The alterations in the extracellular matrix composition guide the repair of damaged liver tissue

• Published in: Scientific reports Vol. 6; no. 1; p. 27398
• Main Authors: Klaas, Mariliis, Kangur, Triin, Viil, Janeli, Mäemets-Allas, Kristina, Minajeva, Ave, Vadi, Krista, Antsov, Mikk, Lapidus, Natalia, Järvekülg, Martin, Jaks, Viljar
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 06.06.2016; Nature Publishing Group
• Subjects: 101/28; 101/47; 101/58; 13/106; 13/51; 14/3; 14/34; 38/109; 631/535/1262; 631/57/2272/2274; 631/80/304; 631/80/79/750; 692/4020/4021/288/2032; Animals; Cell Proliferation; Cells, Cultured; Collagen; Electron microscopes; Extracellular matrix; Extracellular Matrix - metabolism; Female; Fibers; Humanities and Social Sciences; Humans; Laboratory animals; Liver; Liver - metabolism; Liver - pathology; Liver - ultrastructure; Liver cirrhosis; Liver Regeneration; Male; Medicin och hälsovetenskap; Mice; Mice, Inbred CBA; Microscopy, Atomic Force; Microscopy, Electron, Scanning; Microscopy, Fluorescence; multidisciplinary; Peptides; Proteins; Scanning electron microscopy; Science; Scientific imaging; Germany; Estonia
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep27398

While the cellular mechanisms of liver regeneration have been thoroughly studied, the role of extracellular matrix (ECM) in liver regeneration is still poorly understood. We utilized a proteomics-based approach to identify the shifts in ECM composition after CCl 4 or DDC treatment and studied their effect on the proliferation of liver cells by combining biophysical and cell culture methods. We identified notable alterations in the ECM structural components (eg collagens I, IV, V, fibronectin, elastin) as well as in non-structural proteins (eg olfactomedin-4, thrombospondin-4, armadillo repeat-containing x-linked protein 2 (Armcx2)). Comparable alterations in ECM composition were seen in damaged human livers. The increase in collagen content and decrease in elastic fibers resulted in rearrangement and increased stiffness of damaged liver ECM. Interestingly, the alterations in ECM components were nonhomogenous and differed between periportal and pericentral areas and thus our experiments demonstrated the differential ability of selected ECM components to regulate the proliferation of hepatocytes and biliary cells. We define for the first time the alterations in the ECM composition of livers recovering from damage and present functional evidence for a coordinated ECM remodelling that ensures an efficient restoration of liver tissue.