Failla Memorial Lecture - A sense of danger from radiation

被引:272
作者
McBride, WH [1 ]
Chiang, CS
Olson, JL
Wang, CC
Hong, JH
Pajonk, F
Dougherty, GJ
Iwamoto, KS
Pervan, M
Liao, YP
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiat Oncol, Los Angeles, CA 90095 USA
[2] Natl Tsing Hua Univ, Dept Atom Sci, Hsinchu 30013, Taiwan
[3] St Jude Childrens Res Hosp, Med Therapies Lab Oncol, Memphis, TN 38105 USA
[4] Chang Gung Mem Hosp, Dept Radiat Oncol, Tao Yuan, Taiwan
[5] Univ Clin Freiburg, Dept Radiat Oncol, D-79106 Freiburg, Germany
关键词
D O I
10.1667/RR3196
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tissue damage caused by exposure to pathogens, chemicals and physical agents such as ionizing radiation triggers production of generic "danger" signals that mobilize the innate and acquired immune system to deal with the intrusion and effect tissue repair with the goal of maintaining the integrity of the tissue and the body. Ionizing radiation appears to do the same, but less is known about the role of "danger" signals in tissue responses to this agent. This review deals with the nature of putative "danger" signals that may be generated by exposure to ionizing radiation and their significance. There are a number of potential consequences of "danger" signaling in response to radiation exposure. "Danger" signals could mediate the pathogenesis of, or recovery from, radiation damage. They could alter intrinsic cellular radiosensitivity or initiate radioadaptive responses to subsequent exposure. They may spread outside the locally damaged site and mediate bystander or "out-of-field" radiation effects. Finally, an important aspect of classical "danger" signals is that they link initial nonspecific immune responses in a pathological site to the development of specific adaptive immunity. Interestingly, in the case of radiation, there is little evidence that "danger" signals efficiently translate radiation-induced tumor cell death into the generation of tumor-specific immunity or normal tissue damage into autoimmunity. The suggestion is that radiation-induced "danger" signals may be inadequate in this respect or that radiation interferes with the generation of specific immunity. There are many issues that need to be resolved regarding "danger" signaling after exposure to ionizing radiation. Evidence of their importance is, in some areas, scant, but the issues are worthy of consideration, if for no other reason than that manipulation of these pathways has the potential to improve the therapeutic benefit of radiation therapy. This article focuses on how normal tissues and tumors sense and respond to danger from ionizing radiation, on the nature of the signals that are sent, and on the impact on the eventual consequences of exposure. (C) 2004 by Radiation Research Society.
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页码:1 / 19
页数:19
相关论文
共 236 条
[1]  
AbdelWahab Z, 1996, CELL IMMUNOL, V171, P246, DOI 10.1006/cimm.1996.0200
[2]   INTERLEUKIN-6 MEDIATED DIFFERENTIATION AND RESCUE OF CELL REDOX IN PC12 CELLS EXPOSED TO IONIZING-RADIATION [J].
ABEYAMA, K ;
KAWANO, K ;
NAKAJIMA, T ;
TAKASAKI, I ;
KITAJIMA, I ;
MARUYAMA, I .
FEBS LETTERS, 1995, 364 (03) :298-300
[3]   The radioprotective effect of the 24 kDa FGF-2 isoform in HeLa cells is related to an increased expression and activity of the DNA dependent protein kinase (DNA-PK) catalytic subunit [J].
Ader, I ;
Muller, C ;
Bonnet, J ;
Favre, G ;
Cohen-Jonathan, E ;
Salles, B ;
Toulas, C .
ONCOGENE, 2002, 21 (42) :6471-6479
[4]   Using plasma transforming growth factor beta-1 during radiotherapy to select patients for dose escalation [J].
Anscher, MS ;
Marks, LB ;
Shafman, TD ;
Clough, R ;
Huang, H ;
Tisch, A ;
Munley, M ;
Herndon, JE ;
Garst, J ;
Crawford, J ;
Jirtle, RL .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (17) :3758-3765
[5]   BB-10010, an analog of macrophage inflammatory protein-1α, protects murine small intestine against radiation [J].
Arango, D ;
Ettarh, RR ;
Holden, G ;
Moriarty, M ;
Brennan, PC .
DIGESTIVE DISEASES AND SCIENCES, 2001, 46 (12) :2608-2614
[6]   COMPARISON OF INTERLEUKIN-1-ALPHA GENE-EXPRESSION AND PROTEIN-LEVELS IN THE MURINE SPLEEN AFTER LETHAL AND SUBLETHAL TOTAL-BODY IRRADIATION [J].
BAKER, WH ;
LIMANNI, A ;
CHANG, CM ;
JACKSON, WE ;
SEEMANN, R ;
PATCHEN, ML .
RADIATION RESEARCH, 1995, 143 (03) :320-326
[7]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[8]  
BARCELLOSHOFF MH, 1993, CANCER RES, V53, P3880
[9]   CD91 is a common receptor for heat shock proteins gp96, hsp90, hsp70, and calreticulin [J].
Basu, S ;
Binder, RJ ;
Ramalingam, T ;
Srivastava, PK .
IMMUNITY, 2001, 14 (03) :303-313
[10]  
Beetz A, 1997, INT J RADIAT BIOL, V72, P33, DOI 10.1080/095530097143518