Control of respiration by nitric oxide in Keilin-Hartree particles, mitochondria and SH-SY5Y neuroblastoma cells

被引:28
|
作者
Mastronicola, D
Genova, ML
Arese, M
Barone, MC
Giuffrè, A
Bianchi, C
Brunori, M
Lenaz, G
Sarti, P
机构
[1] Univ Roma La Sapienza, Dipartimento Sci Biochim A Rossi Fanelli, I-00185 Rome, Italy
[2] IFO, Regina Elena Canc Inst, SAFU, SSD, I-00100 Rome, Italy
[3] Univ Bologna, Dept Biochem, I-40126 Bologna, Italy
[4] Univ Roma La Sapienza, CNR, Inst Mol Biol & Pathol, I-00185 Rome, Italy
关键词
reaction mechanism; NO scavenging; haemoprotein; tumour cells; control of respiration;
D O I
10.1007/s00018-003-3127-3
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
The pattern of cytochrome c oxidase inhibition by nitric oxide (NO) was investigated polarographically using Keilin-Hartree particles, mitochondria and human neuroblastoma cells. NO reacts with purified cytochrome c oxidase forming either a nitrosyl- or a nitrite-inhibited derivative, displaying distinct kinetics and light sensitivity of respiration recovery in the absence of free NO. Keilin-Hartree particles or cells, respiring either on endogenous substrates alone or in the presence of ascorbate, Das well as state 3 and state 4 mitochondria respiring on glutamate and malate, displayed the rapid recovery characteristic of the nitrite derivative. All systems, when respiring in the presence of tetramethyl-p-phenylenediamine, were characterised by the slower, light-sensitive recovery typical of the nitrosyl derivative. Together the results suggest that the reaction of NO with cytochrome c oxidase in situ follows two alternative inhibition pathways, depending on the electron flux through the respiratory chain.
引用
收藏
页码:1752 / 1759
页数:8
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