Remyelination after Lysophosphatidyl Choline-Induced Demyelination Is Stimulated by Bone Marrow Stromal Cell-Derived Oligoprogenitor Cell Transplantation

• Published in: Cells, tissues, organs Vol. 200; no. 5; pp. 300 - 306
• Main Authors: Nazm Bojnordi, M., Ghasemi, H.H., Akbari, E.
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.01.2014
• Subjects: Animals; Bone Marrow - metabolism; Cell Differentiation - physiology; Cells, Cultured; Demyelinating Diseases - chemically induced; Demyelinating Diseases - therapy; Disease Models, Animal; Lysophosphatidylcholines - toxicity; Mesenchymal Stem Cell Transplantation; Mesenchymal Stromal Cells - cytology; Myelin Sheath - metabolism; Nerve Regeneration - physiology; Original Paper; Rats, Sprague-Dawley; Bone marrow stromal cell; Multiple sclerosis; Demyelination model; Oligoprogenitor cell; Cell transplantation
• ISSN: 1422-6405; 1422-6421
• DOI: 10.1159/000437350

Bone marrow stromal cells (BMSCs) are a desirable cell source that may be useful for the treatment of neurodegenerative diseases given their capacity to differentiate into various types of cells. The current study aimed to investigate whether oligoprogenitor cell (OPC)-derived BMSCs have therapeutic benefits in an animal model of local demyelination. BMSCs were transdifferentiated into OPCs using a defined culture medium supplemented with a combination of inducers. The differentiation capacity of the BMSCs was evaluated at the end of the induction phase by assessing the expression levels of the glial-specific markers oligodendrocyte transcription factor 2 and O4 surface antigen. Local demyelination was induced in the corpus callosum of adult female rats via direct injection of lysophosphatidylcholine (LPC) followed by engraftment of BMSC-generated OPCs. The rats were divided into sham control, vehicle control, and cell-transplanted groups. The changes in the extent of demyelination and the robustness of the remyelination event were assessed using Luxol Fast Blue staining and immunohistochemical analysis 1 week after LPC injection and 2 weeks after cell transplantation. Consequently, transplantation of OPCs into the demyelinated corpus callosum model resulted in differentiation of the cells into mature oligodendrocytes that were immunopositive for myelin basic protein. Furthermore, OPC transplantation mitigated demyelination and augmented remyelination relative to controls. These findings suggest that BMSC-derived OPCs can be utilized in therapeutic approaches for the management of demyelination-associated diseases such as multiple sclerosis.