Cargando…
Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry
BACKGROUND: Pituitary adenomas, the third most common intracranial tumor, comprise nearly 16.7% of intracranial neoplasm and 25%-44% of pituitary adenomas are prolactinomas. Prolactinoma represents a complex heterogeneous mixture of cells including prolactin (PRL), endothelial cells, fibroblasts, an...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825229/ https://www.ncbi.nlm.nih.gov/pubmed/20205839 http://dx.doi.org/10.1186/1477-5956-8-2 |
_version_ | 1782177797711593472 |
---|---|
author | Liu, Yingchao Wu, Jinsong Yan, Guoquan Hou, Ruiping Zhuang, Dongxiao Chen, Luping Pang, Qi Zhu, Jianhong |
author_facet | Liu, Yingchao Wu, Jinsong Yan, Guoquan Hou, Ruiping Zhuang, Dongxiao Chen, Luping Pang, Qi Zhu, Jianhong |
author_sort | Liu, Yingchao |
collection | PubMed |
description | BACKGROUND: Pituitary adenomas, the third most common intracranial tumor, comprise nearly 16.7% of intracranial neoplasm and 25%-44% of pituitary adenomas are prolactinomas. Prolactinoma represents a complex heterogeneous mixture of cells including prolactin (PRL), endothelial cells, fibroblasts, and other stromal cells, making it difficult to dissect the molecular and cellular mechanisms of prolactin cells in pituitary tumorigenesis through high-throughout-omics analysis. Our newly developed immuno-laser capture microdissection (LCM) method would permit rapid and reliable procurement of prolactin cells from this heterogeneous tissue. Thus, prolactin cell specific molecular events involved in pituitary tumorigenesis and cell signaling can be approached by proteomic analysis. RESULTS: Proteins from immuno-LCM captured prolactin cells were digested; resulting peptides were separated by two dimensional-nanoscale liquid chromatography (2D-nanoLC/MS) and characterized by tandem mass spectrometry. All MS/MS spectrums were analyzed by SEQUEST against the human International Protein Index database and a specific prolactinoma proteome consisting of 2243 proteins was identified. This collection of identified proteins by far represents the largest and the most comprehensive database of proteome for prolactinoma. Category analysis of the proteome revealed a widely unbiased access to various proteins with diverse functional characteristics. CONCLUSIONS: This manuscript described a more comprehensive proteomic profile of prolactinomas compared to other previous published reports. Thanks to the application of immuno-LCM combined with online two-dimensional nano-scale liquid chromatography here permitted identification of more proteins and, to our best knowledge, generated the largest prolactinoma proteome. This enlarged proteome would contribute significantly to further understanding of prolactinoma tumorigenesis which is crucial to the management of prolactinomas. |
format | Text |
id | pubmed-2825229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28252292010-02-20 Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry Liu, Yingchao Wu, Jinsong Yan, Guoquan Hou, Ruiping Zhuang, Dongxiao Chen, Luping Pang, Qi Zhu, Jianhong Proteome Sci Research BACKGROUND: Pituitary adenomas, the third most common intracranial tumor, comprise nearly 16.7% of intracranial neoplasm and 25%-44% of pituitary adenomas are prolactinomas. Prolactinoma represents a complex heterogeneous mixture of cells including prolactin (PRL), endothelial cells, fibroblasts, and other stromal cells, making it difficult to dissect the molecular and cellular mechanisms of prolactin cells in pituitary tumorigenesis through high-throughout-omics analysis. Our newly developed immuno-laser capture microdissection (LCM) method would permit rapid and reliable procurement of prolactin cells from this heterogeneous tissue. Thus, prolactin cell specific molecular events involved in pituitary tumorigenesis and cell signaling can be approached by proteomic analysis. RESULTS: Proteins from immuno-LCM captured prolactin cells were digested; resulting peptides were separated by two dimensional-nanoscale liquid chromatography (2D-nanoLC/MS) and characterized by tandem mass spectrometry. All MS/MS spectrums were analyzed by SEQUEST against the human International Protein Index database and a specific prolactinoma proteome consisting of 2243 proteins was identified. This collection of identified proteins by far represents the largest and the most comprehensive database of proteome for prolactinoma. Category analysis of the proteome revealed a widely unbiased access to various proteins with diverse functional characteristics. CONCLUSIONS: This manuscript described a more comprehensive proteomic profile of prolactinomas compared to other previous published reports. Thanks to the application of immuno-LCM combined with online two-dimensional nano-scale liquid chromatography here permitted identification of more proteins and, to our best knowledge, generated the largest prolactinoma proteome. This enlarged proteome would contribute significantly to further understanding of prolactinoma tumorigenesis which is crucial to the management of prolactinomas. BioMed Central 2010-01-29 /pmc/articles/PMC2825229/ /pubmed/20205839 http://dx.doi.org/10.1186/1477-5956-8-2 Text en Copyright ©2010 Liu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Liu, Yingchao Wu, Jinsong Yan, Guoquan Hou, Ruiping Zhuang, Dongxiao Chen, Luping Pang, Qi Zhu, Jianhong Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title | Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title_full | Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title_fullStr | Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title_full_unstemmed | Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title_short | Proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
title_sort | proteomic analysis of prolactinoma cells by immuno-laser capture microdissection combined with online two-dimensional nano-scale liquid chromatography/mass spectrometry |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825229/ https://www.ncbi.nlm.nih.gov/pubmed/20205839 http://dx.doi.org/10.1186/1477-5956-8-2 |
work_keys_str_mv | AT liuyingchao proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT wujinsong proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT yanguoquan proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT houruiping proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT zhuangdongxiao proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT chenluping proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT pangqi proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry AT zhujianhong proteomicanalysisofprolactinomacellsbyimmunolasercapturemicrodissectioncombinedwithonlinetwodimensionalnanoscaleliquidchromatographymassspectrometry |