Evidence map›Paper›PMID 36285332›Full record

ArticlePeerJ2022

Tubular epithelial progenitors are excreted in urine during recovery from severe acute kidney injury and are able to expand and differentiate

Daniela Gerges, Zsofia Hevesi, Sophie H Schmidt, Sebastian Kapps, Sahra Pajenda, Barbara Geist, Alice Schmidt, Ludwig Wagner, Wolfgang Winnicki

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Daniela GergesDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.ORCID 0000-0001-6810-615X
Zsofia HevesiCenter for Brain Research, Medical University Vienna, Vienna, Austria.
Sophie H SchmidtDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.
Sebastian KappsDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.
Sahra PajendaDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.
Barbara GeistDepartment of Biochemical Imaging and Image-guided Therapy, Division of Nuclear Medicine, Medical University Vienna, Vienna, Austria.
Alice SchmidtDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.
Ludwig WagnerDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.
Wolfgang WinnickiDivision of Nephrology and Dialysis, Department of Medicine III, Medical University Vienna, Vienna, Austria.ORCID 0000-0002-0511-6120
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acute kidney injury (AKI) is a serious condition associated with chronic kidney disease, dialysis requirement and a high risk of death. However, there are specialized repair mechanisms for the nephron, and migrated committed progenitor cells are the key players. Previous work has described a positive association between renal recovery and the excretion of tubular progenitor cells in the urine of kidney transplant recipients. The aim of this work was to describe such structures in non-transplanted AKI patients and to focus on their differentiation. Methods: Morning urine was obtained from four patients with AKI stage 3 and need for RRT on a consecutive basis. Urine sediment gene expression was performed to assess which part of the tubular or glomerular segment was affected by injury, along with measurement of neprilysin. Urine output and sediment morphology were monitored, viable hyperplastic tubular epithelial clusters were isolated and characterized by antibody or cultured Results: Urinary neprilysin decreased rapidly with increasing urinary volume in ischemic, toxic, nephritic, and infection-associated AKI, whereas the decrease in sCr required at least 2 weeks. While urine output increased, dead cells were present in the sediment along with debris followed by hyperplastic agglomerates. Monitoring of urine sediment for tubular cell-specific gene transcript levels NPHS2 (podocyte), AQP1 and AQP6 (proximal tubule), and SLC12A1 (distal tubule) by qPCR revealed different components depending on the cause of AKI. Confocal immunofluorescence staining confirmed the presence of intact nephron-specific epithelial cells, some of which appeared in clusters expressing AQP1 and PAX8 and were 53% positive for the stem cell marker PROM1. Isolated tubule epithelial progenitor cells were grown Conclusion: During renal recovery, a high replicatory potential of tubular epithelial progenitor cells is found in urine.

Indexed as

Acute Kidney InjuryNeprilysinHumansIschemiaKidneyKidney Tubules, ProximalNeprilysinAcute kidney injury (AKI)Cell cultureDifferentiationGene expressionNephrosphereTubular epithelial progenitorsTubular regeneration

Identifiers

PMID36285332
PMCPMC9588302
OpenAlexW4306860300

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.