Lipocalin-2-mediated upregulation of various antioxidants and growth factors protects bone marrow-derived mesenchymal stem cells against unfavorable microenvironments

被引:0
作者
Raheleh Halabian
Hossein Abdul Tehrani
Ali Jahanian-Najafabadi
Mehryar Habibi Roudkenar
机构
[1] Tarbiat Modares University,Department of Medical Biotechnology, Faculty of Medical Sciences
[2] Isfahan University of Medical Sciences and Health Services,Department of Pharmaceutical Biotechnology, School of Pharmacy
[3] High Institute for Research and Education in Transfusion Medicine,Blood Transfusion Research Center
来源
Cell Stress and Chaperones | 2013年 / 18卷
关键词
Mesenchymal stem cells; Lcn2; Oxidative stress; Apoptosis; Antioxidants; Growth factors;
D O I
暂无
中图分类号
学科分类号
摘要
Despite many advantages of mesenchymal stem cells (MSCs) that make them suitable for cell therapy purposes, their therapeutic application has been limited due to their susceptibility to several stresses (e.g., nutrient-poor environment, oxidative stress, and hypoxic and masses of cytotoxic factors) to which they are exposed during their preparation and following transplantation. Hence, reinforcing MSCs against these stresses is a challenge for both basic and clinician scientists. Recently, much attention has been directed toward equipping MSCs with cytoprotective factors to strengthen them against unfavorable microenvironments. Here, we engineered MSCs with lipocalin 2 (Lcn2), a cytoprotective factor that is naturally induced following exposure of cells to stresses imposed by the microenvironment. Lcn2 overexpression not only did not interfere with the multidifferentiation capacity of the MSCs but also granted many protective properties to them. Lcn2 potentiated MSCs to withstand oxidative, hypoxia, and serum deprivation (SD) conditions via antagonizing their induced cytotoxicity and apoptosis. Adhesion rate of MSCs to coated culture plates was also enhanced by Lcn2 overexpression. In addition, Lcn2 induced antioxidants and upregulated some growth factors in MSCs. Our findings suggested a new strategy for prevention of graft cell death in MSC-based cell therapy.
引用
收藏
页码:785 / 800
页数:15
相关论文
共 450 条
[1]  
Abdel-Mageed AS(2009)Intravenous administration of mesenchymal stem cells genetically modified with extracellular superoxide dismutase improves survival in irradiated mice Blood 113 1201-II-252
[2]  
Senagore AJ(2003)Transplantation of autologous fresh bone marrow into infarcted myocardium: a word of caution Circulation 108 II-247-1839
[3]  
Pietryga DW(2006)Lipocalin 2-deficient mice exhibit increased sensitivity to Proc Natl Acad Sci USA 103 1834-H2203
[4]  
Connors RH(2006) infection but not to ischemia–reperfusion injury Am J Physiol Heart Circ Physiol 290 H2196-2434
[5]  
Giambernardi TA(2002)Mesenchymal stem cell injection after myocardial infarction improves myocardial compliance J Neurol Sci 199 2417-2061
[6]  
Hay RV(2011)Caspase inhibition by Z-VAD increase the survival of grafted bone marrow cells and improves functional outcome after MCAO rats Circ J 75 2060-231
[7]  
Deng W(2011)Adipose tissue or bone marrow, store for purchasing mesenchymal stem cells? Cell Transplant 20 217-247
[8]  
Bel A(1968)Long-term contribution of human bone marrow mesenchymal stromal cells to skeletal muscle regeneration in mice Transplantation 6 230-2691
[9]  
Messas E(2011)Heterotopic of bone marrow. Analysis of precursor cells for osteogenic and hematopoietic tissues Circ J 75 2683-190
[10]  
Agbulut O(2011)Overexpression of Csx/Nkx2.5 and GATA-4 enhances the efficacy of mesenchymal stem cell transplantation after myocardial infarction Cell Stress Chaperon 17 181-858