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

被引:84
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
相关论文
共 36 条
[1]   METABOLISM OF PROLINE AND THE HYDROXYPROLINES [J].
ADAMS, E ;
FRANK, L .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :1005-1061
[2]   Redox-linked cell surface-oriented signaling for T-cell death [J].
Akhand, AA ;
Du, J ;
Liu, W ;
Hossain, K ;
Miyata, T ;
Nagase, F ;
Kato, M ;
Suzuki, H ;
Nakashima, I .
ANTIOXIDANTS & REDOX SIGNALING, 2002, 4 (03) :445-454
[3]   Functional consequences of PRODH missense mutations [J].
Bender, HU ;
Almashanu, S ;
Steel, G ;
Hu, CA ;
Lin, WW ;
Willis, A ;
Pulver, A ;
Valle, D .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (03) :409-420
[4]   MITOCHONDRIAL PROLINE DEHYDROGENASE-DEFICIENCY IN HYPERPROLINEMIC PRO-RE MICE - GENETIC AND ENZYMATIC ANALYSES [J].
BLAKE, RL ;
HALL, JG ;
RUSSELL, ES .
BIOCHEMICAL GENETICS, 1976, 14 (9-10) :739-757
[6]   Mitochondrial signaling: The retrograde response [J].
Butow, RA ;
Avadhani, NG .
MOLECULAR CELL, 2004, 14 (01) :1-15
[7]  
Donald SP, 2001, CANCER RES, V61, P1810
[8]   PROLINE OXIDASE IN CULTURED MAMMALIAN-CELLS [J].
DOWNING, SJ ;
PHANG, JM ;
KOWALOFF, EM ;
VALLE, D ;
SMITH, RJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1977, 91 (03) :369-376
[9]   Organelle-specific initiation of cell death pathways [J].
Ferri, KF ;
Kroemer, G .
NATURE CELL BIOLOGY, 2001, 3 (11) :E255-E263
[10]   Mutations in the Δ1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia [J].
Geraghty, MT ;
Vaughn, D ;
Nicholson, AJ ;
Lin, WW ;
Jimenez-Sanchez, G ;
Obie, C ;
Flynn, MP ;
Valle, D ;
Hu, CAA .
HUMAN MOLECULAR GENETICS, 1998, 7 (09) :1411-1415