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鉴定原发性皮肤黏蛋白病中黏蛋白的潜在来源——一项基于组织病理学和多重荧光染色的回顾性研究和分析。

Identifying the potential origin of mucin in primary cutaneous mucinoses-A retrospective study and analysis using histopathology and multiplex fluorescence staining.

机构信息

Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.

Medical Faculty, University of Zurich, Zurich, Switzerland.

出版信息

J Eur Acad Dermatol Venereol. 2023 Jul;37(7):1302-1310. doi: 10.1111/jdv.18992. Epub 2023 Mar 10.

Abstract

BACKGROUND

Primary cutaneous mucinoses (PCM) are rare diseases characterized by dermal or follicular mucin deposits.

OBJECTIVES

A retrospective study characterizing PCM to compare dermal with follicular mucin to identify its potential origin on a single-cell level.

MATERIAL AND METHODS

Patients diagnosed with PCM between 2010 and 2020 at our department were included in this study. Biopsy specimens were stained using conventional mucin stains (Alcian blue, PAS) and MUC1 immunohistochemical staining. Multiplex fluorescence staining (MFS) was used to investigate which cells were associated with MUC1 expression in select cases.

RESULTS

Thirty-one patients with PCM were included, 14 with follicular mucinosis (FM), 8 with reticular erythematous mucinosis, 2 with scleredema, 6 with pretibial myxedema and one patient with lichen myxedematosus. In all 31 specimens, mucin stained positive for Alcian blue and negative for PAS. In FM, mucin deposition was exclusively found in hair follicles and sebaceous glands. None of the other entities showed mucin deposits in follicular epithelial structures. Using MFS, all cases showed CD4+ and CD8+ T cells, tissue histiocytes, fibroblasts and pan-cytokeratin+ cells. These cells expressed MUC1 at different intensities. MUC1 expression in tissue histiocytes, fibroblasts, CD4+ and CD8+ T cells, and follicular epithelial cells of FM was significantly higher than the same cell types in the dermal mucinoses (p < 0.001). CD8+ T cells were significantly more involved in expression of MUC1 than all other analysed cell types in FM. This finding was also significant in comparison with dermal mucinoses.

CONCLUSION

Various cell types seem to contribute to mucin production in PCM. Using MFS, we showed that CD8+ T cells seem to be more involved in the production of mucin in FM than in dermal mucinoses, which could indicate that mucin in dermal and follicular epithelial mucinoses have different origins.

摘要

背景

原发性皮肤黏蛋白病(PCM)是一种罕见的疾病,其特征为真皮或毛囊黏蛋白沉积。

目的

对 PCM 进行回顾性研究,比较真皮与毛囊黏蛋白,以在单细胞水平上确定其潜在来源。

材料和方法

本研究纳入了 2010 年至 2020 年期间在我科诊断为 PCM 的患者。对活检标本进行常规黏蛋白染色(阿辛蓝、 PAS)和 MUC1 免疫组化染色。选择病例进行多重荧光染色(MFS),以研究哪些细胞与 MUC1 表达相关。

结果

共纳入 31 例 PCM 患者,其中 14 例为滤泡黏蛋白病(FM),8 例为网状红斑性黏蛋白病,2 例为硬肿病,6 例为胫前黏液水肿,1 例为苔藓样黏蛋白水肿。所有 31 例标本的黏蛋白均阿辛蓝染色阳性,PAS 染色阴性。在 FM 中,黏蛋白沉积仅见于毛囊和皮脂腺。其他病变均未见黏蛋白沉积于毛囊上皮结构。使用 MFS,所有病例均显示 CD4+和 CD8+T 细胞、组织组织细胞、成纤维细胞和泛细胞角蛋白+细胞。这些细胞的 MUC1 表达强度不同。FM 中的组织组织细胞、成纤维细胞、CD4+和 CD8+T 细胞以及毛囊上皮细胞的 MUC1 表达显著高于真皮黏蛋白病中的相同细胞类型(p<0.001)。与其他分析的细胞类型相比,CD8+T 细胞在 FM 中 MUC1 的表达更为显著。与真皮黏蛋白病相比,这一发现也具有统计学意义。

结论

各种细胞类型似乎都参与了 PCM 中的黏蛋白产生。使用 MFS,我们发现 CD8+T 细胞在 FM 中产生黏蛋白的作用似乎比真皮黏蛋白病更为显著,这可能表明真皮和毛囊上皮黏蛋白病中的黏蛋白具有不同的起源。

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