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Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats

The present study evaluated the effects of calcitonin gene-related peptide (CGRP) on bone marrow mesenchymal stem cells (BMMSCs) in vitro and in a rat model of mandibular distraction osteogenesis (MDO). Rat BMMSCs were isolated then treated with CGRP or CGRP antagonist (CGRP8-37). The proliferation...

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Autores principales: Jia, Sen, Zhang, Shi-Jian, Wang, Xu-Dong, Yang, Zi-Hui, Sun, Ya-Nan, Gupta, Anand, Hou, Rui, Lei, De-Lin, Hu, Kai-Jin, Ye, Wei-Min, Wang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601389/
https://www.ncbi.nlm.nih.gov/pubmed/31316600
http://dx.doi.org/10.3892/etm.2019.7659
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author Jia, Sen
Zhang, Shi-Jian
Wang, Xu-Dong
Yang, Zi-Hui
Sun, Ya-Nan
Gupta, Anand
Hou, Rui
Lei, De-Lin
Hu, Kai-Jin
Ye, Wei-Min
Wang, Lei
author_facet Jia, Sen
Zhang, Shi-Jian
Wang, Xu-Dong
Yang, Zi-Hui
Sun, Ya-Nan
Gupta, Anand
Hou, Rui
Lei, De-Lin
Hu, Kai-Jin
Ye, Wei-Min
Wang, Lei
author_sort Jia, Sen
collection PubMed
description The present study evaluated the effects of calcitonin gene-related peptide (CGRP) on bone marrow mesenchymal stem cells (BMMSCs) in vitro and in a rat model of mandibular distraction osteogenesis (MDO). Rat BMMSCs were isolated then treated with CGRP or CGRP antagonist (CGRP8-37). The proliferation and migration ability of BMMSCs was determined using 5-bromo-2′-deoxyuridine and Transwell assays, respectively. Osteogenic-related gene expression was analyzed with reverse transcription-quantitative polymerase chain reaction. For the in vivo analysis, thirty MDO rats were randomly assigned to control, CGRP or CGRP8-37 groups. To evaluate the mobilization of BMMSCs, nestin and stromal cell-derived factor 1 (SDF-1) were detected by immunohistochemistry and ELISA. Rats were sacrificed following 14 days and new bone formation was assessed by histological and micro-computed tomography analysis. In the in vitro results, the CGRP group demonstrated significantly higher migration and proliferation, as well as enhanced alkaline phosphatase and runt-related transcription factor 2 expression compared with the control. In the in vivo experiments, bone mineral density of the newly formed bone in the CGRP group was significantly higher than controls. The nestin and SDF-1 expression in the CGRP group was also significantly upregulated. In conclusion, the present study demonstrated that CGRP administration increased new bone formation, possibly via enhancing BMMSC migration and differentiation in MDO rats.
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spelling pubmed-66013892019-07-17 Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats Jia, Sen Zhang, Shi-Jian Wang, Xu-Dong Yang, Zi-Hui Sun, Ya-Nan Gupta, Anand Hou, Rui Lei, De-Lin Hu, Kai-Jin Ye, Wei-Min Wang, Lei Exp Ther Med Articles The present study evaluated the effects of calcitonin gene-related peptide (CGRP) on bone marrow mesenchymal stem cells (BMMSCs) in vitro and in a rat model of mandibular distraction osteogenesis (MDO). Rat BMMSCs were isolated then treated with CGRP or CGRP antagonist (CGRP8-37). The proliferation and migration ability of BMMSCs was determined using 5-bromo-2′-deoxyuridine and Transwell assays, respectively. Osteogenic-related gene expression was analyzed with reverse transcription-quantitative polymerase chain reaction. For the in vivo analysis, thirty MDO rats were randomly assigned to control, CGRP or CGRP8-37 groups. To evaluate the mobilization of BMMSCs, nestin and stromal cell-derived factor 1 (SDF-1) were detected by immunohistochemistry and ELISA. Rats were sacrificed following 14 days and new bone formation was assessed by histological and micro-computed tomography analysis. In the in vitro results, the CGRP group demonstrated significantly higher migration and proliferation, as well as enhanced alkaline phosphatase and runt-related transcription factor 2 expression compared with the control. In the in vivo experiments, bone mineral density of the newly formed bone in the CGRP group was significantly higher than controls. The nestin and SDF-1 expression in the CGRP group was also significantly upregulated. In conclusion, the present study demonstrated that CGRP administration increased new bone formation, possibly via enhancing BMMSC migration and differentiation in MDO rats. D.A. Spandidos 2019-08 2019-06-11 /pmc/articles/PMC6601389/ /pubmed/31316600 http://dx.doi.org/10.3892/etm.2019.7659 Text en Copyright: © Jia et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Jia, Sen
Zhang, Shi-Jian
Wang, Xu-Dong
Yang, Zi-Hui
Sun, Ya-Nan
Gupta, Anand
Hou, Rui
Lei, De-Lin
Hu, Kai-Jin
Ye, Wei-Min
Wang, Lei
Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title_full Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title_fullStr Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title_full_unstemmed Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title_short Calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
title_sort calcitonin gene-related peptide enhances osteogenic differentiation and recruitment of bone marrow mesenchymal stem cells in rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601389/
https://www.ncbi.nlm.nih.gov/pubmed/31316600
http://dx.doi.org/10.3892/etm.2019.7659
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