4.1 Article

The Extracts of Human Fetal Brain Induce the Differentiation of Human Umbilical Cord Mesenchymal Stem Cells into Dopaminergic Neuron Containing Cells

Journal

CELLULAR REPROGRAMMING
Volume 22, Issue 5, Pages 254-261

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/cell.2020.0029

Keywords

EHFBT; hUCMSCs; dopaminergic neuron-like cells; Parkinson's disease

Funding

  1. Project of Science and Technology Department of Henan Province [162102310493, 162102210117]
  2. Key Project of Science and Technology Research of Henan Provincial Education Department [18A180029, 19A180027]
  3. National Natural Science Foundation of China [81671619, U1804186]
  4. National Undergraduate Training Programs for Innovation and Entrepreneurship [201510472013]

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Mesenchymal stem cells (MSCs) have the potential to differentiate into neuron-like cells, which may provide a new strategy for the clinical treatment of neurodegenerative diseases such as Parkinson's disease (PD). However, the application of MSCs in the patients is still limited as the reason of efficiency and safety of transplantation. The aim of this study is to develop a new method and induce human umbilical cord MSCs (hUCMSCs) into neuron-like cells. Results from flow cytometry indicate that the isolated MSCs from hUCMSCs exhibited a typical phenotype of adult stem cells and express CD44, CD54, CD73, CD90, CD105, CD166, and HLA-ABC. Furthermore, the induced cells from hUCMSCs could spontaneously express different neural cell markers [neuron-specific enolase (NSE) and glial fibrillary acidic protein (GFAP)], even transcription factors related to dopaminergic neuron's development (Nurr1, Wnt-1, and En-1). Moreover, after treatment of EHFBT (extracts of human fetal brain tissue), hUCMSCs can express neuronal markers such as Nestin, LIM homeobox transcription factor 1 beta (LMX1B), dopamine beta hydroxylase (DBH) , and dopamine transporter (DAT). In summary, a method that can induce hUCMSCs into dopaminergic neuron containing cells is establishedin vitroby the treatment of EHFBT. This would provide us a new cell source for PD in clinical treatment in the future.

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