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Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc

BACKGROUND: Human adipose-derived mesenchymal stem cells (ADMSCs) may be ideal source of cells for intervertebral disc (IVD) regeneration, but the harsh chemical microenvironment of IVD may significantly influence the biological and metabolic vitality of ADMSCs and impair their repair potential. Thi...

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Autores principales: Liang, Chengzhen, Li, Hao, Tao, Yiqing, Zhou, Xiaopeng, Li, Fangcai, Chen, Gang, Chen, Qixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338074/
https://www.ncbi.nlm.nih.gov/pubmed/22424131
http://dx.doi.org/10.1186/1479-5876-10-49
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author Liang, Chengzhen
Li, Hao
Tao, Yiqing
Zhou, Xiaopeng
Li, Fangcai
Chen, Gang
Chen, Qixin
author_facet Liang, Chengzhen
Li, Hao
Tao, Yiqing
Zhou, Xiaopeng
Li, Fangcai
Chen, Gang
Chen, Qixin
author_sort Liang, Chengzhen
collection PubMed
description BACKGROUND: Human adipose-derived mesenchymal stem cells (ADMSCs) may be ideal source of cells for intervertebral disc (IVD) regeneration, but the harsh chemical microenvironment of IVD may significantly influence the biological and metabolic vitality of ADMSCs and impair their repair potential. This study aimed to investigate the viability, proliferation and the expression of main matrix proteins of ADMSCs in the chemical microenvironment of IVD under normal and degeneration conditions. METHODS: ADMSCs were harvested from young (aged 8-12 years, n = 6) and mature (aged 33-42 years, n = 6) male donors and cultured under standard condition and IVD-like conditions (low glucose, acidity, high osmolarity, and combined conditions) for 2 weeks. Cell viability was measured by annexin V-FITC and PI staining and cell proliferation was measured by MTT assay. The expression of aggrecan and collagen-I was detected by real-time quantitative polymerase chain reaction and Western blot analysis. RESULTS: IVD-like glucose condition slightly inhibited cell viability, but increased the expression of aggrecan. In contrast, IVD-like osmolarity, acidity and the combined conditions inhibited cell viability and proliferation and the expression of aggrecan and collagen-I. ADMSCs from young and mature donors exhibited similar responses to the chemical microenvironments of IVD. CONCLUSION: IVD-like low glucose is a positive factor but IVD-like high osmolarity and low pH are deleterious factors that affect the survival and biological behaviors of ADMSCs. These findings may promote the translational research of ADMSCs in IVD regeneration for the treatment of low back pain.
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spelling pubmed-33380742012-04-27 Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc Liang, Chengzhen Li, Hao Tao, Yiqing Zhou, Xiaopeng Li, Fangcai Chen, Gang Chen, Qixin J Transl Med Research BACKGROUND: Human adipose-derived mesenchymal stem cells (ADMSCs) may be ideal source of cells for intervertebral disc (IVD) regeneration, but the harsh chemical microenvironment of IVD may significantly influence the biological and metabolic vitality of ADMSCs and impair their repair potential. This study aimed to investigate the viability, proliferation and the expression of main matrix proteins of ADMSCs in the chemical microenvironment of IVD under normal and degeneration conditions. METHODS: ADMSCs were harvested from young (aged 8-12 years, n = 6) and mature (aged 33-42 years, n = 6) male donors and cultured under standard condition and IVD-like conditions (low glucose, acidity, high osmolarity, and combined conditions) for 2 weeks. Cell viability was measured by annexin V-FITC and PI staining and cell proliferation was measured by MTT assay. The expression of aggrecan and collagen-I was detected by real-time quantitative polymerase chain reaction and Western blot analysis. RESULTS: IVD-like glucose condition slightly inhibited cell viability, but increased the expression of aggrecan. In contrast, IVD-like osmolarity, acidity and the combined conditions inhibited cell viability and proliferation and the expression of aggrecan and collagen-I. ADMSCs from young and mature donors exhibited similar responses to the chemical microenvironments of IVD. CONCLUSION: IVD-like low glucose is a positive factor but IVD-like high osmolarity and low pH are deleterious factors that affect the survival and biological behaviors of ADMSCs. These findings may promote the translational research of ADMSCs in IVD regeneration for the treatment of low back pain. BioMed Central 2012-03-16 /pmc/articles/PMC3338074/ /pubmed/22424131 http://dx.doi.org/10.1186/1479-5876-10-49 Text en Copyright ©2012 Liang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Liang, Chengzhen
Li, Hao
Tao, Yiqing
Zhou, Xiaopeng
Li, Fangcai
Chen, Gang
Chen, Qixin
Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title_full Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title_fullStr Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title_full_unstemmed Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title_short Responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
title_sort responses of human adipose-derived mesenchymal stem cells to chemical microenvironment of the intervertebral disc
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338074/
https://www.ncbi.nlm.nih.gov/pubmed/22424131
http://dx.doi.org/10.1186/1479-5876-10-49
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