Yang Donghai, Tang Ming, Zhang Mingming, Ren Hongmei, Li Xiaoping, Zhang Ziyue, He Bo, Peng Song, Wang Wei, Fang Dandong, Song Yi, Xiong Yao, Liu Zhi Zhao, Liang Lijia, Shi Weibin, Fu Chunjiang, Hu Yijie, Jose Pedro A, Zhou Lin, Han Yu, Zeng Chunyu
Department of Cardiology, Daping Hospital, The Third Military Medical University (Army Medical University), Chongqing, People's Republic of China; Chongqing Key Laboratory for Hypertension Research, Chongqing Cardiovascular Clinical Research Center, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Department of Urology, Daping Hospital, The Third Military Medical University, Chongqing, People's Republic of China.
Kidney Int. 2023 Apr;103(4):719-734. doi: 10.1016/j.kint.2022.12.023. Epub 2023 Jan 18.
Ischemia/reperfusion injury of the kidney is associated with high morbidity and mortality, and treatment of this injury remains a challenge. G protein-coupled receptor kinase 4 (GRK4) plays a vital role in essential hypertension and myocardial infarction, but its function in kidney ischemia/reperfusion injury remains undetermined. Among the GRK subtypes (GRK2-6) expressed in kidneys, the increase in GRK4 expression was much more apparent than that of the other four GRKs 24 hours after injury and was found to accumulate in the nuclei of injured mouse and human renal tubule cells. Gain- and loss-of-function experiments revealed that GRK4 overexpression exacerbated acute kidney ischemia/reperfusion injury, whereas kidney tubule-specific knockout of GRK4 decreased injury-induced kidney dysfunction. Necroptosis was the major type of tubule cell death mediated by GRK4, because GRK4 significantly increased receptor interacting kinase (RIPK)1 expression and phosphorylation, subsequently leading to RIPK3 and mixed lineage kinase domain-like protein (MLKL) phosphorylation after kidney ischemia/reperfusion injury, but was reversed by necrostatin-1 pretreatment (an RIPK1 inhibitor). Using co-immunoprecipitation, mass spectrometry, and siRNA screening studies, we identified signal transducer and activator of transcription (STAT)1 as a GRK4 binding protein, which co-localized with GRK4 in the nuclei of renal tubule cells. Additionally, GRK4 phosphorylated STAT1 at serine 727, whose inactive mutation effectively reversed GRK4-mediated RIPK1 activation and tubule cell death. Kidney-targeted GRK4 silencing with nanoparticle delivery considerably ameliorated kidney ischemia/reperfusion injury. Thus, our findings reveal that GRK4 triggers necroptosis and aggravates kidney ischemia/reperfusion injury, and its downregulation may provide a promising therapeutic strategy for kidney protection.
肾脏缺血/再灌注损伤与高发病率和死亡率相关,对这种损伤的治疗仍然是一项挑战。G蛋白偶联受体激酶4(GRK4)在原发性高血压和心肌梗死中起着至关重要的作用,但其在肾脏缺血/再灌注损伤中的功能仍未明确。在肾脏中表达的GRK亚型(GRK2 - 6)中,损伤后24小时GRK4表达的增加比其他四种GRK更明显,并且发现其在损伤的小鼠和人类肾小管细胞核中积累。功能获得和功能丧失实验表明,GRK4过表达加剧了急性肾脏缺血/再灌注损伤,而肾小管特异性敲除GRK4则降低了损伤诱导的肾功能障碍。坏死性凋亡是GRK4介导的肾小管细胞死亡的主要类型,因为GRK4显著增加了受体相互作用激酶(RIPK)1的表达和磷酸化,随后导致肾脏缺血/再灌注损伤后RIPK3和混合谱系激酶结构域样蛋白(MLKL)的磷酸化,但坏死抑制剂-1预处理(一种RIPK1抑制剂)可逆转这种情况。通过免疫共沉淀、质谱和siRNA筛选研究,我们确定信号转导和转录激活因子(STAT)1为GRK4结合蛋白,其与GRK4在肾小管细胞核中共定位。此外,GRK4在丝氨酸727处磷酸化STAT1,其失活突变有效地逆转了GRK4介导的RIPK1激活和肾小管细胞死亡。用纳米颗粒递送进行肾脏靶向GRK4沉默可显著改善肾脏缺血/再灌注损伤。因此,我们的研究结果表明,GRK4触发坏死性凋亡并加重肾脏缺血/再灌注损伤,下调GRK4可能为肾脏保护提供一种有前景的治疗策略。