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Aggrecan, aging and assembly in articular cartilage.
Dudhia, J.
Afiliación
  • Dudhia J; Department of Veterinary Clinical Sciences, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Herts, AL9 7TA, United Kingdom. jdudhia@rvc.ac.uk
Cell Mol Life Sci ; 62(19-20): 2241-56, 2005 Oct.
Article en En | MEDLINE | ID: mdl-16143826
The primary function of articular cartilage to act as a self-renewing, low frictional material that can distribute load efficiently at joints is critically dependent upon the composition and organisation of the extracellular matrix. Aggrecan is a major component of the extracellular matrix, forming high molecular weight aggregates necessary for the hydration of cartilage and to meet its weight-bearing mechanical demands. Aggregate assembly is a highly ordered process requiring the formation of a ternary complex between aggrecan, link protein and hyaluronan. There is extensive age-associated heterogeneity in the structure and molecular stoichiometry of these components in adult human articular cartilage, resulting in diverse populations of complexes with a range of stabilities that have implications for cartilage mechanobiology and integrity. Recent findings have demonstrated that aggrecan can form ligands with other matrix proteins. These findings provide new insights into mechanisms for aggregate assembly and functional protein networks in different cartilage compartments with maturation and aging.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Envejecimiento / Cartílago Articular / Proteínas de la Matriz Extracelular / Lectinas Tipo C Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cell Mol Life Sci Asunto de la revista: BIOLOGIA MOLECULAR Año: 2005 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Suiza
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Envejecimiento / Cartílago Articular / Proteínas de la Matriz Extracelular / Lectinas Tipo C Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cell Mol Life Sci Asunto de la revista: BIOLOGIA MOLECULAR Año: 2005 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Suiza