Carbon monoxide modulates the response of human basophils to FcepsilonRI stimulation through the heme oxygenase pathway.
Carbon monoxide modulates the response of human basophils to FcepsilonRI stimulation through the heme oxygenase pathway.
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一氧化碳通过血红素加氧酶途径调节人类嗜碱性粒细胞对 FcepsilonRI 刺激的反应。
DOI:
10.1016/s0014-2999(03)01489-4
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发表时间:
2003
影响因子:
5
通讯作者:
E. Masini
中科院分区:
文献类型:
--
作者:
A. Vannacci;R. Baronti;G. Zagli;C. Marzocca;S. Pierpaoli;D. Bani;M. Passani;P. Mannaioni;E. Masini
We report the effects of exogenous and endogenous carbon monoxide (CO) on the immunological activation of human basophils. Hemin (1−100 μM), a heme oxygenase substrate analogue, significantly increased the formation of bilirubin from partially purified human basophils, thus indicating that these cells express heme oxygenase. This effect was reversed by preincubating the cells for 30 min with Zn-protoporphyrin IX (100 μM), a heme oxygenase inhibitor. Hemin (100 μM) also decreased immunoglobulin G anti-Fcε(anti-IgE)-induced activation of basophils, measured by the expression of a membrane granule-associated protein, identified as cluster differentiation protein 63 (CD63), and by histamine release. These effects were reversed by Zn-protoporphyrin IX (100 μM), by oxyhemoglobin (HbO2), a CO scavenger (100 μM), and by 1H-[1,2,4]oxadiazolo[4,3-a] quinoxalin-1-one (ODQ), an inhibitor of the soluble guanylyl cyclase (100 μM). Exposure of basophils to exogenous CO (10 μM for 30 min) also decreased their activation, while nitrogen (N2) was ineffective. HbO2and ODQ reversed the inhibition, reversing both membrane protein CD63 expression and histamine release to basal values. Both hemin and exogenous CO significantly raised cGMP levels in basophils and blunted the rise of calcium levels caused by immunological activation. This study suggests that CO increases cGMP formation, which in turn induces a fall in intracellular Ca2+concentration, thereby resulting in the inhibition of human basophil activation.
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DOI:
10.1016/s0034-5687(98)00072-3
发表时间:
1998
期刊:
Respiration physiology
影响因子:
--
作者:
Prabhakar,NR
通讯作者:
Prabhakar,NR
DOI:
10.1073/pnas.92.7.2568
发表时间:
1995-03-28
影响因子:
11.1
作者:
KHARITONOV, VG;SHARMA, VS;KOESLING, D
通讯作者:
KOESLING, D
影响因子:
20.1
作者:
Motterlini, R;Gonzales, A;Winslow, RM
通讯作者:
Winslow, RM
DOI:
10.1073/pnas.92.5.1475
发表时间:
1995-02-28
影响因子:
11.1
作者:
MORITA, T;PERRELLA, MA;KOUREMBANAS, S
通讯作者:
KOUREMBANAS, S
影响因子:
--
作者:
Maines,M
通讯作者:
Maines,M