Embryonic stem cells promote motor recovery and affect inflammatory cell infiltration in spinal cord injured mice

被引:60
作者
Bottai, Daniele [1 ,2 ]
Cigognini, Daniela [1 ]
Madaschi, Laura [1 ]
Adami, Raffaella [1 ]
Nicora, Emanuela [1 ]
Menarini, Mauro [3 ]
Di Giulio, Anna Maria [1 ]
Gorio, Alfredo [1 ,2 ]
机构
[1] Univ Milan, Fac Med, Dept Med Surg & Dent, I-20142 Milan, Italy
[2] Clin Pharmacol IRCCS Humanitas, I-20089 Milan, Italy
[3] Fdn Montecatone Onlus, I-40026 Imola, BO, Italy
关键词
i.v. cell injection; confocal microscopy; inflammation; stem cells; traumatic spinal cord injury; ADULT-RAT; LOCOMOTOR RECOVERY; FUNCTIONAL RECOVERY; NEUROTROPHIC FACTOR; NEURAL PRECURSORS; NEURONS; TRANSPLANTATION; OLIGODENDROCYTES; DIFFERENTIATE; DEGENERATION;
D O I
10.1016/j.expneurol.2010.01.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The purpose of this study was to determine the fate and the effects of undifferentiated embryonic stem cells (ESCs) in mice after contusive lesion of the spinal cord (SCI). Reproducible traumatic lesion to the cord was performed at 18 level by means of the Infinite Horizon Device, and was followed by intravenous injection of one million of undifferentiated ESCs through the tail vein within 2 h from the lesion. The ESCs-treated animals showed a significant improvement of the recovery of motor function 28 days after lesion, with an average score of 4.61 +/- 0.13 points of the Basso Mouse Scale (n=14), when compared to the average score of vehicle treated mice, 3.58 +/- 0.23 (n=10). The number of identified ESCs found at the lesion site was 0.6% of the injected cells at 1 week after transplantation, and further reduced to 0.04% at 1 month. It is, thus, apparent that the promoted hind-limb recovery cannot be correlated to a substitution of the lost tissue performed by the exogenous ESC. The extensive evaluation of production of several neuroprotective and inflammatory cytokines did not reveal any effect by ESC-treatment, but unexpectedly the number of invading macrophages and neutrophils was greatly reduced. This may explain the improved preservation of lesion site ventral myelin, at both 1 week (29 +/- 11%) and 1 month (106 +/- 14%) after injury. No teratoma formation was observed, although an inappropriate colonization of the sacral cord by differentiated nestin-and beta-tubulin III-positive ESCs was detected. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:452 / 463
页数:12
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