Novel parietal epithelial cell subpopulations contribute to focal segmental glomerulosclerosis and glomerular tip lesions
Year: 2019
Type: article
Abstract: Beside the classical flat parietal epithelial cells (PECs), we investigated proximal tubular epithelial-like cells, a neglected subgroup of PECs. These cells, termed cuboidal PECs, make up the most proximal part of the proximal tubule and may also line parts of Bowman's capsule. Additionally, a third intermediate PEC subgroup was identified at the junction between the flat and cuboidal PEC subgroups at the tubular orifice. The transgenic mouse line PEC-rtTA labeled all three PEC subgroups. Here we show that the inducible Pax8-rtTA mouse line specifically labeled only cuboidal and intermediate PECs, but not flat PECs. In aging Pax8-rtTA mice, cell fate mapping showed no evidence for significant transdifferentiation from flat PECs to cuboidal or intermediate PECs or vice versa. In murine glomerular disease models of crescentic glomerulonephritis, and focal segmental glomerulosclerosis (FSGS), intermediate PECs became more numerous. These intermediate PECs preferentially expressed activation markers CD44 and Ki-67, suggesting that this subgroup of PECs was activated more easily than the classical flat PECs. In mice with FSGS, cuboidal and intermediate PECs formed sclerotic lesions. In patients with FSGS, cells forming the tip lesions expressed markers of intermediate PECs. These novel PEC subgroups form sclerotic lesions and were more prone to cellular activation compared to the classical flat PECs in disease. Thus, colonization of Bowman's capsule by cuboidal PECs may predispose to lesion formation and chronic kidney disease. We propose that tip lesions originate from this novel subgroup of PECs in patients with FSGS.
Source: Kidney International
Institutions: RWTH Aachen University, Monash Health, Monash University, Radboud University Nijmegen, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Radboud Institute for Health Sciences, Universitätsmedizin Göttingen, Friedrich-Alexander-Universität Erlangen-Nürnberg, German Cancer Research Center, Vanderbilt University Medical Center
Language: English
Subfield: Nephrology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $3,200
Funders: Alexander von Humboldt-Stiftung, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, RWTH Aachen University, Medical Research Council, National Health and Medical Research Council, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: Novel signalling pathways leading to the activation of glomerular parietal epithelial cells, G3421341489, Resolution of Glomerulosclerosis, G3599332668, Verbundprojekt: Translationale Forschung zur Verbesserung von Diagnostik und Therapie der der FSGS TP1 + TP4, Pathology of the FSGS Kidney, G824575502, G894468893
OpenAlex ID: W2916933789
