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Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold
BACKGROUND: Nowadays, cartilage tissue engineering is the best candidate for regeneration of cartilage defects. This study evaluates the function of herbal extracts icariin (ICA), the major pharmacological constituent of herba Epimedium, compared with transforming growth factor β3 (TGFβ3) to prove i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840972/ https://www.ncbi.nlm.nih.gov/pubmed/29531934 http://dx.doi.org/10.4103/2277-9175.225925 |
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author | Bahrami, Maryam Valiani, Ali Amirpour, Noushin Ra Rani, Mohammad Zamani Hashemibeni, Batool |
author_facet | Bahrami, Maryam Valiani, Ali Amirpour, Noushin Ra Rani, Mohammad Zamani Hashemibeni, Batool |
author_sort | Bahrami, Maryam |
collection | PubMed |
description | BACKGROUND: Nowadays, cartilage tissue engineering is the best candidate for regeneration of cartilage defects. This study evaluates the function of herbal extracts icariin (ICA), the major pharmacological constituent of herba Epimedium, compared with transforming growth factor β3 (TGFβ3) to prove its potential effect for cartilage tissue engineering. MATERIALS AND METHODS: ICA, TGFβ3, and TGFβ3 + ICA were added fibrin-cell constructions derived from adipose tissue stem cells. After 14 days, cell viability analyzed by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H- tetrazolium bromide assay and the expression of cartilage genes was evaluated with real-time polymerase chain reaction (RT-PCR). RESULTS: The results showed ICA, TGFβ3, and TGFβ3 + ICA increased the rate of proliferation and viability of cells; but there were no significant differences between them (P > 0.05). Furthermore, quantitative RT-PCR analysis demonstrated that cooperation of ICA with TGFβ3 showed a better effect in expression of cartilaginous specific genes and increased Sox9, type II collagen, and aggrecan expression significantly. Furthermore, the results of the expression of type I and X collagens revealed that TGFβ3 increased the expression of them (P < 0.01); However, treatment with ICA + TGFβ3 down regulated the expression of these genes significantly. CONCLUSION: The results indicated ICA could be a potential factor for chondrogenesis and in cooperation with TGFβ3 could reduce its hypertrophic effects and it is a promising factor for cartilage tissue engineering. |
format | Online Article Text |
id | pubmed-5840972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58409722018-03-12 Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold Bahrami, Maryam Valiani, Ali Amirpour, Noushin Ra Rani, Mohammad Zamani Hashemibeni, Batool Adv Biomed Res Original Article BACKGROUND: Nowadays, cartilage tissue engineering is the best candidate for regeneration of cartilage defects. This study evaluates the function of herbal extracts icariin (ICA), the major pharmacological constituent of herba Epimedium, compared with transforming growth factor β3 (TGFβ3) to prove its potential effect for cartilage tissue engineering. MATERIALS AND METHODS: ICA, TGFβ3, and TGFβ3 + ICA were added fibrin-cell constructions derived from adipose tissue stem cells. After 14 days, cell viability analyzed by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H- tetrazolium bromide assay and the expression of cartilage genes was evaluated with real-time polymerase chain reaction (RT-PCR). RESULTS: The results showed ICA, TGFβ3, and TGFβ3 + ICA increased the rate of proliferation and viability of cells; but there were no significant differences between them (P > 0.05). Furthermore, quantitative RT-PCR analysis demonstrated that cooperation of ICA with TGFβ3 showed a better effect in expression of cartilaginous specific genes and increased Sox9, type II collagen, and aggrecan expression significantly. Furthermore, the results of the expression of type I and X collagens revealed that TGFβ3 increased the expression of them (P < 0.01); However, treatment with ICA + TGFβ3 down regulated the expression of these genes significantly. CONCLUSION: The results indicated ICA could be a potential factor for chondrogenesis and in cooperation with TGFβ3 could reduce its hypertrophic effects and it is a promising factor for cartilage tissue engineering. Medknow Publications & Media Pvt Ltd 2018-02-21 /pmc/articles/PMC5840972/ /pubmed/29531934 http://dx.doi.org/10.4103/2277-9175.225925 Text en Copyright: © 2018 Advanced Biomedical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Bahrami, Maryam Valiani, Ali Amirpour, Noushin Ra Rani, Mohammad Zamani Hashemibeni, Batool Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title | Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title_full | Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title_fullStr | Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title_full_unstemmed | Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title_short | Cartilage Tissue Engineering Via Icariin and Adipose-derived Stem Cells in Fibrin Scaffold |
title_sort | cartilage tissue engineering via icariin and adipose-derived stem cells in fibrin scaffold |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840972/ https://www.ncbi.nlm.nih.gov/pubmed/29531934 http://dx.doi.org/10.4103/2277-9175.225925 |
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