Evidence map›Paper›PMID 40902080›Full record

ArticleDiabetes2025

Cell Type-Specific Expression of Long Noncoding RNAs in Human Diabetic Kidneys Identifies TARID as a Key Regulator of Podocyte Function.

Juliette A de Klerk, Roderick C Slieker, Wilson C Parker, Haojia Wu, Yoshiharu Muto, Rudmer J Postma, Leen M 't Hart, Janneke H D Peerlings, Floris Herrewijnen, Heein Song and 11 more

Abstract read
In one paragraph

Article in Diabetes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. S100A1 Promotes MDM2-Mediated KLF15 Ubiquitination to Regulate ID1-Driven Tubular Injury in Diabetic Kidney Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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

21 authors.

Juliette A de KlerkDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Roderick C SliekerDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
Wilson C ParkerDivision of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO.
Haojia WuDivision of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO.
Yoshiharu MutoDivision of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO.
Rudmer J PostmaDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Leen M 't HartDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
Janneke H D PeerlingsDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
Floris HerrewijnenDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
Heein SongDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
H Siebe SpijkerDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Sébastien J DumasDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Marije KoningDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Loïs A K van der PluijmDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Hans J BaeldeDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Tessa GerritsDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Joris I RotmansDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Anton Jan van ZonneveldDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Coen van SolingenCardiovascular Research Center, Department of Medicine, New York University Grossman School of Medicine, New York, NY.
Benjamin D HumphreysDivision of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO.
Roel BijkerkDivision of Nephrology and the Einthoven Laboratory for Vascular and Regenerative Medicine. Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-6438-4133

Funding

The Single Cell Landscape of Early Human Diabetic NephropathyK08DK126847 · NIDDK · WASHINGTON UNIVERSITY · PI Parker C. Wilson · 2022 to 2026
$840k
American Heart Association 23SCEFIA1153739Dutch Kidney Foundation 20OK015European Foundation for the Study of Diabetes NNF23SA0087433NIDDK NIH HHS K08 DK126847Novo Nordisk Fonden NNF21CC0073729
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play essential roles in cellular processes, often exhibiting cell type-specific expression and influencing kidney function. While single-cell RNA sequencing (scRNA-seq) has advanced our understanding of cellular specificity, past studies focus solely on protein-coding genes. We hypothesize that lncRNAs, due to their cell-specific nature, have crucial functions within particular renal cells and thereby play essential roles in renal cell function and disease. Using single-nucleus RNA-seq (snRNA-seq) data from kidney samples of five healthy individuals and six patients with diabetic kidney disease (DKD), we explored the noncoding transcriptome. Cell type-specific lncRNAs were identified, and their differential expression in DKD was assessed. Integrative analyses included expression quantitative trait loci (eQTL), genome-wide association studies (GWAS) for estimated glomerular filtration rate (eGFR), and gene regulatory networks. Functional studies focused on TCF21 antisense RNA inducing promoter demethylation (TARID), a lncRNA with podocyte-specific expression, to elucidate its role in podocyte health. We identified 174 lncRNAs with cell type-specific expression across kidney cell types. Of these, 54 lncRNAs were differentially expressed in DKD. Integrative analyses, including eQTL data, GWAS results for eGFR, and gene regulatory networks, pinpointed TARID, a podocyte-specific lncRNA, as a key candidate upregulated in DKD. Functional studies confirmed TARID's podocyte-specific expression and revealed its central role in actin cytoskeleton reorganization. Our study provides a comprehensive resource of single-cell lncRNA expression in the human kidney and highlights the importance of cell type-specific lncRNAs in kidney function and disease. Specifically, we demonstrate the functional relevance of TARID in podocyte health. ARTICLE HIGHLIGHTS: This study provides a resource for kidney (cell type-specific) long noncoding (lnc)RNA expression and demonstrates the importance of lncRNAs in renal health. We identified 174 cell type-specific lncRNAs in the human kidney, with 54 showing altered expression in diabetic kidney disease. TCF21 antisense RNA inducing promoter demethylation (TARID), a podocyte-specific lncRNA upregulated in diabetic kidney disease, is crucial for actin cytoskeleton reorganization in podocytes.

Indexed as

Diabetic NephropathiesPodocytesRNA, Long NoncodingFemaleGene Expression RegulationGene Regulatory NetworksGenome-Wide Association StudyGlomerular Filtration RateHumansMaleMiddle AgedQuantitative Trait LociRNA, Long Noncoding

Identifiers

PMID40902080
PMCPMC12585169

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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.