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Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells

OBJECTIVE(S): This research is to study the influences of different concentrations of simvastatin on the biological activities of nucleus pulposus-derived mesenchymal stem cells (NPMSC). MATERIALS AND METHODS: NPMSC were cultured with different concentrations of simvastatin (0, 0.01, 0.1, and 1 μM)...

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Autores principales: Huang, Zenan, Cheng, Xiaofei, Zhao, Jie, Liu, Zhongjun, Wang, Jingcheng, Feng, Xinmin, Zhang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043879/
https://www.ncbi.nlm.nih.gov/pubmed/32133066
http://dx.doi.org/10.22038/IJBMS.2019.14068
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author Huang, Zenan
Cheng, Xiaofei
Zhao, Jie
Liu, Zhongjun
Wang, Jingcheng
Feng, Xinmin
Zhang, Liang
author_facet Huang, Zenan
Cheng, Xiaofei
Zhao, Jie
Liu, Zhongjun
Wang, Jingcheng
Feng, Xinmin
Zhang, Liang
author_sort Huang, Zenan
collection PubMed
description OBJECTIVE(S): This research is to study the influences of different concentrations of simvastatin on the biological activities of nucleus pulposus-derived mesenchymal stem cells (NPMSC). MATERIALS AND METHODS: NPMSC were cultured with different concentrations of simvastatin (0, 0.01, 0.1, and 1 μM) and assessed to determine the possible effects of simvastatin. The cell proliferation was assessed with CCK-8 assay. The flowcytometry and multilineage differentiation were also performed to identify the stem characterization of the cells. The mRNA expressions of aggrecan, collagen type II, glucose transporter 1 (GLUT-1), vascular endothelial growth factor (VEGF) and hypoxia-inducible factor-1α (HIF-1α) were determined by qRT-PCR. RESULTS: The results demonstrated that the cells isolated from nucleus pulposus of healthy Sprague-Dawley (SD) rat met the criteria of MSC. NPMSC could form sunflower-like colonies and strongly expressed stem cell-related genes. In addition, NPMSC showed strong ability of chondrogenic, adipogenic and osteogenic differentiation. Simvastatin at certain range concentrations (0.01 μM-0.1 μM)) significantly promoted colony-forming rate and cell proliferation, and inhibited cell apoptosis. Simvastatin could promote expressions of aggrecan, collagen type II, HIF-1α, VEGF and GLUT-1, while 0.1 μmol/l concentration reached the maximum effect. Our study further demonstrated that HIF-1α-intermediated signaling pathway might participate in regulating the biological activities of NPMSC. CONCLUSION: Proper concentration of simvastatin can promote the biological behavior of NPMSC, and HIF-1α-intermediated signaling pathway might participate in the mechanism.
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spelling pubmed-70438792020-03-04 Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells Huang, Zenan Cheng, Xiaofei Zhao, Jie Liu, Zhongjun Wang, Jingcheng Feng, Xinmin Zhang, Liang Iran J Basic Med Sci Original Article OBJECTIVE(S): This research is to study the influences of different concentrations of simvastatin on the biological activities of nucleus pulposus-derived mesenchymal stem cells (NPMSC). MATERIALS AND METHODS: NPMSC were cultured with different concentrations of simvastatin (0, 0.01, 0.1, and 1 μM) and assessed to determine the possible effects of simvastatin. The cell proliferation was assessed with CCK-8 assay. The flowcytometry and multilineage differentiation were also performed to identify the stem characterization of the cells. The mRNA expressions of aggrecan, collagen type II, glucose transporter 1 (GLUT-1), vascular endothelial growth factor (VEGF) and hypoxia-inducible factor-1α (HIF-1α) were determined by qRT-PCR. RESULTS: The results demonstrated that the cells isolated from nucleus pulposus of healthy Sprague-Dawley (SD) rat met the criteria of MSC. NPMSC could form sunflower-like colonies and strongly expressed stem cell-related genes. In addition, NPMSC showed strong ability of chondrogenic, adipogenic and osteogenic differentiation. Simvastatin at certain range concentrations (0.01 μM-0.1 μM)) significantly promoted colony-forming rate and cell proliferation, and inhibited cell apoptosis. Simvastatin could promote expressions of aggrecan, collagen type II, HIF-1α, VEGF and GLUT-1, while 0.1 μmol/l concentration reached the maximum effect. Our study further demonstrated that HIF-1α-intermediated signaling pathway might participate in regulating the biological activities of NPMSC. CONCLUSION: Proper concentration of simvastatin can promote the biological behavior of NPMSC, and HIF-1α-intermediated signaling pathway might participate in the mechanism. Mashhad University of Medical Sciences 2019-12 /pmc/articles/PMC7043879/ /pubmed/32133066 http://dx.doi.org/10.22038/IJBMS.2019.14068 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Huang, Zenan
Cheng, Xiaofei
Zhao, Jie
Liu, Zhongjun
Wang, Jingcheng
Feng, Xinmin
Zhang, Liang
Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title_full Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title_fullStr Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title_full_unstemmed Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title_short Influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
title_sort influence of simvastatin on the biological behavior of nucleus pulposus-derived mesenchymal stem cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043879/
https://www.ncbi.nlm.nih.gov/pubmed/32133066
http://dx.doi.org/10.22038/IJBMS.2019.14068
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