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富含脯氨酸的小分子蛋白在肿瘤性和炎症性皮肤病中的表达

Expression of small proline rich proteins in neoplastic and inflammatory skin diseases.

作者信息

De Heller-Milev M, Huber M, Panizzon R, Hohl D

机构信息

Department of Dermatology, CHUV/DHURDV, CH-1011 Lausanne, Switzerland.

出版信息

Br J Dermatol. 2000 Oct;143(4):733-40. doi: 10.1046/j.1365-2133.2000.03768.x.

Abstract

BACKGROUND

The formation of the cornified cell envelope (CE) during the late stages of epidermal differentiation is essential for epidermal barrier function and protects the body against environmental attack and water loss. Formation of the CE involves the replacement of the plasma membrane by cross-linkage of precursor proteins such as involucrin, small proline rich proteins (SPRR) and loricrin. In normal epidermis, SPRR1 is restricted to appendages, SPRR2 is also expressed in interfollicular areas, while SPRR3 is completely absent; the latter is most abundant in oral epithelium. This differential expression indicates an important part for SPRRs in specific barrier requirements, and reflects their importance in the biomechanical properties of the CE.

OBJECTIVES

We report here on the expression of SPRR1, SPRR2 and SPRR3 in a wide range of cutaneous neoplastic and inflammatory diseases.

METHODS

We used immunohistochemistry; in addition, Northern blot analysis of malignant tumours was performed.

RESULTS

Increased suprabasal expression of SPRR1 and SPRR2, but no SPRR3 expression, was noted in inflammatory dermatoses with orthokeratotic and parakeratotic squamous differentiation. By contrast, differentiating epidermal tumours such as Bowen's disease, keratoacanthoma and squamous cell carcinoma expressed SPRR3.

CONCLUSIONS

As SPRRs were originally cloned on the basis of their expression in ultraviolet light-irradiated keratinocytes, the expression of SPRR3 in actinic lesions is of interest, and might serve as a diagnostic tool.

摘要

背景

表皮分化后期角质化细胞包膜(CE)的形成对于表皮屏障功能至关重要,可保护身体免受环境侵害和水分流失。CE的形成涉及通过前体蛋白如兜甲蛋白、富含脯氨酸的小分子蛋白(SPRR)和loricrin的交联来替代质膜。在正常表皮中,SPRR1局限于附属器,SPRR2也在毛囊间区域表达,而SPRR3完全缺失;后者在口腔上皮中最为丰富。这种差异表达表明SPRR在特定屏障需求中起重要作用,并反映了它们在CE生物力学特性中的重要性。

目的

我们在此报告SPRR1、SPRR2和SPRR3在多种皮肤肿瘤性和炎性疾病中的表达情况。

方法

我们采用免疫组织化学方法;此外,对恶性肿瘤进行了Northern印迹分析。

结果

在具有正角化和不全角化鳞状分化的炎性皮肤病中,观察到SPRR1和SPRR2在基底层以上表达增加,但无SPRR3表达。相比之下,分化型表皮肿瘤如鲍温病、角化棘皮瘤和鳞状细胞癌表达SPRR3。

结论

由于SPRR最初是基于它们在紫外线照射的角质形成细胞中的表达而克隆的,因此SPRR3在光化性病变中的表达值得关注,可能用作诊断工具。

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