Literature DB >> 28702926

The stability evaluation of mesenchymal stem cells differentiation toward endothelial cells by chemical and mechanical stimulation.

Elham Hasanzadeh1,2, Ghassem Amoabediny3,4, Nooshin Haghighipour5, Nasim Gholami2,6, Javad Mohammadnejad2, Shahrokh Shojaei7, Nasim Salehi-Nik8,6.   

Abstract

Adipose-derived mesenchymal stem cells (ADSCs) are adult multipotent cells able to differentiate into several cell lineages. Vascular endothelial growth factor (VEGF) and the shear stress associated with blood flow are considered as the most important chemical and mechanical cues that play major roles in endothelial differentiation. However, the stability of endothelial-specific gene expression has not been completely addressed yet. ADSCs in passage 3 were cultured inside the tubular silicon tubes and then exposed to VEGF or shear stress produced in a perfusion bioreactor. To investigate the differentiation, the expression levels of Flk-1, von Willebrand factor (vWF), and vascular endothelial-cadherin (VE-cadherin) were studied using Real-Time PCR. For studying the endothelial differentiation stability, mRNA levels of the genes were evaluated in certain time intervals after completion of the tests so as to determine whether the expression level of each gene in different time points was stable and remained constant or not. Application of VEGF and shear stress caused an elevation in endothelial cells' specific genes. Although there are some changes following the days after application of mechanical and chemical stimuli, the gene expression results depicted significantly higher gene expression between sequential chemically and mechanically incited groups. In conclusion, stress alone can be a differentiating factor, by itself. Our results verified the efficient stable differentiation ability of the chemical and mechanical factors.

Entities:  

Keywords:  Differentiation; Endothelial cell; Shear stress; Stem cell

Mesh:

Substances:

Year:  2017        PMID: 28702926     DOI: 10.1007/s11626-017-0165-y

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol Anim        ISSN: 1071-2690            Impact factor:   2.416


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