Soo Jin Kim, Yeseul Park, Yuri Cho, Heeyoun Hwang, Dong Jin Joo, Kyu Ha Huh and Juhan Lee*,
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引用次数: 0
摘要
在心肌梗死中,由于缺乏有效的治疗方法,缺血再灌注损伤(IRI)是一项重大挑战。胆红素是一种天然化合物,以其抗炎和抗氧化特性而闻名,已被确定为治疗 IRI 的潜在药物。目前,还没有与 IRI 和胆红素治疗相关的蛋白质组学研究报告。在本研究中,我们探讨了胆红素纳米颗粒对大鼠心肌梗死模型的影响。我们使用 LC-MS/MS 方法鉴定了由 76,681 个不同肽段组成的 3616 个蛋白质组,其中我们区分了两类蛋白质组:一类在 IRI 中表达增加,另一类在胆红素治疗的 IRI 中表达减少,反之亦然,分别占 202 个和 35 个蛋白质组。我们的蛋白质组分析发现,Wnt 和胰岛素信号通路的表达明显上调,高尔基体标记物的表达也有所增加,这表明它们在介导胆红素纳米粒子的保护作用方面发挥了作用。这项研究有助于人们从蛋白质组学角度了解心肌梗死,并表明胆红素纳米粒子是一种很有前景的心脏保护策略,值得在人体模型中进一步研究。
Proteomics Profiling of Bilirubin Nanoparticle Treatment against Myocardial Ischemia-Reperfusion Injury
In myocardial infarction, ischemia-reperfusion injury (IRI) poses a significant challenge due to a lack of effective treatments. Bilirubin, a natural compound known for its anti-inflammatory and antioxidant properties, has been identified as a potential therapeutic agent for IRI. Currently, there are no reports about proteomic studies related to IRI and bilirubin treatment. In this study, we explored the effects of bilirubin nanoparticles in a rat model of myocardial IRI. A total of 3616 protein groups comprising 76,681 distinct peptides were identified using LC-MS/MS, where we distinguished two kinds of protein groups: those showing increased expression in IRI and decreased expression in IRI with bilirubin treatment, and vice versa, accounting for 202 and 35 proteins, respectively. Our proteomic analysis identified significant upregulation in the Wnt and insulin signaling pathways and increased Golgi markers, indicating their role in mediating bilirubin nanoparticle’s protective effects. This research contributes to the proteomic understanding of myocardial IRI and suggests bilirubin nanoparticles as a promising strategy for cardiac protection, warranting further investigation in human models.