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Trypsin-induced proteome alteration during cell subculture in mammalian cells
BACKGROUND: It is essential to subculture the cells once cultured cells reach confluence. For this, trypsin is frequently applied to dissociate adhesive cells from the substratum. However, due to the proteolytic activity of trypsin, cell surface proteins are often cleaved, which leads to dysregulati...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873939/ https://www.ncbi.nlm.nih.gov/pubmed/20459778 http://dx.doi.org/10.1186/1423-0127-17-36 |
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author | Huang, Hsiang-Ling Hsing, Hsiang-Wei Lai, Tzu-Chia Chen, Yi-Wen Lee, Tian-Ren Chan, Hsin-Tsu Lyu, Ping-Chiang Wu, Chieh-Lin Lu, Ying-Chieh Lin, Szu-Ting Lin, Cheng-Wen Lai, Chih-Ho Chang, Hao-Teng Chou, Hsiu-Chuan Chan, Hong-Lin |
author_facet | Huang, Hsiang-Ling Hsing, Hsiang-Wei Lai, Tzu-Chia Chen, Yi-Wen Lee, Tian-Ren Chan, Hsin-Tsu Lyu, Ping-Chiang Wu, Chieh-Lin Lu, Ying-Chieh Lin, Szu-Ting Lin, Cheng-Wen Lai, Chih-Ho Chang, Hao-Teng Chou, Hsiu-Chuan Chan, Hong-Lin |
author_sort | Huang, Hsiang-Ling |
collection | PubMed |
description | BACKGROUND: It is essential to subculture the cells once cultured cells reach confluence. For this, trypsin is frequently applied to dissociate adhesive cells from the substratum. However, due to the proteolytic activity of trypsin, cell surface proteins are often cleaved, which leads to dysregulation of the cell functions. METHODS: In this study, a triplicate 2D-DIGE strategy has been performed to monitor trypsin-induced proteome alterations. The differentially expressed spots were identified by MALDI-TOF MS and validated by immunoblotting. RESULTS: 36 proteins are found to be differentially expressed in cells treated with trypsin, and proteins that are known to regulate cell metabolism, growth regulation, mitochondrial electron transportation and cell adhesion are down-regulated and proteins that regulate cell apoptosis are up-regulated after trypsin treatment. Further study shows that bcl-2 is down-regulated, p53 and p21 are both up-regulated after trypsinization. CONCLUSIONS: In summary, this is the first report that uses the proteomic approach to thoroughly study trypsin-induced cell physiological changes and provides researchers in carrying out their experimental design. |
format | Text |
id | pubmed-2873939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28739392010-05-21 Trypsin-induced proteome alteration during cell subculture in mammalian cells Huang, Hsiang-Ling Hsing, Hsiang-Wei Lai, Tzu-Chia Chen, Yi-Wen Lee, Tian-Ren Chan, Hsin-Tsu Lyu, Ping-Chiang Wu, Chieh-Lin Lu, Ying-Chieh Lin, Szu-Ting Lin, Cheng-Wen Lai, Chih-Ho Chang, Hao-Teng Chou, Hsiu-Chuan Chan, Hong-Lin J Biomed Sci Research BACKGROUND: It is essential to subculture the cells once cultured cells reach confluence. For this, trypsin is frequently applied to dissociate adhesive cells from the substratum. However, due to the proteolytic activity of trypsin, cell surface proteins are often cleaved, which leads to dysregulation of the cell functions. METHODS: In this study, a triplicate 2D-DIGE strategy has been performed to monitor trypsin-induced proteome alterations. The differentially expressed spots were identified by MALDI-TOF MS and validated by immunoblotting. RESULTS: 36 proteins are found to be differentially expressed in cells treated with trypsin, and proteins that are known to regulate cell metabolism, growth regulation, mitochondrial electron transportation and cell adhesion are down-regulated and proteins that regulate cell apoptosis are up-regulated after trypsin treatment. Further study shows that bcl-2 is down-regulated, p53 and p21 are both up-regulated after trypsinization. CONCLUSIONS: In summary, this is the first report that uses the proteomic approach to thoroughly study trypsin-induced cell physiological changes and provides researchers in carrying out their experimental design. BioMed Central 2010-05-11 /pmc/articles/PMC2873939/ /pubmed/20459778 http://dx.doi.org/10.1186/1423-0127-17-36 Text en Copyright ©2010 Huang 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 Huang, Hsiang-Ling Hsing, Hsiang-Wei Lai, Tzu-Chia Chen, Yi-Wen Lee, Tian-Ren Chan, Hsin-Tsu Lyu, Ping-Chiang Wu, Chieh-Lin Lu, Ying-Chieh Lin, Szu-Ting Lin, Cheng-Wen Lai, Chih-Ho Chang, Hao-Teng Chou, Hsiu-Chuan Chan, Hong-Lin Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title | Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title_full | Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title_fullStr | Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title_full_unstemmed | Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title_short | Trypsin-induced proteome alteration during cell subculture in mammalian cells |
title_sort | trypsin-induced proteome alteration during cell subculture in mammalian cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873939/ https://www.ncbi.nlm.nih.gov/pubmed/20459778 http://dx.doi.org/10.1186/1423-0127-17-36 |
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