Inflammatory Microenvironment Changes the Secretory Profile of Mesenchymal Stem Cells to Recruit Mesenchymal Stem Cells

被引:18
|
作者
Xing, Junchao [1 ,2 ,3 ,4 ]
Hou, Tianyong [1 ,2 ,3 ,4 ]
Jin, Huiyong [1 ,2 ,3 ,4 ]
Luo, Fei [1 ,2 ,3 ,4 ]
Chang, Zhengqi [1 ,2 ,3 ,4 ]
Li, Zhiqiang [1 ,2 ,3 ,4 ]
Xie, Zhao [1 ,2 ,3 ,4 ]
Xu, Jianzhong [1 ,2 ,3 ,4 ]
机构
[1] Third Mil Med Univ, Natl & Local United Engn Lab Tissue Engn, Dept Orthopaed, Southwest Hosp, Chongqing, Peoples R China
[2] Third Mil Med Univ, Ctr Tissue Engn Res & Applicat, Chongqing, Peoples R China
[3] Lab Tissue Engn Chongqing City, Chongqing, Peoples R China
[4] Ctr Regenet & Reconstruct Engn Technol Chongqing, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesenchymal stem cells; Cell migration; Inflammatory microenvironment; Chemokine secretion; MARROW STROMAL CELLS; MYOCARDIAL-INFARCTION; CHEMOKINE RECEPTORS; TISSUE REGENERATION; CXC CHEMOKINES; GROWTH; REPAIR; MIGRATION; ALPHA; TRANSDIFFERENTIATION;
D O I
10.1159/000358663
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Human bone-marrow mesenchymal stem cells (hBMSCs) are widely transplanted into inflammatory microenvironment to accelerate tissue regeneration. Transplanted hBMSCs recruit host hBMSCs through a poorly understood mechanism. This study was aimed to determine whether and how inflammatory microenvironment influenced the host-hBMSCs-recruiting capability of transplanted hBMSCs. Methods: Pro-inflammatory factors, including IL-1 beta, IL-6 and TNF-alpha, were utilized to mimic inflammatory microenvironment. hBMSCs were cultured and conditioned media (CM) were collected. The effects of inflammatory microenvironment on the host-hBMSCs-recruting capability of cultured hBMSCs were revealed by transwell migration assays. Employing semi-quantitative and quantitative cytokine antibody assays, we examined the secretory profile of cultured hBMSCs. Results: CM from cultured hBMSCs exerted excellent host-hBMSCs-recruting capability, which was significantly promoted by exposure to inflammatory microenvironment. Within inflammatory microenvironment, hBMSCs secreted more chemokines related to cell migration. Finally, 21 cytokines were verified as potential factors accounting for the enhanced host-hBMSCs-recruting capability of cultured hBMSCs exposed to inflammatory microenvironment. Conclusion: These results strongly suggested that in clinic, inflammatory microenvironment might promote the host-hBMSCs-recruiting capacity of transplanted hBMSCs by increasing chemokines secretion. Modulation of such characteristics of hBMSCs might provide novel therapeutic ideas in the context of hBMSCs. Copyright (C) 2014 S. Karger AG, Basel
引用
收藏
页码:905 / 919
页数:15
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