Transplantation of hematopoietic stem cells: intra-arterial versus intravenous administration impacts stroke outcomes in a murine model

被引:21
作者
Kasahara, Yukiko
Yamahara, Kenichi
Soma, Toshihiro
Stern, David M.
Nakagomi, Takayuki
Matsuyama, Tomohiro
Taguchi, Akihiko
机构
[1] Inst Biomed Res & Innovat, Dept Regenerat Med Res, Kobe, Hyogo, Japan
[2] Natl Cerebral & Cardiovasc Ctr Res Inst, Dept Regenerat Med & Tissue Engn, Suita, Osaka, Japan
[3] Hyogo Coll Med, Dept Hematol, Nishinomiya, Hyogo, Japan
[4] Univ Tennessee, Knoxville, TN 37996 USA
[5] Hyogo Coll Med, Dept Neurogenesis & CNS Repair, Nishinomiya, Hyogo, Japan
基金
日本学术振兴会;
关键词
BONE-MARROW MONONUCLEAR; COLONY-STIMULATING FACTOR; FOCAL CEREBRAL-ISCHEMIA; ACUTE MYOCARDIAL-INFARCTION; THERAPEUTIC ANGIOGENESIS; BRAIN-INJURY; CORD BLOOD; INFUSION; DELIVERY; BIODISTRIBUTION;
D O I
10.1016/j.trsl.2016.04.003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Based on results of hematopoietic stem cell transplantation in animal models of stroke, clinical trials with hematopoietic stem cells administered intro-arterially or intravenously have been initiated in patients. Although intra-arterial injection is expected to deliver transplanted cells more directly to the ischemic tissue, the optimal route for enhancing clinical outcomes has not been identified in the setting of stroke. In this study, we compared the therapeutic potential of intro-arterial versus intravenous injection of bone marrow derived-mononuclear cells (BM-MNCs) and CD133-positive (CD133(+)) cells in a murine stroke model. We have found that intra-arterial injection of BM-MNCs exaggerates inflammation with accompanying loss of micro vascular structures in poststroke brain and no improvement in cortical function. In contrast, intravenous injection of BM-MNCs did not similarly enhance inflammation and improved cortical function. Our results indicate that the optimal route of cell transplantation can vary with different cell populations and highlight possible issues that might arise with intro-arterial cell administration for acute ischemic cerebrovascular disease.
引用
收藏
页码:69 / 80
页数:12
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