hyaluronan in leukocyte trafficking. Front Immunol 6:68
Mehal WZ, Schuppan D (2015) Antifibrotic therapies in the liver. Semin Liver Dis 35(2):184–198. https://doi.org/10.1055/s-0035-1550055
Michalopoulos GK, DeFrances M (2005) Liver regeneration. Adv Biochem Eng Biotechnol 93:101–134
Monneau Y, Arenzana-Seisdedos F, Lortat-Jacob H (2016) The sweet spot: how GAGs help chemokines guide migrating cells. J Leukoc Biol 99(6):935–953. https://doi.org/10.1189/jlb.3MR0915-440R
Morrison ED, Kowdley KV (2000) Genetic liver disease in adults. Early recognition of the three most common causes. Postgrad Med 107(2):147–152. https://doi.org/10.3810/pgm.2000.02.872
Naba A, Clauser KR, Hoersch S, Liu H, Carr SA, Hynes RO (2012) The matrisome: in silico definition and in vivo characterization by proteomics of normal and tumor extracellular matrices. Mol Cell Proteomics 11(4). https://doi.org/10.1074/mcp.M111.014647
Naba A, Clauser KR, Ding H, Whittaker CA, Carr SA, Hynes RO (2016) The extracellular matrix: tools and insights for the “omics” era. Matrix Biol 49:10–24. https://doi.org/10.1016/j.matbio.2015.06.003
Nargis NN, Aldredge RC, Guy RD (2018) The influence of soluble fragments of extracellular matrix (ECM) on tumor growth and morphology. Math Biosci 296:1–16. https://doi.org/10.1016/j.mbs.2017.11.014
Oliveira THC, Marques PE, Proost P, Teixeira MMM (2018) Neutrophils: a cornerstone of liver ischemia and reperfusion injury. Lab Investig 98(1):51–62. https://doi.org/10.1038/labinvest.2017.90
Omenetti A, Porrello A, Jung Y, Yang L, Popov Y, Choi SS, Witek RP, Alpini G, Venter J, Vandongen HM, Syn WK, Baroni GS, Benedetti A, Schuppan D, Diehl AM (2008) Hedgehog signaling regulates epithelial-mesenchymal transition during biliary fibrosis in rodents and humans. J Clin Invest 118(10):3331–3342. https://doi.org/10.1172/JCI35875
Ozaki I, Hamajima H, Matsuhashi S, Mizuta T (2011) Regulation of TGF-beta1-induced pro-apoptotic signaling by growth factor receptors and extracellular matrix receptor integrins in the liver. Front Physiol 2:78. https://doi.org/10.3389/fphys.2011.00078
Patel VN, Pineda DL, Hoffman MP (2017) The function of heparan sulfate during branching morphogenesis. Matrix Biol 57–58:311–323. https://doi.org/10.1016/j.matbio.2016.09.004
Patouraux S, Rousseau D, Bonnafous S, Lebeaupin C, Luci C, Canivet CM, Schneck AS, Bertola A, Saint-Paul MC, Iannelli A, Gugenheim J, Anty R, Tran A, Bailly-Maitre B, Gual P (2017) CD44 is a key player in non-alcoholic steatohepatitis. J Hepatol 67(2):328–338. https://doi.org/10.1016/j.jhep.2017.03.003
Patsenker E, Stickel F (2011) Role of integrins in fibrosing liver diseases. Am J Physiol Gastrointest Liver Physiol 301(3):G425–G434. https://doi.org/10.1152/ajpgi.00050.2011
Pellicoro A, Aucott RL, Ramachandran P, Robson AJ, Fallowfield JA, Snowdon VK, Hartland SN, Vernon M, Duffield JS, Benyon RC, Forbes SJ, Iredale JP (2012) Elastin accumulation is regulated at the level of degradation by macrophage metalloelastase (MMP-12) during experimental liver fibrosis. Hepatology 55(6):1965–1975. https://doi.org/10.1002/hep.25567
Pellicoro A, Ramachandran P, Iredale JP, Fallowfield JA (2014) Liver fibrosis and repair: immune regulation of wound healing in a solid organ. Nat Rev Immunol 14(3):181–194. https://doi.org/10.1038/nri3623
Phillip JM, Aifuwa I, Walston J, Wirtz D (2015) The mechanobiology of aging. Annu Rev Biomed Eng 17:113–141. https://doi.org/10.1146/annurev-bioeng-071114-040829
Poole LG, Arteel GE (2016) Transitional remodeling of the hepatic extracellular matrix in alcohol-induced liver injury. Biomed Res Int 2016:3162670. https://doi.org/10.1155/2016/3162670
Poole LG, Dolin CE, Arteel GE (2017) Organ-organ crosstalk and alcoholic liver disease. Biomol Ther 7(3). https://doi.org/10.3390/biom7030062
Poynard T, McHutchison J, Manns M, Trepo C, Lindsay K, Goodman Z, Ling MH, Albrecht J (2002) Impact of pegylated interferon alfa-2b and ribavirin on liver fibrosis in patients with chronic hepatitis C. Gastroenterology 122(5):1303–1313. https://doi.org/10.1053/gast.2002.33023
Preziosi ME, Monga SP (2017) Update on the mechanisms of liver regeneration. Semin Liver Dis 37(2):141–151. https://doi.org/10.1055/s-0037-1601351
Pritchard MT, McCracken JM (2015) Identifying novel targets for treatment of liver fibrosis: what can we learn from injured tissues which heal without a scar? Curr Drug Targets 16(12):1332–1346
Proudfoot AE, Handel TM, Johnson Z, Lau EK, LiWang P, Clark-Lewis I, Borlat F, Wells TN, Kosco-Vilbois MH (2003) Glycosaminoglycan binding and oligomerization are essential for the in vivo activity of certain chemokines. Proc Natl Acad Sci USA 100(4):1885–1890. https://doi.org/10.1073/pnas.0334864100
Ramachandran P, Pellicoro A, Vernon MA, Boulter L, Aucott RL, Ali A, Hartland SN, Snowdon VK, Cappon A, Gordon-Walker TT, Williams MJ, Dunbar DR, Manning JR, van Rooijen N, Fallowfield JA, Forbes SJ, Iredale JP (2012) Differential Ly-6C expression identifies the recruited macrophage phenotype, which orchestrates the regression of murine liver fibrosis. Proc Natl Acad Sci USA 109(46):E3186–E3195. https://doi.org/10.1073/pnas.1119964109
Ramaiah SK, Rittling S (2008) Pathophysiological role of osteopontin in hepatic inflammation, toxicity, and cancer. Toxicol Sci 103(1):4–13. https://doi.org/10.1093/toxsci/kfm246
Randles M, Lennon R (2015) Applying proteomics to investigate extracellular matrix in health and disease. Curr Top Membr 76:171–196. https://doi.org/10.1016/bs.ctm.2015.06.001
Rauniyar N, Yates JR (2014) Isobaric labeling-based relative quantification in shotgun proteomics. J Proteome Res 13(12):5293–5309. https://doi.org/10.1021/pr500880b
Reddig PJ, Juliano RL (2005) Clinging to life: cell to matrix adhesion and cell survival. Cancer Metastasis Rev 24(3):425–439. https://doi.org/10.1007/s10555-005-5134-3
Robertson H, Kirby JA, Yip WW, Jones DE, Burt AD (2007) Biliary epithelial-mesenchymal transition in posttransplantation recurrence of primary biliary cirrhosis. Hepatology 45(4):977–981. https://doi.org/10.1002/hep.21624
Robinson MW, Harmon C, O'Farrelly C (2016) Liver immunology and its role in inflammation and homeostasis. Cell Mol Immunol 13(3):267–276. https://doi.org/10.1038/cmi.2016.3
Roderfeld M (2018) Matrix metalloproteinase functions in hepatic injury and fibrosis. Matrix Biol 68-69:452–462. https://doi.org/10.1016/j.matbio.2017.11.011
Rousselle P, Braye F, Dayan G (2018) Re-epithelialization of adult skin wounds: cellular mechanisms and therapeutic strategies. Adv Drug Deliv Rev. https://doi.org/10.1016/j.addr.2018.06.019
Rozario T, DeSimone DW (2010) The extracellular matrix in development and morphogenesis: a dynamic view. Dev Biol 341(1):126–140. https://doi.org/10.1016/j.ydbio.2009.10.026
Sacca SC, Gandolfi S, Bagnis A, Manni G, Damonte G, Traverso CE, Izzotti A (2016) From DNA damage to functional changes of the trabecular meshwork in aging and glaucoma. Ageing Res Rev 29:26–41. https://doi.org/10.1016/j.arr.2016.05.012
Sadeghi S, Vink RL (2015) Membrane sorting via the extracellular matrix. Biochim Biophys Acta 1848(2):527–531. https://doi.org/10.1016/j.bbamem.2014.10.035
Sand JM, Leeming DJ, Byrjalsen I, Bihlet AR, Lange P, Tal-Singer R, Miller BE, Karsdal MA, Vestbo J (2016) High levels of biomarkers of collagen remodeling are associated with increased mortality in COPD - results from the ECLIPSE study. Respir Res 17(1):125. https://doi.org/10.1186/s12931-016-0440-6
Santambrogio L, Rammensee HG (2019) Contribution of the plasma and lymph degradome and peptidome to the MHC ligandome. Immunogenetics 71(3):203–216. https://doi.org/10.1007/s00251-018-1093-z
Schnittert J, Bansal R, Storm G, Prakash J (2018) Integrins in wound healing, fibrosis and tumor stroma: high potential targets for therapeutics and drug delivery. Adv Drug Deliv Rev 129:37–53. https://doi.org/10.1016/j.addr.2018.01.020
Schuppan D, Ashfaq-Khan M, Yang AT, Kim YO (2018) Liver fibrosis: direct antifibrotic agents and targeted therapies. Matrix Biol 68-69:435–451. https://doi.org/10.1016/j.matbio.2018.04.006
Schuster S, Cabrera D, Arrese M, Feldstein AE (2018) Triggering and resolution of inflammation in NASH. Nat Rev Gastroenterol Hepatol 15(6):349–364. https://doi.org/10.1038/s41575-018-0009-6
Schwartz JM, Reinus JF (2012) Prevalence and natural history of alcoholic liver disease. Clin Liver Dis 16(4):659–666. https://doi.org/10.1016/j.cld.2012.08.001
Sessions AO, Engler AJ (2016) Mechanical regulation of cardiac aging in model systems. Circ Res 118(10):1553–1562. https://doi.org/10.1161/CIRCRESAHA.116.307472
Seth D, Haber PS, Syn WK, Diehl AM, Day CP (2011) Pathogenesis of alcohol-induced liver disease: classical concepts and recent advances. J Gastroenterol Hepatol 26(7):1089–1105. https://doi.org/10.1111/j.1440-1746.2011.06756.x
Seth D, Duly A, Kuo PC, McCaughan GW, Haber PS (2014) Osteopontin is an important mediator of alcoholic liver disease via hepatic stellate cell activation. World J Gastroenterol 20(36):13088–13104. https://doi.org/10.3748/wjg.v20.i36.13088
Shao X, Taha IN, Clauser KR, Gao YT, Naba A (2020) MatrisomeDB: the ECM-protein knowledge database. Nucleic Acids Res 48(D1):D1136–D1144. https://doi.org/10.1093/nar/gkz849
Shimizu Y, Shaw S (1991) Lymphocyte interactions with extracellular matrix. FASEB J 5(9):2292–2299. https://doi.org/10.1096/fasebj.5.9.1860621
Shirin H, Bruck R, Aeed H, Frenkel D, Kenet G, Zaidel L, Avni Y, Halpern Z, Hershkoviz R (1998) Pentoxifylline prevents concanavalin A-induced hepatitis by reducing tumor necrosis factor alpha levels and inhibiting adhesion of T lymphocytes to extracellular matrix. J Hepatol 29(1):60–67. https://doi.org/10.1016/s0168-8278(98)80179-7
Simons K, Toomre D (2000) Lipid rafts and signal transduction. Nat Rev Mol Cell Biol 1(1):31–39. https://doi.org/10.1038/35036052
Singh S, Osna NA, Kharbanda KK (2017) Treatment options for alcoholic and non-alcoholic fatty liver disease: a review. World J Gastroenterol 23(36):6549–6570. https://doi.org/10.3748/wjg.v23.i36.6549
Song KS, Kim HS, Park KE, Kwon OH (1993) The fibrinogen degradation products (FgDP) levels in liver disease. Yonsei Med J 34(3):234–238. https://doi.org/10.3349/ymj.1993.34.3.234
Sorokin L (2010) The impact of the extracellular matrix on inflammation. Nat Rev Immunol 10(10):712–723. https://doi.org/10.1038/nri2852
Srivastava A, Jong S, Gola A, Gailer R, Morgan S, Sennett K, Tanwar S, Pizzo E, O'Beirne J, Tsochatzis E, Parkes J, Rosenberg W (2019) Cost-comparison analysis of FIB-4, ELF and fibroscan in community pathways for non-alcoholic fatty liver disease. BMC Gastroenterol 19(1):122. https://doi.org/10.1186/s12876-019-1039-4
Sullivan DC, Mirmalek-Sani SH, Deegan DB, Baptista PM, Aboushwareb T, Atala A, Yoo JJ (2012) Decellularization methods of porcine kidneys for whole organ engineering using a high-throughput system. Biomaterials 33(31):7756–7764. https://doi.org/10.1016/j.biomaterials.2012.07.023
Sun BK, Siprashvili Z, Khavari PA (2014) Advances in skin grafting and treatment of cutaneous wounds. Science 346(6212):941–945. https://doi.org/10.1126/science.1253836
Sweet PH, Khoo T, Nguyen S (2017) Nonalcoholic fatty liver disease. Prim Care 44(4):599–607. https://doi.org/10.1016/j.pop.2017.07.003
Tatsukawa H, Furutani Y, Hitomi K, Kojima S (2016) Transglutaminase 2 has opposing roles in the regulation of cellular functions as well as cell growth and death. Cell Death Dis 7(6):e2244. https://doi.org/10.1038/cddis.2016.150
Thiele GM, Duryee MJ, Freeman TL, Sorrell MF, Willis MS, Tuma DJ, Klassen LW (2005) Rat sinusoidal liver endothelial cells (SECs) produce pro-fibrotic factors in response to adducts formed from the metabolites of ethanol. Biochem Pharmacol 70(11):1593–1600. https://doi.org/10.1016/j.bcp.2005.08.014
Vempati P, Popel AS, Mac Gabhann F (2014) Extracellular regulation of VEGF: isoforms, proteolysis, and vascular patterning. Cytokine Growth Factor Rev 25(1):1–19. https://doi.org/10.1016/j.cytogfr.2013.11.002
Verstegen MMA, Willemse J, van den Hoek S, Kremers GJ, Luider TM, van Huizen NA, Willemssen F, Metselaar HJ, JNM IJ, van der Laan LJW, de Jonge J (2017) Decellularization of whole human liver grafts using controlled perfusion for transplantable organ bioscaffolds. Stem Cells Dev 26(18):1304–1315. https://doi.org/10.1089/scd.2017.0095
Vispo E, Barreiro P, Del Valle J, Maida I, de Ledinghen V, Quereda C, Moreno A, Macias J, Castera L, Pineda JA, Soriano V (2009) Overestimation of liver fibrosis staging using transient elastography in patients with chronic hepatitis C and significant liver inflammation. Antivir Ther 14(2):187–193
Wang S, Voisin MB, Larbi KY, Dangerfield J, Scheiermann C, Tran M, Maxwell PH, Sorokin L, Nourshargh S (2006) Venular basement membranes contain specific matrix protein low expression regions that act as exit points for emigrating neutrophils. J Exp Med 203(6):1519–1532. https://doi.org/10.1084/jem.20051210
Wasmuth HE, Tacke F, Trautwein C (2010) Chemokines in liver inflammation and fibrosis. Semin Liver Dis 30(3):215–225. https://doi.org/10.1055/s-0030-1255351
Widgerow AD (2012) Cellular resolution of inflammation—catabasis. Wound Repair Regen 20(1):2–7. https://doi.org/10.1111/j.1524-475X.2011.00754.x
Willemse J, Verstegen MMA, Vermeulen A, Schurink IJ, Roest HP, van der Laan LJW, de Jonge J (2020) Fast, robust and effective decellularization of whole human livers using mild detergents and pressure controlled perfusion. Mater Sci Eng C Mater Biol Appl 108:110200. https://doi.org/10.1016/j.msec.2019.110200
Wisniewski JR, Zougman A, Mann M (2009) Combination of FASP and StageTip-based fractionation allows in-depth analysis of the hippocampal membrane proteome. J Proteome Res 8(12):5674–5678. https://doi.org/10.1021/pr900748n
Wong J, Johnston B, Lee SS, Bullard DC, Smith CW, Beaudet AL, Kubes P (1997) A minimal role for selectins in the recruitment of leukocytes into the inflamed liver microvasculature. J Clin Invest 99(11):2782–2790. https://doi.org/10.1172/JCI119468
Woodfin A, Voisin MB, Nourshargh S (2010) Recent developments and complexities in neutrophil transmigration. Curr Opin Hematol 17(1):9–17. https://doi.org/10.1097/MOH.0b013e3283333930
Wree A, Marra F (2016) The inflammasome in liver disease. J Hepatol 65(5):1055–1056. https://doi.org/10.1016/j.jhep.2016.07.002
Wu D, Birukov K (2019) Endothelial cell mechano-metabolomic coupling to disease states in the lung microvasculature. Front Bioeng Biotechnol 7:172. https://doi.org/10.3389/fbioe.2019.00172
Zang S, Wang L, Ma X, Zhu G, Zhuang Z, Xun Y, Zhao F, Yang W, Liu J, Luo Y, Liu Y, Ye D, Shi J (2015) Neutrophils play a crucial role in the early stage of nonalcoholic steatohepatitis via neutrophil Elastase in mice. Cell Biochem Biophys 73(2):479–487. https://doi.org/10.1007/s12013-015-0682-9
Zeisberg M, Yang C, Martino M, Duncan MB, Rieder F, Tanjore H, Kalluri R (2007) Fibroblasts derive from hepatocytes in liver fibrosis via epithelial to mesenchymal transition. J Biol Chem 282(32):23337–23347. https://doi.org/10.1074/jbc.M700194200
Zhou HF, Chan HW, Wickline SA, Lanza GM, Pham CT (2009) Alphavbeta3-targeted nanotherapy suppresses inflammatory arthritis in mice. FASEB J 23(9):2978–2985. https://doi.org/10.1096/fj.09-129874
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Dolin, C.E., Sato, T., Merchant, M.L., Arteel, G.E. (2020). Detecting Changes to the Extracellular Matrix in Liver Diseases. In: Ricard-Blum, S. (eds) Extracellular Matrix Omics. Biology of Extracellular Matrix, vol 7. Springer, Cham. https://doi.org/10.1007/978-3-030-58330-9_3
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