Delayed transplantation of human neural precursor cells improves outcome from focal cerebral ischemia in aged rats

被引:58
作者
Jin, Kunlin [1 ]
Mao, XiaoOu [1 ]
Xie, Lin [1 ]
Greenberg, Rose B. [1 ]
Peng, Botao [1 ]
Moore, Alexander [1 ]
Greenberg, Maeve B. [1 ]
Greenberg, David A. [1 ]
机构
[1] Buck Inst Age Res, Novato, CA 94945 USA
关键词
brain; ischemia; neural precursor; stroke; transplant; PROMOTES FUNCTIONAL RECOVERY; ENDOTHELIAL GROWTH-FACTOR; STEM-CELLS; DENTATE GYRUS; STROKE MODEL; ADULT-RAT; BRAIN; NEUROGENESIS; PROLIFERATION; INFARCTION;
D O I
10.1111/j.1474-9726.2010.00638.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P>Neural precursor cell (NPC) transplantation may have a role in restoring brain function after stroke, but how aging might affect the brain's receptivity to such transplants is unknown. We reported previously that transplantation of human embryonic stem cell (hESC)-derived NPCs together with biomaterial (Matrigel) scaffolding into the brains of young adult Sprague-Dawley rats 3 weeks after distal middle cerebral artery occlusion (MCAO) reduced infarct volume and improved neurobehavioral performance. In this study, we compared the effect of NPC and Matrigel transplants in young adult (3-month-old) and aged (24-month-old) Fisher 344 rats from the National Institute on Aging's aged rodent colony. Distal MCAO was induced by electrocoagulation, and hESC-derived NPCs were transplanted into the infarct cavity 3 weeks later. Aged rats developed larger infarcts, but infarct volume and performance on the cylinder and elevated body swing tests, measured 6-8 weeks post-transplant, were improved by transplantation. We conclude that advanced age does not preclude a beneficial response to NPC transplantation following experimental stroke.
引用
收藏
页码:1076 / 1083
页数:8
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