Identification of aging related proteins in human normal colonic epithelium.
- Author:
Guo ZHU
1
;
Zhi-qiang XIAO
;
Zhu-chu CHEN
;
Jian-ling LI
;
Peng-fei ZHANG
;
Yi-xuan YANG
;
Xue-ping FENG
;
Wei-jian YUAN
Author Information
1. Key Laboratory of Cancer Proteomics of Chinese Ministry of Public Health, Xiangya Hospital, Central South University, Changsha.
- Publication Type:Journal Article
- MeSH:
Aging;
metabolism;
Cells, Cultured;
Cellular Senescence;
genetics;
Chloride Channels;
biosynthesis;
genetics;
Colon;
cytology;
Electron-Transferring Flavoproteins;
biosynthesis;
genetics;
Epithelial Cells;
cytology;
Humans;
Intestinal Mucosa;
cytology;
Proteins;
metabolism
- From:
Journal of Central South University(Medical Sciences)
2005;30(6):625-630
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the molecular mechanisms of colonic epithelial aging related proteins and aged colonic epithelial susceptibility to tumor.
METHODS:The proteins of normal human colonic epithelial tissue from young and old people were separated by 2-dimensional gel electrophoresis (2DGE), respectively. Then gels were stained by silver, scanned by imagescanner and analyzed with PDQuest software. The differentially expressed protein spots of colonic epithelium between the old and the young groups were identified by peptide mass fingerprint based on matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) and database searching.
RESULTS:Well-resolved and reproducible 2DGE maps of normal human colonic epithelium from the young and the old were acquired. Nineteen more than 2 fold differentially expressed protein spots were identified representing 17 different proteins by MALDI-TOF-MS. The functions of these proteins involve in metabolism, energy generation, transportation, antioxidation, translation and protein folding.
CONCLUSION:Seventeen aging related proteins of human colonic epithelium identified indicate that injury of mitochondrial function and decline of antioxidant capability are important reasons for the aging of human colonic epithelium. These data provided useful clues for elucidating the mechanisms of colonic epithelial aging and aged colonic epithelial susceptibility to cancer.
