Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bahrami, Maryam, Valiani, Ali, Amirpour, Noushin, Ra Rani, Mohammad Zamani, Hashemibeni, Batool
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
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
_version_ 1783304676597301248
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
work_keys_str_mv AT bahramimaryam cartilagetissueengineeringviaicariinandadiposederivedstemcellsinfibrinscaffold
AT valianiali cartilagetissueengineeringviaicariinandadiposederivedstemcellsinfibrinscaffold
AT amirpournoushin cartilagetissueengineeringviaicariinandadiposederivedstemcellsinfibrinscaffold
AT raranimohammadzamani cartilagetissueengineeringviaicariinandadiposederivedstemcellsinfibrinscaffold
AT hashemibenibatool cartilagetissueengineeringviaicariinandadiposederivedstemcellsinfibrinscaffold