A threshold of mechanical strain intensity for the direct activation of osteoblast function exists in a murine maxilla loading model
Language English Country Germany Media print-electronic
Document type Journal Article
PubMed
26578077
DOI
10.1007/s10237-015-0746-1
PII: 10.1007/s10237-015-0746-1
Knihovny.cz E-resources
- Keywords
- Bone formation, Inflammation, Mechanical strain intensity, Murine maxilla, Numerical analyses, Sclerostin,
- MeSH
- Adaptor Proteins, Signal Transducing MeSH
- Models, Biological * MeSH
- Glycoproteins metabolism MeSH
- Bone Density MeSH
- Maxilla cytology physiology MeSH
- Stress, Mechanical * MeSH
- Intercellular Signaling Peptides and Proteins MeSH
- Mice, Inbred C57BL MeSH
- Osteoblasts physiology MeSH
- Osteocytes cytology MeSH
- Osteogenesis MeSH
- Cell Count MeSH
- Weight-Bearing MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Adaptor Proteins, Signal Transducing MeSH
- Glycoproteins MeSH
- Intercellular Signaling Peptides and Proteins MeSH
- Sost protein, mouse MeSH Browser
The response to the mechanical loading of bone tissue has been extensively investigated; however, precisely how much strain intensity is necessary to promote bone formation remains unclear. Combination studies utilizing histomorphometric and numerical analyses were performed using the established murine maxilla loading model to clarify the threshold of mechanical strain needed to accelerate bone formation activity. For 7 days, 191 kPa loading stimulation for 30 min/day was applied to C57BL/6J mice. Two regions of interest, the AWAY region (away from the loading site) and the NEAR region (near the loading site), were determined. The inflammatory score increased in the NEAR region, but not in the AWAY region. A strain intensity map obtained from [Formula: see text] images was superimposed onto the images of the bone formation inhibitor, sclerostin-positive cell localization. The number of sclerostin-positive cells significantly decreased after mechanical loading of more than [Formula: see text] in the AWAY region, but not in the NEAR region. The mineral apposition rate, which shows the bone formation ability of osteoblasts, was accelerated at the site of surface strain intensity, namely around [Formula: see text], but not at the site of lower surface strain intensity, which was around [Formula: see text] in the AWAY region, thus suggesting the existence of a strain intensity threshold for promoting bone formation. Taken together, our data suggest that a threshold of mechanical strain intensity for the direct activation of osteoblast function and the reduction of sclerostin exists in a murine maxilla loading model in the non-inflammatory region.
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