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干细胞因子通过多种机制增强组胺分泌,但不影响大鼠肥大细胞释放肿瘤坏死因子-α。

Stem cell factor potentiates histamine secretion by multiple mechanisms, but does not affect tumour necrosis factor-alpha release from rat mast cells.

作者信息

Lin T J, Bissonnette E Y, Hirsh A, Befus A D

机构信息

Department of Medicine, University of Alberta, Edmonton, Canada.

出版信息

Immunology. 1996 Oct;89(2):301-7. doi: 10.1046/j.1365-2567.1996.d01-733.x.

Abstract

The effect of stem cell factor (SCF) on histamine and tumour necrosis factor-alpha (TNF-alpha) release from rat peritoneal mast cells (PMC) was determined and the intracellular pathways involved in the potentiation of histamine secretion were investigated. The effects of SCF (2-100 ng/ml) were examined following both short-term (0 and 20 min) and long-term (up to 24hr) preincubations with SCF. Pretreatment of PMC with SCF for 0 min (concurrent) or 20 min did not induce histamine secretion directly, but significantly increased antigen (Ag)-induced histamine secretion. SCF potentiated Ag-induced intracellular Ca2+ increase and calcium ionophore A23187-induced histamine secretion. Pertussis toxin (PT) inhibited SCF-induced potentiation of IgE-dependent histamine secretion, indicating that PT-sensitive G-proteins are involved in the immediate effects of SCF. In long-term incubation experiments, SCF pretreatment for 18-24 hr significantly enhanced Ag-induced histamine secretion, but did not affect Ag-induced intracellular Ca2+ levels. The effects of long-term incubation with SCF, but not the short-term effects, were blocked by cycloheximide. Interestingly, spontaneous and Ag-induced TNF-alpha release from rat PMC were not affected by pretreatment with SCF (2-500 ng/ml) for 1 to 24 hr. Thus, through immediate and delayed mechanisms, SCF potentiates histamine release from PMC, but has not effect on TNF-alpha release. The regulation of MC by SCF may be important in allergic and other inflammatory diseases.

摘要

研究了干细胞因子(SCF)对大鼠腹膜肥大细胞(PMC)组胺和肿瘤坏死因子-α(TNF-α)释放的影响,并探讨了参与组胺分泌增强的细胞内信号通路。在短期(0和20分钟)和长期(长达24小时)预孵育SCF后,检测了SCF(2-100 ng/ml)的作用。用SCF预处理PMC 0分钟(同时)或20分钟不会直接诱导组胺分泌,但会显著增加抗原(Ag)诱导的组胺分泌。SCF增强了Ag诱导的细胞内Ca2+增加和钙离子载体A23187诱导的组胺分泌。百日咳毒素(PT)抑制了SCF诱导的IgE依赖性组胺分泌增强,表明PT敏感的G蛋白参与了SCF的即时作用。在长期孵育实验中,SCF预处理18-24小时显著增强了Ag诱导的组胺分泌,但不影响Ag诱导的细胞内Ca2+水平。SCF长期孵育的作用而非短期作用被放线菌酮阻断。有趣的是,大鼠PMC自发和Ag诱导的TNF-α释放不受SCF(2-500 ng/ml)预处理1至24小时的影响。因此,通过即时和延迟机制,SCF增强了PMC组胺释放,但对TNF-α释放无影响。SCF对肥大细胞的调节在过敏性和其他炎症性疾病中可能很重要。

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本文引用的文献

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Biochim Biophys Acta. 1994 Aug 24;1194(1):155-65. doi: 10.1016/0005-2736(94)90215-1.

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