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Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals

Externally visible body and longitudinal bone growth is a result of proliferation of chondrocytes. In growth disorder, there is delay in the age associated increase in height. The present study evaluates the effect of extract from transgenic tomato fruit expressing AtMYB12 transcription factor on bo...

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Autores principales: Choudhary, Dharmendra, Pandey, Ashutosh, Adhikary, Sulekha, Ahmad, Naseer, Bhatia, Chitra, Bhambhani, Sweta, Trivedi, Prabodh Kumar, Trivedi, Ritu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768317/
https://www.ncbi.nlm.nih.gov/pubmed/26917158
http://dx.doi.org/10.1038/srep21668
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author Choudhary, Dharmendra
Pandey, Ashutosh
Adhikary, Sulekha
Ahmad, Naseer
Bhatia, Chitra
Bhambhani, Sweta
Trivedi, Prabodh Kumar
Trivedi, Ritu
author_facet Choudhary, Dharmendra
Pandey, Ashutosh
Adhikary, Sulekha
Ahmad, Naseer
Bhatia, Chitra
Bhambhani, Sweta
Trivedi, Prabodh Kumar
Trivedi, Ritu
author_sort Choudhary, Dharmendra
collection PubMed
description Externally visible body and longitudinal bone growth is a result of proliferation of chondrocytes. In growth disorder, there is delay in the age associated increase in height. The present study evaluates the effect of extract from transgenic tomato fruit expressing AtMYB12 transcription factor on bone health including longitudinal growth. Constitutive expression of AtMYB12 in tomato led to a significantly enhanced biosynthesis of flavonoids in general and the flavonol biosynthesis in particular. Pre-pubertal ovary intact BALB/c mice received daily oral administration of vehicle and ethanolic extract of wild type (WT-TOM) and transgenic AtMYB12-tomato (MYB12-TOM) fruits for six weeks. Animal fed with MYB12-TOM showed no inflammation in hepatic tissues and normal sinusoidal Kupffer cell morphology. MYB12-TOM extract significantly increased tibial and femoral growth and subsequently improved the bone length as compared to vehicle and WT-TOM. Histomorphometry exhibited significantly wider distal femoral and proximal tibial growth plate, increased number and size of hypertrophic chondrocytes in MYB12-TOM which corroborated with micro-CT and expression of BMP-2 and COL-10, marker genes for hypertrophic cells. We conclude that metabolic reprogramming of tomato by AtMYB12 has the potential to improve longitudinal bone growth thus helping in achievement of greater peak bone mass during adolescence.
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spelling pubmed-47683172016-03-02 Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals Choudhary, Dharmendra Pandey, Ashutosh Adhikary, Sulekha Ahmad, Naseer Bhatia, Chitra Bhambhani, Sweta Trivedi, Prabodh Kumar Trivedi, Ritu Sci Rep Article Externally visible body and longitudinal bone growth is a result of proliferation of chondrocytes. In growth disorder, there is delay in the age associated increase in height. The present study evaluates the effect of extract from transgenic tomato fruit expressing AtMYB12 transcription factor on bone health including longitudinal growth. Constitutive expression of AtMYB12 in tomato led to a significantly enhanced biosynthesis of flavonoids in general and the flavonol biosynthesis in particular. Pre-pubertal ovary intact BALB/c mice received daily oral administration of vehicle and ethanolic extract of wild type (WT-TOM) and transgenic AtMYB12-tomato (MYB12-TOM) fruits for six weeks. Animal fed with MYB12-TOM showed no inflammation in hepatic tissues and normal sinusoidal Kupffer cell morphology. MYB12-TOM extract significantly increased tibial and femoral growth and subsequently improved the bone length as compared to vehicle and WT-TOM. Histomorphometry exhibited significantly wider distal femoral and proximal tibial growth plate, increased number and size of hypertrophic chondrocytes in MYB12-TOM which corroborated with micro-CT and expression of BMP-2 and COL-10, marker genes for hypertrophic cells. We conclude that metabolic reprogramming of tomato by AtMYB12 has the potential to improve longitudinal bone growth thus helping in achievement of greater peak bone mass during adolescence. Nature Publishing Group 2016-02-26 /pmc/articles/PMC4768317/ /pubmed/26917158 http://dx.doi.org/10.1038/srep21668 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Choudhary, Dharmendra
Pandey, Ashutosh
Adhikary, Sulekha
Ahmad, Naseer
Bhatia, Chitra
Bhambhani, Sweta
Trivedi, Prabodh Kumar
Trivedi, Ritu
Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title_full Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title_fullStr Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title_full_unstemmed Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title_short Genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
title_sort genetically engineered flavonol enriched tomato fruit modulates chondrogenesis to increase bone length in growing animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768317/
https://www.ncbi.nlm.nih.gov/pubmed/26917158
http://dx.doi.org/10.1038/srep21668
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