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
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.
引用
收藏
页数:13
相关论文
共 50 条
[1]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[2]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[3]   Lentiviral gene transfer of SDF-1 α to wounds improves diabetic wound healing [J].
Badillo, Andrea T. ;
Chung, Sophie ;
Zhang, Liping ;
Zoltick, Philip ;
Liechty, Kenneth W. .
JOURNAL OF SURGICAL RESEARCH, 2007, 143 (01) :35-42
[4]   Inhibition of stromal cell-derived factor-1α further impairs diabetic wound healing [J].
Bermudez, Dustin M. ;
Xu, Junwang ;
Herdrich, Benjamin J. ;
Radu, Antoneta ;
Mitchell, Marc E. ;
Liechty, Kenneth W. .
JOURNAL OF VASCULAR SURGERY, 2011, 53 (03) :774-784
[5]   Bone marrow grafts restore cerebral blood flow and blood brain barrier in stroke rats [J].
Borlongan, CV ;
Lind, JG ;
Dillon-Carter, O ;
Yu, GL ;
Hadman, M ;
Cheng, C ;
Carroll, J ;
Hess, DC .
BRAIN RESEARCH, 2004, 1010 (1-2) :108-116
[6]   Decreasing intracellular superoxide corrects defective ischemia-induced new vessel formation in diabetic mice [J].
Ceradini, Daniel J. ;
Yao, Dachun ;
Grogan, Raymon H. ;
Callaghan, Matthew J. ;
Edelstein, Diane ;
Brownlee, Michael ;
Gurtner, Geoffrey C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (16) :10930-10938
[7]   Circulating endothelial progenitor cells and cellular membrane microparticles in db/db diabetic mouse: possible implications in cerebral ischemic damage [J].
Chen, Ji ;
Chen, Shuzhen ;
Chen, Yusen ;
Zhang, Cheng ;
Wang, Jinju ;
Zhang, Wenfeng ;
Liu, Gang ;
Zhao, Bin ;
Chen, Yanfang .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2011, 301 (01) :E62-E71
[8]   Ischemia-induced brain damage is enhanced in human renin and angiotensinogen double-transgenic mice [J].
Chen, Shuzhen ;
Li, Guangze ;
Zhang, Wenfeng ;
Wang, Jinju ;
Sigmund, Curt D. ;
Olson, James E. ;
Chen, Yanfang .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2009, 297 (05) :R1526-R1531
[9]   Effects of rapamycin on number activity and eNOS of endothelial progenitor cells from peripheral blood [J].
Chen, TG ;
Chen, JZ ;
Wang, XX .
CELL PROLIFERATION, 2006, 39 (02) :117-125
[10]   High glucose impairs early and late endothelial progenitor cells by modifying nitric oxide-related but not oxidative stress-mediated mechanisms [J].
Chen, Yung-Hsiang ;
Lin, Shing-Jong ;
Lin, Feng-Yen ;
Wu, Tao-Cheng ;
Tsao, Chen-Rong ;
Huang, Po-Hsun ;
Liu, Po-Len ;
Chen, Yuh-Lien ;
Chen, Jaw-Wen .
DIABETES, 2007, 56 (06) :1559-1568