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迈向“白发自由基理论”:衰老人类毛囊中的黑素细胞凋亡是氧化应激诱导组织损伤的一个指标。

Towards a "free radical theory of graying": melanocyte apoptosis in the aging human hair follicle is an indicator of oxidative stress induced tissue damage.

作者信息

Arck Petra Clara, Overall Rupert, Spatz Katharina, Liezman Christiane, Handjiski Bori, Klapp Burghard F, Birch-Machin Mark A, Peters Eva Milena Johanne

机构信息

Cutaneous Neuroimmunology, Biomedical Research Center, Rm. Nr. 2.0549, University Medicine Charité, Virchow Campus, Humboldt University of Berlin, Augustenburger Platz 1, Berlin 13353, Germany.

出版信息

FASEB J. 2006 Jul;20(9):1567-9. doi: 10.1096/fj.05-4039fje. Epub 2006 May 24.

Abstract

Oxidative stress is generated by a multitude of environmental and endogenous challenges such as radiation, inflammation, or psychoemotional stress. It also speeds the aging process. Graying is a prominent but little understood feature of aging. Intriguingly, the continuous melanin synthesis in the growing (anagen) hair follicle generates high oxidative stress. We therefore hypothesize that hair bulb melanocytes are especially susceptible to free radical-induced aging. To test this hypothesis, we subjected human scalp skin anagen hair follicles from graying individuals to macroscopic and immunohistomorphometric analysis and organ culture. We found evidence of melanocyte apoptosis and increased oxidative stress in the pigmentary unit of graying hair follicles. The "common" deletion, a marker mitochondrial DNA-deletion for accumulating oxidative stress damage, occurred most prominently in graying hair follicles. Cultured unpigmented hair follicles grew better than pigmented follicles of the same donors. Finally, cultured pigmented hair follicles exposed to exogenous oxidative stress (hydroquinone) showed increased melanocyte apoptosis in the hair bulb. We conclude that oxidative stress is high in hair follicle melanocytes and leads to their selective premature aging and apoptosis. The graying hair follicle, therefore, offers a unique model system to study oxidative stress and aging and to test antiaging therapeutics in their ability to slow down or even stop this process.

摘要

氧化应激是由多种环境和内源性挑战引发的,如辐射、炎症或心理情绪压力。它还会加速衰老过程。头发变白是衰老的一个显著但却鲜为人知的特征。有趣的是,在生长(生长期)毛囊中持续的黑色素合成会产生高氧化应激。因此,我们推测毛球黑素细胞特别容易受到自由基诱导的衰老影响。为了验证这一假设,我们对来自头发变白个体的人头皮皮肤生长期毛囊进行了宏观和免疫组织形态计量分析以及器官培养。我们发现了白发毛囊色素单元中黑素细胞凋亡和氧化应激增加的证据。“常见”缺失,一种用于累积氧化应激损伤的线粒体DNA缺失标记,在白发毛囊中最为显著。培养的无色素毛囊比同一供体的有色素毛囊生长得更好。最后,暴露于外源性氧化应激(对苯二酚)的培养有色素毛囊在毛球中显示黑素细胞凋亡增加。我们得出结论,毛囊黑素细胞中的氧化应激水平很高,会导致其选择性过早衰老和凋亡。因此,白发毛囊为研究氧化应激和衰老以及测试抗衰老疗法减缓甚至阻止这一过程的能力提供了一个独特的模型系统。

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