AI Article Synopsis

  • The study investigates the neuroprotective effects of bone marrow mesenchymal stem cells (BM-MSCs) in a mouse model of multiple sclerosis using cuprizone, a chemical that induces demyelination.
  • BM-MSCs were injected intraperitoneally over two weeks after cuprizone treatment, and results showed a reduction in demyelination in the corpus callosum and improved myelin basic protein expression.
  • The findings suggest that BM-MSCs have potential for remyelination and may offer therapeutic benefits in conditions like multiple sclerosis.

Article 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 6 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058183PMC
http://dx.doi.org/10.29252/ibj.22.5.312DOI Listing

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