Wu Ping-Hsun, Lin Yi-Ting, Wu Pei-Yu, Lee Hei-Hwa, Lee Su-Chu, Hung Szu-Chun, Chen Szu-Chia, Kuo Mei-Chuan, Chiu Yi-Wen
Graduate Institute of Clinical Medicine, College of Medicines, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
J Clin Med. 2020 Jan 2;9(1):124. doi: 10.3390/jcm9010124.
Protein-bound uremic toxin is a cardiovascular (CV) risk factor for patients with end-stage renal disease. Indole-3-acetic acid (IAA) was found to be associated with CV disease but the detailed pathophysiology remains unknown. Moreover, mitogen-activated protein kinase (MAPK) signaling cascades play an important role in the pathogenesis of CV disease. Thus, we explored the association between circulating IAA levels and forty MAPK cascade associated proteins in patients undergoing hemodialysis (HD). Circulating total form IAA was quantified by mass spectrometry and forty MAPK cascade associated proteins by a proximity extension assay in 331 prevalent HD patients. Accounting for multiple testing, and in multivariable-adjusted linear regression models, circulating total form IAA levels were positively associated with stem cell factor (β coefficient 0.13, 95% confidence interval 0.04 to 0.21, = 0.004). A bioinformatics approach using the search tool for interactions of chemicals (STITCH) tool provided information that IAA may be involved in the regulation of cell proliferation, hematopoietic cells, and the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling pathway. The knowledge gained here can be generalized, thereby impacting the non-traditional CV risk factors in patients with kidney disease. Further in vitro work is necessary to validate the translation of the mechanistic pathways.
蛋白结合型尿毒症毒素是终末期肾病患者的心血管(CV)危险因素。吲哚 - 3 - 乙酸(IAA)被发现与心血管疾病有关,但其详细的病理生理学仍不清楚。此外,丝裂原活化蛋白激酶(MAPK)信号级联在心血管疾病的发病机制中起重要作用。因此,我们探讨了血液透析(HD)患者循环IAA水平与40种MAPK级联相关蛋白之间的关联。通过质谱法定量331例HD患者的循环总形式IAA,并通过邻近延伸分析法定量40种MAPK级联相关蛋白。在多变量调整线性回归模型中,考虑多重检验后,循环总形式IAA水平与干细胞因子呈正相关(β系数0.13,95%置信区间0.04至0.21,P = 0.004)。使用化学物质相互作用搜索工具(STITCH)工具的生物信息学方法提供的信息表明,IAA可能参与细胞增殖、造血细胞以及Janus激酶(JAK)-信号转导子和转录激活子(STAT)信号通路的调节。这里获得的知识可以推广,从而影响肾病患者的非传统心血管危险因素。需要进一步的体外研究来验证机制途径的转化。