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皮肤刺激诱导胸腺基质淋巴细胞生成素的产生不依赖于肿瘤坏死因子-α,但依赖于白细胞介素-1。

Thymic stromal lymphopoietin induction by skin irritation is independent of tumour necrosis factor-α, but supported by interleukin-1.

机构信息

Klinik für Dermatologie und Allergologie, Allergie-Centrum-Charité, CCM, Charité - Universitätsmedizin, 10117, Berlin, Germany.

出版信息

Br J Dermatol. 2015 Apr;172(4):951-60. doi: 10.1111/bjd.13465. Epub 2015 Feb 27.

Abstract

BACKGROUND

Thymic stromal lymphopoietin (TSLP) is an extensively studied cytokine linked to the pathogenesis of allergic diseases, but the inherent activities behind TSLP expression are not well defined.

OBJECTIVES

To explore the conditions favourable to TSLP induction outside of a typically allergic set-up and determine the associated mechanisms, and to assess whether TSLP is similarly controlled in murine and human skin.

METHODS

A combination of primary keratinocytes, skin explants/epidermal sheets and in vivo strategies was employed. The skin of wild-type and tumour necrosis factor knockout (TNF-/-) mice was subjected to acute irritation. Cells and specimens were stimulated with a range of TSLP inducers in the presence or absence of neutralizing antibodies. TSLP was quantitated by quantitative reverse-transcriptase polymerase chain reaction, enzyme-linked immunosorbent assay and immunohistochemistry.

RESULTS

In addition to cytokines, skin irritation brought about by various causes (e.g. shaving, scratching and chemical perturbation) elicited uniformly high-level production of TSLP, which entered the circulatory system. Despite the potency of TNF-α as an in vitro TSLP inducer, the use of TNF-/- mice revealed that this mechanism was completely independent of endogenous TNF-α. Conversely, irritation-elicited TSLP depended on interleukin (IL)-1, which had a more pronounced influence in human skin than in murine skin. Murine and human skin differed considerably regarding TSLP regulation.

CONCLUSIONS

Thymic stromal lymphopoietin is a general responder to disrupted skin homeostasis and may have a role in triggering the alarm system of the skin. TSLP induction is rapid, transient and driven by a mechanism that does not involve TNF-α, but partially relies on the evolutionarily ancient IL-1 system. The irritated skin secretes TSLP into the circulatory system. TSLP regulation varies between species.

摘要

背景

胸腺基质淋巴细胞生成素(TSLP)是一种广泛研究的细胞因子,与过敏疾病的发病机制有关,但 TSLP 表达的内在活性尚未得到很好的定义。

目的

探索在非典型过敏环境下有利于 TSLP 诱导的条件,并确定相关机制,并评估 TSLP 是否在鼠类和人类皮肤中受到类似的控制。

方法

采用原代角质形成细胞、皮肤标本/表皮片和体内策略相结合的方法。对野生型和肿瘤坏死因子敲除(TNF-/-)小鼠的皮肤进行急性刺激。在存在或不存在中和抗体的情况下,用一系列 TSLP 诱导剂刺激细胞和标本。通过定量逆转录聚合酶链反应、酶联免疫吸附试验和免疫组织化学定量 TSLP。

结果

除细胞因子外,各种原因(如剃须、抓挠和化学干扰)引起的皮肤刺激均导致高水平 TSLP 的一致产生,并进入循环系统。尽管 TNF-α作为体外 TSLP 诱导剂具有很强的作用,但 TNF-/- 小鼠的使用表明,这种机制完全独立于内源性 TNF-α。相反,刺激引起的 TSLP 依赖于白细胞介素(IL)-1,其在人类皮肤中的影响比在鼠类皮肤中更为显著。鼠类和人类皮肤在 TSLP 调节方面存在显著差异。

结论

胸腺基质淋巴细胞生成素是对皮肤稳态破坏的一般反应者,可能在触发皮肤报警系统中发挥作用。TSLP 诱导迅速、短暂,并由一种不涉及 TNF-α的机制驱动,但部分依赖于进化古老的 IL-1 系统。受刺激的皮肤将 TSLP 分泌到循环系统中。TSLP 调节在不同物种之间存在差异。

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