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Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis
Secretomes produced by mesenchymal stromal cells (MSCs) were considered to be therapeutic potential. However, harvesting enough primary MSCs from tissue was time-consuming and costly, which impeded the application of MSCs secretomes. This study was to immortalize MSCs and compare the secretomes prof...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544752/ https://www.ncbi.nlm.nih.gov/pubmed/28779163 http://dx.doi.org/10.1038/s41598-017-07467-3 |
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author | Dou, Lei Wu, Yan Yan, Qifang Wang, Jinhua Zhang, Yan Ji, Ping |
author_facet | Dou, Lei Wu, Yan Yan, Qifang Wang, Jinhua Zhang, Yan Ji, Ping |
author_sort | Dou, Lei |
collection | PubMed |
description | Secretomes produced by mesenchymal stromal cells (MSCs) were considered to be therapeutic potential. However, harvesting enough primary MSCs from tissue was time-consuming and costly, which impeded the application of MSCs secretomes. This study was to immortalize MSCs and compare the secretomes profile of immortalized and original MSCs. Human dental follicle cells (DFCs) were isolated and immortalized using pMPH86. The secretome profile of immortalized DFCs (iDFCs) was investigated and compared using iTRAQ labeling combined with mass spectrometry (MS) quantitative proteomics. The MS data was analyzed using ProteinPilotTM software, and then bioinformatic analysis of identified proteins was done. A total of 2092 secreted proteins were detected in conditioned media of iDFCs. Compared with primary DFCs, 253 differently expressed proteins were found in iDFCs secretome (142 up-regulated and 111 down-regulated). Intensive bioinformatic analysis revealed that the majority of secreted proteins were involved in cellular process, metabolic process, biological regulation, cellular component organization or biogenesis, immune system process, developmental process, response to stimulus and signaling. Proteomic profile of cell secretome wasn’t largely affected after immortalization converted by this piggyBac immortalization system. The secretome of iDFCs may be a good candidate of primary DFCs for regenerative medicine. |
format | Online Article Text |
id | pubmed-5544752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55447522017-08-09 Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis Dou, Lei Wu, Yan Yan, Qifang Wang, Jinhua Zhang, Yan Ji, Ping Sci Rep Article Secretomes produced by mesenchymal stromal cells (MSCs) were considered to be therapeutic potential. However, harvesting enough primary MSCs from tissue was time-consuming and costly, which impeded the application of MSCs secretomes. This study was to immortalize MSCs and compare the secretomes profile of immortalized and original MSCs. Human dental follicle cells (DFCs) were isolated and immortalized using pMPH86. The secretome profile of immortalized DFCs (iDFCs) was investigated and compared using iTRAQ labeling combined with mass spectrometry (MS) quantitative proteomics. The MS data was analyzed using ProteinPilotTM software, and then bioinformatic analysis of identified proteins was done. A total of 2092 secreted proteins were detected in conditioned media of iDFCs. Compared with primary DFCs, 253 differently expressed proteins were found in iDFCs secretome (142 up-regulated and 111 down-regulated). Intensive bioinformatic analysis revealed that the majority of secreted proteins were involved in cellular process, metabolic process, biological regulation, cellular component organization or biogenesis, immune system process, developmental process, response to stimulus and signaling. Proteomic profile of cell secretome wasn’t largely affected after immortalization converted by this piggyBac immortalization system. The secretome of iDFCs may be a good candidate of primary DFCs for regenerative medicine. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5544752/ /pubmed/28779163 http://dx.doi.org/10.1038/s41598-017-07467-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dou, Lei Wu, Yan Yan, Qifang Wang, Jinhua Zhang, Yan Ji, Ping Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title | Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title_full | Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title_fullStr | Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title_full_unstemmed | Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title_short | Secretome profiles of immortalized dental follicle cells using iTRAQ-based proteomic analysis |
title_sort | secretome profiles of immortalized dental follicle cells using itraq-based proteomic analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544752/ https://www.ncbi.nlm.nih.gov/pubmed/28779163 http://dx.doi.org/10.1038/s41598-017-07467-3 |
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