Institute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine of the Slovak Academy of Sciences, 841 04 Bratislava, Slovakia.
Faculty of Natural Sciences, Comenius University, 841 04 Bratislava, Slovakia.
Cells. 2024 Nov 9;13(22):1860. doi: 10.3390/cells13221860.
Sarco/endoplasmic reticulum Ca-ATPase (SERCA) is an important regulatory protein responsible for maintaining calcium homeostasis within cells. Impairment of SERCA associated with activity/expression decrease has been implicated in multiple chronic conditions, including cardiovascular diseases, diabetes, cancer, neurodegenerative diseases, and skeletal muscle pathologies. Natural polyphenols have been recognized to interact with several target proteins involving SERCA. To date, only a limited number of polyphenolic compounds or their derivatives have been described either to increase SERCA activity/expression directly or to affect Ca signaling pathways. In this study, we tested polyphenols for their ability to activate SERCA1a in the absence or presence of methylglyoxal or palmitate and to impact insulin release in pancreatic beta cells. The protective effects of these compounds against methylglyoxal- or palmitate-induced injury were evaluated. Results indicate that 6-gingerol, resveratrol, and ellagic acid activate SERCA1a and protect against activity decrease induced by methylglyoxal and palmitate. Molecular docking analysis revealed the binding of these polyphenols to Glu439 in the SERCA1a P-domain, suggesting a critical role in the stimulation of enzyme activity. Ellagic acid was found to directly stimulate the activity of SERCA1a, marking the first instance of such an observation.
肌浆/内质网 Ca-ATP 酶(SERCA)是一种重要的调节蛋白,负责维持细胞内钙的动态平衡。与 SERCA 相关的活性/表达降低与多种慢性疾病有关,包括心血管疾病、糖尿病、癌症、神经退行性疾病和骨骼肌病理。已经认识到天然多酚类化合物可以与涉及 SERCA 的几种靶蛋白相互作用。迄今为止,只有少数几种多酚类化合物或其衍生物被描述为直接增加 SERCA 活性/表达,或影响 Ca 信号通路。在这项研究中,我们测试了多酚类化合物在没有或存在甲基乙二醛或棕榈酸的情况下激活 SERCA1a 的能力,并测试了它们对胰腺β细胞胰岛素释放的影响。评估了这些化合物对甲基乙二醛或棕榈酸诱导损伤的保护作用。结果表明,6-姜酚、白藜芦醇和鞣花酸可激活 SERCA1a 并防止甲基乙二醛和棕榈酸诱导的活性降低。分子对接分析显示这些多酚类化合物与 SERCA1a P 结构域中的 Glu439 结合,提示其在刺激酶活性方面的关键作用。鞣花酸被发现可直接刺激 SERCA1a 的活性,这是首次观察到这种现象。