Proteomics analysis of apoptosis-regulating proteins in tissues with different radiosensitivity

被引:17
作者
An, Jeung Hee [1 ]
Seong, Jin Sil [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Radiat Oncol, Brain Korea 21 Project Med Sci, Seoul 120749, South Korea
关键词
radiation; proteomics; apoptosis; radiosusceptibility;
D O I
10.1269/jrr.47.147
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The aim of this study was to identify of radiosusceptibility proteins in tissues with different radiosensitivity. C3H/HeJ mice were exposed to 10 Gy. The tissues were processed for proteins extraction and were analyzed by 2-dimensional electrophoresis. The proteins were identified by matrix-assisted laser desorption ionizing time-of-flight mass spectrometry and validated by immunohistochemical staining and Western blotting. The peaks of apoptosis levels were 35.3 +/- 1.7% and 0.6 +/- 0.2% in the spleen and the liver, respectively, after ionizing radiation. Analysis of liver tissue showed that the expression level of ROS related proteins such as cytochrome c, glutathione S transferase, NADH dehydrogenase and peroxiredoxin VI increased after radiation. The expression level of cytochrome c increased to 3-fold after ionizing radiation in both tissues. However in spleen tissue, the expression level of various kinds of apoptosis regulating proteins increased after radiation. These involved iodothyronine, CD 59A glycoprotein precursor, fas antigen and tumor necrosis factor -inducible protein TSG-6nprecursor after radiation. The difference in the apoptosis index between the liver and spleen tissues is closely associated with the expression of various kinds of apoptosis-related proteins. The result suggests that the expression of apoptosis-related protein and redox proteins play important roles in this radiosusceptibility.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 25 条
[1]
Redox signaling by ionizing radiation in mouse liver [J].
An, JH ;
Kim, J ;
Seong, J .
SIGNAL TRANSDUCTION PATHWAYS, CHROMATIN STRUCTURE, AND GENE EXPRESSION MECHANISMS AS THERAPEUTIC TARGETS, 2004, 1030 :86-94
[2]
The death substrate Gas2 binds m-calpain and increases susceptibility to p53-dependent apoptosis [J].
Benetti, R ;
Del Sal, G ;
Monte, M ;
Paroni, G ;
Brancolini, C ;
Schneider, C .
EMBO JOURNAL, 2001, 20 (11) :2702-2714
[3]
COMPARISON BETWEEN INVITRO RADIOSENSITIVITY AND INVIVO RADIORESPONSE IN MURINE TUMOR-CELL LINES .2. INVIVO RADIORESPONSE FOLLOWING FRACTIONATED TREATMENT AND INVITRO INVIVO CORRELATIONS [J].
BRISTOW, RG ;
HILL, RP .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 18 (02) :331-345
[4]
The late increase in intracellular free radical oxygen species during apoptosis is associated with cytochrome c release, caspase activation, and mitochondrial dysfunction [J].
Chen, Q ;
Chai, YC ;
Mazumder, S ;
Jiang, C ;
Macklis, R ;
Chisolm, GM ;
Almasan, A .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (03) :323-334
[5]
Hall EJ, 2000, RADIOBIOLOGY RADIOLO, P314
[6]
THE INTERACTION BETWEEN RECOMBINANT HUMAN TUMOR-NECROSIS-FACTOR AND RADIATION IN 13 HUMAN TUMOR-CELL LINES [J].
HALLAHAN, DE ;
BECKETT, MA ;
KUFE, D ;
WEICHSELBAUM, RR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (01) :69-74
[7]
INGOLD JA, 1965, AMER J ROENTGENOL RA, V93, P200
[8]
Kerr NCH, 1998, J PATHOL, V186, P24
[9]
KIM SH, 2002, J KOREA SOC THER RAD, V21, P222
[10]
Radiation and ceramide-induced apoptosis [J].
Kolesnick, R ;
Fuks, Z .
ONCOGENE, 2003, 22 (37) :5897-5906