Renal Division, Department of Medicine, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany.
Renal Division, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Kidney Int. 2022 Jun;101(6):1216-1231. doi: 10.1016/j.kint.2021.12.031. Epub 2022 Feb 1.
Risk variants of the apolipoprotein-L1 (APOL1) gene are associated with severe kidney disease, putting homozygous carriers at risk. Since APOL1 lacks orthologs in all major model organisms, a wide range of mechanisms frequently in conflict have been described for APOL1-associated nephropathies. The genetic toolkit in Drosophila allows unique in vivo insights into disrupted cellular homeostasis. To perform a mechanistic analysis, we expressed human APOL1 control and gain-of-function kidney risk variants in the podocyte-like garland cells of Drosophila nephrocytes and a wing precursor tissue. Expression of APOL1 risk variants was found to elevate endocytic function of garland cell nephrocytes that simultaneously showed early signs of cell death. Wild-type APOL1 had a significantly milder effect, while a control transgene with deletion of the short BH3 domain showed no overt phenotype. Nephrocyte endo-lysosomal function and slit diaphragm architecture remained unaffected by APOL1 risk variants, but endoplasmic reticulum (ER) swelling, chaperone induction, and expression of the reporter Xbp1-EGFP suggested an ER stress response. Pharmacological inhibition of ER stress diminished APOL1-mediated cell death and direct ER stress induction enhanced nephrocyte endocytic function similar to expression of APOL1 risk variants. We confirmed APOL1-dependent ER stress in the Drosophila wing precursor where silencing the IRE1-dependent branch of ER stress signaling by inhibition with Xbp1-RNAi abrogated cell death, representing the first rescue of APOL1-associated cytotoxicity in vivo. Thus, we uncovered ER stress as an essential consequence of APOL1 risk variant expression in vivo in Drosophila, suggesting a central role of this pathway in the pathogenesis of APOL1-associated nephropathies.
载脂蛋白-L1(APOL1)基因的风险变体与严重的肾脏疾病有关,使纯合子携带者面临风险。由于 APOL1 在所有主要的模式生物中都没有同源物,因此经常会描述与 APOL1 相关的肾病相关的多种机制。果蝇中的遗传工具包允许对细胞内稳态的破坏进行独特的体内洞察。为了进行机制分析,我们在果蝇肾细胞的足突样花环细胞和翅膀前体细胞中表达了人类 APOL1 对照和功能获得性肾脏风险变体。发现表达 APOL1 风险变体可提高花环细胞肾细胞的内吞功能,同时表现出早期细胞死亡的迹象。野生型 APOL1 的作用明显较轻,而具有短 BH3 结构域缺失的对照转基因则没有明显的表型。APOL1 风险变体对肾细胞的内体-溶酶体功能和裂孔隔膜结构没有影响,但内质网(ER)肿胀、伴侣蛋白诱导和报告基因 Xbp1-EGFP 的表达表明存在 ER 应激反应。ER 应激的药理学抑制可减少 APOL1 介导的细胞死亡,而直接诱导 ER 应激可增强肾细胞的内吞功能,类似于表达 APOL1 风险变体。我们在果蝇翅膀前体细胞中证实了依赖 APOL1 的 ER 应激,其中通过 Xbp1-RNAi 抑制 IRE1 依赖性 ER 应激信号传导分支可消除细胞死亡,这代表了首次在体内挽救 APOL1 相关细胞毒性。因此,我们发现 ER 应激是 APOL1 风险变体在果蝇体内表达的重要后果,表明该途径在 APOL1 相关肾病的发病机制中起核心作用。