Propionibacteria induce apoptosis of colorectal carcinoma cells via short-chain fatty acids acting on mitochondria

被引:287
作者
Jan, G
Belzacq, AS
Haouzi, D
Rouault, A
Métivier, D
Kroemer, G
Brenner, C
机构
[1] Univ Technol Compiegne, UMR 6022, Ctr Natl Rech Sci, F-60205 Compiegne, France
[2] INRA, UR 121, Lab Rech Technol Laitiere, F-35042 Rennes, France
[3] Inst Gustave Roussy, UMR 1599, Ctr Natl Rech Sci, F-94805 Villejuif, France
关键词
adenine nucleotide translocator; apoptosis; cancer; mitochondria; probiotic; propionibacteria; short-chain fatty acid;
D O I
10.1038/sj.cdd.4400935
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genus Propionibacterium is composed of dairy and cutaneous bacteria which produce short-chain fatty acids (SCFA), mainly propionate and acetate, by fermentation. Here, we show that P. acidipropionici and freudenreichii, two species which can survive in the human intestine, can kill two human colorectal carcinoma cell lines by apoptosis. Propionate and acetate were identified as the major cytotoxic components secreted by the bacteria. Bacterial culture supernatants as well as pure SCFA induced typical signs of apoptosis including a loss of mitochondrial transmembrane potential, the generation of reactive oxygen species, caspase-3 processing, and nuclear chromatin condensation. The oncoprotein Bcl-2, which is known to prevent apoptosis via mitochondrial effects, and the cytomegalovirus-encoded protein vMIA, which inhibits apoptosis and interacts with the mitochondrial adenine nucleotide translocator (ANT), both inhibited cell death induced by propionibacterial SCFA, suggesting that mitochondria and ANT are involved in the cell death pathway. Accordingly, propionate and acetate induced mitochondrial swelling when added to purified mitochondria in vitro. Moreover, they specifically permeabi-lize proteoliposomes containing ANT, indicating that ANT can be a critical target in SCFA-induced apoptosis. We suggest that propionibacteria could constitute probiotics efficient in digestive cancer prophylaxis via their ability to produce apoptosis-inducing SCFA.
引用
收藏
页码:179 / 188
页数:10
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