Evaluation of hsa-miR-۷۶۶-۵p as a new regulator of mitochondrial apoptosis pathway and cardiomyocyte differentiation of Human embryonic stem cells (hESCs)

Publish Year: 1399
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:

CIGS16_394

تاریخ نمایه سازی: 14 اردیبهشت 1400

Abstract:

Background and Aim: miRNAs are small non coding mediator RNAs with potential role in development, cellular proliferation, differentiation, and apoptosis. These agnets can be used as new regulator of mitochondrial apoptosis pathway. The aim of this study is examination of the role of hsa-miR-۷۶۶-۵p during the apoptosis and cardiomyocyte differentiation of Human embryonic stem cells (hESCs).Results: Flow cytometry and MTT assay indicated cell death reduction and viability elevation effect of hsa-miR-۷۶۶ in SW۴۸۰ cells after its overexpression. Endogenous expression of hsa-miR-۷۶۶ during the course of human embryonic stem cells (hESCs) differentiation into cardiomyocytes revealed an inverse expression status of this miRNA with BOK. However, the expression of this miRNA was inversely related to BAX and BAK for some time points of differentiation.Conclusion: Based on this study, the involvement of hsa-miR-۷۶۶ in regulation of mitochondrial apoptosis pathway was approved.

Authors

Hadi Zare Zardini

Hematology and Oncology Research Center, Shahid Sadoughi University of Medical Sciences and Health Services,Yazd, Iran

Hossein Soltaninejad

Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Sadat Dokaneheifard

Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Parisa Ghiasi

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Bahram M. Soltani

Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Hossein Baharvand

Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR.