Evidence map›Paper›PMID 33850129›Full record

ArticleNature communications2021

Single cell transcriptional and chromatin accessibility profiling redefine cellular heterogeneity in the adult human kidney.

Yoshiharu Muto, Parker C Wilson, Nicolas Ledru, Haojia Wu, Henrik Dimke, Sushrut S Waikar, Benjamin D Humphreys

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 319 papers.

0numbers the graph read from it
0cells of the map it votes in
319citing papers in PubMed
28.4field-weighted citation impact, top 1% 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

319 citing papers in PubMed, 452 citations in OpenAlex.

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  6. Differential regulation of basal and interferon-inducedAmerican journal of physiology. Renal physiology · 2026
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  12. Renal TRPM6 but not Kv1.1 is required for magnesium homeostasis in mice.American journal of physiology. Renal physiology · 2026
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  13. Biomolecules · 2026
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259 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 2 countries.

Yoshiharu Muto *Division of Nephrology, Department of Medicine, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-0358-9442
Parker C Wilson *Department of Pathology and Immunology, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0001-8647-9662
Nicolas LedruDivision of Nephrology, Department of Medicine, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-9237-3634
Haojia WuDivision of Nephrology, Department of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Henrik DimkeDepartment of Cardiovascular and Renal Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.ORCID 0000-0002-9170-2168
Sushrut S WaikarSection of Nephrology, Department of Medicine, Boston University School of Medicine and Boston Medical Center, Boston, MA, USA.ORCID 0000-0003-4004-326X
Benjamin D HumphreysDivision of Nephrology, Department of Medicine, Washington University in St. Louis, St. Louis, MO, USA. humphreysbd@wustl.edu.ORCID 0000-0002-6420-8703
Washington University in St. Louis · USBoston University · USUniversity of Southern Denmark · DK

Funding

Chronic Kidney Disease (CKD) Biomarkers Consortium Data Coordinating CenterU01DK103225 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SCHRAUBEN, SARAH JEANNE · 2014 to 2020
$5.5M
NIDDK NIH HHS U01 DK103225
6 · The paper itself

Abstract

The integration of single cell transcriptome and chromatin accessibility datasets enables a deeper understanding of cell heterogeneity. We performed single nucleus ATAC (snATAC-seq) and RNA (snRNA-seq) sequencing to generate paired, cell-type-specific chromatin accessibility and transcriptional profiles of the adult human kidney. We demonstrate that snATAC-seq is comparable to snRNA-seq in the assignment of cell identity and can further refine our understanding of functional heterogeneity in the nephron. The majority of differentially accessible chromatin regions are localized to promoters and a significant proportion are closely associated with differentially expressed genes. Cell-type-specific enrichment of transcription factor binding motifs implicates the activation of NF-κB that promotes VCAM1 expression and drives transition between a subpopulation of proximal tubule epithelial cells. Our multi-omics approach improves the ability to detect unique cell states within the kidney and redefines cellular heterogeneity in the proximal tubule and thick ascending limb.

Indexed as

Genetic HeterogeneityTranscriptomeAdultChromatinGene Expression RegulationHepatocyte Nuclear Factor 4HumansKidneyMiddle AgedNF-kappa BPromoter Regions, GeneticRNA, Small NuclearTranscription Factor AP-2Transcription FactorsTransposasesVascular Cell Adhesion Molecule-1ChromatinHepatocyte Nuclear Factor 4HNF4A protein, humanNF-kappa BRNA, Small NuclearTFAP2B protein, humanTranscription Factor AP-2Transcription FactorsTransposasesVascular Cell Adhesion Molecule-1

Identifiers

PMID33850129
PMCPMC8044133
OpenAlexW3155656876

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.