Volume 32, Issue 10 (January 2022)
Studies in Medical Sciences 2022, 32(10): 773-781 |
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Research code: 62233
Ethics code: IR.TBZMED.VCR.REC.1397.485
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Bandarian N, Rahbarghazi R, Mahdipour M, Ahmadi M, Rezabakhsh A, Haiaty S et al . INHIBITION OF WNT3A DIMINISHED ANGIOGENIC DIFFERENTIATION CAPACITY OF RAT CARDIAC PROGENITOR CELLS. Studies in Medical Sciences 2022; 32 (10) :773-781
URL: http://umj.umsu.ac.ir/article-1-5683-en.html
URL: http://umj.umsu.ac.ir/article-1-5683-en.html
Nasim Bandarian 
, Reza Rahbarghazi * 
, Mahdi Mahdipour , Mahdi Ahmadi , Aysa Rezabakhsh , Sanya Haiaty , Majid Khaksar
, Reza Rahbarghazi * , Mahdi Mahdipour , Mahdi Ahmadi , Aysa Rezabakhsh , Sanya Haiaty , Majid Khaksar
Department of Applied Cell Sciences, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran (Corresponding Author) , rezarahbardvm@gmail.com
Abstract: (2809 Views)
Background & Aims: Myocardial infarction is a leading cause of human mortality in industrialized and developing societies. Limited restorative ability of of cardiomyocytes after ischemic changes can causes extensive damage lead to prominent chronic heart failure. At present, the application of certain drugs is touted as one of the main available approaches to inhibit the spread of the lesion and to maintain the integrity of the myocardial tissue after infarction. Today, the transplantation of stem cells to restore structure and maintain heart function has opened new hopes for clinicians in human medicine. These cells accelerate the healing process by secreting a variety of factors and differentiation into varient cell lines, including vascular cells. Here, we investigated the inhibitory role of Wnt3a factor on the process of differentiation of rat cardiomyoblast (H9C2) to endothelial cells.
Materials & Methods: In this experimental study, rat cardiomyoblast (H9C2) were expanded in DMEM/HG and exposed to 10 µM LGK-974 (a Wnt3a inhibitor) for 48 hours. The viability of cells was determined using MTT method. The ability to differentiation into endothelial cells was assessed by measuring expression and protein levels of VE-Cadherin and vWF using real-time PCR and western blotting.
Results: The inhibition of Wnt3a in H9C2 cells could significantly reduce cell survival rate after 48 hours compared to the control cells (p<0.05). Based on data, expression and protein levels of VE-Cadherin and vWF were significantly diminished in group incubated with LGK-974
Conclusion: The inhibition of Wnt3a can suppress the angiogenic potential of rat cardio myoblasts
Materials & Methods: In this experimental study, rat cardiomyoblast (H9C2) were expanded in DMEM/HG and exposed to 10 µM LGK-974 (a Wnt3a inhibitor) for 48 hours. The viability of cells was determined using MTT method. The ability to differentiation into endothelial cells was assessed by measuring expression and protein levels of VE-Cadherin and vWF using real-time PCR and western blotting.
Results: The inhibition of Wnt3a in H9C2 cells could significantly reduce cell survival rate after 48 hours compared to the control cells (p<0.05). Based on data, expression and protein levels of VE-Cadherin and vWF were significantly diminished in group incubated with LGK-974
Conclusion: The inhibition of Wnt3a can suppress the angiogenic potential of rat cardio myoblasts
Type of Study: Research |
Subject:
قلب و عروق
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