Activation of NADPH oxidase-related proton and electron currents in human eosinophils by arachidonic acid

被引:70
作者
Cherny, VV
Henderson, LM
Xu, W
Thomas, LL
DeCoursey, TE
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Mol Biophys & Physiol, Chicago, IL 60612 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Immunol Microbiol, Chicago, IL 60612 USA
[3] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2001年 / 535卷 / 03期
关键词
D O I
10.1111/j.1469-7793.2001.00783.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Effects of arachidonic acid (AA) on proton and electron currents in human eosinophils were studied using the permeabilized-patch voltage-clamp technique, using an applied NH4+ gradient to control pH(i). 2. Superoxide anion (O-2(-)) release was assessed by cytochrome c reduction in human eosinophils. Significant O-2(-) release was stimulated by 5-10 muM AA. 3. AA activated diphenylene iodinium (DPI)-inhibitable inward current reflecting electron efflux through NADPH oxidase. These electron currents (I-e) were elicited in human eosinophils at AA concentrations (3-10 muM) similar to those that induced O-2(-) release. 4. The voltage-gated proton conductance (g(H)) in eosinophils stimulated with AA was profoundly enhanced: H+ current amplitude (I-H) increased 4.6 times, activation was 4 times faster, and the H+ conductance-voltage (g(H) - V) relationship was shifted to substantially more negative voltages. The electrophysiological effects of AA resembled those reported for PMA, except that zn AA did not consistently slow tau (tail) (deactivation of H+ currents). 5. The stimulation of both proton and electron currents by AA was reversible upon washout. Repeated exposure elicited repeated responses. The activation of H+ currents by AA wa's dissociable from its activation of NADPH oxidase; H+ currents were enhanced at low concentrations of AA that did not elicit detectable I, or when NADPH oxidase was inhibited by DPI. 6. Most of the effects of AA on H+ currents qualitatively resemble those reported in whole-cell studies, reflecting a more direct action than PMA. The results are compatible with AA being an immediate activator of both NADPH oxidase and proton channels in human eosinophils.
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页码:783 / 794
页数:12
相关论文
共 47 条
[31]   ACTIVATION OF H+ CONDUCTANCE IN NEUTROPHILS REQUIRES ASSEMBLY OF COMPONENTS OF THE RESPIRATORY BURST OXIDASE BUT NOT ITS REDOX FUNCTION [J].
NANDA, A ;
CURNUTTE, JT ;
GRINSTEIN, S .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1770-1775
[32]   PROTEIN-KINASE-C ACTIVATES AN H+ (EQUIVALENT) CONDUCTANCE IN THE PLASMA-MEMBRANE OF HUMAN NEUTROPHILS [J].
NANDA, A ;
GRINSTEIN, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10816-10820
[33]  
ODONNELL VB, 1994, MOL PHARMACOL, V46, P778
[34]   Activation of the leukocyte NADPH oxidase subunit p47(phox) by protein kinase C. A phosphorylation-dependent change in the conformation of the C-terminal end of p47(phox) [J].
Park, JW ;
Babior, BM .
BIOCHEMISTRY, 1997, 36 (24) :7474-7480
[35]  
QUINN MT, 1993, J BIOL CHEM, V268, P20983
[36]   THE USE OF DIPHENYLENE IODONIUM, AN INHIBITOR OF NADPH OXIDASE, TO INVESTIGATE THE ANTIMICROBIAL ACTION OF HUMAN MONOCYTE DERIVED MACROPHAGES [J].
ROBERTSON, AK ;
CROSS, AR ;
JONES, OTG ;
ANDREW, PW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 133 (02) :175-179
[37]   ARACHIDONIC-ACID INCREASES THE ACTIVITY OF THE ASSEMBLED NADPH OXIDASE IN CYTOPLASMIC MEMBRANES AND ENDOSOMES [J].
RUBINEK, T ;
LEVY, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1176 (1-2) :51-58
[38]   Electron currents generated by the human phagocyte NADPH oxidase [J].
Schrenzel, J ;
Serrander, L ;
Bánfi, B ;
Nüsse, O ;
Fouyouzi, R ;
Lew, DP ;
Demaurex, N ;
Krause, KH .
NATURE, 1998, 392 (6677) :734-737
[39]   Proton currents in human eosinophils [J].
Schrenzel, J ;
Lew, DP ;
Krause, KH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (06) :C1861-C1871
[40]   Arachidonic acid and phosphorylation synergistically induce a conformational change of p47phox to activate the phagocyte NADPH oxidase [J].
Shiose, A ;
Sumimoto, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (18) :13793-13801