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Effect of remifentanil on pre-osteoclast cell differentiation in vitro

BACKGROUND: The structure and function of bone tissue is maintained through a constant remodeling process, which is maintained by the balance between osteoblasts and osteoclasts. The failure of bone remodeling can lead to pathological conditions of bone structure and function. Remifentanil is curren...

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Autores principales: Jeon, Hyun-Ook, Choi, In-Seok, Yoon, Ji-Young, Kim, Eun-Jung, Yoon, Ji-Uk, Cho, Ah-Reum, Kim, Hyung-Joon, Kim, Cheul-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dental Society of Anesthsiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858013/
https://www.ncbi.nlm.nih.gov/pubmed/29556554
http://dx.doi.org/10.17245/jdapm.2018.18.1.9
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author Jeon, Hyun-Ook
Choi, In-Seok
Yoon, Ji-Young
Kim, Eun-Jung
Yoon, Ji-Uk
Cho, Ah-Reum
Kim, Hyung-Joon
Kim, Cheul-Hong
author_facet Jeon, Hyun-Ook
Choi, In-Seok
Yoon, Ji-Young
Kim, Eun-Jung
Yoon, Ji-Uk
Cho, Ah-Reum
Kim, Hyung-Joon
Kim, Cheul-Hong
author_sort Jeon, Hyun-Ook
collection PubMed
description BACKGROUND: The structure and function of bone tissue is maintained through a constant remodeling process, which is maintained by the balance between osteoblasts and osteoclasts. The failure of bone remodeling can lead to pathological conditions of bone structure and function. Remifentanil is currently used as a narcotic analgesic agent in general anesthesia and sedation. However, the effect of remifentanil on osteoclasts has not been studied. Therefore, we investigated the effect of remifentanil on pre-osteoclast (pre-OCs) differentiation and the mechanism of osteoclast differentiation in the absence of specific stimulus. METHODS: Pre-OCs were obtained by culturing bone marrow-derived macrophages (BMMs) in osteoclastogenic medium for 2 days and then treated with various concentration of remifentanil. The mRNA expression of NFATc1 and c-fos was examined by using real-time PCR. We also examined the effect of remifentanil on the osteoclast-specific genes TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. Finally, we examined the influence of remifentanil on the migration of pre-OCs by using the Boyden chamber assay. RESULTS: Remifentanil increased pre-OC differentiation and osteoclast size, but did not affect the mRNA expression of NFATc1 and c-fos or significantly affect the expression of TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. However, remifentanil increased the migration of pre-OCs. CONCLUSIONS: This study suggested that remifentanil promotes the differentiation of pre-OCs and induces maturation, such as increasing osteoclast size. In addition, the increase in osteoclast size was mediated by the enhancement of pre-OC migration and cell fusion.
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spelling pubmed-58580132018-03-19 Effect of remifentanil on pre-osteoclast cell differentiation in vitro Jeon, Hyun-Ook Choi, In-Seok Yoon, Ji-Young Kim, Eun-Jung Yoon, Ji-Uk Cho, Ah-Reum Kim, Hyung-Joon Kim, Cheul-Hong J Dent Anesth Pain Med Original Article BACKGROUND: The structure and function of bone tissue is maintained through a constant remodeling process, which is maintained by the balance between osteoblasts and osteoclasts. The failure of bone remodeling can lead to pathological conditions of bone structure and function. Remifentanil is currently used as a narcotic analgesic agent in general anesthesia and sedation. However, the effect of remifentanil on osteoclasts has not been studied. Therefore, we investigated the effect of remifentanil on pre-osteoclast (pre-OCs) differentiation and the mechanism of osteoclast differentiation in the absence of specific stimulus. METHODS: Pre-OCs were obtained by culturing bone marrow-derived macrophages (BMMs) in osteoclastogenic medium for 2 days and then treated with various concentration of remifentanil. The mRNA expression of NFATc1 and c-fos was examined by using real-time PCR. We also examined the effect of remifentanil on the osteoclast-specific genes TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. Finally, we examined the influence of remifentanil on the migration of pre-OCs by using the Boyden chamber assay. RESULTS: Remifentanil increased pre-OC differentiation and osteoclast size, but did not affect the mRNA expression of NFATc1 and c-fos or significantly affect the expression of TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. However, remifentanil increased the migration of pre-OCs. CONCLUSIONS: This study suggested that remifentanil promotes the differentiation of pre-OCs and induces maturation, such as increasing osteoclast size. In addition, the increase in osteoclast size was mediated by the enhancement of pre-OC migration and cell fusion. The Korean Dental Society of Anesthsiology 2018-02 2018-02-27 /pmc/articles/PMC5858013/ /pubmed/29556554 http://dx.doi.org/10.17245/jdapm.2018.18.1.9 Text en Copyright © 2018 Journal of Dental Anesthesia and Pain Medicine http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jeon, Hyun-Ook
Choi, In-Seok
Yoon, Ji-Young
Kim, Eun-Jung
Yoon, Ji-Uk
Cho, Ah-Reum
Kim, Hyung-Joon
Kim, Cheul-Hong
Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title_full Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title_fullStr Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title_full_unstemmed Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title_short Effect of remifentanil on pre-osteoclast cell differentiation in vitro
title_sort effect of remifentanil on pre-osteoclast cell differentiation in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858013/
https://www.ncbi.nlm.nih.gov/pubmed/29556554
http://dx.doi.org/10.17245/jdapm.2018.18.1.9
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