Laboratory of Cellular Biology and Functional Anatomy, Department of Anatomy, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 2415, Cidade Universitária, São Paulo, SP, 05508-000, Brazil.
Department of Pharmacology, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, SP, Brazil.
Pflugers Arch. 2018 Mar;470(3):549-558. doi: 10.1007/s00424-017-2088-6. Epub 2017 Nov 25.
We have previously demonstrated that calcium-binding protein S100A8 and myeloid differentiation factor-88 (MyD88) are important mediators of nuclear transcription factor kappa-B (NF-κB) activation in cardiomyocytes and that signalling molecules are involved in the hypertrophic response that is stimulated by thyroid hormones (TH). Angiotensin II (Ang II), the main active peptide of the renin-angiotensin system (RAS), binds to type 1 Ang II receptor (AT1R) and subsequently promotes cardiac hypertrophy and the inflammatory response with NF-κB activation underlying the cardiovascular effects. Considering the amount of evidence that RAS is an important mediator of TH actions on the cardiovascular system, we aimed to investigate whether cardiac expression of NF-κB and upstream associated molecules could be altered in hyperthyroidism, as well as whether AT1R could mediate the effects of TH on cardiac tissue and in cardiomyocytes in culture. Wistar rats were subjected to hyperthyroidism with or without the AT1R blocker losartan. The TH serum levels, haemodynamic parameters and cardiac mass were assessed to confirm the hyperthyroid status. The S100A8, MyD88 and nuclear NF-κB expression levels were increased in the hearts of the hyperthyroid rats, and the losartan treatment attenuated these TH effects. In addition, the cultured cardiomyocytes that had been stimulated with losartan exhibited blunted S100A8 upregulation and NF-κB activation compared with the TH-treated cells. Together, our results suggest that AT1R participates in TH-induced cardiac hypertrophy partly by mediating S100A8, MyD88 and NF-κB activation via TH. These findings indicate the important crosstalk between TH and RAS, highlighting the participation of AT1R in the triggered mechanisms of TH that contribute to the cardiac hypertrophy response.
我们之前已经证明,钙结合蛋白 S100A8 和髓样分化因子-88(MyD88)是心肌细胞中核转录因子 κB(NF-κB)激活的重要介质,信号分子参与甲状腺激素(TH)刺激的肥大反应。血管紧张素 II(Ang II)是肾素-血管紧张素系统(RAS)的主要活性肽,与 1 型 Ang II 受体(AT1R)结合,随后通过 NF-κB 激活促进心肌肥大和炎症反应,这是心血管效应的基础。考虑到 RAS 是 TH 对心血管系统作用的重要介质的大量证据,我们旨在研究甲状腺功能亢进症是否会改变 NF-κB 和上游相关分子在心脏中的表达,以及 AT1R 是否可以介导 TH 对心脏组织和培养的心肌细胞的作用。Wistar 大鼠通过给予甲状腺素或给予 AT1R 阻滞剂氯沙坦来建立甲状腺功能亢进症模型。通过检测血清 TH 水平、血流动力学参数和心脏质量来评估甲状腺功能亢进状态。结果显示,甲状腺功能亢进大鼠心脏中 S100A8、MyD88 和核 NF-κB 的表达水平增加,氯沙坦治疗可减弱这些 TH 作用。此外,与 TH 处理的细胞相比,用氯沙坦刺激的培养心肌细胞中 S100A8 的上调和 NF-κB 的激活减弱。综上所述,这些结果表明 AT1R 通过介导 S100A8、MyD88 和 NF-κB 的激活参与 TH 诱导的心脏肥大,这部分是通过 TH 介导的。这些发现表明 TH 和 RAS 之间存在重要的串扰,强调了 AT1R 参与 TH 触发机制在心脏肥大反应中的作用。