Methionine restriction alters bone morphology and affects osteoblast differentiation

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 an...

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Main Authors: Amadou Ouattara, Diana Cooke, Raj Gopalakrishnan, Tsang-hai Huang, Gene P. Ables
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Bone Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2352187216300067
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author Amadou Ouattara
Diana Cooke
Raj Gopalakrishnan
Tsang-hai Huang
Gene P. Ables
author_facet Amadou Ouattara
Diana Cooke
Raj Gopalakrishnan
Tsang-hai Huang
Gene P. Ables
author_sort Amadou Ouattara
collection DOAJ
description 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. Keywords: Methionine restriction, Aged mice, Micro-computed tomography, Nanoindentation, MC3T3-E1 subclone 4
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spelling doaj.art-371f980d0ab84c05a8794f5f7951421e2022-12-22T02:30:59ZengElsevierBone Reports2352-18722016-12-0153342Methionine restriction alters bone morphology and affects osteoblast differentiationAmadou Ouattara0Diana Cooke1Raj Gopalakrishnan2Tsang-hai Huang3Gene P. Ables4Orentreich Foundation for the Advancement of Science, Inc, 855 Route 301, Cold Spring, NY 10516, USAOrentreich Foundation for the Advancement of Science, Inc, 855 Route 301, Cold Spring, NY 10516, USASchool of Dentistry, University of Minnesota, Minneapolis, MN 55455, USAInstitute of Physical Education, Health and Leisure Studies, National Cheng Kung University, Tainan City, TaiwanOrentreich Foundation for the Advancement of Science, Inc, 855 Route 301, Cold Spring, NY 10516, USA; Corresponding author at: Orentreich Foundation for the Advancement of Science, Inc., 855 Route 301, Cold Spring, NY 10516, USA.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. Keywords: Methionine restriction, Aged mice, Micro-computed tomography, Nanoindentation, MC3T3-E1 subclone 4http://www.sciencedirect.com/science/article/pii/S2352187216300067
spellingShingle Amadou Ouattara
Diana Cooke
Raj Gopalakrishnan
Tsang-hai Huang
Gene P. Ables
Methionine restriction alters bone morphology and affects osteoblast differentiation
Bone Reports
title Methionine restriction alters bone morphology and affects osteoblast differentiation
title_full Methionine restriction alters bone morphology and affects osteoblast differentiation
title_fullStr Methionine restriction alters bone morphology and affects osteoblast differentiation
title_full_unstemmed Methionine restriction alters bone morphology and affects osteoblast differentiation
title_short Methionine restriction alters bone morphology and affects osteoblast differentiation
title_sort methionine restriction alters bone morphology and affects osteoblast differentiation
url http://www.sciencedirect.com/science/article/pii/S2352187216300067
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