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Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
Published on: December 3, 2016
Methionine restriction alters bone morphology and affects osteoblast differentiation
Amadou Ouattara1, Diana Cooke1, Raj Gopalakrishnan2
1Orentreich Foundation for the Advancement of Science, Inc, 855 Route 301, Cold Spring, NY 10516, USA.
Abstract:
Methionine restriction (MR) extends the lifespan of a wide variety of species, including rodents, drosophila, nematodes, and yeasts. MR has also been demonstrated to affect the overall growth of mice and rats. The objective of this study was to evaluate the effect of MR on bone structure in young and aged male and female C57BL/6J mice. This study indicated that MR affected the growth rates of males and young females, but not aged females. MR reduced volumetric bone mass density (vBMD) and bone mineral content (BMC), while bone microarchitecture parameters were decreased in males and young females, but not in aged females compared to control-fed (CF) mice. However, when adjusted for bodyweight, the effect of MR in reducing vBMD, BMC and microarchitecture measurements was either attenuated or reversed suggesting that the smaller bones in MR mice is appropriate for its body size. In addition, CF and MR mice had similar intrinsic strength properties as measured by nanoindentation. Plasma biomarkers suggested that the low bone mass in MR mice could be due to increased collagen degradation, which may be influenced by leptin, IGF-1, adiponectin and FGF21 hormone levels. Mouse preosteoblast cell line cultured under low sulfur amino acid growth media attenuated gene expression levels of Col1al, Runx2, Bglap, Alpl and Spp1 suggesting delayed collagen formation and bone differentiation. Collectively, our studies revealed that MR altered bone morphology which could be mediated by delays in osteoblast differentiation.
Insights
Methionine restriction (MR) impacts bone structure, reducing bone mass and altering microarchitecture in young mice. However, these effects appear appropriate for reduced body size and do not compromise bone strength.
Area of Science:
- Gerontology
- Nutritional Science
- Skeletal Biology
Background:
- Methionine restriction (MR) is known to extend lifespan across various species.
- MR has been shown to influence overall growth in rodents.
Purpose of the Study:
- To investigate the effects of MR on bone structure in young and aged male and female C57BL/6J mice.
- To determine if observed changes in bone parameters are due to MR itself or secondary to body weight reduction.
Main Methods:
- Comparison of bone structure (vBMD, BMC, microarchitecture) between MR and control-fed (CF) mice of different ages and sexes.
- Nanoindentation for intrinsic strength assessment.
- Analysis of plasma biomarkers (leptin, IGF-1, adiponectin, FGF21) and gene expression in preosteoblast cells.
Main Results:
- MR affected growth rates in males and young females, but not aged females.
- MR reduced bone mass and microarchitecture in males and young females, but these changes were attenuated or reversed when adjusted for body weight.
- Intrinsic bone strength was similar between MR and CF groups.
- Plasma biomarkers suggested increased collagen degradation, potentially influenced by hormonal changes.
- In vitro studies showed attenuated gene expression related to collagen formation and osteoblast differentiation under MR conditions.
Conclusions:
- MR alters bone morphology, potentially through delayed osteoblast differentiation.
- The observed reduction in bone mass and microarchitecture in MR mice is largely appropriate for their reduced body size.
- MR does not appear to compromise intrinsic bone strength despite changes in bone morphology.
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