Abstract

Doc number: 36

Abstract

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.

Details

Title
Trypsin-induced proteome alteration during cell subculture in mammalian cells
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
Pages
36
Publication year
2010
Publication date
2010
Publisher
BioMed Central
ISSN
10217770
e-ISSN
14230127
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1030086748
Copyright
© 2010 Huang et al; licensee BioMed Central Ltd. 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.