Role of vicinal protein thiols in radiation and cytotoxic responses

被引:14
作者
Biaglow, JE
Ayene, IS
Tuttle, SW
Koch, CJ
Donahue, J
Mieyal, JJ
机构
[1] Univ Penn, Sch Med, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Biochem, Philadelphia, PA 19104 USA
[3] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
关键词
D O I
10.1667/RR3505.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glutathione (GSH) and more recently protein thiols (P-SH) have been found to play a major role in cellular radiation response. However, the effects of protein vicinal thiols, which are important for the functions of several major enzymes, on cellular responses to radiation have not been clearly delineated. Here we investigated the effects of depleting GSH and protein vicinal thiols (HS-P-SH) and P-SH on cell toxicity and radiation response. We used hydroxyethyldisulfide (HEDS, beta-mercaptoethanol-disulfide) alone and in combination with phenylarsine oxide (PAO) to alter P-SH, HS-P-SH and GSH. HEDS, a direct substrate for thioredoxin reductase and an indirect substrate for glutaredoxin (thioltransferase), did not alter protein vicinal thiols in cells. However, PAO, which specifically forms a covalent adduct with vicinal thiols, blocked bioreduction of HEDS; there was a concomitant and yet unexplained decrease in K1 cell GSH in the presence of HEDS and PAO. G6PD(+) (K1) and G6PD(-) (E89) cells treated with L-buthionine sulfoximine (L-BSO) for 72 h to deplete GSH followed by PAO showed an increased cytotoxic response. However, the surviving E89 cells showed a 10,000-fold greater radiation lethality than the K1 cells. The effects of rapid depletion of GSH by a combination Of L-BSO and dimethyfomarate (DMF), a glutathione-S-transferase substrate, were also investigated. Under these conditions, PAO radiosensitized the E89 cells more than 1000-fold over the K1 cells. The potential mechanisms for the altered response may be related to the inhibition of thioredoxin reductase and glutaredoxin. Both are key enzymes involved in DNA synthesis, protein homeostasis and cell survival. With GSH removed, vicinal thiols appear to play a critical role in determining cell survival and radiosensitivity. Decreasing P-SH and removing GSH and vicinal thiols is extremely toxic to K1 and E89 cells. We conclude that radiation sensitivity and cell survival are dependent on vicinal thiol and GSH. In the former and latter cases, the protein thiols are also important. (C) 2006 by Radiation Research Society.
引用
收藏
页码:307 / 317
页数:11
相关论文
共 35 条
[1]   Mutation in the glucose-6-phosphate dehydrogenase gene leads to inactivation of Ku DNA end binding during oxidative stress [J].
Ayene, IS ;
Stamato, TD ;
Mauldin, SK ;
Biaglow, JE ;
Tuttle, SW ;
Jenkins, SF ;
Koch, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (12) :9929-9935
[2]  
Ayene IS, 2000, INT J RADIAT BIOL, V76, P1523
[3]   DIAMIDE INDUCED SHIFT IN PROTEIN AND GLUTATHIONE THIOL - DISULFIDE STATUS DELAYS DNA REJOINING AFTER X-IRRADIATION OF HUMAN CANCER-CELLS [J].
BAKER, MA ;
HAGNER, BA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1037 (01) :39-47
[4]   Roles of superoxide radical anion in signal transduction mediated by reversible regulation of protein-tyrosine phosphatase 1B [J].
Barrett, WC ;
DeGnore, JP ;
Keng, YF ;
Zhang, ZY ;
Yim, MB ;
Chock, PB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) :34543-34546
[5]  
Biaglow JE, 2005, CANCER BIOL THER, V4, P6
[6]  
Biaglow JE, 2003, ADV EXP MED BIOL, V530, P153
[7]  
Biaglow JE, 2003, RADIAT RES, V159, P484, DOI 10.1667/0033-7587(2003)159[0484:RROCDA]2.0.CO
[8]  
2
[9]   G6PD deficient cells and the bioreduction of disulfides: Effects of DHEA, GSH depletion and phenylarsine oxide [J].
Biaglow, JE ;
Ayene, IS ;
Koch, CJ ;
Donahue, J ;
Stamato, TD ;
Tuttle, SW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (03) :846-852
[10]   A method for measuring disulfide reduction by cultured mammalian cells: Relative contributions of glutathione-dependent and glutathione-independent mechanisms [J].
Biaglow, JE ;
Donahue, J ;
Tuttle, S ;
Held, K ;
Chrestensen, C ;
Mieyal, J .
ANALYTICAL BIOCHEMISTRY, 2000, 281 (01) :77-86