Article

p53 activation inhibits ochratoxin A-induced apoptosis in monkey and human kidney epithelial cells via suppression of JNK activation.

Division of Nutrition and Health, College of Food Science and Nutritional Engineering, China Agricultural University, No. 17 Qinghua East Road, Haidian District, Beijing 100083, China.
Biochemical and Biophysical Research Communications (impact factor: 2.48). 07/2011; 411(2):458-63. DOI:10.1016/j.bbrc.2011.06.190 pp.458-63
Source: PubMed

ABSTRACT Ochratoxin A (OTA), one of the major food-borne mycotoxins, induces apoptosis in various types of cells. Induction of apoptosis is suggested to be one of the major cellular mechanisms behind OTA-induced diverse toxic effects. However, the molecular mechanisms involved, especially the role of p53 in OTA-induced apoptosis have not been clearly elucidated. In the present study, we find that p53 activation exerts pro-survival function to inhibit apoptosis induction in MARC-145, Vero monkey kidney cells and HEK293 human kidney cells in response to ochratoxin A treatment. We further demonstrate that the pro-survival activity of p53 is attributed to its ability to suppress JNK activation that mediates apoptotic signaling through down-regulation of Bcl-xL. To our knowledge, this is first report of pro-survival role of p53 in OTA-induced apoptosis in kidney epithelial cells. Our findings provide a novel insight into the mechanisms of OTA-induced apoptosis in kidney epithelial cells.

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Keywords

apoptosis
 
apoptosis induction
 
HEK293 human kidney cells
 
induces apoptosis
 
JNK activation
 
major cellular mechanisms
 
major food-borne mycotoxins
 
mediates apoptotic signaling
 
molecular mechanisms
 
novel insight
 
ochratoxin
 
OTA
 
OTA-induced apoptosis
 
OTA-induced diverse toxic effects
 
pro-survival activity
 
Vero monkey kidney cells