Literature DB >> 26295200

Effect of Laminin-A4 inhibition on cluster formation of human osteoarthritic chondrocytes.

Florentine C Moazedi-Fuerst1, Gerald Gruber2, Martin H Stradner1, Diego Guidolin3, Jonathan C Jones4, Koppany Bodo5, Karin Wagner6, Daniela Peischler1, Verena Krischan1, Jennifer Weber1, Patrick Sadoghi2, Mathias Glehr2, Andreas Leithner2, Winfried B Graninger1.   

Abstract

Formation of chondrocyte clusters is not only a morphological sign of osteoarthritis but it is also observed in cell culture. Active locomotion of chondrocytes is controlled by integrins in vitro. Integrins bind to Laminin-A4 (LAMA4), a protein that is highly expressed in vivo in clusters of hypertrophic chondrocytes. We tested if LAMA4 is relevant for cluster formation. Human chondrocytes were cultured in a 2D matrigel model and treated with different concentrations of a monoclonal inhibitory anti-LAMA4-antibody. Migration and cluster formation was analysed using live cell imaging technique. Full genome gene expression analysis was performed to assess the effect of LAMA4 inhibition. The data set were screened for genes relevant to cell motility. F-actin staining was performed to document cytoskeletal changes. Anti-LAMA4 treatment significantly reduced the rate of cluster formation in human chondrocytes. Cells changed their surface morphology and exhibited fewer protrusions. Expression of genes associated with cellular motility and migration was affected by anti-LAMA4 treatment. LAMA4-integrin signalling affects chondrocyte morphology and gene expression in vitro, thereby contributing to cluster formation in human osteoarthritic chondrocytes.
© 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.

Entities:  

Keywords:  LAMA4; chondrocytes; cluster; migration; osteoarthritis

Mesh:

Substances:

Year:  2015        PMID: 26295200      PMCID: PMC5727909          DOI: 10.1002/jor.23036

Source DB:  PubMed          Journal:  J Orthop Res        ISSN: 0736-0266            Impact factor:   3.494


  48 in total

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3.  The Role of Extracellular Matrix Expression, ERK1/2 Signaling and Cell Cohesiveness for Cartilage Yield from iPSCs.

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4.  A Meta-Analysis of Non-Osteoarthritis and Osteoarthritis Chondrocyte Gene Expression to Determine the Efficacy of Autologous Chondrocyte Transplantation as a Viable Treatment Option.

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