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http://dx.doi.org/10.17555/jvc.2021.38.6.261

Carboxymethyl Chitosan Promotes Migration and Inhibits Lipopolysaccharide-Induced Inflammatory Response in Canine Bone Marrow-Derived Mesenchymal Stem Cells  

Ryu, Ho-Sung (College of Veterinary Medicine, Kyungpook National University)
Ryou, Seong-Hwan (College of Veterinary Medicine, Kyungpook National University)
Jang, Min (College of Veterinary Medicine, Kyungpook National University)
Ku, Sae-Kwang (Department of Anatomy and Histology, College of Korean Medicine, Daegu Haany University)
Kwon, Young-Sam (College of Veterinary Medicine, Kyungpook National University)
Seo, Min-Soo (Laboratory Animal Center, Daegu-Gyeongbuk Medical Innovation Foundation)
Publication Information
Journal of Veterinary Clinics / v.38, no.6, 2021 , pp. 261-268 More about this Journal
Abstract
The study was conducted to evaluate the effects of carboxymethyl chitosan (CMC) on proliferation, migration, and lipopolysaccharide (LPS)-induced inflammatory response in canine bone marrow-derived mesenchymal stem cells (BMSCs). The proliferation and migration of BMSCs were examined after treatment with CMC. The effect of CMC on the mRNA expression of inflammatory cytokines, such as interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF)-α, IL-10, and transforming growth factor (TGF)-β, was also evaluated by reverse transcription polymerase chain reaction (RT-PCR). In the proliferation assay, no significant changes were found at all CMC concentrations compared with controls. The migration assay showed that CMC dose-dependently stimulated the migration of BMSCs in normal and LPS-treated conditions. RT-PCR showed that TNF-α and IL-10 expressions were suppressed in the BMSCs after CMC treatment. However, other genes were not affected. Taken together, CMC promoted BMSC migration and inhibited TNF-α and IL-10. Therefore, CMC may be possible to regulate wound healing when mesenchymal stem cells are applied in inflammatory diseases.
Keywords
chitosan; migration; inflammatory response; stem cells;
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