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Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens

The present study concerned the effect of ageing in laying hens, from 23 to 90 weeks of age, on the regulation of Ca metabolism related to the requirement for eggshell mineralization. Samples were collected from parathyroid gland (PG), liver, jejunum, medullary bone (MB) and kidney for a quantitativ...

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Autores principales: Gloux, A., Le Roy, N., Même, N., Piketty, M. L., Prié, D., Benzoni, G., Gautron, J., Nys, Y., Narcy, A., Duclos, M. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713066/
https://www.ncbi.nlm.nih.gov/pubmed/33273568
http://dx.doi.org/10.1038/s41598-020-78106-7
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author Gloux, A.
Le Roy, N.
Même, N.
Piketty, M. L.
Prié, D.
Benzoni, G.
Gautron, J.
Nys, Y.
Narcy, A.
Duclos, M. J.
author_facet Gloux, A.
Le Roy, N.
Même, N.
Piketty, M. L.
Prié, D.
Benzoni, G.
Gautron, J.
Nys, Y.
Narcy, A.
Duclos, M. J.
author_sort Gloux, A.
collection PubMed
description The present study concerned the effect of ageing in laying hens, from 23 to 90 weeks of age, on the regulation of Ca metabolism related to the requirement for eggshell mineralization. Samples were collected from parathyroid gland (PG), liver, jejunum, medullary bone (MB) and kidney for a quantitative study of candidate gene expression. Although parathyroid hormone (PTH) gene expression in the PG did not vary with age, a stronger challenge to Ca homeostasis was suggested in aged hens. Indeed gene expression of Ca transporters , Vitamin D Receptor (VDR) in the jejunum, and that of transient receptor potential channel subfamily V member 5 (TRPV5) in the kidney decreased. This could exacerbate bone resorption and impair bone accretion, as attested by a higher expression of the Carbonic Anhydrase 2 (CA2) gene and a lower expression of collagen type I alpha 1 chain (COL1A1) in the MB. The increased expression of Fibroblast Growth Factor 23 (FGF23) in the MB likely contributed to the decreased plasma levels of 1.25(OH)(2)D(3) and the altered expression of target genes under its regulation. Our data highlights the molecular mechanisms underlying the osteoporotic syndrome previously documented in aged laying hens, thus providing new perspectives for future interventions.
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spelling pubmed-77130662020-12-03 Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens Gloux, A. Le Roy, N. Même, N. Piketty, M. L. Prié, D. Benzoni, G. Gautron, J. Nys, Y. Narcy, A. Duclos, M. J. Sci Rep Article The present study concerned the effect of ageing in laying hens, from 23 to 90 weeks of age, on the regulation of Ca metabolism related to the requirement for eggshell mineralization. Samples were collected from parathyroid gland (PG), liver, jejunum, medullary bone (MB) and kidney for a quantitative study of candidate gene expression. Although parathyroid hormone (PTH) gene expression in the PG did not vary with age, a stronger challenge to Ca homeostasis was suggested in aged hens. Indeed gene expression of Ca transporters , Vitamin D Receptor (VDR) in the jejunum, and that of transient receptor potential channel subfamily V member 5 (TRPV5) in the kidney decreased. This could exacerbate bone resorption and impair bone accretion, as attested by a higher expression of the Carbonic Anhydrase 2 (CA2) gene and a lower expression of collagen type I alpha 1 chain (COL1A1) in the MB. The increased expression of Fibroblast Growth Factor 23 (FGF23) in the MB likely contributed to the decreased plasma levels of 1.25(OH)(2)D(3) and the altered expression of target genes under its regulation. Our data highlights the molecular mechanisms underlying the osteoporotic syndrome previously documented in aged laying hens, thus providing new perspectives for future interventions. Nature Publishing Group UK 2020-12-03 /pmc/articles/PMC7713066/ /pubmed/33273568 http://dx.doi.org/10.1038/s41598-020-78106-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gloux, A.
Le Roy, N.
Même, N.
Piketty, M. L.
Prié, D.
Benzoni, G.
Gautron, J.
Nys, Y.
Narcy, A.
Duclos, M. J.
Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title_full Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title_fullStr Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title_full_unstemmed Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title_short Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens
title_sort increased expression of fibroblast growth factor 23 is the signature of a deteriorated ca/p balance in ageing laying hens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713066/
https://www.ncbi.nlm.nih.gov/pubmed/33273568
http://dx.doi.org/10.1038/s41598-020-78106-7
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