Chinese Journal of Tissue Engineering Research ›› 2017, Vol. 21 ›› Issue (1): 6-12.doi: 10.3969/j.issn.2095-4344.2017.01.002

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Influence of apelin on survival and vascularization potential of bone marrow mesenchymal stem cells under hypoxic and ischemic conditions

Hou Jing-ying, Wang Lei, Zhong Ting-ting, Zhou Chang-qing, Guo Tian-zhu, Long Hui-bao, Wu Quan-hua, Zheng Shao-xin, Wu Hao, Wang Tong   

  1. Department of Emergency, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China
  • Revised:2016-11-28 Online:2017-01-08 Published:2017-03-15
  • Contact: Wang Tong, M.D., Doctoral supervisor, Professor, Chief physician, Researcher, Department of Emergency, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China
  • About author:Hou Jing-ying, Master, Attending physician, Department of Emergency, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China
  • Supported by:

    the National Natural Science Foundation of China, No. 81070125, 81270213, 81670306; the Scientific Plan Projects of Guangdong Province, No. 2014A020211002, 2010B031600032; Fundamental Research Funds for the Universities for Young Teachers Cultivation in Sun Yat-sen University, No. 13ykzd16; the Medical Science Research Fund of Guangdong Province, No. A2016264

Abstract:

BACKGROUND: Our previous work demonstrated that bone marrow mesenchymal stem cells (BMSCs) transplantation could improve cardiac function in rats with myocardial infarction. However, the overall efficacy was not satisfactory. The implanted cells presented a low survival rate and newly formed vascular-like structures were sparse in the local infarct tissues.
OBJECTIVE: To observe the influence of putative receptor protein related to the angiotensin receptor AT1 endogenous ligand (apelin) on the survival and vascularization potential of BMSCs in hypoxic and ischemic conditions and to investigate relevant mechanisms.
METHODS: The bone marrow mesenchymal stem cells were obtained and cultured in vitro with or without apelin-13
(5 μmol/L) stimulation under hypoxic-ischemic condition (serum-free medium, 1% O2) for 24 hours, or cultured under normoxia (complete culture medium, 20% O2) as a negative control during the whole process. All the experimental groups were further co-cultured with human umbilical vein endothelial cells to promote vascular differentiation for another 6 hours. Cell proliferation, apoptosis, and vascular density were assessed and the expression of vascular endothelial growth factor was detected using western blot assay thereafter.
RESULTS AND CONCLUSION: Compared with the BMSCs group, BMSCs+apelin group presented more rapid cell growth, higher proliferation rate, and lower apoptosis percentage under normoxic and hypoxic conditions. In the BMSCs+apelin group, a larger number of vascular branches formed on matrigel under normoxic and hypoxic-ischemic conditions; and the expression of vascular endothelial growth factor was significantly enhanced. These findings suggest that apelin could effectively promote BMSCs survival and vascularization under hypoxic-ischemic conditions in vitro. It might function via upregulating the expression of vascular endothelial growth factor.

 

 

Key words: Bone Marrow, Mesenchymal Stem Cells, Receptor, Angiotensin, Type 1, Ligands, Cell Proliferation, Apoptosis, Cardiovascular Physiological Processes, Tissue Engineering

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