Literature DB >> 23707199

Skeletal diseases caused by mutations that affect collagen structure and function.

William V Arnold1, Andrzej Fertala.   

Abstract

Collagens form critical elements of extracellular matrices that provide mechanical strength to skeletal tissues and serve as a binding platform for cells of bone and cartilage. The formation of collagen-rich extracellular matrices is a complex process that involves intracellular and extracellular steps. Mutations in genes that encode individual chains of triple-helical collagens present in bone and cartilage are associated with heritable diseases of skeletal tissues. In addition, mutations in genes encoding proteins involved in the intracellular and extracellular modifications of collagens are also responsible for developing skeletal abnormalities. In this review, we will summarize the pathomechanisms of molecular and cellular consequences of mutations that alter collagen structure and function. Moreover, we will discuss the prospects and limitations of therapeutic approaches to minimize the effects of mutations that affect collagens of skeletal tissues.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Bone; Cartilage; Collagen; ER stress; Heritable diseases

Mesh:

Substances:

Year:  2013        PMID: 23707199     DOI: 10.1016/j.biocel.2013.05.017

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  19 in total

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Review 4.  Trafficking mechanisms of extracellular matrix macromolecules: insights from vertebrate development and human diseases.

Authors:  Gokhan Unlu; Daniel S Levic; David B Melville; Ela W Knapik
Journal:  Int J Biochem Cell Biol       Date:  2013-12-09       Impact factor: 5.085

5.  Target-Specific Delivery of an Antibody That Blocks the Formation of Collagen Deposits in Skin and Lung.

Authors:  Jolanta Fertala; Freddy Romero; Ross Summer; Andrzej Fertala
Journal:  Monoclon Antib Immunodiagn Immunother       Date:  2017-10-03

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Authors:  Cheng Wang; Zhijia Tan; Ben Niu; Kwok Yeung Tsang; Andrew Tai; Wilson C W Chan; Rebecca L K Lo; Keith K H Leung; Nelson W F Dung; Nobuyuki Itoh; Michael Q Zhang; Danny Chan; Kathryn Song Eng Cheah
Journal:  Elife       Date:  2018-07-19       Impact factor: 8.140

7.  Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasia.

Authors:  E B Cadoff; R Sheffer; S Wientroub; D Ovadia; V Meiner; J E Schwarzbauer
Journal:  Clin Genet       Date:  2018-09-03       Impact factor: 4.438

Review 8.  Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.

Authors:  David N Cooper; Michael Krawczak; Constantin Polychronakos; Chris Tyler-Smith; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2013-07-03       Impact factor: 4.132

9.  Morphological and Biochemical Effects on the Skeletal Muscle of Ovariectomized Old Female Rats Submitted to the Intake of Diets with Vegetable or Animal Protein and Resistance Training.

Authors:  Glaucia Figueiredo Braggion; Elisabete Ornelas; Jurema Carmona Sattin Cury; Natália Edviges Alves Lima; Rita C Aquino; Fernando Luiz Affonso Fonseca; Laura Beatriz Mesiano Maifrino
Journal:  Oxid Med Cell Longev       Date:  2016-01-14       Impact factor: 6.543

10.  New therapeutic targets in rare genetic skeletal diseases.

Authors:  Michael D Briggs; Peter A Bell; Michael J Wright; Katarzyna A Pirog
Journal:  Expert Opin Orphan Drugs       Date:  2015-09-24       Impact factor: 0.694

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