DocumentCode :
380161
Title :
Mammalian cell death model of p53 induced apoptosis
Author :
Okazaki, T. ; Nagakura, T.
Author_Institution :
Graduate Sch. of Medicine, Osaka Univ., Japan
Volume :
3
fYear :
2001
fDate :
2001
Firstpage :
2934
Abstract :
Although apoptosis is a physiological pathway to cell suicide that is critical to normal development and homeostasis, the mechanism of cell death has not been well elucidated because of the complicated multiple signal pathways involved. The p53 tumor suppressor gene is a transcriptional factor that induces cell cycle arrest and apoptosis and recognized as a central component of the apoptosis system. In this study, we try to establish the cell system in which apoptosis can be induced spontaneously by introducing temperature sensitive dominant negative p53 mutant into mammalian epithelial cell lines. Using this cell system the time-course of changes of the number of cells were evaluated from the onset of apoptosis cell death signal. After activating wild type p53, the number of cells continued to increase until around 18 hours, and began to decrease logarithmically rather than linearly. Based on molecular biological findings for p53-induced apoptosis, it can be estimated that once cell death signal is introduced, cell cycle arrest precedes apoptosis in the passage of cell death. These cell death model concerning apoptosis could be useful for further understanding of the life span of human beings.
Keywords :
biothermics; cellular biophysics; genetics; living systems; molecular biophysics; physiological models; proteins; skin; 18 h; 80 h; apoptosis cell death signal; cell cycle arrest; cell suicide; central component; culture temperature; homeostasis; life span; mammalian cell death model; mammalian epithelial cell lines; molecular biological findings; multiple signal pathways; normal development; p53 induced apoptosis; p53 tumor suppressor gene; physiological pathway; temperature sensitive dominant negative p53 mutant; time-course; total protein concentration; transcriptional factor; wild type p53; Biological system modeling; Biomedical engineering; Cells (biology); Humans; Microscopy; Neoplasms; Pediatrics; Proteins; Temperature sensors; Time measurement;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Engineering in Medicine and Biology Society, 2001. Proceedings of the 23rd Annual International Conference of the IEEE
ISSN :
1094-687X
Print_ISBN :
0-7803-7211-5
Type :
conf
DOI :
10.1109/IEMBS.2001.1017406
Filename :
1017406
Link To Document :
بازگشت