Calcium movement and membrane potential changes in the early phase of neutrophil activation by phorbol myristate acetate: a study with ion-selective electrodes.
Calcium movement and membrane potential changes in the early phase of neutrophil activation by phorbol myristate acetate: a study with ion-selective electrodes.
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DOI:
10.1083/jcb.93.1.129
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发表时间:
1982-04
期刊:
影响因子:
--
通讯作者:
Romeo D
中科院分区:
文献类型:
--
作者:
Mottola C;Romeo D
To quantitate calcium movements and membrane potential changes in stimulated neutrophils, we have measured net fluxes of Ca2+ and of the lipophilic cation tetraphenyl phosphonium by a very sensitive ion- selective electrode system. Activation of neutrophils by 3 X 10(-8) M phorbol 12-myristate, 13-acetate induces a release of approximately 20% of total cell calcium, with an initial lag period of less than 10 s. The Ca2+ outflux is markedly reduced in ATP-depleted cells and in the presence of a calmodulin inhibitor, thereby suggesting that it occurs by activation of the ATP-driven Ca2+ pump of the neutrophil plasmalemma. Activation of neutrophils also induces a transiently increased exchange of medium 45Ca with cell calcium, which is measurable a few seconds after cell exposure to the stimulant and peaks at approximately 40 s. Stimulation of neutrophils after attainment of steady-state accumulation of tetraphenyl phosphonium (resting potential of -67 mV) results in a marked depolarization, with a lag period of approximately 60 s. The rate and extent of depolarization are reduced by 40 and 65%, respectively, in a low Na+ medium but are not modified by an inhibitor of anion exchange across membranes. A high-K+ medium depolarizes neutrophils without either modifying their resting oxidative metabolism or impairing stimulability by the phorbol ester. Phorbol 12-myristate, which also exhibits no effect on the oxidative metabolism of neutrophils, does not induce Ca2+ extrusion and membrane potential changes. The causal relationship between Ca2+ mobilization, membrane potential changes and activation of neutrophil functions is discussed.
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DOI:
10.1083/jcb.82.2.369
发表时间:
1979-08
期刊:
The Journal of cell biology
影响因子:
--
作者:
Cramer EB;Gallin JI
通讯作者:
Gallin JI
影响因子:
56.9
作者:
BOUCEK, MM;SNYDERMAN, R
通讯作者:
SNYDERMAN, R
DOI:
10.1073/pnas.77.5.2721
发表时间:
1980-01-01
期刊:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES
影响因子:
--
作者:
KORCHAK, HM;EISENSTAT, BA;WEISSMANN, G
通讯作者:
WEISSMANN, G
影响因子:
64.8
作者:
ESTENSEN, RD;HILL, HR;GOLDBERG, ND
通讯作者:
GOLDBERG, ND
DOI:
10.1016/0005-2736(73)90389-1
发表时间:
1973-01-01
期刊:
BIOCHIMICA ET BIOPHYSICA ACTA
影响因子:
--
作者:
HORVATH, C;SOVAK, M
通讯作者:
SOVAK, M