Shyfrin Sophie R, Ferren Marion, Perrin-Cocon Laure, Espi Maxime, Charmetant Xavier, Brailly Manon, Decimo Didier, Iampietro Mathieu, Canus Lola, Horvat Branka, Lotteau Vincent, Vidalain Pierre-Olivier, Thaunat Olivier, Mathieu Cyrille
CIRI, Centre International de Recherche en Infectiologie, Team Neuro-Invasion, TROpism and VIRal Encephalitis, Univ Lyon, Inserm, U1111, CNRS, UMR5308, Université Claude Bernard Lyon 1, Ecole Normale Supérieure de Lyon, Lyon, France.
CIRI, Centre International de Recherche en Infectiologie, Team Immunobiology of the Viral infections, Univ Lyon, Inserm, U1111, CNRS, UMR5308, Université Claude Bernard Lyon 1, Ecole Normale Supérieure de Lyon, Lyon, France.
J Tissue Eng. 2022 Sep 6;13:20417314221122130. doi: 10.1177/20417314221122130. eCollection 2022 Jan-Dec.
Kidney pathology is frequently reported in patients hospitalized with COVID-19, the pandemic disease caused by the Severe acute respiratory coronavirus 2 (SARS-CoV-2). However, due to a lack of suitable study models, the events occurring in the kidney during the earliest stages of infection remain unknown. We have developed hamster organotypic kidney cultures (OKCs) to study the early stages of direct renal infection. OKCs maintained key renal structures in their native three-dimensional arrangement. SARS-CoV-2 productively replicated in hamster OKCs, initially targeting endothelial cells and later disseminating into proximal tubules. We observed a delayed interferon response, markers of necroptosis and pyroptosis, and an early repression of pro-inflammatory cytokines transcription followed by a strong later upregulation. While it remains an open question whether an active replication of SARS-CoV-2 takes place in the kidneys of COVID-19 patients with AKI, our model provides new insights into the kinetics of SARS-CoV-2 kidney infection and can serve as a powerful tool for studying kidney infection by other pathogens and testing the renal toxicity of drugs.
在因严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的大流行疾病新冠肺炎住院的患者中,肾脏病理学报告屡见不鲜。然而,由于缺乏合适的研究模型,感染最早阶段肾脏中发生的事件仍不清楚。我们开发了仓鼠肾组织器官培养物(OKCs)来研究肾脏直接感染的早期阶段。OKCs维持了关键肾脏结构的天然三维排列。SARS-CoV-2在仓鼠OKCs中有效复制,最初靶向内皮细胞,随后扩散到近端小管。我们观察到干扰素反应延迟、坏死性凋亡和炎性小体介导的细胞死亡标志物,以及促炎细胞因子转录的早期抑制,随后是强烈的后期上调。虽然SARS-CoV-2在患有急性肾损伤的新冠肺炎患者肾脏中是否进行活跃复制仍是一个悬而未决的问题,但我们的模型为SARS-CoV-2肾脏感染的动力学提供了新的见解,并且可以作为研究其他病原体肾脏感染和测试药物肾毒性的有力工具。