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Medical Science Monitor Basic Research

AmJCaseRep
MedSciTechnol

eISSN: 2329-0358

Effects of Reactive Oxygen Species on Differentiation of Bone Marrow Mesenchymal Stem Cells

Yao Shi, Yiwen Hu, Chen Lv, Guanjun Tu

Department of Orthopaedic Surgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China (mainland)

Ann Transplant 2016; 21:695-700

DOI: 10.12659/AOT.900463

Available online:

Published: 2016-11-14


#900463

BACKGROUND: The low differentiation rates for transplanted stem cells are challenging problems in spinal cord injury (SCI) treatment. Studies have demonstrated that the inhibition of the Notch1 pathway in bone marrow mesenchymal stem cells (BMSCs) contributed to the differentiation of these cells. Research findings that certain antioxidants induce BMSCs to differentiate into neuronal cells suggest that BMSC differentiation is related to the level of reactive oxygen species (ROS) in cells. This study aimed to define the effect of ROS on the differentiation of BMSCs.
MATERIAL AND METHODS: In this study, after BMSCs were induced with the antioxidant β-mercaptoethanol (β-ME), related proteins were analyzed by Western blotting and immunofluorescence. In order to find the role of ROS in the differentiation, DCFH-DA was used to detect ROS levels in antioxidant-treated BMSCs, H2O2-treated BMSCs, and normal BMSCs, and the expression levels of Notch1 and its downstream transcriptional suppressor Hes1 were analyzed.
RESULTS: Induced with β-ME, Western blotting and immunofluorescence revealed gradual increases in the expression of Nestin (a neural stem cell-specific protein) and neuron-specific enolase (NSE) but decreases in Notch1 expression. The expression levels of Notch1 and Hes1 were positively correlated with changes in ROS level.
CONCLUSIONS: These data suggest that the antioxidant-induced differentiation of BMSCs into neurons may be related to ROS-based regulation of the Notch1 signalling pathway.

Keywords: Cell Differentiation, mesenchymal stromal cells, Reactive Oxygen Species, Receptor, Notch1



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