Pressure simulation of orthodontic force in osteoblasts: a pilot study

Structured Authors – Baumert U, Golan I, Becker B, Hrala BP, Redlich M, Roos HA, Reichenberg E, Palmon A, Müßig D Objectives – To elucidate the RUNX2 gene expression induction in human osteoblasts after mechanical loading. Design – Using a stringent pulse‐chase protocol human osteoblasts were expose...

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Veröffentlicht in:Clinical orthodontics and research 2004-02, Vol.7 (1), p.3-9
Hauptverfasser: Baumert, U., Golan, I., Becker, B., Hrala, B.P., Redlich, M., Roos, H.A., Palmon, A., Reichenberg, E., Müßig, D.
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Sprache:eng
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Zusammenfassung:Structured Authors – Baumert U, Golan I, Becker B, Hrala BP, Redlich M, Roos HA, Reichenberg E, Palmon A, Müßig D Objectives – To elucidate the RUNX2 gene expression induction in human osteoblasts after mechanical loading. Design – Using a stringent pulse‐chase protocol human osteoblasts were exposed to centrifugal pressure force for 30 and 90 min. Untreated control cells were processed in parallel. Before, and at defined times after centrifugation, total RNA was isolated. RUNX2 gene expression was measured using real‐time quantitative reverse transcriptase polymerase chain reaction. The stress/control ratio was used to illustrate possible stimulatory or diminishing effects of force application. Results – Immediately after 30 min of force application the RUNX2 gene expression was induced by a factor of 1.7 ± 0.14 as compared with the negative control. This induction decreased rapidly and reached its pre‐load levels within 30 min. Longer force applications (up to 90 min) did not change the RUNX2 gene expression. Conclusion – In mature osteoblasts centrifugal pressure force stimulates RUNX2 gene expression within a narrow time frame: loading of mature cells results in a temporary increase of RUNX2 expression and a fast downregulation back to its pre‐load expression level. With this pilot study the gene expression behavior after mechanical stimuli could be determined with a simple laboratory setup.
ISSN:1601-6335
1397-5927
1601-6343
DOI:10.1046/j.1601-6335.2003.00270.x