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二羟丙酮暴露改变 NAD(P)H 并诱导 HEK293T 细胞线粒体应激和自噬。

Dihydroxyacetone Exposure Alters NAD(P)H and Induces Mitochondrial Stress and Autophagy in HEK293T Cells.

机构信息

Department of Physiology and Cell Biology , University of South Alabama College of Medicine , Mobile , Alabama 36688 , United States.

Mitchell Cancer Institute , University of South Alabama , 1660 Springhill Avenue , Mobile , Alabama 36604-1405 , United States.

出版信息

Chem Res Toxicol. 2019 Aug 19;32(8):1722-1731. doi: 10.1021/acs.chemrestox.9b00230. Epub 2019 Aug 2.

Abstract

Dihydroxyacetone phosphate (DHAP) is the endogenous byproduct of fructose metabolism. Excess DHAP in cells can induce advanced glycation end products and oxidative stress. Dihydroxyacetone (DHA) is the triose precursor to DHAP. DHA is used as the active ingredient in sunless tanning products, including aerosolized spray tans, and is formed by the combustion of solvents found in electronic cigarettes. Human exposure to DHA has been increasing as the popularity of sunless tanning products and electronic cigarettes has grown. Topically applied DHA is absorbed through the viable layers of the skin and into the bloodstream. Exogenous exposure to DHA is cytotoxic in immortalized keratinocytes and melanoma cells with cell cycle arrest induced within 24 h and cell death occurring by apoptosis at consumer-relevant concentrations of DHA within 72 h. Less is known about systemic exposures to DHA that occur following absorption through skin, and now through inhalation of the aerosolized DHA used in spray tanning. In the present study, HEK293T cells were exposed to consumer-relevant concentrations of DHA to examine the cytotoxicity of systemic exposures. HEK293T cells were sensitive to consumer-relevant doses of DHA with an IC value of 2.4 ± 0.3 mM. However, cell cycle arrest did not begin until 48 h after DHA exposure. DHA-exposed cells showed altered metabolic activity with decreased mitochondrial function and decreased lactate and ATP production observed within 24 h of exposure. Autofluorescent imaging and NAD sensors also revealed an imbalance in the redox cofactors NAD/NADH within 24 h of exposure. Cell death occurred by autophagy indicated by increases in LC3B and SIRT1. Despite DHA's ability to be converted to DHAP and integrated into metabolic pathways, the metabolic dysfunction and starvation responses observed in the HEK293T cells indicate that DHA does not readily contribute to the energetic pool in these cells.

摘要

二羟丙酮磷酸(DHAP)是果糖代谢的内源性副产物。细胞内过量的 DHAP 可诱导晚期糖基化终产物和氧化应激。二羟丙酮(DHA)是 DHAP 的三碳前体。DHA 被用作无阳光晒黑产品(包括气溶胶喷雾晒黑)的活性成分,它是由电子烟中发现的溶剂燃烧形成的。随着无阳光晒黑产品和电子烟的普及,人们接触 DHA 的情况越来越多。局部应用的 DHA 通过皮肤的有活力层吸收到血液中。外源性接触 DHA 在永生化角质形成细胞和黑色素瘤细胞中具有细胞毒性,在 24 小时内诱导细胞周期停滞,并在消费者相关浓度的 DHA 下在 72 小时内通过细胞凋亡发生细胞死亡。在皮肤吸收后,以及现在通过吸入喷雾晒黑中使用的气溶胶化 DHA 后,对全身暴露于 DHA 的了解较少。在本研究中,暴露于消费者相关浓度的 DHA 的 HEK293T 细胞被用来检查全身暴露的细胞毒性。HEK293T 细胞对消费者相关剂量的 DHA 敏感,IC 值为 2.4 ± 0.3 mM。然而,细胞周期停滞直到 DHA 暴露后 48 小时才开始。DHA 暴露的细胞表现出代谢活性改变,线粒体功能下降,暴露 24 小时内乳酸和 ATP 生成减少。在暴露后 24 小时内,通过自荧光成像和 NAD 传感器也发现了氧化还原辅因子 NAD/NADH 的失衡。自噬引起的细胞死亡由 LC3B 和 SIRT1 的增加表明。尽管 DHA 能够转化为 DHAP 并整合到代谢途径中,但在 HEK293T 细胞中观察到的代谢功能障碍和饥饿反应表明,DHA 不易为这些细胞的能量池做出贡献。

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