Tang Li-Qun, Wang Ling-Ling, Tang Qi-Feng, Wang Wei
Geriatric Medicine Center, Department of Geriatric Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, No.156 Shangtang Road, Xiacheng District, Hangzhou, 310016, China.
Department of Critical Care Medicine, Central Hospital of Dinghai District, Zhoushan, 316000, China.
Sci Rep. 2025 Apr 11;15(1):12511. doi: 10.1038/s41598-025-97874-8.
Solute carrier family 26 member 4 (SLC26A4) plays an essential role in the progression of pathological cardiac hypertrophy. This study aimed to examine the involvement of SLC26A4 in cardiac hypertrophy by regulation of autophagy and activation of the NOD-like receptor thermal protein domain associated protein 3 (NLRP3) inflammasome. Cardiomyocytes were treated with 200 µmol/L phenylephrine (PE) to induce cardiac hypertrophy, followed by treatment with 10 mmol/L INF39, an NLRP3 inhibitor. Furthermore, the pLL3.7 lentiviral vector was used to construct a sh-SLC26A4 interference plasmid and a PLL3.7-cardiomyocytesv-SLC26A4 overexpression plasmid to intervene in PE-induced cardiac hypertrophy. Quantitative reverse transcription polymerase chain reaction and Western blotting were performed to measure the expression of ANP, BNP, β-MHC, SLC26A4, NLRP3, apoptosis associated speck-like protein containing a C-terminal caspase recruitment domain (ASC), and caspase-1. Immunofluorescence was used to detect the level of α-smooth muscle actin (α-SMA) to indicate the cardiomyocyte area. The expression levels of the autophagy proteins LC3, beclin-1, and p62 were determined by Western blotting. Finally, an SD rats model of cardiac hypertrophy was established using transverse aortic constriction (TAC) surgery. SLC26A4, NLRP3, IL-1β, ACS and caspase-1 were further examined at gene and protein levels. SLC26A4 expression was associated with cardiac hypertrophy in cell experiments. SLC26A4 promoted autophagy and activation of the NLRP3 inflammasome pathway, regulating the gene and protein expression of LC3, beclin-1, p62, ACS, NLRP3, and caspase-1. Similar results were observed in the TAC rat model, in which SLC26A4 expression was associated with cardiomyocyte enlargement and cardiac interstitial and perivascular fibrosis. SLC26A4 was involved in cardiac hypertrophy by promoting autophagy and activating the NLRP3 inflammasome pathway. Targeting the expression of SLC26A4 may provide a new treatment option for cardiac hypertrophy.
溶质载体家族26成员4(SLC26A4)在病理性心肌肥厚进展中起重要作用。本研究旨在通过调节自噬和激活NOD样受体热蛋白结构域相关蛋白3(NLRP3)炎性小体来研究SLC26A4在心肌肥厚中的作用。用200μmol/L去甲肾上腺素(PE)处理心肌细胞以诱导心肌肥厚,随后用10 mmol/L INF39(一种NLRP3抑制剂)处理。此外,使用pLL3.7慢病毒载体构建sh - SLC26A4干扰质粒和PLL3.7 - cardiomyocytesv - SLC26A4过表达质粒,以干预PE诱导的心肌肥厚。进行定量逆转录聚合酶链反应和蛋白质免疫印迹法检测心钠素(ANP)、脑钠肽(BNP)、β - 肌球蛋白重链(β - MHC)、SLC26A4、NLRP3、含半胱天冬酶招募结构域的凋亡相关斑点样蛋白(ASC)和半胱天冬酶 - 1的表达。采用免疫荧光法检测α - 平滑肌肌动蛋白(α - SMA)水平以指示心肌细胞面积。通过蛋白质免疫印迹法测定自噬蛋白微管相关蛋白轻链3(LC3)、自噬相关蛋白beclin - 1和p62的表达水平。最后,采用横向主动脉缩窄(TAC)手术建立心肌肥厚的SD大鼠模型。在基因和蛋白水平进一步检测SLC26A4、NLRP3、白细胞介素 - 1β(IL - 1β)、ASC和半胱天冬酶 - 1。在细胞实验中,SLC26A4表达与心肌肥厚相关。SLC26A4促进自噬和NLRP3炎性小体途径的激活,调节LC3、beclin - 1、p62、ASC、NLRP3和半胱天冬酶 - 1的基因和蛋白表达。在TAC大鼠模型中观察到类似结果,其中SLC26A4表达与心肌细胞增大以及心脏间质和血管周围纤维化相关。SLC26A4通过促进自噬和激活NLRP3炎性小体途径参与心肌肥厚。靶向SLC26A4的表达可能为心肌肥厚提供新的治疗选择。