Department of Chemistry and Biochemistry, The University of Toledo, Toledo, OH 43606, USA.
Department of Chemistry, Kenyon College, Gambier, OH 43022, USA.
Cell Signal. 2020 May;69:109547. doi: 10.1016/j.cellsig.2020.109547. Epub 2020 Jan 23.
The chemical- and photo- toxicity of chromophore retinal on cells have long been debated. Although we recently showed that retinal and blue light exposure interrupt cellular signaling, a comprehensive study examining molecular underpinnings of this perturbation and its consequences to cellular fate is lacking. Here, we report molecular evidence for blue light excited-retinal induced oxidative damage of polyunsaturated lipid anchors in membrane-interacting signaling molecules and DNA damage in cells using live-cell imaging and in vitro experimentation. The incurred molecular damage irreversibly disrupted subcellular localization of these molecules, a crucial criterion for their signaling. We further show retinal accumulation in lipid-bilayers of cell membranes could enhance the lifetime of retinal in cells. Comparative response-signatures suggest that retinal triggers reactions upon photoexcitation similar to photodynamic therapy agents and generate reactive oxygen species in cells. Additionally, data also shows that exposing retinal-containing cells to sunlight induces substantial cytotoxicity. Collectively, our results explain a likely in vivo mechanism and reaction conditions under which bio-available retinal in physiological light conditions damages cells.
色基视黄醛对细胞的化学毒性和光毒性一直存在争议。虽然我们最近表明,视黄醛和蓝光暴露会中断细胞信号转导,但缺乏对这种干扰的分子基础及其对细胞命运影响的全面研究。在这里,我们使用活细胞成像和体外实验报告了分子证据,证明蓝光激发的视黄醛会导致膜相互作用信号分子中多不饱和脂质锚的氧化损伤,以及细胞中的 DNA 损伤。这种损伤会不可逆地破坏这些分子的亚细胞定位,这是它们信号转导的关键标准。我们进一步表明,视黄醛在细胞膜的脂质双层中的积累可以延长细胞内视黄醛的寿命。比较反应特征表明,视黄醛在光激发后引发类似于光动力疗法药物的反应,并在细胞中产生活性氧物质。此外,数据还表明,使含有视黄醛的细胞暴露在阳光下会引起明显的细胞毒性。总的来说,我们的结果解释了在生理光照条件下生物可利用的视黄醛在体内损伤细胞的可能机制和反应条件。