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Netherton 综合征:蛋白酶抑制丧失导致的皮肤炎症和过敏。

Netherton syndrome: skin inflammation and allergy by loss of protease inhibition.

机构信息

Laboratory of Genetic Skin Diseases, INSERM U781, Paris, France.

出版信息

Cell Tissue Res. 2013 Feb;351(2):289-300. doi: 10.1007/s00441-013-1558-1. Epub 2013 Jan 24.

Abstract

Netherton syndrome (NS) is a rare autosomal recessive skin disease with severe skin inflammation and scaling, a specific hair shaft defect and constant allergic manifestations. NS is caused by loss-of-function mutations in SPINK5 (serine protease inhibitor of kazal type 5) encoding LEKTI-1 (lympho-epithelial kazal type related inhibitor type 5) expressed in stratified epithelia. In vitro and in vivo studies in murine models and in NS patients have cast light on the pathogenesis of the disease and shown that LEKTI deficiency results in unopposed kallikrein-related peptidase 5 (KLK5) and KLK7 activities and to the overactivity of a new epidermal protease, elastase 2 (ELA2). Two main cascades initiated by KLK5 activity have emerged. One results in desmoglein 1 degradation and desmosome cleavage leading to stratum corneum detachment. KLK5 also activates KLK7 and ELA2, which contribute to a defective skin barrier. This facilitates allergen and microbe penetration and generates danger signals leading to caspase 1 activation and the production of active interleukin-1β. In parallel, KLK5 activates a specific cascade of allergy and inflammation by activating protease-activated receptor-2 (PAR-2) receptors. PAR-2 activation triggers the production of the major pro-Th2 cytokine TSLP (thymic stromal lymphopoietin) and several inflammatory cytokines, including tumour necrosis factor-α. Levels of thymus and activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC) also contribute to allergy in a PAR-2-independent manner. Patient investigations have confirmed these abnormalities and revealed a wide spectrum of disease expression, sometimes associated with residual LEKTI expression. These results have demonstrated that the tight regulation of epidermal protease activity is essential for skin homeostasis and identified new targets for therapeutic intervention. They also provide a link with atopic dermatitis through deregulated protease activity, as recently supported by functional studies of the E420K LEKTI variant.

摘要

Netherton 综合征(NS)是一种罕见的常染色体隐性皮肤疾病,具有严重的皮肤炎症和鳞屑、特定的毛发轴缺陷和持续的过敏表现。NS 是由编码 LEKTI-1(淋巴上皮 Kazal 型相关抑制剂 5 型)的 SPINK5(丝氨酸蛋白酶抑制剂 Kazal 型 5)功能丧失突变引起的,LEKTI-1 在角化上皮中表达。在鼠模型和 NS 患者的体外和体内研究揭示了疾病的发病机制,并表明 LEKTI 缺乏导致 Kallikrein-related peptidase 5(KLK5)和 KLK7 活性无拮抗作用,并导致新的表皮蛋白酶弹性蛋白酶 2(ELA2)过度活跃。KLK5 活性引发的两个主要级联反应已经出现。一个导致桥粒芯糖蛋白 1 降解和桥粒裂解,导致角质层脱落。KLK5 还激活 KLK7 和 ELA2,导致皮肤屏障缺陷。这促进了过敏原和微生物的渗透,并产生危险信号,导致半胱天冬酶 1 激活和活性白细胞介素-1β的产生。同时,KLK5 通过激活蛋白酶激活受体-2(PAR-2)受体激活特定的过敏和炎症级联反应。PAR-2 激活触发主要的 Th2 细胞因子 TSLP(胸腺基质淋巴细胞生成素)和几种炎症细胞因子的产生,包括肿瘤坏死因子-α。胸腺和激活调节趋化因子(TARC)和巨噬细胞衍生趋化因子(MDC)的水平也通过 PAR-2 非依赖性方式促进过敏。患者研究证实了这些异常,并揭示了广泛的疾病表达谱,有时与残留的 LEKTI 表达有关。这些结果表明,表皮蛋白酶活性的严格调节对于皮肤稳态至关重要,并确定了新的治疗干预靶点。它们还通过最近对 E420K LEKTI 变体的功能研究,与特应性皮炎通过调节蛋白酶活性建立了联系。

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