Author/Authors :
Marzban, Mohsen Department of Neuroscience - School of Advanced Technologies in Medicine - Tehran University of Medical Sciences, Tehran, Iran , Mousavizadeh, Kazem Cellular and Molecular Research Center and Department of Molecular Medicine - Faculty of Advanced Technologies in Medicine - Iran University of Medical Sciences, Tehran, Iran , Bakhshayesh, Masoomeh Cellular and Molecular Research Center and Department of Molecular Medicine - Faculty of Advanced Technologies in Medicine - Iran University of Medical Sciences, Tehran, Iran , Vousooghi, Nasim Department of Neuroscience - School of Advanced Technologies in Medicine - Tehran University of Medical Sciences, Tehran, Iran , Vakilzadeh, Gelareh Department of Neuroscience - School of Advanced Technologies in Medicine - Tehran University of Medical Sciences, Tehran, Iran , Torkaman-Boutorabi, Anahita Department of Neuroscience - School of Advanced Technologies in Medicine - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Background: Bone marrow mesenchymal stem cells (BM-MSCs) elicit neuroprotective effects, and their repair
ability has been investigated in different experimental models. We aimed to investigate the effect of multiple i.p.
BM-MSCs injections in the cuprizone model of multiple sclerosis in mice. Methods: Adult male C57BL/6 mice (n =
40) were fed a regular diet or a diet containing cuprizone (0.2% w/w) for six weeks. Bone marrow samples were
taken from patients with spinal cord injury. BM-MSCs (2 × 106 in 1 milliliter medium) were administered
intraperitoneally for two consecutive weeks at the end of the forth weeks of cuprizone administration. Animals (n =
12) were perfused with 10% paraformaldehyde at the end of sixth week. The brains were sectioned coronally in 6-
8-μm thickness (-2.3 to 1.8 mm from bregma). The sections were stained by luxol fast blue-cresyl violet, and
images were captured via a microscope. Demyelination ratio was estimated in corpus callosum in a blind manner.
A quantitative real-time PCR was used to measure the myelin basic protein gene expression at sixth week.
Results: Histologically, cuprizone induced demyelination in the corpus callosum. Demyelinated area was
diminished in the corpus callosum of cell-administered group. Cuprizone could decrease myelin-binding protein
mRNAs expression in corpus callosum, which was significantly recovered after BM-MSCs injections. Conclusion:
Our data indicated a remyelination potency of multiple i.p. BM-MSCs in the cuprizone model of multiple sclerosis
in mice.
Keywords :
Multiple sclerosis , Mice , Mesenchymal stem cells , Cuprizone