Characterization of immortalized human podocytes infected with lentivirus as an in vitro model of viral infection-associated podocytopathy.

IF 1.4 Q4 IMMUNOLOGY American journal of clinical and experimental immunology Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.62347/BBCX1142
Peng Yu, Xi Jin, Weijun Huang, Jingjing Wang, Sipang Zhang, Lu Ren, Haitao Zhang, Shaolin Shi
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Abstract

A large number of studies have shown the association of kidney disease with viral infections in the body. Viral infections cause kidney injury in two manners, the systemic inflammation (cytokine storm) and the direct infection of kidney cells. Concerning direct viral infection of podocytes, the mechanism underlying virus-induced podocyte injury remains largely unknown and requires effective experimental models to facilitate its study. Here, we performed molecular characterization of immortalized human podocyte cell line (HPC) infected with lentivirus by RNA-seq. Bioinformatics analysis revealed a strong innate immune response in the cells, including interferon production and signaling. Meanwhile, activations of ferroptosis pathway and TNF-alpha signaling were also found, consistent with an impaired viability of the cells. Lentiviral infection also upregulated expression of APOL1 as observed in patients with HIV associated nephropathy (HIVAN) and diabetic nephropathy (DN). Interestingly, when the lentiviral infected cells were treated with Adriamycin (ADR), the ADR-associated signaling pathways were not interfered and remained activated as that in the cells treated with ADR only, suggesting that the virus and ADR have distinct mechanisms in damaging podocytes. Thus, the lentivirus-infected HPC cells represent a useful in vitro model of viral infection-associated podocytopathy.

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用慢病毒感染永生化人类荚膜细胞作为病毒感染相关荚膜细胞病的体外模型的特征。
大量研究表明,肾脏疾病与体内病毒感染有关。病毒感染导致肾脏损伤的方式有两种,一种是全身性炎症(细胞因子风暴),另一种是直接感染肾脏细胞。关于病毒直接感染荚膜细胞,病毒诱导荚膜细胞损伤的机制在很大程度上仍是未知的,需要有效的实验模型来促进研究。在这里,我们通过 RNA-seq 对感染慢病毒的永生化人荚膜细胞系(HPC)进行了分子鉴定。生物信息学分析表明,细胞中存在强烈的先天性免疫反应,包括干扰素的产生和信号转导。同时,还发现了铁变态反应通路和 TNF-α 信号的激活,这与细胞活力受损相一致。慢病毒感染还能上调 APOL1 的表达,这在 HIV 相关性肾病(HIVAN)和糖尿病肾病(DN)患者中也能观察到。有趣的是,当用阿霉素(ADR)处理慢病毒感染的细胞时,与 ADR 相关的信号通路没有受到干扰,仍然与只用 ADR 处理的细胞一样处于激活状态,这表明病毒和 ADR 在损伤荚膜细胞方面具有不同的机制。因此,慢病毒感染的 HPC 细胞是病毒感染相关荚膜细胞病变的有用体外模型。
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