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Title: Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway

Abstract

Ghrelin is a 28-amino-acid peptide that acts as a natural endogenous ligand of the growth hormone secretagogue receptor (GHSR) and strongly stimulates the release of growth hormone from the hypothalamus–pituitary axis. Previous studies have identified the important physiological effects of ghrelin on bone metabolism, such as regulating proliferation and differentiation of osteoblasts, independent of GH/IGF-1 axis. However, research on effects and mechanisms of ghrelin on osteoblast apoptosis is still rare. In this study, we identified expression of GHSR in MC3T3-E1 cells and determined the effects of ghrelin on the apoptosis of osteoblastic MC3T3-E1 cells and the mechanism involved. Our data demonstrated that ghrelin inhibited the apoptosis of osteoblastic MC3T3-E1 cells induced by serum deprivation, as determined by terminal deoxynucleotidyl transferase-mediated deoxyribonucleotide triphosphate nick end-labeling (TUNEL) and ELISA assays. Moreover, ghrelin upregulated Bcl-2 expression and downregulated Bax expression in a dose-dependent manner. Our study also showed decreased activated caspase-3 activity under the treatment of ghrelin. Further study suggested that ghrelin stimulated the phosphorylation of ERK and AKT. Pretreatment of cells with the ERK inhibitor PD98059, PI3K inhibitor LY294002, and GHSR-siRNA blocked the ghrelin-induced activation of ERK and AKT, respectively; however, ghrelin did not stimulate the phosphorylation of p38 or JNK. PD90859,more » LY294002 and GHSR-siRNA attenuated the anti-apoptosis effect of ghrelin in MC3T3-E1 cells. In conclusion, ghrelin inhibits the apoptosis of osteoblastic MC3T3-E1 cells induced by serum deprivation, which may be mediated by activating the GHSR/ERK and GHSR/PI3K/AKT signaling pathways. - Highlights: • We explored the effects of ghrelin on serum deprivation-induced MC3T3-E1 cells apoptosis. • Both ELISA and TUNEL were used to detect the apoptosis. • The receptor of ghrelin, GHSR, was expressed in MC3T3-E1 cells. • Both Akt and ERK are critical adaptor molecules to mediate the effects of ghrelin.« less

Authors:
; ; ; ; ;
Publication Date:
OSTI Identifier:
22285451
Resource Type:
Journal Article
Resource Relation:
Journal Name: Toxicology and Applied Pharmacology; Journal Volume: 272; Journal Issue: 3; Other Information: Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; AMINO ACIDS; APOPTOSIS; CONNECTIVE TISSUE CELLS; ENZYME IMMUNOASSAY; LIGANDS; METABOLISM; MOLECULES; PEPTIDES; RECEPTORS; SKELETON; STH

Citation Formats

Liang, Qiu-Hua, Liu, Yuan, Wu, Shan-Shan, Cui, Rong-Rong, Yuan, Ling-Qing, E-mail: allenylq@hotmail.com, and Liao, Er-Yuan, E-mail: eyliao@21cn.com. Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway. United States: N. p., 2013. Web. doi:10.1016/J.TAAP.2013.07.018.
Liang, Qiu-Hua, Liu, Yuan, Wu, Shan-Shan, Cui, Rong-Rong, Yuan, Ling-Qing, E-mail: allenylq@hotmail.com, & Liao, Er-Yuan, E-mail: eyliao@21cn.com. Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway. United States. doi:10.1016/J.TAAP.2013.07.018.
Liang, Qiu-Hua, Liu, Yuan, Wu, Shan-Shan, Cui, Rong-Rong, Yuan, Ling-Qing, E-mail: allenylq@hotmail.com, and Liao, Er-Yuan, E-mail: eyliao@21cn.com. 2013. "Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway". United States. doi:10.1016/J.TAAP.2013.07.018.
@article{osti_22285451,
title = {Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway},
author = {Liang, Qiu-Hua and Liu, Yuan and Wu, Shan-Shan and Cui, Rong-Rong and Yuan, Ling-Qing, E-mail: allenylq@hotmail.com and Liao, Er-Yuan, E-mail: eyliao@21cn.com},
abstractNote = {Ghrelin is a 28-amino-acid peptide that acts as a natural endogenous ligand of the growth hormone secretagogue receptor (GHSR) and strongly stimulates the release of growth hormone from the hypothalamus–pituitary axis. Previous studies have identified the important physiological effects of ghrelin on bone metabolism, such as regulating proliferation and differentiation of osteoblasts, independent of GH/IGF-1 axis. However, research on effects and mechanisms of ghrelin on osteoblast apoptosis is still rare. In this study, we identified expression of GHSR in MC3T3-E1 cells and determined the effects of ghrelin on the apoptosis of osteoblastic MC3T3-E1 cells and the mechanism involved. Our data demonstrated that ghrelin inhibited the apoptosis of osteoblastic MC3T3-E1 cells induced by serum deprivation, as determined by terminal deoxynucleotidyl transferase-mediated deoxyribonucleotide triphosphate nick end-labeling (TUNEL) and ELISA assays. Moreover, ghrelin upregulated Bcl-2 expression and downregulated Bax expression in a dose-dependent manner. Our study also showed decreased activated caspase-3 activity under the treatment of ghrelin. Further study suggested that ghrelin stimulated the phosphorylation of ERK and AKT. Pretreatment of cells with the ERK inhibitor PD98059, PI3K inhibitor LY294002, and GHSR-siRNA blocked the ghrelin-induced activation of ERK and AKT, respectively; however, ghrelin did not stimulate the phosphorylation of p38 or JNK. PD90859, LY294002 and GHSR-siRNA attenuated the anti-apoptosis effect of ghrelin in MC3T3-E1 cells. In conclusion, ghrelin inhibits the apoptosis of osteoblastic MC3T3-E1 cells induced by serum deprivation, which may be mediated by activating the GHSR/ERK and GHSR/PI3K/AKT signaling pathways. - Highlights: • We explored the effects of ghrelin on serum deprivation-induced MC3T3-E1 cells apoptosis. • Both ELISA and TUNEL were used to detect the apoptosis. • The receptor of ghrelin, GHSR, was expressed in MC3T3-E1 cells. • Both Akt and ERK are critical adaptor molecules to mediate the effects of ghrelin.},
doi = {10.1016/J.TAAP.2013.07.018},
journal = {Toxicology and Applied Pharmacology},
number = 3,
volume = 272,
place = {United States},
year = 2013,
month =
}
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