Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells

Objective Ghrelin is a peptide which has a proliferative and antiapoptotic effect in many cells including bone marrow stromal cells (BMSCs). Homeobox protein B4 (HOXB4) is a transcription factor involved in stem cell regeneration and survival. The aim of the study was to find out the effect of ghre...

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Main Authors: Alireza Abdanipour, Behnaz Shahsavandi, Mohsen Alipour, Hadi Feizi
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2018-04-01
Series:Cell Journal
Subjects:
Online Access:http://celljournal.org/journal/article/19671/download
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author Alireza Abdanipour
Behnaz Shahsavandi
Mohsen Alipour
Hadi Feizi
author_facet Alireza Abdanipour
Behnaz Shahsavandi
Mohsen Alipour
Hadi Feizi
author_sort Alireza Abdanipour
collection DOAJ
description Objective Ghrelin is a peptide which has a proliferative and antiapoptotic effect in many cells including bone marrow stromal cells (BMSCs). Homeobox protein B4 (HOXB4) is a transcription factor involved in stem cell regeneration and survival. The aim of the study was to find out the effect of ghrelin on Hoxb4 expression in BMSCs. Materials and Methods In this experimental study, rat BMSCs were cultivated in Dulbecco’s Modified Eagle Medium (DMEM). Passage three BMSCs were treated with ghrelin 100 μM for 48 hours. Real-time polymerase chain reaction (PCR) was carried out from the untreated BMSCs (B), BMSCs treated with 125 µM H2O2 (BH), BMSCs treated with 100 µM ghrelin then 125 µM H2O2(BGH) and BMSCs treated with 100 µM ghrelin (BG) groups. For immunofluorescence, cells were incubated with an anti-HOXB4 monoclonal antibody. Primary antibodies were visualized using the Fluorescein isothiocyanate (FITC) method. All data are presented as mean ± SEM and P<0.05 was considered as statistical significant. Results Hoxb4 expression significantly increased in the BG compared with BH and BGH groups. Furthermore, 100 µM ghrelin, increased the mean of HOXB4 positive immunoreactive cells compared to the BH group. Conclusion Ghrelin probably enhances proliferation and viability of BMSCs through Hoxb4 upregulation. However, the signaling pathway and other biological outcomes of this effect should be elucidated in different stem cells.
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spelling doaj.art-d08db5d2362149788c2b61d3752da8cf2022-12-22T02:22:08ZengRoyan Institute (ACECR), TehranCell Journal2228-58062228-58142018-04-0120218318710.22074/cellj.2018.5164Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal CellsAlireza Abdanipour0Behnaz Shahsavandi1Mohsen Alipour2Hadi Feizi3Department of Anatomical Sciences, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Physiology and Pharmacology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Physiology and Pharmacology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Physiology and Pharmacology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, IranObjective Ghrelin is a peptide which has a proliferative and antiapoptotic effect in many cells including bone marrow stromal cells (BMSCs). Homeobox protein B4 (HOXB4) is a transcription factor involved in stem cell regeneration and survival. The aim of the study was to find out the effect of ghrelin on Hoxb4 expression in BMSCs. Materials and Methods In this experimental study, rat BMSCs were cultivated in Dulbecco’s Modified Eagle Medium (DMEM). Passage three BMSCs were treated with ghrelin 100 μM for 48 hours. Real-time polymerase chain reaction (PCR) was carried out from the untreated BMSCs (B), BMSCs treated with 125 µM H2O2 (BH), BMSCs treated with 100 µM ghrelin then 125 µM H2O2(BGH) and BMSCs treated with 100 µM ghrelin (BG) groups. For immunofluorescence, cells were incubated with an anti-HOXB4 monoclonal antibody. Primary antibodies were visualized using the Fluorescein isothiocyanate (FITC) method. All data are presented as mean ± SEM and P<0.05 was considered as statistical significant. Results Hoxb4 expression significantly increased in the BG compared with BH and BGH groups. Furthermore, 100 µM ghrelin, increased the mean of HOXB4 positive immunoreactive cells compared to the BH group. Conclusion Ghrelin probably enhances proliferation and viability of BMSCs through Hoxb4 upregulation. However, the signaling pathway and other biological outcomes of this effect should be elucidated in different stem cells.http://celljournal.org/journal/article/19671/download Bone Marrow Stromal CellsGhrelinHOXB4Rat
spellingShingle Alireza Abdanipour
Behnaz Shahsavandi
Mohsen Alipour
Hadi Feizi
Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
Cell Journal
Bone Marrow Stromal Cells
Ghrelin
HOXB4
Rat
title Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
title_full Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
title_fullStr Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
title_full_unstemmed Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
title_short Ghrelin Upregulates Hoxb4 Gene Expression in Rat Bone Marrow Stromal Cells
title_sort ghrelin upregulates hoxb4 gene expression in rat bone marrow stromal cells
topic Bone Marrow Stromal Cells
Ghrelin
HOXB4
Rat
url http://celljournal.org/journal/article/19671/download
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AT behnazshahsavandi ghrelinupregulateshoxb4geneexpressioninratbonemarrowstromalcells
AT mohsenalipour ghrelinupregulateshoxb4geneexpressioninratbonemarrowstromalcells
AT hadifeizi ghrelinupregulateshoxb4geneexpressioninratbonemarrowstromalcells