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在进展期白癜风患者皮肤中检测到的表皮朗格汉斯细胞的形态学改变及S100B表达增加

Morphological Alterations and Increased S100B Expression in Epidermal Langerhans Cells Detected in Skin from Patients with Progressive Vitiligo.

作者信息

Yang Fei, Yang Lingli, Teng Lanting, Zhang Huimin, Katayama Ichiro

机构信息

Department of Pigmentation Research and Therapeutics, Graduate School of Medicine, Osaka City University, Osaka 5450051, Japan.

Department of Dermatology, Course of Integrated Medicine, Graduate School of Medicine, Osaka University, Osaka 5650871, Japan.

出版信息

Life (Basel). 2021 Jun 18;11(6):579. doi: 10.3390/life11060579.

Abstract

The role of Langerhans cells (LCs) in vitiligo pathogenesis remains unclear, with published studies reporting contradictory results regarding the quantity of LCs and no data on the features of LCs in vitiligo. Here, we aimed to analyze the presence, density, and morphological features of LCs in the epidermis of patients with vitiligo. Skin biopsies were stained for LCs using anti-CD1a/anti-langerin antibodies and analyzed by immunocytochemistry with light and electron microscopy. Compared with healthy controls, we detected significantly increased numbers of epidermal LCs in lesional skin from vitiligo in the progressive state. These LCs exhibited striking morphological alterations, including an elevated number of dendrites, with increased length and more branches than dendrites from controls. Ultrastructure examination via immuno-electron microscopy revealed markedly reduced Birbeck granules (BGs) and shorter BG rods in LCs from progressive vitiligo, with higher expression of langerin. Additionally, expression of S100B, the activity biomarker of vitiligo, was increased in these LCs. This work provides new insight on the cellular composition of LCs in vitiliginous skin, revealing altered morphology and increased LC numbers, with elevated S100B expression. Our data suggest LCs might play a critical role in vitiligo pathogenesis and thus may represent a novel therapeutic target for this disease.

摘要

朗格汉斯细胞(LCs)在白癜风发病机制中的作用仍不清楚,已发表的研究报告了关于LCs数量的相互矛盾的结果,且尚无关于白癜风中LCs特征的数据。在此,我们旨在分析白癜风患者表皮中LCs的存在情况、密度和形态特征。使用抗CD1a/抗朗格蛋白抗体对皮肤活检组织进行LCs染色,并通过免疫细胞化学结合光学和电子显微镜进行分析。与健康对照相比,我们在进展期白癜风的皮损中检测到表皮LCs数量显著增加。这些LCs表现出明显的形态改变,包括树突数量增加,与对照的树突相比,长度增加且分支更多。通过免疫电子显微镜进行的超微结构检查显示,进展期白癜风的LCs中伯贝克颗粒(BGs)明显减少且BG杆缩短,同时朗格蛋白表达升高。此外,白癜风活性生物标志物S100B在这些LCs中的表达增加。这项工作为白癜风皮肤中LCs的细胞组成提供了新的见解,揭示了形态改变、LCs数量增加以及S100B表达升高。我们的数据表明LCs可能在白癜风发病机制中起关键作用,因此可能代表该疾病的一个新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d4/8235069/0943459dc201/life-11-00579-g001.jpg

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