Oxidative stress-induced calcium signalling in Aspergillus nidulans

被引:36
作者
Greene, V
Cao, H
Schanne, FAX
Bartelt, DC
机构
[1] St Johns Univ, Dept Biol Sci, Jamaica, NY 11439 USA
[2] St Johns Univ, Coll Pharm & Allied Hlth Sci, Jamaica, NY 11439 USA
关键词
oxidative stress; calcium; signalling; Aspergillus; luminescence; aequorin;
D O I
10.1016/S0898-6568(01)00266-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The effect; of oxidative stress on levels of calcium ion (Ca2+) in Aspergillus nidulans were measured using strains expressing aequorin in the cytoplasm (Aeq(cyt)) and mitochondria (Aeq(mt)). When oxidative stress was induced by exposure to 10-mM H2O2 the mitochondrial calcium response (C a,;) was greater than the change in cytoplasmic calcium (Ca-c(2+)). The Ca-mt(2+) response to H2O2 was dose dependent, while the increase in [Ca-c(2+)] did not change with increasing H2O2. The increase in both [Ca-c(2+)] and [Ca-mt(2+)] in response to oxidative stress was enhanced by exposure of cells to Ca2+. The presence of chelator in the external medium only partially inhibited the Ca-mt(2+) and Ca-c(2+) responses to oxidative stress. Reagents that alter calcium fluxes had varied effects on the Cap response to peroxide. Ruthenium red blocked the increase in [Ca-mt(2+)], while neomycin caused an even greater increase in [Ca-mt(2+)]. Treatment with ruthenium red and neomycin had no effect on the Ca-c(2+) response. Bafilomycin A and oligomycin had no effect on either the mitochondrial or cytoplasmic response. Inhibitors of both voltage-regulated calcium channels and intracellular calcium release channels inhibited the Ca2+-dependent component of the Ca-mt(2+) response to oxidative stress. We conclude that the more significant Ca2+ response to oxidatve stress occurs in the mitochondria and that both intracellular and extracellular calcium pools can contribute to the increases in [Ca-c(2+)] and [Ca-mt(2+)] induced by oxidative stress. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:437 / 443
页数:7
相关论文
共 39 条
[31]  
RIZZUTO R, 1994, METHOD CELL BIOL, V40, P339
[32]   Communicating with calcium [J].
Sanders, D ;
Brownlee, C ;
Harper, JF .
PLANT CELL, 1999, 11 (04) :691-706
[33]   THE RELATIVE RATE OF AEQUORIN REGENERATION FROM APOAEQUORIN AND COELENTERAZINE ANALOGS [J].
SHIMOMURA, O ;
KISHI, Y ;
INOUYE, S .
BIOCHEMICAL JOURNAL, 1993, 296 :549-551
[34]   LIGHT-EMITTING PROPERTIES OF RECOMBINANT SEMISYNTHETIC AEQUORINS AND RECOMBINANT FLUORESCEIN-CONJUGATED AEQUORIN FOR MEASURING CELLULAR CALCIUM [J].
SHIMOMURA, O ;
MUSICKI, B ;
KISHI, Y ;
INOUYE, S .
CELL CALCIUM, 1993, 14 (05) :373-378
[35]   SEMI-SYNTHETIC AEQUORINS WITH IMPROVED SENSITIVITY TO CA-2+ IONS [J].
SHIMOMURA, O ;
MUSICKI, B ;
KISHI, Y .
BIOCHEMICAL JOURNAL, 1989, 261 (03) :913-920
[36]   Membrane permeability of coelenterazine analogues measured with fish eggs [J].
Shimomura, O .
BIOCHEMICAL JOURNAL, 1997, 326 :297-298
[37]  
WANG X, 2001, J BIOL CHEM
[38]  
WOJTCZAK L, 1972, ACTA BIOCHIM POL, V19, P227
[39]   Dantrolene inhibition of ryanodine receptor Ca2+ release channels -: Molecular mechanism and isoform selectivity [J].
Zhao, FY ;
Li, P ;
Chen, SRW ;
Fruen, BR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (17) :13810-13816