Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosis

被引:83
作者
Hu, Chien-an A.
Donald, Steven P.
Yu, Jian
Lin, Wei-Wen
Liu, Zhihe
Steel, Gary
Obie, Cassandra
Valle, David
Phang, James M.
机构
[1] Univ New Mexico, Sch Med, Dept Biochem & Mol Biol, Albuquerque, NM 87131 USA
[2] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15260 USA
[3] Tri Serv Gen Hosp, Dept Psychiat, Taipei, Taiwan
[4] Natl Def Med Inst, Taipei, Taiwan
[5] Johns Hopkins Univ, Howard Hughes Med Inst, McKusick Nathans Inst Genet Med, Sch Med, Baltimore, MD 21218 USA
关键词
proline oxidase; apoptosis; reactive oxygen species; mitochondria; p53; proline-P5C cycle;
D O I
10.1007/s11010-006-9276-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proline oxidase (POX), a mitochondrial inner-membrane protein, catalyzes the rate-limiting oxidation of proline to pyrroline-5-carboxylate (P5C). Previously we showed that overexpression of POX is associated with generation of reactive oxygen species (ROS) and apoptosis in POX-inducible colorectal cancer cells, DLD-1.POX. We also showed expression of mitochondrial MnSOD partially blunts POX-induced ROS generation and apoptosis. To further investigate the molecular basis of POX-induced apoptosis, we utilized the DLD-1.POX cells to show that cells overproducing POX exhibit an L-proline-dependent apoptotic response. The apoptotic effect is specific for L-proline, detectable at 0.2 mM, maximal at 1 mM, and occurs during 48-72 h following the addition of L-proline to cells with maximally induced POX. The apoptotic response is mitochondria-mediated with release of cytochrome c, activation of caspase-9, chromatin condensation/DNA fragmentation, and cell shrinkage. We conclude that in the presence of proline, high POX activity is sufficient to induce mitochondria-mediated apoptosis.
引用
收藏
页码:85 / 92
页数:8
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