Spatially resolved cellular responses to singlet oxygen

被引:364
作者
Redmond, Robert W. [1 ]
Kochevar, Irene E. [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Wellman Ctr Photomed, Boston, MA 02115 USA
关键词
D O I
10.1562/2006-04-14-IR-874
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Singlet oxygen (O-1(2)) is unique amongst reactive oxygen species formed in cells in that it is an excited state molecule with an inherent upper lifetime of 4 mu s in water. Whether the lifetime Of O-1(2) in cells is shortened by reactions with cellular molecules or reaches the inherent maximum value is still unclear. However, even with the maximum lifetime, the diffusion radius is only similar to 220 nm during three lifetimes (similar to 5% O-1(2) remaining), much shorter than cellular dimensions indicating that the primary reactions Of O-1(2) will be subcellularly localized near the site Of O-1(2) formation. This fact has raised the question of whether spatially resolved cellular responses to O-1(2) occur, i.e. whether responses can be initiated by generation and reaction Of O-1(2) at a particular subcellular location that would not have been produced by O-1(2) generation at other subcellular sites. In this paper, we discuss examples of spatially resolved responses initiated by O-1(2) as a function of distance from the site of generation Of O-1(2). Three levels are recognized, namely, a molecular level where the primary oxidation product directly modifies the behavior of a cell, an organelle level where the initial photo-oxidation products initiate mechanisms that are unique to the organelle and the cellular level where mediators diffuse from their site of formation to the target molecules that initiate the response. These examples indicate that, indeed, spatially resolved responses to O-1(2) occur in cells.
引用
收藏
页码:1178 / 1186
页数:9
相关论文
共 82 条
[71]   Genetically targeted chromophore-assisted light inactivation [J].
Tour, O ;
Meijer, RM ;
Zacharias, DA ;
Adams, SR ;
Tsien, RY .
NATURE BIOTECHNOLOGY, 2003, 21 (12) :1505-1508
[72]  
Trauner KB, 1998, PHOTOCHEM PHOTOBIOL, V67, P133
[73]  
Usuda J, 2003, PHOTOCHEM PHOTOBIOL, V78, P1, DOI 10.1562/0031-8655(2003)078<0001:ABTPLO>2.0.CO
[74]  
2
[75]   The genetic basis of singlet oxygen-induced stress responses of Arabidopsis thaliana [J].
Wagner, D ;
Przybyla, D ;
Camp, ROD ;
Kim, C ;
Landgraf, F ;
Lee, KP ;
Würsch, M ;
Laloi, C ;
Nater, M ;
Hideg, E ;
Apel, K .
SCIENCE, 2004, 306 (5699) :1183-1185
[76]   Photodynamic antimicrobial chemotherapy (PACT) [J].
Wainwright, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 42 (01) :13-28
[77]   Photo-oxidation of cells generates long-lived intracellular protein peroxides [J].
Wright, A ;
Hawkins, CL ;
Davies, MJ .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 34 (06) :637-647
[78]   Singlet oxygen-mediated protein oxidation: evidence for the formation of reactive peroxides [J].
Wright, A ;
Hawkins, CL ;
Davies, MJ .
REDOX REPORT, 2000, 5 (2-3) :159-161
[79]   Photodamage to multiple Bcl-xL isoforms by photodynamic therapy with the phthalocyanine photosensitizer Pc 4 [J].
Xue, LY ;
Chiu, SM ;
Fiebig, A ;
Andrews, DW ;
Oleinick, NL .
ONCOGENE, 2003, 22 (58) :9197-9204
[80]   Factors affecting DNA damage caused by lipid hydroperoxides and aldehydes [J].
Yang, MH ;
Schaich, KM .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (02) :225-236