Chimerization of Astroglial Population in the Lumbar Spinal Cord after Mesenchymal Stem Cell Transplantation Prolongs Survival in a Rat Model of Amyotrophic Lateral Sclerosis

被引:76
作者
Boucherie, Cedric [1 ,2 ,3 ]
Schaefer, Sabrina [1 ,2 ,3 ]
Lavand'homme, Patricia [4 ]
Maloteaux, Jean-Marie [1 ,2 ]
Hermans, Emmanuel [1 ,2 ]
机构
[1] Catholic Univ Louvain, Lab Expt Pharmacol, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Inst Neurosci, INES, B-1200 Brussels, Belgium
[3] European Grad Sch Neurosci EURON, Maastricht, Netherlands
[4] Catholic Univ Louvain, Lab Anesthesiol, B-1200 Brussels, Belgium
关键词
astrocytes; glial differentiation; mesenchymal stem cells; ALS; MOTOR-NEURON DEGENERATION; TRANSGENIC MOUSE MODEL; WILD-TYPE MICROGLIA; DISEASE PROGRESSION; GLUTAMATE TRANSPORTER; FAMILIAL ALS; CEREBROSPINAL-FLUID; PARKINSONS-DISEASE; MULTIPLE-SCLEROSIS; EXTEND SURVIVAL;
D O I
10.1002/jnr.22038
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adult mesenchymal stem cells (MSCs) exhibit neuroprotective properties when introduced into the degenerating central nervous system through different putative mechanisms including secretion of growth factors and transdifferentiation. In the present study, we injected MSCs into the cerebrospinal fluid of symptomatic hSOD1(G93A) rats, a transgenic animal model of familial amyotrophic lateral sclerosis (ALS) expressing a mutated form of the human superoxide dismutase. MSCs were found to infiltrate the nervous parenchyma and migrate substantially into the ventral gray matter, where motor neurons degenerate. Even though overall astrogliosis was not modified, MSCs differentiated massively into astrocytes at the site of degeneration. The intrathecal delivery of MSCs and the subsequent generation of healthy astrocytes at symptomatic stage decreased motor neuron loss in the lumbar spinal cord, preserving motor functions and extending the survival of hSOD1(G93A) rats. This neuroprotection was correlated with decreased inflammation, as shown by the lower proliferation of microglial cells and the reduced expressiontion of COX-2 and NOX-2. Together, these data highlight the protective capacity of adult MSC-derived astrocytes when grafted into the central nervous system and illustrate an attractive strategy to target excessive inflammation in ALS. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2034 / 2046
页数:13
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