Topographic changes of focal adhesion components and modulation of p125FAK activation in stretched human periodontal ligament fibroblasts
| Autor: | T. Molina, Annette Kohl, Pascal Tomakidi, Kirsten Kabsch, Angel Alonso, Gerda Komposch |
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| Rok vydání: | 2002 |
| Předmět: |
0301 basic medicine
Dental Stress Analysis Periodontal Ligament Integrin Immunoblotting Focal adhesion 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Periodontal fiber Humans Phosphorylation Fluorescent Antibody Technique Indirect Phosphotyrosine General Dentistry Paxillin Cells Cultured Focal Adhesions biology Chemistry Integrin beta1 Tyrosine phosphorylation 030206 dentistry Fibroblasts Protein-Tyrosine Kinases Phosphoproteins Enzyme Activation Cytoskeletal Proteins 030104 developmental biology Biochemistry Cytoplasm Focal Adhesion Kinase 1 Focal Adhesion Protein-Tyrosine Kinases biology.protein Biophysics Stress Mechanical Signal transduction Signal Transduction |
| Zdroj: | Journal of dental research. 80(11) |
| ISSN: | 0022-0345 |
| Popis: | Mechanical stress has been shown in vitro to modulate integrin-β1-mediated activation of p125FAK/FAK. To test the hypothesis whether this also applies to periodontal ligament fibroblasts (PDLs), we subjected human PDLs to mechanical stretch and analyzed stress-induced changes of p125FAKactivation by quantitative immunoprecipitation of p125FAKand changes in the topography of molecules localizing in focal adhesions by indirect immunofluorescence. Generally, all components of focal contacts under study-including detection of phosphotyrosine, i.e., integrin-β1, p125FAK, and paxillin-revealed a relative co-localization during stretch application. Under stretch, we observed a re-distribution of all components from the cell periphery to the cytoplasm following the main axes. Tyrosine phosphorylation of p125FAKwas monitored up to 72 hours under stretch. While the amount of p125FAKremained essentially constant, the activation of p125FAKwas clearly modulated. Tyrosine phosphorylation of p125FAKincreased from 15 minutes up to 1 hour and declined after stretching periods of 24, 48, and 72 hours. The analysis of our data indicated a stretch-induced re-distribution of focal adhesion components and a modulation of p125FAKactivation, suggesting alterations in focal adhesions and their associated signal cascade. |
| Databáze: | OpenAIRE |
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