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银屑病皮肤病变样本中的中性粒细胞趋化因子和白细胞介素-1样活性。进一步的特性研究。

Neutrophil chemoattractant and IL-1-like activity in samples from psoriatic skin lesions. Further characterization.

作者信息

Fincham N J, Camp R D, Gearing A J, Bird C R, Cunningham F M

机构信息

Institute of Dermatology, St. Thomas's Hospital, London, England.

出版信息

J Immunol. 1988 Jun 15;140(12):4294-9.

PMID:3286771
Abstract

The IL-1-like neutrophil chemoattractant activity previously reported by us to be present in the stratum corneum of psoriatic skin lesions has now been characterized further. Aqueous extracts of stratum corneum samples from psoriatic lesions and from the heels of normal volunteers were ultrafiltered to yield 10- to 30-kDa fractions. The ultrafiltered psoriatic preparations consistently contained greater neutrophil chemokinetic activity than the normal heel preparations, but in contrast the latter contained markedly greater IL-1 activity than the former. Successive chromatographic purification of psoriatic lesional stratum corneum extracts showed that the neutrophil chemokinetic material previously reported to co-elute with IL-1 activity on reversed phase HPLC, but to be distinct from C5a des arg, could now be separated by anion exchange HPLC into at least four different chemokinetic compounds that were also resolved from the IL-1 activity. The reversed phase HPLC-purified chemokinetic material from psoriatic stratum corneum was also active in a neutrophil chemotaxis assay. These findings show that samples from psoriatic skin lesions contain a group of novel 10- to 30-kDa neutrophil chemoattractant compounds that are distinct from both C5a des arg and IL-1. The contrasting neutrophil chemokinetic and IL-1 activities in psoriatic lesional and normal heel stratum corneum preparations support the finding that the two activities are produced by different compounds. These neutrophil chemoattractant and IL-1-like compounds may be of pathogenic importance in inflammatory skin disease.

摘要

我们之前报道过,银屑病皮损角质层中存在白细胞介素-1样中性粒细胞趋化活性,现在我们对其进行了进一步的特性研究。对银屑病皮损和正常志愿者足跟部角质层样本的水提取物进行超滤,得到10至30 kDa的组分。超滤后的银屑病样本始终比正常足跟样本含有更高的中性粒细胞化学趋动活性,但相比之下,后者含有的白细胞介素-1活性明显高于前者。对银屑病皮损角质层提取物进行连续色谱纯化,结果显示,之前报道的在反相高效液相色谱上与白细胞介素-1活性共洗脱,但与C5a去精氨酸不同的中性粒细胞化学趋动物质,现在可以通过阴离子交换高效液相色谱分离成至少四种不同的化学趋动化合物,这些化合物也与白细胞介素-1活性分离。来自银屑病角质层的经反相高效液相色谱纯化的化学趋动物质在中性粒细胞趋化试验中也具有活性。这些发现表明,银屑病皮损样本中含有一组新型的10至30 kDa中性粒细胞趋化剂化合物,它们与C5a去精氨酸和白细胞介素-1都不同。银屑病皮损和正常足跟角质层制剂中中性粒细胞化学趋动和白细胞介素-1活性的对比,支持了这两种活性由不同化合物产生的发现。这些中性粒细胞趋化剂和白细胞介素-1样化合物可能在炎症性皮肤病中具有致病重要性。

相似文献

1
Neutrophil chemoattractant and IL-1-like activity in samples from psoriatic skin lesions. Further characterization.银屑病皮肤病变样本中的中性粒细胞趋化因子和白细胞介素-1样活性。进一步的特性研究。
J Immunol. 1988 Jun 15;140(12):4294-9.
2
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Psoriatic skin lesions contain a novel lipid neutrophil chemokinetic compound which is distinct from known chemoattractant eicosanoids.银屑病皮肤损伤含有一种新型脂质中性粒细胞趋化化合物,它不同于已知的趋化性类二十烷酸。
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Aberrant expression of a chemokinetic glycoprotein in psoriatic skin.
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IL-1 alpha, IL-1 beta and psoriasis: conflicting results in the literature. Opposite behaviour of the two cytokines in lesional or non-lesional extracts of whole skin.白细胞介素-1α、白细胞介素-1β与银屑病:文献中的矛盾结果。两种细胞因子在全皮肤病变或非病变提取物中的相反表现。
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Mediators Inflamm. 2014;2014:472625. doi: 10.1155/2014/472625. Epub 2014 Feb 10.
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Mediators of increased blood flow in porcine skin.增加猪皮血流量的介质。
Mediators Inflamm. 1992;1(1):55-9. doi: 10.1155/S0962935192000115.
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Surprisingly high levels of anaphylatoxin C5a des Arg are extractable from psoriatic scales.令人惊讶的是,从银屑病鳞屑中可提取出高水平的过敏毒素C5a去精氨酸。
Arch Dermatol Res. 1993;285(3):131-4. doi: 10.1007/BF01112914.
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Proceedings of the British Pharmacological Society. London, 19th-21st December. Abstracts.英国药理学会会议记录。伦敦,12月19日至21日。摘要。
Br J Pharmacol. 1989 Mar;96 Suppl(Suppl):1P-368P.
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Immunology. 1989 Jun;67(2):181-3.
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IL-8 causes in vivo neutrophil migration by a cell-dependent mechanism.白细胞介素-8通过一种细胞依赖机制引起体内中性粒细胞迁移。
Immunology. 1991 Aug;73(4):472-7.
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In situ expression of messenger RNA of interleukin-1 and interleukin-6 in psoriasis: interleukin-6 involved in formation of psoriatic lesions.白细胞介素-1和白细胞介素-6信使核糖核酸在银屑病中的原位表达:白细胞介素-6参与银屑病皮损形成。
Arch Dermatol Res. 1991;283(6):351-6. doi: 10.1007/BF00371814.
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Arch Dermatol Res. 1992;284 Suppl 1:S2-9. doi: 10.1007/BF00638232.