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Kidney Organoids Generated Using an Allelic Series of NPHS2 Point Variants Reveal Distinct Intracellular Podocin Mistrafficking.

journal contribution
posted on 2024-06-13, 04:31 authored by Aude DorisonAude Dorison, Irene Ghobrial, Alison Graham, Thanushi Peiris, Thomas ForbesThomas Forbes, Michael SeeMichael See, Mithun Das, Moin A Saleem, Catherine QuinlanCatherine Quinlan, Kynan LawlorKynan Lawlor, Mirana RamialisonMirana Ramialison, Sara HowdenSara Howden, Melissa LittleMelissa Little
BACKGROUND: NPHS2 variants are the most common cause of steroid-resistant nephrotic syndrome in children >1 month old. Missense NPHS2 variants were reported to cause mistrafficking of the encoded protein, PODOCIN, but this conclusion was on the basis of overexpression in some nonpodocyte cell lines. METHODS: We generated a series of human induced pluripotent stem cell (iPSC) lines bearing pathogenic missense variants of NPHS2 , encoding the protein changes p.G92C, p.P118L, p.R138Q, p.R168H, and p.R291W, and control lines. iPSC lines were also generated from a patient with steroid-resistant nephrotic syndrome (p.R168H homozygote) and a healthy heterozygous parent. All lines were differentiated into kidney organoids. Immunofluorescence assessed PODOCIN expression and subcellular localization. Podocytes were transcriptionally profiled and PODOCIN-NEPHRIN interaction interrogated. RESULTS: All variant lines revealed reduced levels of PODOCIN protein in the absence of reduced transcription. Although wild-type PODOCIN localized to the membrane, distinct variant proteins displayed unique patterns of subcellular protein trafficking, some unreported. P118L and R138Q were preferentially retained in the endoplasmic reticulum (ER); R168H and R291W accumulated in the Golgi. Podocyte profiling demonstrated minimal disease-associated transcriptional change. All variants displayed podocyte-specific apoptosis, which was not linked to ER stress. NEPHRIN-PODOCIN colocalization elucidated the variant-specific effect on NEPHRIN association and hence NEPHRIN trafficking. CONCLUSIONS: Specific variants of endogenous NPHS2 result in distinct subcellular PODOCIN localization within organoid podocytes. Understanding the effect of each variant on protein levels and localization and the effect on NEPHRIN provides additional insight into the pathobiology of NPHS2 variants. PODCAST: This article contains a podcast at https://dts.podtrac.com/redirect.mp3/www.asn-online.org/media/podcast/JASN/2023_01_05_JASN2022060707.mp3.

Funding

Stem cell models of glomerular kidney disease for understanding disease and developing treatments : Medical Research Future Fund | DOH-MRFF APP2007287

Regenerating the kidney using an understanding of normal development : National Health and Medical Research Council | 1136085

Generating a higher order kidney by understanding and controlling nephron connectivity : National Health and Medical Research Council | 2011314

History

Pagination

88-109

Volume

34

Publisher

Wolters Kluwer

Issue

1

Journal

J Am Soc Nephrol

Language

eng

Location

United States

Medium

Print-Electronic

PII

00001751-202301000-00013

Publisher licence

CC BY-NC-ND

Online publication date

2022-09-27

Publication date

2023-01-01

Associated identifiers

grant.7876321 (dimensions-grant-id)

Publication status

  • Published