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Fibrillins in Tendon

Tendons among connective tissue, mainly collagen, contain also elastic fibers (EF) made of fibrillin 1, fibrillin 2 and elastin that are broadly distributed in tendons and represent 1–2% of the dried mass of the tendon. Only in the last years, studies on structure and function of EF in tendons have...

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Detalles Bibliográficos
Autores principales: Giusti, Betti, Pepe, Guglielmina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071311/
https://www.ncbi.nlm.nih.gov/pubmed/27812333
http://dx.doi.org/10.3389/fnagi.2016.00237
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author Giusti, Betti
Pepe, Guglielmina
author_facet Giusti, Betti
Pepe, Guglielmina
author_sort Giusti, Betti
collection PubMed
description Tendons among connective tissue, mainly collagen, contain also elastic fibers (EF) made of fibrillin 1, fibrillin 2 and elastin that are broadly distributed in tendons and represent 1–2% of the dried mass of the tendon. Only in the last years, studies on structure and function of EF in tendons have been performed. Aim of this review is to revise data on the organization of EF in tendons, in particular fibrillin structure and function, and on the clinical manifestations associated to alterations of EF in tendons. Indeed, microfibrils may contribute to tendon mechanics; therefore, their alterations may cause joint hypermobility and contractures which have been found to be clinical features in patients with Marfan syndrome (MFS) and Beals syndrome. The two diseases are caused by mutations in genes FBN1 and FBN2 encoding fibrillin 1 and fibrillin 2, respectively.
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spelling pubmed-50713112016-11-03 Fibrillins in Tendon Giusti, Betti Pepe, Guglielmina Front Aging Neurosci Neuroscience Tendons among connective tissue, mainly collagen, contain also elastic fibers (EF) made of fibrillin 1, fibrillin 2 and elastin that are broadly distributed in tendons and represent 1–2% of the dried mass of the tendon. Only in the last years, studies on structure and function of EF in tendons have been performed. Aim of this review is to revise data on the organization of EF in tendons, in particular fibrillin structure and function, and on the clinical manifestations associated to alterations of EF in tendons. Indeed, microfibrils may contribute to tendon mechanics; therefore, their alterations may cause joint hypermobility and contractures which have been found to be clinical features in patients with Marfan syndrome (MFS) and Beals syndrome. The two diseases are caused by mutations in genes FBN1 and FBN2 encoding fibrillin 1 and fibrillin 2, respectively. Frontiers Media S.A. 2016-10-20 /pmc/articles/PMC5071311/ /pubmed/27812333 http://dx.doi.org/10.3389/fnagi.2016.00237 Text en Copyright © 2016 Giusti and Pepe. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Giusti, Betti
Pepe, Guglielmina
Fibrillins in Tendon
title Fibrillins in Tendon
title_full Fibrillins in Tendon
title_fullStr Fibrillins in Tendon
title_full_unstemmed Fibrillins in Tendon
title_short Fibrillins in Tendon
title_sort fibrillins in tendon
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071311/
https://www.ncbi.nlm.nih.gov/pubmed/27812333
http://dx.doi.org/10.3389/fnagi.2016.00237
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