Mattinzoli Deborah, Ikehata Masami, D'Alonzo Daniele, De Fenza Maria, Diana Alberto, Li Min, Armelloni Silvia, Tosoni Antonella, Del Gobbo Alessandro, Collino Federica, Mastrangelo Antonio, Morello William, Zanoni Francesca, Bianchi Gaia, Alfieri Carlo, Messa Piergiorgio, Nebuloni Manuela, Montini Giovanni, Del Giacco Luca, Pavone Vincenzo, Podestà Manuel Alfredo, Castellano Giuseppe
Renal Research Laboratory, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Chemical Sciences, University of Naples Federico II, Naples, Italy.
Am J Transplant. 2025 Jun 13. doi: 10.1016/j.ajt.2025.06.010.
Primary podocytopathies are a group of disorders characterized by nephrotic syndrome and frequent progression to kidney failure, with high rates of posttransplant recurrence. Increased expression of the urokinase-type plasminogen activator receptor (uPAR) has been associated with podocyte dysfunction in primary podocytopathies. uPAR can interact with formyl peptide receptors (FPRs) in podocytes, but the relevance of this signaling pathway in these diseases remains unclear. We retrospectively evaluated uPAR-FPR expression in renal biopsies from patients with primary podocytopathies with recurrent disease after transplantation. Upregulation of uPAR-FPR signaling was consistently observed in podocytes from kidney biopsies of patients with primary podocytopathies and in cultured podocytes exposed to sera from patients with recurrent disease. Pharmacologic inhibition of uPAR-FPR interactions with UPARANT restored podocyte plasticity, reversing cytoskeletal alterations and protecting against damage. This treatment also led to significant functional recovery in an in vitro glomerular filtration barrier model. Finally, targeting uPAR-FPR crosstalk in a zebrafish model of podocytopathy reversed podocyte foot process effacement and reduced glomerular loss of high-molecular weight dextran, effectively alleviating the disease phenotype. Our data indicate that pharmacologic targeting of the uPAR-FPR axis protects podocytes from damage and may preserve renal function in primary podocytopathies, potentially reducing recurrence after transplantation.
原发性足细胞病是一组以肾病综合征为特征、常进展为肾衰竭且移植后复发率高的疾病。尿激酶型纤溶酶原激活物受体(uPAR)表达增加与原发性足细胞病中的足细胞功能障碍有关。uPAR可与足细胞中的甲酰肽受体(FPR)相互作用,但该信号通路在这些疾病中的相关性仍不清楚。我们回顾性评估了移植后复发的原发性足细胞病患者肾活检组织中uPAR-FPR的表达。在原发性足细胞病患者的肾活检足细胞以及暴露于复发患者血清的培养足细胞中,均一致观察到uPAR-FPR信号上调。用UPARANT对uPAR-FPR相互作用进行药理学抑制可恢复足细胞可塑性,逆转细胞骨架改变并防止损伤。这种治疗还导致体外肾小球滤过屏障模型出现显著的功能恢复。最后,在足细胞病斑马鱼模型中靶向uPAR-FPR串扰可逆转足细胞足突消失,并减少高分子量葡聚糖的肾小球丢失,有效减轻疾病表型。我们的数据表明,对uPAR-FPR轴进行药理学靶向可保护足细胞免受损伤,并可能在原发性足细胞病中保留肾功能, potentially reducing recurrence after transplantation.(此处英文原文有误,根据前文推测可能是“potentially reducing recurrence after transplantation”,直译为“可能降低移植后复发率”) 从而可能降低移植后复发率。