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二羟蒽酮诱导人角质形成细胞凋亡的作用研究。

An investigation of the effects of dithranol-induced apoptosis in a human keratinocyte cell line.

机构信息

Sunderland Pharmacy School, University of Sunderland, Sunderland, UK.

出版信息

J Pharm Pharmacol. 2013 Apr;65(4):552-60. doi: 10.1111/jphp.12019. Epub 2013 Jan 10.

Abstract

OBJECTIVES

Dithranol, one of the most successful topical agents for the treatment of psoriasis, has been shown to exert its therapeutic effect by inducing keratinocyte apoptosis. To gain further insights into dithranol-induced apoptotic events in vitro, a detailed investigation of its time- and dose-dependent effects has been performed through the evaluation of selected apoptotic markers, using a human keratinocyte cell line (HaCaT) as a model.

METHODS

The time- and dose-dependent effects of dithranol on a human keratinocyte cell line (HaCaT) were investigated through the evaluation of a series of apoptotic markers; morphological changes (electron microscopy), phosphatidylserine externalisation (flow cytometry), and caspase-3/7 activation.

KEY FINDINGS

The dithranol-induced apoptotic cascade was found to follow a well-defined dose and time-course, with the concentration and the period of exposure to the drug acting as the two major factors influencing the events and nature of cell death. The earliest apoptotic event detected was caspase activation (after 6 h), followed by the occurrence of phosphatidylserine externalisation (after 9 h) and subsequently the morphological characteristics associated with early and late stage apoptosis/necrosis (after 12 h).

CONCLUSIONS

This study has elucidated the dose- and time-response effects of dithranol-induced apoptosis in human keratinocytes in vitro.

摘要

目的

蒽林是治疗银屑病最成功的外用药物之一,其治疗作用已被证明是通过诱导角质形成细胞凋亡来实现的。为了更深入地了解蒽林在体外诱导凋亡的事件,我们通过评估选定的凋亡标志物,使用人角质形成细胞系(HaCaT)作为模型,对其时间和剂量依赖性效应进行了详细研究。

方法

通过评估一系列凋亡标志物,研究了蒽林对人角质形成细胞系(HaCaT)的时间和剂量依赖性效应;形态变化(电子显微镜)、磷脂酰丝氨酸外化(流式细胞术)和半胱天冬酶-3/7 的激活。

主要发现

蒽林诱导的凋亡级联反应呈现出明确的剂量和时间曲线,药物的浓度和暴露时间是影响细胞死亡事件和性质的两个主要因素。检测到的最早的凋亡事件是半胱天冬酶激活(6 小时后),随后发生磷脂酰丝氨酸外化(9 小时后),随后出现与早晚期凋亡/坏死相关的形态特征(12 小时后)。

结论

本研究阐明了蒽林在体外诱导人角质形成细胞凋亡的剂量和时间反应。

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