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Extracellular matrix composition of connective tissues: a systematic review and meta-analysis

The function of connective tissues depends on the physical and biochemical properties of their extracellular matrix (ECM), which are in turn dictated by ECM protein composition. With the primary objective of obtaining quantitative estimates for absolute and relative amounts of ECM proteins, we perfo...

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Autores principales: McKee, Turney J., Perlman, George, Morris, Martin, Komarova, Svetlana V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646303/
https://www.ncbi.nlm.nih.gov/pubmed/31332239
http://dx.doi.org/10.1038/s41598-019-46896-0
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author McKee, Turney J.
Perlman, George
Morris, Martin
Komarova, Svetlana V.
author_facet McKee, Turney J.
Perlman, George
Morris, Martin
Komarova, Svetlana V.
author_sort McKee, Turney J.
collection PubMed
description The function of connective tissues depends on the physical and biochemical properties of their extracellular matrix (ECM), which are in turn dictated by ECM protein composition. With the primary objective of obtaining quantitative estimates for absolute and relative amounts of ECM proteins, we performed a systematic review of papers reporting protein composition of human connective tissues. Articles were included in meta-analysis if they contained absolute or relative quantification of proteins found in the ECM of human bone, adipose tissue, tendon, ligament, cartilage and skeletal muscle. We generated absolute quantitative estimates for collagen in articular cartilage, intervertebral disk (IVD), skeletal muscle, tendon, and adipose tissue. In addition, sulfated glycosaminoglycans were quantified in articular cartilage, tendon and skeletal muscle; total proteoglycans in IVD and articular cartilage, fibronectin in tendon, ligament and articular cartilage, and elastin in tendon and IVD cartilage. We identified significant increases in collagen content in the annulus fibrosus of degenerating IVD and osteoarthritic articular cartilage, and in elastin content in degenerating disc. In contrast, collagen content was decreased in the scoliotic IVD. Finally, we built quantitative whole-tissue component breakdowns. Quantitative estimates improve our understanding of composition of human connective tissues, providing insights into their function in physiology and pathology.
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spelling pubmed-66463032019-07-29 Extracellular matrix composition of connective tissues: a systematic review and meta-analysis McKee, Turney J. Perlman, George Morris, Martin Komarova, Svetlana V. Sci Rep Article The function of connective tissues depends on the physical and biochemical properties of their extracellular matrix (ECM), which are in turn dictated by ECM protein composition. With the primary objective of obtaining quantitative estimates for absolute and relative amounts of ECM proteins, we performed a systematic review of papers reporting protein composition of human connective tissues. Articles were included in meta-analysis if they contained absolute or relative quantification of proteins found in the ECM of human bone, adipose tissue, tendon, ligament, cartilage and skeletal muscle. We generated absolute quantitative estimates for collagen in articular cartilage, intervertebral disk (IVD), skeletal muscle, tendon, and adipose tissue. In addition, sulfated glycosaminoglycans were quantified in articular cartilage, tendon and skeletal muscle; total proteoglycans in IVD and articular cartilage, fibronectin in tendon, ligament and articular cartilage, and elastin in tendon and IVD cartilage. We identified significant increases in collagen content in the annulus fibrosus of degenerating IVD and osteoarthritic articular cartilage, and in elastin content in degenerating disc. In contrast, collagen content was decreased in the scoliotic IVD. Finally, we built quantitative whole-tissue component breakdowns. Quantitative estimates improve our understanding of composition of human connective tissues, providing insights into their function in physiology and pathology. Nature Publishing Group UK 2019-07-22 /pmc/articles/PMC6646303/ /pubmed/31332239 http://dx.doi.org/10.1038/s41598-019-46896-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
McKee, Turney J.
Perlman, George
Morris, Martin
Komarova, Svetlana V.
Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title_full Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title_fullStr Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title_full_unstemmed Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title_short Extracellular matrix composition of connective tissues: a systematic review and meta-analysis
title_sort extracellular matrix composition of connective tissues: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646303/
https://www.ncbi.nlm.nih.gov/pubmed/31332239
http://dx.doi.org/10.1038/s41598-019-46896-0
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