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干扰素-γ抑制黑素生成并诱导黑素细胞凋亡:CD8 + 细胞毒性T淋巴细胞在白癜风中的关键作用

Interferon-gamma Inhibits Melanogenesis and Induces Apoptosis in Melanocytes: A Pivotal Role of CD8+ Cytotoxic T Lymphocytes in Vitiligo.

作者信息

Yang Lili, Wei Yi, Sun Yue, Shi Weimin, Yang Ji, Zhu Lubing, Li Ming

机构信息

Department of Dermatology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Acta Derm Venereol. 2015 Jul;95(6):664-70. doi: 10.2340/00015555-2080.

Abstract

Increased expression of the cytokine interferon (IFN)-γ plays a pivotal role in vitiligo-induced depigmentation. However, the major source of IFN-γ in vitiligo patients and the mechanisms underlying melanocyte destruction are unknown. In this study, a large number of skin infiltrating IFN-γ+ cells and CD8+ T cells were detected in progressive vitiligo. Among the peripheral blood mononuclear cells (PBMCs) of vitiligo patients, CD8+ cytotoxic T lymphocytes (CTLs) that express IFN-γ exhibited significant expansion, which suggests that activated CTLs are the main source of increased IFN-γ in progressive vitiligo. An in vitro analysis demonstrated that IFN-γ inhibits melanogenesis in primary cultured human melanocytes by altering melanogenic enzyme mRNA expression and, more importantly, that IFN-γ directly induces melanocyte apoptosis. Our data indicate that vitiligo pathophysiology may be linked to globally activated CD8+ CTL subpopulations, which produce increased IFN-γ and induce melanocyte dysfunction and apoptosis.

摘要

细胞因子干扰素(IFN)-γ表达增加在白癜风所致色素脱失中起关键作用。然而,白癜风患者中IFN-γ的主要来源以及黑素细胞破坏的潜在机制尚不清楚。在本研究中,在进展期白癜风中检测到大量皮肤浸润的IFN-γ+细胞和CD8+ T细胞。在白癜风患者的外周血单个核细胞(PBMC)中,表达IFN-γ的CD8+细胞毒性T淋巴细胞(CTL)显著扩增,这表明活化的CTL是进展期白癜风中IFN-γ增加的主要来源。体外分析表明,IFN-γ通过改变黑素生成酶mRNA表达抑制原代培养的人黑素细胞中的黑素生成,更重要的是,IFN-γ直接诱导黑素细胞凋亡。我们的数据表明,白癜风的病理生理学可能与整体活化的CD8+ CTL亚群有关,该亚群产生增加的IFN-γ并诱导黑素细胞功能障碍和凋亡。

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