Deferoxamine Preconditioning of Neural-Like Cells Derived from Human Wharton's Jelly Mesenchymal Stem Cells as a Strategy to Promote Their Tolerance and Therapeutic Potential: An In Vitro Study

被引:22
作者
Nouri, Fatemeh [1 ]
Salehinejad, Parvin [2 ]
Nematollahi-mahani, Seyed Noureddin [2 ]
Kamarul, Tunku [3 ]
Zarrindast, Mohammad Reza [4 ]
Sharifi, Ali Mohammad [1 ,3 ,5 ]
机构
[1] Iran Univ Med Sci, Sch Med, Dept Pharmacol, Razi Drug Res Ctr, Tehran, Iran
[2] Kerman Univ Med Sci, Dept Anat, Afzalipour Sch Med, Kerman, Iran
[3] Univ Malaya, Dept Orthoped, Fac Med, Tissue Engn Grp TEG & Res,NOCERAL, Kuala Lumpur, Malaysia
[4] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Neurosci, Tehran, Iran
[5] Iran Univ Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Regenerat Med, Tehran, Iran
关键词
Deferoxamine; Neural-like cells; Preconditioning; BDNF; VEGF; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR-I; STROMAL CELLS; NEUROVASCULAR NICHE; SIGNAL-TRANSDUCTION; OXIDATIVE STRESS; DNA-BINDING; HYPOXIA; EXPRESSION; ACTIVATION;
D O I
10.1007/s10571-015-0249-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transplantation of neural-like cells is considered as a promising therapeutic strategy developed for neurodegenerative disease in particular for ischemic stroke. Since cell survival is a major concern following cell implantation, a number of studies have underlined the protective effects of preconditioning with hypoxia or hypoxia mimetic pharmacological agents such as deferoxamine (DFO), induced by activation of hypoxia inducible factor-1 (HIF-1) and its target genes. The present study has investigated the effects of DFO preconditioning on some factors involved in cell survival, angiogenesis, and neurogenesis of neural-like cells derived from human Wharton's jelly mesenchymal stem cells (HWJ-MSCs) in presence of hydrogen peroxide (H2O2). HWJ-MSCs were differentiated toward neural-like cells for 14 days and neural cell markers were identified using immunocytochemistry. HWJ-MSC-derived neural-like cells were then treated with 100 A mu M DFO, as a known hypoxia mimetic agent for 48 h. mRNA and protein expression of HIF-1 target genes including brain-derived neurotrophic factors (BDNF) and vascular endothelial growth factor (VEGF) significantly increased using RT-PCR and Western blotting which were reversed by HIF-1 alpha inhibitor, while, gene expression of Akt-1, Bcl-2, and Bax did not change significantly but pAkt-1 was up-regulated as compared to poor DFO group. However, addition of H2O2 to DFO-treated cells resulted in higher resistance to H2O2-induced cell death. Western blotting analysis also showed significant up-regulation of HIF-1 alpha, BDNF, VEGF, and pAkt-1, and decrease of Bax/Bcl-2 ratio as compared to poor DFO. These results may suggest that DFO preconditioning of HWJ-MSC-derived neural-like cells improves their tolerance and therapeutic potential and might be considered as a valuable strategy to improve cell therapy.
引用
收藏
页码:689 / 700
页数:12
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