The differential role of extracellular signal-regulated kinases and p38 mitogen-activated protein kinase in eosinophil functions

被引:87
作者
Adachi, T [1 ]
Choudhury, BK [1 ]
Stafford, S [1 ]
Sur, S [1 ]
Alam, R [1 ]
机构
[1] Univ Texas, Med Branch, Dept Internal Med, Div Allergy & Immunol, Galveston, TX 77555 USA
关键词
D O I
10.4049/jimmunol.165.4.2198
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The activation of eosinophils by cytokines is a major event in the pathogenesis of allergic diseases. We have investigated the activation of mitogen-activated protein (MAP) kinases and their functional relevance in eosinophil differentiation, survival, degranulation, and cytokine production. IL-5 induced phosphorylation and activation of extracellular signal-regulated kinases (ERK) and p38 MAP kinases in eosinophils. PD98059, a MAP/ERK kinase inhibitor, blocked phosphorylation of ERK1/2 in a dose-dependent manner. SB202190, a p38 inhibitor, blocked p38-dependent phosphorylation of activating transcription factor-2, To study the importance of the MAP kinases on eosinophil differentiation, we cultured mouse bone marrow cells with IL-3 and IL-5 in the presence of the inhibitors. SB202190 dramatically inhibited eosinophil differentiation by 72%, PD98059 was less potent and reduced eosinophil differentiation by 28%, Both inhibitors marginally inhibited eosinophil survival only at the highest doses. Prolonged incubation of eosinophils with IL-5 induced significant eosinophil-derived neurotoxin release. Both PD98059 and SB202190 nearly completely inhibited (87% and 100% inhibition, respectively) IL-5-stimulated eosinophil-derived neurotoxin release in a dose-dependent manner. Next, we examined the effect of the MAP kinase inhibitors on eosinophil production of the cytokine macrophage-inflammatory protein (MIP)-1 alpha. PD98059 blocked C5a- but not ionomycin-induced MIP-1 alpha production (59% inhibition at 50 mu M concentration). In contrast, SB202190 nearly completely inhibited (99%) C5a-induced MIP-1 alpha production, Further, it blocked ionomycin-stimulated production by 66%, Our results suggest that both p38 and ERK1/2 MAP kinases play an important role in eosinophil differentiation, cytokine production, and degranulation, The p38 MAP kinase plays a greater role than ERK1/2 in eosinophil differentiation and cytokine production.
引用
收藏
页码:2198 / 2204
页数:7
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