Cargando…

iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells

As the only known organ that can completely regenerate in mammals, deer antler is of real significance in the field of regenerative medicine. Recent studies have shown that the regenerative capacity of the antlers comes from the pedicle periosteum and the cells resident in the periosteum possess the...

Descripción completa

Detalles Bibliográficos
Autores principales: Dong, Zhen, Ba, Hengxing, Zhang, Wei, Coates, Dawn, Li, Chunyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133779/
https://www.ncbi.nlm.nih.gov/pubmed/27792145
http://dx.doi.org/10.3390/ijms17111778
_version_ 1782471336437743616
author Dong, Zhen
Ba, Hengxing
Zhang, Wei
Coates, Dawn
Li, Chunyi
author_facet Dong, Zhen
Ba, Hengxing
Zhang, Wei
Coates, Dawn
Li, Chunyi
author_sort Dong, Zhen
collection PubMed
description As the only known organ that can completely regenerate in mammals, deer antler is of real significance in the field of regenerative medicine. Recent studies have shown that the regenerative capacity of the antlers comes from the pedicle periosteum and the cells resident in the periosteum possess the attributes of stem cells. Currently, the molecular mechanism of antler regeneration remains unclear. In the present study, we compared the potentiated and dormant antler stem cells using isobaric tags for the relative and absolute quantification (iTRAQ) labeling of the peptides, coupled with two-dimensional liquid chromatography-tandem mass spectrometry (LC-MS/MS) to compare the proteome profiles. Proteins were identified by searching against the NCBI nr database and our own Cervine transcriptome database, and bioinformatics analysis was conducted to identify the differentially expressed proteins. Based on this searching strategy, we identified 169 differentially expressed proteins in total, consisting of 70 up- and 99 down-regulated in the potentiated vs. dormant antler stem cells. Reliability of the iTRAQ was confirmed via quantitative real-time polymerase chain reaction (qRT-PCR) to measure the expression of selected genes. We identified transduction pathways through the Kyoto Encyclopedia of Genes and Genomes (KEGG) database, such as HIF-1 and PI3K-AKT signaling pathways that play important roles in regulating the regeneration of antlers. In summary, the initiation stage of antler regeneration, a process from dormant to potentiated states in antler stem cells, is regulated by multiple proteins and complicated signal networks.
format Online
Article
Text
id pubmed-5133779
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-51337792016-12-12 iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells Dong, Zhen Ba, Hengxing Zhang, Wei Coates, Dawn Li, Chunyi Int J Mol Sci Article As the only known organ that can completely regenerate in mammals, deer antler is of real significance in the field of regenerative medicine. Recent studies have shown that the regenerative capacity of the antlers comes from the pedicle periosteum and the cells resident in the periosteum possess the attributes of stem cells. Currently, the molecular mechanism of antler regeneration remains unclear. In the present study, we compared the potentiated and dormant antler stem cells using isobaric tags for the relative and absolute quantification (iTRAQ) labeling of the peptides, coupled with two-dimensional liquid chromatography-tandem mass spectrometry (LC-MS/MS) to compare the proteome profiles. Proteins were identified by searching against the NCBI nr database and our own Cervine transcriptome database, and bioinformatics analysis was conducted to identify the differentially expressed proteins. Based on this searching strategy, we identified 169 differentially expressed proteins in total, consisting of 70 up- and 99 down-regulated in the potentiated vs. dormant antler stem cells. Reliability of the iTRAQ was confirmed via quantitative real-time polymerase chain reaction (qRT-PCR) to measure the expression of selected genes. We identified transduction pathways through the Kyoto Encyclopedia of Genes and Genomes (KEGG) database, such as HIF-1 and PI3K-AKT signaling pathways that play important roles in regulating the regeneration of antlers. In summary, the initiation stage of antler regeneration, a process from dormant to potentiated states in antler stem cells, is regulated by multiple proteins and complicated signal networks. MDPI 2016-10-25 /pmc/articles/PMC5133779/ /pubmed/27792145 http://dx.doi.org/10.3390/ijms17111778 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dong, Zhen
Ba, Hengxing
Zhang, Wei
Coates, Dawn
Li, Chunyi
iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title_full iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title_fullStr iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title_full_unstemmed iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title_short iTRAQ-Based Quantitative Proteomic Analysis of the Potentiated and Dormant Antler Stem Cells
title_sort itraq-based quantitative proteomic analysis of the potentiated and dormant antler stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133779/
https://www.ncbi.nlm.nih.gov/pubmed/27792145
http://dx.doi.org/10.3390/ijms17111778
work_keys_str_mv AT dongzhen itraqbasedquantitativeproteomicanalysisofthepotentiatedanddormantantlerstemcells
AT bahengxing itraqbasedquantitativeproteomicanalysisofthepotentiatedanddormantantlerstemcells
AT zhangwei itraqbasedquantitativeproteomicanalysisofthepotentiatedanddormantantlerstemcells
AT coatesdawn itraqbasedquantitativeproteomicanalysisofthepotentiatedanddormantantlerstemcells
AT lichunyi itraqbasedquantitativeproteomicanalysisofthepotentiatedanddormantantlerstemcells