Evidence map›Paper›PMID 31029503›Full record

ArticleKidney international2019

Novel parietal epithelial cell subpopulations contribute to focal segmental glomerulosclerosis and glomerular tip lesions.

Christoph Kuppe, Katja Leuchtle, Anton Wagner, Nazanin Kabgani, Turgay Saritas, Victor G Puelles, Bart Smeets, Samy Hakroush, Johan van der Vlag, Peter Boor and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Cell-cell crosstalk in kidney health and disease.Nature reviews. Nephrology · 2026
    Review
  3. Article
  4. bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Crosstalk between glomeruli and tubules.Nature reviews. Nephrology · 2025
    Review
  11. Podocytes in health and glomerular disease.Frontiers in cell and developmental biology · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Mice with aAmerican journal of physiology. Renal physiology · 2024
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 4 countries.

Christoph KuppeDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany. Electronic address: ckuppe@ukaachen.de.
Katja LeuchtleDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany.
Anton WagnerDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany.
Nazanin KabganiDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany.
Turgay SaritasDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany.
Victor G PuellesDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany; Cardiovascular Program, Monash Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, School of Biomedical Sciences, and Centre for Inflammatory Diseases, Monash University, Melbourne, Victoria, Australia; Department of Nephrology, Monash Health, Melbourne Australia.
Bart SmeetsDepartment of Pathology, Radboud Institute for Molecular Life Sciences, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Samy HakroushInstitute of Pathology, University Medical Center, Göttingen, Germany.
Johan van der VlagDepartment of Nephrology, Radboud Institute for Molecular Life Sciences, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Peter BoorDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany; Institute of Pathology, RWTH University of Aachen, Aachen, Germany.
Mario SchifferDepartment of Nephrology and Hypertension, University of Erlangen, Erlangen, Germany.
Hermann-Josef GröneCellular and Molecular Pathology, German Cancer Research Center, Heidelberg, Germany.
Agnes FogoVanderbilt University Medical Center, Nashville, Tennessee, USA.
Jürgen FloegeDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany.
Marcus Johannes MoellerDivision of Nephrology and Clinical Immunology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University, Aachen, Germany. Electronic address: mmoeller@ukaachen.de.
RWTH Aachen University · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEGerman Cancer Research Center · DEMonash University · AURadboud Institute for Molecular Life Sciences · NLRadboud University Nijmegen · NLUniversity of Göttingen · DEVanderbilt University Medical Center · US

Funding

RESOLUTION OF GLOMERULOSCLEROSISR01DK056942 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI FOGO, AGNES B. · 2001 to 2021
$4.9M
Pathology of the FSGS KidneyR01DK080095 · NIDDK · VANDERBILT UNIVERSITY · PI FOGO, AGNES B. · 2009 to 2010
$700k
NIDDK NIH HHS R01 DK056942NIDDK NIH HHS R01 DK080095
6 · The paper itself

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.

Indexed as

AdolescentAdultAgedAged, 80 and overAnimalsBowman CapsuleDisease Models, AnimalEpithelial CellsFemaleGlomerulosclerosis, Focal SegmentalHumansHyaluronan ReceptorsKi-67 AntigenKidney GlomerulusKidney Tubules, ProximalMaleCD44 protein, humanCd44 protein, mouseHyaluronan ReceptorsKi-67 AntigenMKI67 protein, humanMki67 protein, mousePax8 protein, mousePAX8 Transcription FactorColumbia classificationFSGSglomerular diseaseparietal epithelial cellstip lesions

Identifiers

PMID31029503
PMCPMC7292612
OpenAlexW2916933789

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.