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过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证

OBJECTIVE: To investigate the proteins expression difference after upregulation of human CD99 in Hodgkin Lymphoma cell line, L428 cell, and verify the function of differential proteins. METHODS: The differential proteins were detected by two-dimensional fluorescence difference gel electrophoresis an...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342398/
https://www.ncbi.nlm.nih.gov/pubmed/31340622
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.008
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collection PubMed
description OBJECTIVE: To investigate the proteins expression difference after upregulation of human CD99 in Hodgkin Lymphoma cell line, L428 cell, and verify the function of differential proteins. METHODS: The differential proteins were detected by two-dimensional fluorescence difference gel electrophoresis and mass spectrometry analysis, cluster analysis was done by GOfact. RESULTS: There were 38 proteins screened out, of which 21 proteins were positively associated with CD99, while 17 proteins were negative. Among the 38 proteins, 32 proteins participated in biological process, and 35 proteins were involved in the composition and construction. And 28 proteins participated in multifaceted biological activities including antioxidation, protein binding, catalytic activity, regulation of enzyme, signal transduction, molecular structure, regulation of translation and ion transport. CONCLUSION: The changes of the differential proteins, correlated with cytoskeleton, cell differentiation, signal pathway and regulating gene expression, are closely relevant to the translation between Hodgkin/Reed-Sternberg and B lymphocyte cell.
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spelling pubmed-73423982020-07-16 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the proteins expression difference after upregulation of human CD99 in Hodgkin Lymphoma cell line, L428 cell, and verify the function of differential proteins. METHODS: The differential proteins were detected by two-dimensional fluorescence difference gel electrophoresis and mass spectrometry analysis, cluster analysis was done by GOfact. RESULTS: There were 38 proteins screened out, of which 21 proteins were positively associated with CD99, while 17 proteins were negative. Among the 38 proteins, 32 proteins participated in biological process, and 35 proteins were involved in the composition and construction. And 28 proteins participated in multifaceted biological activities including antioxidation, protein binding, catalytic activity, regulation of enzyme, signal transduction, molecular structure, regulation of translation and ion transport. CONCLUSION: The changes of the differential proteins, correlated with cytoskeleton, cell differentiation, signal pathway and regulating gene expression, are closely relevant to the translation between Hodgkin/Reed-Sternberg and B lymphocyte cell. Editorial office of Chinese Journal of Hematology 2019-06 /pmc/articles/PMC7342398/ /pubmed/31340622 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.008 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title_full 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title_fullStr 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title_full_unstemmed 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title_short 过表达CD99后霍奇金淋巴瘤细胞株L428细胞蛋白表达变化的蛋白质组学分析及验证
title_sort 过表达cd99后霍奇金淋巴瘤细胞株l428细胞蛋白表达变化的蛋白质组学分析及验证
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342398/
https://www.ncbi.nlm.nih.gov/pubmed/31340622
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.008
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