AKT family and miRNAs expression in IL-2-induced CD4+T cells

Objective(s): Study of non-coding RNAs is considerable to elucidate principal biological questions or design new therapeutic strategies. miRNAs are a group of non-coding RNAs that their functions in PI3K/AKT signaling and apoptosis pathways after T cell activation is not entirely clear. Herein, miRN...

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Main Authors: Najmeh Ranji, Majid Sadeghizadeh, Morteza Karimipoor, Mohammad Ali Shokrgozar, Reza Ebrahimzadeh-Vesal
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2014-11-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
Online Access:http://ijbms.mums.ac.ir/pdf_3740_e90652b47de04422958e2d67863ce080.html
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author Najmeh Ranji
Majid Sadeghizadeh
Morteza Karimipoor
Mohammad Ali Shokrgozar
Reza Ebrahimzadeh-Vesal
author_facet Najmeh Ranji
Majid Sadeghizadeh
Morteza Karimipoor
Mohammad Ali Shokrgozar
Reza Ebrahimzadeh-Vesal
author_sort Najmeh Ranji
collection DOAJ
description Objective(s): Study of non-coding RNAs is considerable to elucidate principal biological questions or design new therapeutic strategies. miRNAs are a group of non-coding RNAs that their functions in PI3K/AKT signaling and apoptosis pathways after T cell activation is not entirely clear. Herein, miRNAs expression and their putative targets in the mentioned pathways were studied in the activated CD4+T cells. Materials and Methods: Herein, proliferation rate and IL-2 secretion were measured in treated and untreated cells by IL-2. Putative targets of up-regulated miRNAs were predicted by bioinformatics approaches in the apoptotic and PI3K/AKT signaling pathways. Then the expression of two putative targets was evaluated by quantitative RT-PCR.  Results: Proliferation rate of treated cells by IL-2 increased in a dose- and time- dependent manner. Naive and activated CD4+T cells  induced by different dose of IL-2 secreted abundant amounts of IL-2. Also, in IL-2 un-induced cells (IL-2 depleted cells) after 3 days, decrease of proliferation has been shown. In silico analysis predicted putative targets of up-regulated miRNAs such as AKT1, AKT3 and apoptotic genes in the activated cells induced or un-induced by IL-2. Decrease of AKT3 was shown by Q-RT-PCR as a potential target of miRNAs overexpressed in IL-2 depleted cells. But there was no significant difference in AKT1 expression in two cell groups. Conclusion:  Our analysis suggests that decrease of AKT3 was likely controlled via up-regulation of specific miRNAs in IL-2 depleted cells. Also it seems that miRNAs play role in induction of different apoptosis pathways in IL-2 induced and un-induced cells.
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spelling doaj.art-da049f08b58e4e0781d3592c47f069542022-12-22T02:59:13ZengMashhad University of Medical SciencesIranian Journal of Basic Medical Sciences2008-38662008-38742014-11-0117118868943740AKT family and miRNAs expression in IL-2-induced CD4+T cellsNajmeh Ranji0Majid Sadeghizadeh1Morteza Karimipoor2Mohammad Ali Shokrgozar3Reza Ebrahimzadeh-Vesal4Department of Genetics, College of Science, Rasht Branch, Islamic Azad University, Rasht, IranDepartment of Genetics, School of Biological Sciences, Tarbiat Modares University, Tehran, IranDepartment of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, IranNational Cell Bank of Iran, Pasteur Institute of Iran, Tehran, IranDepartment of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, IranObjective(s): Study of non-coding RNAs is considerable to elucidate principal biological questions or design new therapeutic strategies. miRNAs are a group of non-coding RNAs that their functions in PI3K/AKT signaling and apoptosis pathways after T cell activation is not entirely clear. Herein, miRNAs expression and their putative targets in the mentioned pathways were studied in the activated CD4+T cells. Materials and Methods: Herein, proliferation rate and IL-2 secretion were measured in treated and untreated cells by IL-2. Putative targets of up-regulated miRNAs were predicted by bioinformatics approaches in the apoptotic and PI3K/AKT signaling pathways. Then the expression of two putative targets was evaluated by quantitative RT-PCR.  Results: Proliferation rate of treated cells by IL-2 increased in a dose- and time- dependent manner. Naive and activated CD4+T cells  induced by different dose of IL-2 secreted abundant amounts of IL-2. Also, in IL-2 un-induced cells (IL-2 depleted cells) after 3 days, decrease of proliferation has been shown. In silico analysis predicted putative targets of up-regulated miRNAs such as AKT1, AKT3 and apoptotic genes in the activated cells induced or un-induced by IL-2. Decrease of AKT3 was shown by Q-RT-PCR as a potential target of miRNAs overexpressed in IL-2 depleted cells. But there was no significant difference in AKT1 expression in two cell groups. Conclusion:  Our analysis suggests that decrease of AKT3 was likely controlled via up-regulation of specific miRNAs in IL-2 depleted cells. Also it seems that miRNAs play role in induction of different apoptosis pathways in IL-2 induced and un-induced cells.http://ijbms.mums.ac.ir/pdf_3740_e90652b47de04422958e2d67863ce080.htmlAKT3 IL-2 induction In silico analysis miRNAs
spellingShingle Najmeh Ranji
Majid Sadeghizadeh
Morteza Karimipoor
Mohammad Ali Shokrgozar
Reza Ebrahimzadeh-Vesal
AKT family and miRNAs expression in IL-2-induced CD4+T cells
Iranian Journal of Basic Medical Sciences
AKT3 IL-2 induction In silico analysis miRNAs
title AKT family and miRNAs expression in IL-2-induced CD4+T cells
title_full AKT family and miRNAs expression in IL-2-induced CD4+T cells
title_fullStr AKT family and miRNAs expression in IL-2-induced CD4+T cells
title_full_unstemmed AKT family and miRNAs expression in IL-2-induced CD4+T cells
title_short AKT family and miRNAs expression in IL-2-induced CD4+T cells
title_sort akt family and mirnas expression in il 2 induced cd4 t cells
topic AKT3 IL-2 induction In silico analysis miRNAs
url http://ijbms.mums.ac.ir/pdf_3740_e90652b47de04422958e2d67863ce080.html
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