Dual-modality in vivo monitoring of subventricular zone stem cell migration and metabolism

被引:22
作者
Cicchetti, Francesca
Gross, Robert E.
Bulte, Jeff W. M.
Owen, Mary
Chen, Iris
Saint-Pierre, Martine
Wang, Xukui
Yu, Meixiang
Brownell, Anna-Liisa
机构
[1] CHU Laval, Ctr Rech & Neurosci, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Dept Med, Quebec City, PQ G1K 7P4, Canada
[3] Emory Univ, Sch Med, Dept Neurosurg, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Ctr Neurodegenerat Dis, Atlanta, GA 30322 USA
[5] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Dept Chem & Biomol Engn, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[7] Simmons Coll, Dept Biol, Boston, MA 02115 USA
[8] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
关键词
positron emission tomography (PET); magnetic resonance imaging (MRI); superparamagnetic iron oxide particles; transplantation; inflammation; dopamine;
D O I
10.1002/cmmi.138
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rat subventricular zone (SVZ) stem cells were labeled with superparamagnetic iron oxide particles (SPIO) to follow their fate and migratory potential with magnetic resonance imaging (MRI) and positron emission tomography (PET). Labeled cells were transplanted into either the right rostral migratory stream (RMS) or striatum of normal adult Sprague-Dawley rats and serially followed for 3 months. Minimal migration of the cells implanted into the striatum was observed after 3 weeks whereas SVZ cells implanted into the RMS migrated toward the olfactory bulb at I week post-transplantation. PET studies of glucose metabolism using F-18-FDG demonstrated enhanced glucose utilization in the striatum of transplanted animals. PET studies conducted 3 months after transplantation showed elevated accumulation of C-11-raclopride (dopamine receptor type 2) and C-11-CFT (dopamine transporter) binding in the striatal grafts. Implanted SVZ cells did not induce significant inflammation as identified by PET using C-11-PK11195, a ligand detecting activated microglia. Histological analysis identified viable SPIO-labeled cells (some of which were nestin-positive) 7 weeks post-transplantation, suggesting a prolonged presence of undifferentiated neural stem cells within transplants. In addition, double immunostaining for neuronal and asttocytic markers (NeuN and GFAP) indicated that differentiation into neuronal and astrocytic phenotypes also occurred. Thus, combining MRI and PET enables monitoring of cell migration and metabolism non-invasively in vivo for extended periods of time. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:130 / 138
页数:9
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