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4-取代酚诱导白癜风和抗黑色素瘤免疫的作用机制。

Mechanism of action of 4-substituted phenols to induce vitiligo and antimelanoma immunity.

机构信息

Department of Dermatology and Netherlands Institute for Pigment Disorders, Amsterdam University Medical Centers, Amsterdam Infection & Immunity Institute, Cancer Center Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.

Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Pigment Cell Melanoma Res. 2019 Jul;32(4):540-552. doi: 10.1111/pcmr.12774. Epub 2019 Mar 18.

Abstract

Monobenzone is a 4-substituted phenol that can induce vitiligo and antimelanoma immunity. We investigated the influence of the chemical structure on the biological activity of a series of structurally related 4-substituted phenols. All phenols inhibited cellular melanin synthesis, and eight of ten phenols inhibited tyrosinase activity, using the MBTH assay. These phenols also induced glutathione (GSH) depletion, indicative of quinone formation and protein thiol binding, which can increase the immunogenicity of melanosomal proteins. Specific T-cell activation was found upon stimulation with phenol-exposed pigmented cells, which also reacted with unexposed cells. In contrast, 4-tertbutylphenol induced immune activation was not restricted to pigment cells, analogous to contact sensitization. We conclude that 4-substituted phenols can induce specific T-cell responses against melanocytes and melanoma cells, also acting at distant, unexposed body sites, and may confer a risk of chemical vitiligo. Conversely, these phenols may be applicable to induce specific antimelanoma immunity.

摘要

单苯氧乙醇是一种 4-取代苯酚,可诱导白癜风和抗黑素瘤免疫。我们研究了化学结构对一系列结构相关的 4-取代苯酚的生物学活性的影响。所有酚类物质均抑制细胞黑色素合成,十种酚类物质中有八种抑制酪氨酸酶活性,使用 MBTH 测定法。这些酚类物质还诱导谷胱甘肽 (GSH) 耗竭,表明醌的形成和蛋白质巯基结合,这可以增加黑素体蛋白的免疫原性。用暴露于酚类的色素细胞刺激发现了特异性 T 细胞激活,这些细胞也与未暴露的细胞反应。相比之下,4-叔丁基苯酚诱导的免疫激活不仅局限于色素细胞,类似于接触致敏。我们得出结论,4-取代苯酚可诱导针对黑素细胞和黑色素瘤细胞的特异性 T 细胞反应,也可在远处未暴露的身体部位发挥作用,并可能导致化学性白癜风的风险。相反,这些酚类物质可能适用于诱导特异性抗黑色素瘤免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3971/6850206/6059cf625a4b/PCMR-32-540-g001.jpg

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