Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (32): 5148-5154.doi: 10.3969/j.issn.2095-4344.2015.32.012

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Wnt signaling promotes the differentiation of adipose mesenchymal stem cells into type II alveolar epithelial cells

Shi Li1, Jie Jing2, Wang Fang3, Zhao Dan2, Zhang Xiu-fang2, Peng Li-ping2   

  1. 1Department of Emergency, the Second Branch, the First Affiliated Hospital of Jilin University, Changchun 130033, Jilin Province, China; 
    2Department of Respiratory Medicine, the First Affiliated Hospital of Jilin University, Changchun 130021, Jilin Province, China; 
    3Department of Endoscopy Center, the China-Japan Union Hospital of Jilin University, Changchun 130033, Jilin Province, China
  • Online:2015-08-06 Published:2015-08-06
  • Contact: Peng Li-ping, M.D., Professor, Doctoral supervisor, Department of Respiratory Medicine, the First Affiliated Hospital of Jilin University, Changchun 130021, Jilin Province, China
  • About author:Shi Li, Senior nurse, Department of Emergency, the Second Branch, the First Affiliated Hospital of Jilin University, Changchun 130033, Jilin Province, China
  • Supported by:

    the National Natural Science Foundation of China, No. 81072368; the Funding Project of Jilin Provincial Department of Health, No. 2012Z053

Abstract:

BACKGROUND: Ability of adipose mesenchymal stem cells differentiating into type II alveolar epithelial cells and the regulating mechanism have not been fully elucidated.
OBJECTIVE: To study the ability of adipose mesenchymal stem cells differentiating into type II alveolar epithelial cells in vitro and the function of Wnt pathway in the regulation of differentiation.
METHODS: Adipose mesenchymal stem cells were obtained from fat tissue of rats and identified by flow cytometry. The adipose mesenchymal stem cells were divided into control group, small airway growth medium (SAGM) group and Wnt3a group. Control group was treated with normal DMEM medium; SAGM and Wnt3a groups were both treated with small airway growth medium, and additionally, the Wnt3a group was treated with Wnt3a, a Wnt signaling pathway agonist. After 10 days, quantitative RT-PCR and immunofluorescence detection were used to test the expression of surfactant proteins B, C, D, type II alveolar epithelial markers. Phosphorylated β-catenin and GSK-3β were detected using western blot after 5 and 10 days of induction.
RESULTS AND CONCLUSION: Adipose mesenchymal stem cells with high purity could be successfully isolated from the adipose tissue of rats, and expressed CD44 and CD29, but not CD11b and CD45. After SAGM treatment, protein and mRNA expressions of surfactant proteins B, C, D were all increased in adipose mesenchymal stem cells (P < 0.01), indicating the ability of adipose mesenchymal stem cells to be induced into type II epithelial cells. Surfactant proteins B, C, D expressions at protein and mRNA levels were significantly higher in the Wnt3a group than the SAGM group (P < 0.01). During the induction progress, the expression of phosphorylated β-catenin gradually increased, but GSK-3β expression gradually decreased in the Wnt3a group (P < 0.01). These findings indicate that Wnt signaling pathways are involved in differentiation of adipose mesenchymal stem cells into type II alveolar epithelial cells.

 

Key words: Stem Cells, Tissue Engineering, Mesenchymal Stem Cells, Pulmonary Alveoli

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