Transfusion of CXCR4-Primed Endothelial Progenitor Cells Reduces Cerebral Ischemic Damage and Promotes Repair in db/db Diabetic Mice

被引:29
作者
Chen, Ji [1 ,2 ,3 ]
Chen, Jianying [2 ,3 ]
Chen, Shuzhen [1 ]
Zhang, Cheng [1 ]
Zhang, Liangqing [2 ,3 ]
Xiao, Xiang [1 ]
Das, Avik [1 ]
Zhao, Yuhui [1 ,4 ]
Yuan, Bin [1 ,2 ,3 ]
Morris, Mariana [1 ]
Zhao, Bin [2 ,3 ]
Chen, Yanfang [1 ,2 ,3 ]
机构
[1] Wright State Univ, Boonshoft Sch Med, Dept Pharmacol & Toxicol, Dayton, OH 45435 USA
[2] Guangdong Med Coll, Affiliated Hosp, Clin Res Ctr, Zhanjiang, Guangdong, Peoples R China
[3] Guangdong Med Coll, Affiliated Hosp, Dept Neurol, Zhanjiang, Guangdong, Peoples R China
[4] Guangxi Med Univ, Affiliated Hosp 1, Dept Neurol, Nanning, Guangxi, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 11期
基金
中国国家自然科学基金;
关键词
MYOCARDIAL-INFARCTION; FUNCTIONAL RECOVERY; TRANSPLANTATION; PROLIFERATION; EXPRESSION; LEPTIN; FACTOR-1-ALPHA; MOBILIZATION; RECRUITMENT; MIGRATION;
D O I
10.1371/journal.pone.0050105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study investigated the role of stromal cell-derived factor-1 alpha (SDF-1 alpha)/CXC chemokine receptor 4 (CXCR4) axis in brain and endothelial progenitor cells (EPCs), and explored the efficacy of CXCR4 primed EPCs in treating ischemic stroke in diabetes. The db/db diabetic and db/+ mice were used in this study. Levels of plasma SDF-1 alpha and circulating CD34+CXCR4+ cells were measured. Brain SDF-1 alpha and CXCR4 expression were quantified at basal and after middle cerebral artery occlusion (MCAO). In in vitro study, EPCs were transfected with adenovirus carrying null (Ad-null) or CXCR4 (Ad-CXCR4) followed with high glucose (HG) treatment for 4 days. For pathway block experiments, cells were pre-incubated with PI3K inhibitor or nitric oxide synthase (NOS) inhibitor for two hours. The CXCR4 expression, function and apoptosis of EPCs were determined. The p-Akt/Akt and p-eNOS/eNOS expression in EPCs were also measured. In in vivo study, EPCs transfected with Ad-null or Ad-CXCR4 were infused into mice via tail vein. On day 2 and 7, the cerebral blood flow, neurologic deficit score, infarct volume, cerebral microvascular density, angiogenesis and neurogenesis were determined. We found: 1) The levels of plasma SDF-1 alpha and circulating CD34+CXCR4+ cells were decreased in db/db mice; 2) The basal level of SDF-1 alpha and MCAO-induced up-regulation of SDF-1 alpha/CXCR4 axis were reduced in the brain of db/db mice; 3) Ad-CXCR4 transfection increased CXCR4 expression in EPCs and enhanced EPC colonic forming capacity; 4) Ad-CXCR4 transfection prevented EPCs from HG-induced dysfunction (migration and tube formation) and apoptosis via activation of PI3K/Akt/eNOS signal pathway; 4) Ad-CXCR4 transfection enhanced the efficacy of EPC infusion in attenuating infarct volume and promoting angiogenesis and neurogenesis. Our data suggest that Ad-CXCR4 primed EPCs have better therapeutic effects for ischemia stroke in diabetes than unmodified EPCs do.
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页数:13
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