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Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice

ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, which regulates the elongation of C12-16 saturated and monounsaturated fatty acids. Elovl6 has been shown to be associated with various pathophysiologies including insulin resistance, atherosclerosis, a...

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Autores principales: Kikuchi, Manami, Shimada, Masako, Matsuzaka, Takashi, Ishii, Kiyoaki, Nakagawa, Yoshimi, Takayanagi, Misa, Yamada, Nobuhiro, Shimano, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965081/
https://www.ncbi.nlm.nih.gov/pubmed/27467521
http://dx.doi.org/10.1371/journal.pone.0159375
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author Kikuchi, Manami
Shimada, Masako
Matsuzaka, Takashi
Ishii, Kiyoaki
Nakagawa, Yoshimi
Takayanagi, Misa
Yamada, Nobuhiro
Shimano, Hitoshi
author_facet Kikuchi, Manami
Shimada, Masako
Matsuzaka, Takashi
Ishii, Kiyoaki
Nakagawa, Yoshimi
Takayanagi, Misa
Yamada, Nobuhiro
Shimano, Hitoshi
author_sort Kikuchi, Manami
collection PubMed
description ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, which regulates the elongation of C12-16 saturated and monounsaturated fatty acids. Elovl6 has been shown to be associated with various pathophysiologies including insulin resistance, atherosclerosis, and non-alcoholic steatohepatitis. To investigate a potential role of Elovl6 during bone development, we here examined a skeletal phenotype of Elovl6 knockout (Elovl6(-/-)) mice. The Elovl6(-/-) skeleton was smaller than that of controls, but exhibited no obvious patterning defects. Histological analysis revealed a reduced length of proliferating and an elongated length of hypertrophic chondrocyte layer, and decreased trabecular bone in Elovl6(-/-) mice compared with controls. These results were presumably due to a modest decrease in chondrocyte proliferation and accelerated differentiation of cells of the chondrocyte lineage. Consistent with the increased length of the hypertrophic chondrocyte layer in Elovl6(-/-) mice, Collagen10α1 was identified as one of the most affected genes by ablation of Elovl6 in chondrocytes. Furthermore, this elevated expression of Collagen10α1 of Elovl6-null chondrocytes was likely associated with increased levels of Foxa2/a3 and Mef2c mRNA expression. Relative increases in protein levels of nuclear Foxa2 and cytoplasmic histone deacethylase 4/5/7 were also observed in Elovl6 knockdown cells of the chondrocyte lineage. Collectively, our data suggest that Elovl6 plays a critical role for proper development of embryonic growth plate.
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spelling pubmed-49650812016-08-18 Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice Kikuchi, Manami Shimada, Masako Matsuzaka, Takashi Ishii, Kiyoaki Nakagawa, Yoshimi Takayanagi, Misa Yamada, Nobuhiro Shimano, Hitoshi PLoS One Research Article ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, which regulates the elongation of C12-16 saturated and monounsaturated fatty acids. Elovl6 has been shown to be associated with various pathophysiologies including insulin resistance, atherosclerosis, and non-alcoholic steatohepatitis. To investigate a potential role of Elovl6 during bone development, we here examined a skeletal phenotype of Elovl6 knockout (Elovl6(-/-)) mice. The Elovl6(-/-) skeleton was smaller than that of controls, but exhibited no obvious patterning defects. Histological analysis revealed a reduced length of proliferating and an elongated length of hypertrophic chondrocyte layer, and decreased trabecular bone in Elovl6(-/-) mice compared with controls. These results were presumably due to a modest decrease in chondrocyte proliferation and accelerated differentiation of cells of the chondrocyte lineage. Consistent with the increased length of the hypertrophic chondrocyte layer in Elovl6(-/-) mice, Collagen10α1 was identified as one of the most affected genes by ablation of Elovl6 in chondrocytes. Furthermore, this elevated expression of Collagen10α1 of Elovl6-null chondrocytes was likely associated with increased levels of Foxa2/a3 and Mef2c mRNA expression. Relative increases in protein levels of nuclear Foxa2 and cytoplasmic histone deacethylase 4/5/7 were also observed in Elovl6 knockdown cells of the chondrocyte lineage. Collectively, our data suggest that Elovl6 plays a critical role for proper development of embryonic growth plate. Public Library of Science 2016-07-28 /pmc/articles/PMC4965081/ /pubmed/27467521 http://dx.doi.org/10.1371/journal.pone.0159375 Text en © 2016 Kikuchi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kikuchi, Manami
Shimada, Masako
Matsuzaka, Takashi
Ishii, Kiyoaki
Nakagawa, Yoshimi
Takayanagi, Misa
Yamada, Nobuhiro
Shimano, Hitoshi
Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title_full Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title_fullStr Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title_full_unstemmed Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title_short Crucial Role of Elovl6 in Chondrocyte Growth and Differentiation during Growth Plate Development in Mice
title_sort crucial role of elovl6 in chondrocyte growth and differentiation during growth plate development in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965081/
https://www.ncbi.nlm.nih.gov/pubmed/27467521
http://dx.doi.org/10.1371/journal.pone.0159375
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