Literature DB >> 19204719

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations.

John F Bateman1, Raymond P Boot-Handford, Shireen R Lamandé.   

Abstract

Tissue-specific extracellular matrices (ECMs) are crucial for normal development and tissue function, and mutations in ECM genes result in a wide range of serious inherited connective tissue disorders. Mutations cause ECM dysfunction by combinations of two mechanisms. First, secretion of the mutated ECM components can be reduced by mutations affecting synthesis or by structural mutations causing cellular retention and/or degradation. Second, secretion of mutant protein can disturb crucial ECM interactions, structure and stability. Moreover, recent experiments suggest that endoplasmic reticulum (ER) stress, caused by mutant misfolded ECM proteins, contributes to the molecular pathology. Targeting ER stress might offer a new therapeutic strategy.

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Year:  2009        PMID: 19204719     DOI: 10.1038/nrg2520

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  108 in total

Review 1.  Chemical chaperones: a pharmacological strategy for disorders of protein folding and trafficking.

Authors:  David H Perlmutter
Journal:  Pediatr Res       Date:  2002-12       Impact factor: 3.756

Review 2.  Endoplasmic reticulum stress in health and disease.

Authors:  Lihong Zhao; Susan L Ackerman
Journal:  Curr Opin Cell Biol       Date:  2006-06-16       Impact factor: 8.382

Review 3.  The endoplasmic reticulum and the unfolded protein response.

Authors:  Jyoti D Malhotra; Randal J Kaufman
Journal:  Semin Cell Dev Biol       Date:  2007-09-08       Impact factor: 7.727

Review 4.  Potential of mesenchymal stem cell therapy.

Authors:  Francesco Dazzi; Nicole J Horwood
Journal:  Curr Opin Oncol       Date:  2007-11       Impact factor: 3.645

5.  Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytes.

Authors:  J T Hecht; E Hayes; M Snuggs; G Decker; D Montufar-Solis; K Doege; F Mwalle; R Poole; J Stevens; P J Duke
Journal:  Matrix Biol       Date:  2001-07       Impact factor: 11.583

Review 6.  Pseudoachondroplasia and multiple epiphyseal dysplasia: mutation review, molecular interactions, and genotype to phenotype correlations.

Authors:  Michael D Briggs; Kathryn L Chapman
Journal:  Hum Mutat       Date:  2002-05       Impact factor: 4.878

7.  Angiotensin II blockade and aortic-root dilation in Marfan's syndrome.

Authors:  Benjamin S Brooke; Jennifer P Habashi; Daniel P Judge; Nishant Patel; Bart Loeys; Harry C Dietz
Journal:  N Engl J Med       Date:  2008-06-26       Impact factor: 91.245

8.  Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies.

Authors:  Luciano Merlini; Alessia Angelin; Tania Tiepolo; Paola Braghetta; Patrizia Sabatelli; Alessandra Zamparelli; Alessandra Ferlini; Nadir M Maraldi; Paolo Bonaldo; Paolo Bernardi
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-24       Impact factor: 11.205

9.  Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutation.

Authors:  Matthew P Leighton; Seema Nundlall; Tobias Starborg; Roger S Meadows; Farhana Suleman; Lynette Knowles; Raimund Wagener; David J Thornton; Karl E Kadler; Raymond P Boot-Handford; Michael D Briggs
Journal:  Hum Mol Genet       Date:  2007-05-21       Impact factor: 6.150

10.  ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.

Authors:  Thomas S Lisse; Frank Thiele; Helmut Fuchs; Wolfgang Hans; Gerhard K H Przemeck; Koichiro Abe; Birgit Rathkolb; Leticia Quintanilla-Martinez; Gabriele Hoelzlwimmer; Miep Helfrich; Eckhard Wolf; Stuart H Ralston; Martin Hrabé de Angelis
Journal:  PLoS Genet       Date:  2008-02       Impact factor: 5.917

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  132 in total

Review 1.  Overview of the matrisome--an inventory of extracellular matrix constituents and functions.

Authors:  Richard O Hynes; Alexandra Naba
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-01-01       Impact factor: 10.005

Review 2.  Chaperoning osteogenesis: new protein-folding disease paradigms.

Authors:  Elena Makareeva; Nydea A Aviles; Sergey Leikin
Journal:  Trends Cell Biol       Date:  2010-12-21       Impact factor: 20.808

Review 3.  Proteostasis strategies for restoring alpha1-antitrypsin deficiency.

Authors:  Marion Bouchecareilh; Juliana J Conkright; William E Balch
Journal:  Proc Am Thorac Soc       Date:  2010-11

4.  Pulse-chase analysis of procollagen biosynthesis by azidohomoalanine labeling.

Authors:  Lynn S Mirigian; Elena Makareeva; Sergey Leikin
Journal:  Connect Tissue Res       Date:  2014-09-22       Impact factor: 3.417

5.  Decorin antagonizes Met receptor activity and down-regulates {beta}-catenin and Myc levels.

Authors:  Simone Buraschi; Nutan Pal; Nadia Tyler-Rubinstein; Rick T Owens; Thomas Neill; Renato V Iozzo
Journal:  J Biol Chem       Date:  2010-10-25       Impact factor: 5.157

Review 6.  Biomechanical relationships between the corneal endothelium and Descemet's membrane.

Authors:  Maryam Ali; VijayKrishna Raghunathan; Jennifer Y Li; Christopher J Murphy; Sara M Thomasy
Journal:  Exp Eye Res       Date:  2016-09-14       Impact factor: 3.467

7.  Heat shock protein 47 and 65-kDa FK506-binding protein weakly but synergistically interact during collagen folding in the endoplasmic reticulum.

Authors:  Yoshihiro Ishikawa; Paul Holden; Hans Peter Bächinger
Journal:  J Biol Chem       Date:  2017-08-31       Impact factor: 5.157

8.  An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1·cartilage-associated protein·cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.

Authors:  Yoshihiro Ishikawa; Hans Peter Bächinger
Journal:  J Biol Chem       Date:  2013-09-16       Impact factor: 5.157

Review 9.  Osteogenesis imperfecta and therapeutics.

Authors:  Roy Morello
Journal:  Matrix Biol       Date:  2018-03-11       Impact factor: 11.583

10.  Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.

Authors:  Ofer Sarig; Sagi Nahum; Debora Rapaport; Akemi Ishida-Yamamoto; Dana Fuchs-Telem; Li Qiaoli; Ksenya Cohen-Katsenelson; Ronen Spiegel; Janna Nousbeck; Shirli Israeli; Zvi-Uri Borochowitz; Gilly Padalon-Brauch; Jouni Uitto; Mia Horowitz; Stavit Shalev; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2012-07-26       Impact factor: 11.025

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