A guide to the composition and functions of the extracellular matrix
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...
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| Published in | The FEBS journal Vol. 288; no. 24; pp. 6850 - 6912 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Blackwell Publishing Ltd
01.12.2021
Wiley |
| Subjects | |
| Online Access | Get full text |
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| Abstract | 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.
Extracellular matrices (ECMs) are well‐orchestrated 3D ultrastructures that supportively encompass cells. ECM macromolecules include collagens, proteoglycans/glycosaminoglycans, laminins, elastin, other proteins/glycoproteins, proteolytic, and glycolytic enzymes. Cell‐matrix interactions via cell surface receptors, such as integrins and CD44, mediate biochemical and biomechanical signals to adapt cellular functions. ECM remodeling is critical in health and disease. This guide condensates main ECM structural components and their ability to cross‐interact and regulate cellular behavior |
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| AbstractList | 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. 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. Extracellular matrices (ECMs) are well‐orchestrated 3D ultrastructures that supportively encompass cells. ECM macromolecules include collagens, proteoglycans/glycosaminoglycans, laminins, elastin, other proteins/glycoproteins, proteolytic, and glycolytic enzymes. Cell‐matrix interactions via cell surface receptors, such as integrins and CD44, mediate biochemical and biomechanical signals to adapt cellular functions. ECM remodeling is critical in health and disease. This guide condensates main ECM structural components and their ability to cross‐interact and regulate cellular behavior 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.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. |
| Author | Troeberg, Linda Masola, Valentina Karamanos, Nikos K. Orian‐Rousseau, Véronique Ricard‐Blum, Sylvie Duca, Laurent Passi, Alberto Schmelzer, Christian E.H. Onisto, Maurizio Skandalis, Spyros S. Durbeej, Madeleine Franchi, Marco Vynios, Demitrios H. Afratis, Nikolaos A. Piperigkou, Zoi Manou, Dimitra Theocharis, Achilleas D. |
| Author_xml | – sequence: 1 givenname: Nikos K. orcidid: 0000-0003-3618-0288 surname: Karamanos fullname: Karamanos, Nikos K. email: n.k.karamanos@upatras.gr organization: Foundation for Research and Technology‐Hellas (FORTH)/Institute of Chemical Engineering Sciences (ICE‐HT) – sequence: 2 givenname: Achilleas D. surname: Theocharis fullname: Theocharis, Achilleas D. email: atheoch@upatras.gr organization: University of Patras – sequence: 3 givenname: Zoi orcidid: 0000-0002-0472-5389 surname: Piperigkou fullname: Piperigkou, Zoi organization: Foundation for Research and Technology‐Hellas (FORTH)/Institute of Chemical Engineering Sciences (ICE‐HT) – sequence: 4 givenname: Dimitra surname: Manou fullname: Manou, Dimitra organization: University of Patras – sequence: 5 givenname: Alberto surname: Passi fullname: Passi, Alberto organization: University of Insubria – sequence: 6 givenname: Spyros S. surname: Skandalis fullname: Skandalis, Spyros S. organization: University of Patras – sequence: 7 givenname: Demitrios H. surname: Vynios fullname: Vynios, Demitrios H. organization: University of Patras – sequence: 8 givenname: Véronique surname: Orian‐Rousseau fullname: Orian‐Rousseau, Véronique organization: Institute of Biological and Chemical Systems‐ Functional Molecular Systems – sequence: 9 givenname: Sylvie surname: Ricard‐Blum fullname: Ricard‐Blum, Sylvie organization: CNRS – sequence: 10 givenname: Christian E.H. orcidid: 0000-0002-1180-0201 surname: Schmelzer fullname: Schmelzer, Christian E.H. organization: Martin Luther University Halle‐Wittenberg – sequence: 11 givenname: Laurent surname: Duca fullname: Duca, Laurent organization: UFR Sciences Exactes et Naturelles – sequence: 12 givenname: Madeleine surname: Durbeej fullname: Durbeej, Madeleine organization: Lund University – sequence: 13 givenname: Nikolaos A. surname: Afratis fullname: Afratis, Nikolaos A. organization: Weizmann Institute of Science – sequence: 14 givenname: Linda surname: Troeberg fullname: Troeberg, Linda organization: Bob Champion Research and Education Building – sequence: 15 givenname: Marco surname: Franchi fullname: Franchi, Marco organization: University of Bologna – sequence: 16 givenname: Valentina surname: Masola fullname: Masola, Valentina organization: University of Padova – sequence: 17 givenname: Maurizio surname: Onisto fullname: Onisto, Maurizio organization: University of Padova |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33605520$$D View this record in MEDLINE/PubMed https://hal.science/hal-04998836$$DView record in HAL https://lup.lub.lu.se/record/c7a99a4d-fc28-4311-8659-06883ff1498d$$DView record from Swedish Publication Index oai:portal.research.lu.se:publications/c7a99a4d-fc28-4311-8659-06883ff1498d$$DView record from Swedish Publication Index |
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| ISSN | 1742-464X 1742-4658 |
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| Issue | 24 |
| Keywords | glycosaminoglycans proteoglycans integrins collagens tenascins hyaluronan laminins heparanase hyaluronidases elastin matrix metalloproteinases extracellular matrix |
| Language | English |
| License | 2021 Federation of European Biochemical Societies. Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0 |
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| Notes | Correction added on 16 April 2021, after first online publication: author name ''Madeleine Durbeej'' has been corrected in this version ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
| ORCID | 0000-0002-1180-0201 0000-0003-3618-0288 0000-0002-0472-5389 |
| OpenAccessLink | https://lup.lub.lu.se/record/c7a99a4d-fc28-4311-8659-06883ff1498d |
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| PublicationDate | December 2021 |
| PublicationDateYYYYMMDD | 2021-12-01 |
| PublicationDate_xml | – month: 12 year: 2021 text: December 2021 |
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| PublicationPlace | England |
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| Publisher | Blackwell Publishing Ltd Wiley |
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34 2015; 23 2020; 197 1997; 242 2017; 98 2015; 22 2015; 21 2019; 378 2019; 139 2012; 279 2004; 117 e_1_2_17_190_1 e_1_2_17_212_1 e_1_2_17_258_1 e_1_2_17_488_1 e_1_2_17_235_1 e_1_2_17_15_1 e_1_2_17_38_1 e_1_2_17_563_1 e_1_2_17_310_1 e_1_2_17_333_1 e_1_2_17_586_1 e_1_2_17_103_1 e_1_2_17_126_1 e_1_2_17_356_1 e_1_2_17_379_1 e_1_2_17_551_1 e_1_2_17_608_1 e_1_2_17_149_1 e_1_2_17_91_1 e_1_2_17_431_1 e_1_2_17_477_1 e_1_2_17_454_1 e_1_2_17_200_1 e_1_2_17_223_1 e_1_2_17_246_1 e_1_2_17_269_1 Esko JD (e_1_2_17_171_1) 2009 e_1_2_17_430_1 e_1_2_17_26_1 e_1_2_17_552_1 e_1_2_17_575_1 Vlodavsky I (e_1_2_17_598_1) 1992; 12 Masola V (e_1_2_17_651_1) 2017; 32 e_1_2_17_321_1 e_1_2_17_115_1 e_1_2_17_344_1 e_1_2_17_367_1 e_1_2_17_540_1 e_1_2_17_138_1 e_1_2_17_442_1 e_1_2_17_465_1 e_1_2_17_213_1 e_1_2_17_236_1 e_1_2_17_489_1 e_1_2_17_650_1 e_1_2_17_259_1 e_1_2_17_16_1 e_1_2_17_541_1 e_1_2_17_564_1 e_1_2_17_587_1 e_1_2_17_39_1 e_1_2_17_334_1 e_1_2_17_311_1 e_1_2_17_125_1 e_1_2_17_148_1 e_1_2_17_102_1 e_1_2_17_357_1 e_1_2_17_609_1 e_1_2_17_92_1 e_1_2_17_432_1 e_1_2_17_455_1 e_1_2_17_478_1 e_1_2_17_201_1 e_1_2_17_247_1 e_1_2_17_224_1 e_1_2_17_27_1 e_1_2_17_530_1 Matsuda K (e_1_2_17_155_1) 2001; 61 e_1_2_17_553_1 e_1_2_17_599_1 e_1_2_17_322_1 e_1_2_17_576_1 e_1_2_17_114_1 e_1_2_17_137_1 e_1_2_17_345_1 e_1_2_17_368_1 e_1_2_17_80_1 e_1_2_17_420_1 e_1_2_17_466_1 e_1_2_17_443_1 e_1_2_17_440_1 e_1_2_17_463_1 e_1_2_17_486_1 e_1_2_17_233_1 e_1_2_17_279_1 e_1_2_17_508_1 e_1_2_17_93_1 e_1_2_17_256_1 e_1_2_17_17_1 e_1_2_17_354_1 e_1_2_17_377_1 e_1_2_17_147_1 e_1_2_17_595_1 e_1_2_17_101_1 e_1_2_17_606_1 e_1_2_17_629_1 e_1_2_17_124_1 e_1_2_17_572_1 e_1_2_17_70_1 e_1_2_17_221_1 e_1_2_17_475_1 e_1_2_17_451_1 e_1_2_17_474_1 e_1_2_17_244_1 e_1_2_17_498_1 e_1_2_17_267_1 e_1_2_17_28_1 e_1_2_17_596_1 e_1_2_17_353_1 e_1_2_17_365_1 e_1_2_17_388_1 e_1_2_17_136_1 e_1_2_17_330_1 e_1_2_17_584_1 e_1_2_17_618_1 Tucker RP (e_1_2_17_51_1) 2019; 7 e_1_2_17_113_1 e_1_2_17_561_1 Murdamoothoo D (e_1_2_17_49_1) 2018 e_1_2_17_159_1 e_1_2_17_81_1 e_1_2_17_232_1 e_1_2_17_211_1 e_1_2_17_234_1 e_1_2_17_257_1 e_1_2_17_441_1 e_1_2_17_487_1 e_1_2_17_71_1 e_1_2_17_94_1 e_1_2_17_509_1 Naba A (e_1_2_17_100_1) 2012; 11 e_1_2_17_18_1 e_1_2_17_111_1 e_1_2_17_585_1 e_1_2_17_332_1 e_1_2_17_320_1 e_1_2_17_355_1 e_1_2_17_123_1 e_1_2_17_146_1 e_1_2_17_550_1 e_1_2_17_573_1 e_1_2_17_378_1 e_1_2_17_169_1 e_1_2_17_453_1 e_1_2_17_476_1 e_1_2_17_245_1 e_1_2_17_268_1 e_1_2_17_222_1 e_1_2_17_452_1 e_1_2_17_499_1 e_1_2_17_82_1 e_1_2_17_29_1 e_1_2_17_574_1 Radhakrishnan AV (e_1_2_17_116_1) 2021; 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| Snippet | Extracellular matrix (ECM) is a dynamic 3‐dimensional network of macromolecules that provides structural support for the cells and tissues. Accumulated... Extracellular matrix (ECM) is a dynamic 3-dimensional network of macromolecules that provides structural support for the cells and tissues. Accumulated... |
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| SubjectTerms | Angiogenesis Animals Autophagy Basic Medicine Bioaccumulation CD44 antigen Cell adhesion Cell and Molecular Biology Cell differentiation Cell migration Cell proliferation Cell signaling Cell surface Cell survival Cell- och molekylärbiologi Collagen collagens Composition Cytology disease progression Elastin Extracellular matrix Extracellular Matrix - chemistry Extracellular Matrix - metabolism Glycoproteins Glycosaminoglycans Glycosidases heparanase human health Humans hyaluronan Hyaluronic acid hyaluronidases immunity Integrins laminin laminins Life Sciences Macromolecules Matrix metalloproteinase Matrix metalloproteinases Medical and Health Sciences Medicin och hälsovetenskap Medicinska och farmaceutiska grundvetenskaper metalloproteinases organogenesis Phagocytosis Proteoglycans tenascins therapeutics |
| Title | A guide to the composition and functions of the extracellular matrix |
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