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皮肤狼疮红斑皮肤活检中的凋亡信号分子:组织微阵列分析。

Apoptotic signal molecules in skin biopsies of cutaneous lupus erythematosus: analysis using tissue microarray.

机构信息

Division of Immunogenetics, Tumorimmunology Program, German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

出版信息

Exp Dermatol. 2013 Oct;22(10):656-9. doi: 10.1111/exd.12216.

Abstract

Cutaneous lupus erythematosus (CLE) is a heterogeneous autoimmune disease. Different pathogenetic mechanisms, including the accumulation of apoptotic keratinocytes in CLE, have been reported. Therefore, we investigated whether CLE and other inflammatory skin diseases differ with regard to the epidermal expression of molecules that are crucial for the initiation and regulation of apoptosis. In this study, 241 skin biopsies from patients with CLE, psoriasis (PSO), lichen planus (LP) and healthy controls (HCs) were analysed immunohistochemically using the tissue microarray (TMA) technique. The TUNEL assay and anti-activated caspase-3 antibodies revealed a significant increase of apoptotic keratinocytes in CLE lesions compared with HCs. Furthermore, we detected a significant increase in the epidermal expression of CD95 in CLE specimens compared with PSO, LP and HCs. These data suggest that the accumulation of apoptotic keratinocytes in CLE might be due to the increased epidermal expression of CD95, resulting in increased activity of the extrinsic apoptotic pathway in the disease.

摘要

皮肤红斑狼疮(CLE)是一种异质性自身免疫性疾病。已经报道了包括 CLE 中凋亡角质形成细胞积累在内的不同发病机制。因此,我们研究了 CLE 和其他炎症性皮肤病在对启动和调节细胞凋亡至关重要的表皮分子表达方面是否存在差异。在这项研究中,使用组织微阵列(TMA)技术对来自 CLE、银屑病(PSO)、扁平苔藓(LP)和健康对照(HCs)患者的 241 个皮肤活检标本进行了免疫组织化学分析。TUNEL 检测和抗活化 caspase-3 抗体显示,与 HCs 相比,CLE 病变中的凋亡角质形成细胞明显增加。此外,我们发现与 PSO、LP 和 HCs 相比,CLE 标本中 CD95 的表皮表达明显增加。这些数据表明,CLE 中凋亡角质形成细胞的积累可能是由于 CD95 的表皮表达增加,导致疾病中外在凋亡途径的活性增加。

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