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干细胞因子增强IgE介导的犬分散皮肤肥大细胞组胺和肿瘤坏死因子-α的释放。

Stem cell factor enhances IgE-mediated histamine and TNF-alpha release from dispersed canine cutaneous mast cells.

作者信息

Brazís P, Queralt M, de Mora F, Ferrer L I, Puigdemont A

机构信息

Departament de Farmacologia, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.

出版信息

Vet Immunol Immunopathol. 2000 Jun 30;75(1-2):97-108. doi: 10.1016/s0165-2427(00)00188-4.

Abstract

Stem cell factor (SCF), the c-kit receptor ligand, plays a critical role in mast cell (MC) development and differentiation. In addition, SCF has recently been found to both modulate and induce MC activation. To investigate the effect of SCF on canine cutaneous MC function, we have characterized the ability of SCF to modulate the release by mature canine MC of preformed (histamine) and newly generated (TNF-alpha) mediators. Mature MC were isolated from skin and cultured in the absence or presence of exogenous SCF (6 ng/ml) for up to 5 days and then challenged with anti-IgE (1 microg/ml) alone for 30 min or with a combination of SCF (50 ng/ml) and anti-IgE. SCF alone failed to trigger either histamine or TNF-alpha release at any time. However, we observed that SCF used as a co-stimulus significantly potentiated histamine and TNF-alpha release in canine MC activated through Fc epsilon RI regardless of whether or not SCF was added to the medium during culturing. Thus, the mean histamine release (%) and TNF-alpha production (pg/ml) were found to be significantly higher if cells were maintained in culture in SCF-supplemented medium compared with cells cultured in the absence of exogenous SCF. We also observed that MC responsiveness to immunological stimulation increased with culture time, the percentage of histamine released being higher in cells cultured for at least 3 days when compared to freshly isolated MC. Taken together these findings suggest that canine skin MC releasability can be enhanced independently either through prolonged incubation with SCF and/or through anti-IgE and SCF co-stimulation.

摘要

干细胞因子(SCF),即c-kit受体配体,在肥大细胞(MC)的发育和分化中起关键作用。此外,最近发现SCF既能调节又能诱导MC活化。为了研究SCF对犬皮肤MC功能的影响,我们已对SCF调节成熟犬MC释放预先形成的(组胺)和新产生的(肿瘤坏死因子-α)介质的能力进行了表征。从皮肤中分离出成熟MC,在无或有外源性SCF(6 ng/ml)的情况下培养长达5天,然后单独用抗IgE(1 μg/ml)刺激30分钟或用SCF(50 ng/ml)与抗IgE联合刺激。单独的SCF在任何时候都未能触发组胺或肿瘤坏死因子-α的释放。然而,我们观察到,作为共刺激剂使用的SCF能显著增强通过FcεRI活化的犬MC中组胺和肿瘤坏死因子-α的释放,无论培养期间培养基中是否添加了SCF。因此,发现与在无外源性SCF的培养基中培养的细胞相比,如果细胞在添加了SCF的培养基中培养,组胺释放的平均百分比(%)和肿瘤坏死因子-α的产生量(pg/ml)会显著更高。我们还观察到,MC对免疫刺激的反应性随培养时间增加,与新鲜分离的MC相比,培养至少3天的细胞中组胺释放的百分比更高。综上所述,这些发现表明,犬皮肤MC的释放能力可通过与SCF长时间孵育和/或通过抗IgE与SCF的共刺激独立增强。

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