Two distinct sources of elicited reactive oxygen species in tobacco epidermal cells

被引:425
作者
Allan, AC [1 ]
Fluhr, R [1 ]
机构
[1] WEIZMANN INST SCI,DEPT PLANT GENET,IL-76100 REHOVOT,ISRAEL
关键词
D O I
10.1105/tpc.9.9.1559
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
Reactive oxygen species (ROS) play a prominent role in early and later stages of the plant pathogenesis response, putatively acting as both cellular signaling molecules and direct antipathogen agents. A single-cell assay, based on the fluorescent probe dichlorofluorescein, was used to scrutinize the generation and movement of ROS in tobacco epidermal tissue, ROS, generated within cells, quickly moved apoplastically as H2O2 into neighboring cells. Two classes of rapidly elicited intracellular ROS, originating from distinct sources, were distinguished. Cryptogein, the fungal elicitor from Phytophthora cryptogea, induced ROS from a flavin-containing oxidase source. ROS accumulation could be inhibited by a number of pharmacological agents, suggesting induction through an active signal transduction pathway. The insensitivity of the increase in ROS to the external addition of enzymes that dissipate ROS suggests that this oxidative increase is primarily intracellular. In contrast, amines and polyamines, compounds that form during wounding and pathogenesis, induced ROS at an apoplastic site from peroxidase-or amine oxidase-type enzyme(s). Salicylic acid, a putative inhibitor of cellular catalases and peroxidases, did not induce cellular ROS, as measured by dichlorofluorescein fluorescence, The physiological relevance of ROS-generated signals was indicated by the rapid alteration of the epidermal cell glutathione pool and the cellular redox state. In addition, induction of ROS by all elicitors was correlated with subsequent cell death.
引用
收藏
页码:1559 / 1572
页数:14
相关论文
共 62 条
[1]   COPPER-CONTAINING PLANT OXIDASES [J].
AGRO, AF ;
ROSSI, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1992, 20 (02) :369-373
[2]   INVOLVEMENT OF POLYAMINES, DIAMINE OXIDASE AND PEROXIDASE IN RESISTANCE OF CHICKPEA TO ASCOCHYTA-RABIEI [J].
ANGELINI, R ;
BRAGALONI, M ;
FEDERICO, R ;
INFANTINO, A ;
PORTAPUGLIA, A .
JOURNAL OF PLANT PHYSIOLOGY, 1993, 142 (06) :704-709
[3]   RAPID STIMULATION OF AN OXIDATIVE BURST DURING ELICITATION OF CULTURED PLANT-CELLS - ROLE IN DEFENSE AND SIGNAL TRANSDUCTION [J].
APOSTOL, I ;
HEINSTEIN, PF ;
LOW, PS .
PLANT PHYSIOLOGY, 1989, 90 (01) :109-116
[4]   Epidermal growth factor (EGF)-induced generation of hydrogen peroxide - Role in EGF receptor-mediated tyrosine phosphorylation [J].
Bae, YS ;
Kang, SW ;
Seo, MS ;
Baines, IC ;
Tekle, E ;
Chock, PB ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (01) :217-221
[5]   ACTIVE OXYGEN IN PLANT PATHOGENESIS [J].
BAKER, CJ ;
ORLANDI, EW .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 1995, 33 :299-321
[6]   MICROTITER PLATE ASSAY FOR THE MEASUREMENT OF GLUTATHIONE AND GLUTATHIONE DISULFIDE IN LARGE NUMBERS OF BIOLOGICAL SAMPLES [J].
BAKER, MA ;
CERNIGLIA, GJ ;
ZAMAN, A .
ANALYTICAL BIOCHEMISTRY, 1990, 190 (02) :360-365
[7]   HYDROGEN-PEROXIDE DOES NOT FUNCTION DOWNSTREAM OF SALICYLIC-ACID IN THE INDUCTION OF PR PROTEIN EXPRESSION [J].
BI, YM ;
KENTON, P ;
MUR, L ;
DARBY, R ;
DRAPER, J .
PLANT JOURNAL, 1995, 8 (02) :235-245
[8]  
BOTTIN A, 1994, PLANT PHYSIOL BIOCH, V32, P373
[9]  
BOWELL GP, 1995, FREE RADICAL RES, V23, P517
[10]   DETECTION OF PICOMOLE LEVELS OF HYDROPEROXIDES USING A FLUORESCENT DICHLOROFLUORESCEIN ASSAY [J].
CATHCART, R ;
SCHWIERS, E ;
AMES, BN .
ANALYTICAL BIOCHEMISTRY, 1983, 134 (01) :111-116