A guide to the composition and functions of the extracellular matrix.

collagens elastin extracellular matrix glycosaminoglycans heparanase hyaluronan hyaluronidases integrins laminins matrix metalloproteinases proteoglycans tenascins

Journal

The FEBS journal
ISSN: 1742-4658
Titre abrégé: FEBS J
Pays: England
ID NLM: 101229646

Informations de publication

Date de publication:
12 2021
Historique:
revised: 13 02 2021
received: 13 01 2021
accepted: 18 02 2021
pubmed: 20 2 2021
medline: 12 1 2022
entrez: 19 2 2021
Statut: ppublish

Résumé

Extracellular matrix (ECM) is a dynamic 3-dimensional network of macromolecules that provides structural support for the cells and tissues. Accumulated knowledge clearly demonstrated over the last decade that ECM plays key regulatory roles since it orchestrates cell signaling, functions, properties and morphology. Extracellularly secreted as well as cell-bound factors are among the major members of the ECM family. Proteins/glycoproteins, such as collagens, elastin, laminins and tenascins, proteoglycans and glycosaminoglycans, hyaluronan, and their cell receptors such as CD44 and integrins, responsible for cell adhesion, comprise a well-organized functional network with significant roles in health and disease. On the other hand, enzymes such as matrix metalloproteinases and specific glycosidases including heparanase and hyaluronidases contribute to matrix remodeling and affect human health. Several cell processes and functions, among them cell proliferation and survival, migration, differentiation, autophagy, angiogenesis, and immunity regulation are affected by certain matrix components. Structural alterations have been also well associated with disease progression. This guide on the composition and functions of the ECM gives a broad overview of the matrisome, the major ECM macromolecules, and their interaction networks within the ECM and with the cell surface, summarizes their main structural features and their roles in tissue organization and cell functions, and emphasizes the importance of specific ECM constituents in disease development and progression as well as the advances in molecular targeting of ECM to design new therapeutic strategies.

Identifiants

pubmed: 33605520
doi: 10.1111/febs.15776
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

6850-6912

Informations de copyright

© 2021 Federation of European Biochemical Societies.

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Auteurs

Nikos K Karamanos (NK)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.
Foundation for Research and Technology-Hellas (FORTH)/Institute of Chemical Engineering Sciences (ICE-HT), Patras, Greece.

Achilleas D Theocharis (AD)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.

Zoi Piperigkou (Z)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.
Foundation for Research and Technology-Hellas (FORTH)/Institute of Chemical Engineering Sciences (ICE-HT), Patras, Greece.

Dimitra Manou (D)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.

Alberto Passi (A)

Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Spyros S Skandalis (SS)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.

Demitrios H Vynios (DH)

Biochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, Greece.

Véronique Orian-Rousseau (V)

Karlsruhe Institute of Technology, Institute of Biological and Chemical Systems- Functional Molecular Systems, Eggenstein-Leopoldshafen, Germany.

Sylvie Ricard-Blum (S)

University of Lyon, UMR 5246, ICBMS, Université Lyon 1, CNRS, Villeurbanne Cedex, France.

Christian E H Schmelzer (CEH)

Fraunhofer Institute for Microstructure of Materials and Systems IMWS, Halle (Saale), Germany.
Institute of Pharmacy, Faculty of Natural Sciences I, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.

Laurent Duca (L)

UMR CNRS 7369 Matrice Extracellulaire et Dynamique Cellulaire (MEDyC), Team 2: Matrix Aging and Vascular Remodelling, Université de Reims Champagne Ardenne (URCA), UFR Sciences Exactes et Naturelles, Reims, France.

Madeleine Durbeej (M)

Department of Experimental Medical Science, Unit of Muscle Biology, Lund University, Sweden.

Nikolaos A Afratis (NA)

Department Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.

Linda Troeberg (L)

Norwich Medical School, University of East Anglia, Bob Champion Research and Education Building, Norwich, UK.

Marco Franchi (M)

Department for Life Quality Study, University of Bologna, Rimini, Italy.

Valentina Masola (V)

Department of Biomedical Sciences, University of Padova, Italy.

Maurizio Onisto (M)

Department of Biomedical Sciences, University of Padova, Italy.

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