Evidence map›Paper›PMID 39271683›Full record

ArticleNature communications2024

Podocyte-specific KLF6 primes proximal tubule CaMK1D signaling to attenuate diabetic kidney disease.

Nehaben A Gujarati, Bismark O Frimpong, Malaika Zaidi, Robert Bronstein, Monica P Revelo, John D Haley, Igor Kravets, Yiqing Guo, Sandeep K Mallipattu

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. New Insights into the Role of Mitochondrial Dysfunction in Diabetic Kidney Disease in the Omics Era.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Review
  10. Article
  11. Aging-related CD8PeerJ · 2026
    Article
  12. Review
  13. Article
  14. Review
  15. Review
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.

Nehaben A Gujarati *Division of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
Bismark O Frimpong *Division of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.ORCID 0000-0002-0689-3968
Malaika ZaidiDivision of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.ORCID 0009-0004-4487-9739
Robert BronsteinDivision of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
Monica P ReveloDepartment of Pathology, University of Utah, Salt Lake City, UT, USA.
John D HaleyDepartment of Pharmacology, Stony Brook University, Stony Brook, NY, USA.
Igor KravetsDivision of Endocrinology, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
Yiqing GuoDivision of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
Sandeep K MallipattuDivision of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, NY, USA. sandeep.mallipattu@stonybrookmedicine.edu.ORCID 0000-0002-6324-7807

Funding

Transcriptional control of mitochondrial function by KLF6 in diabetic kidney diseaseR01DK112984 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI Sandeep K Mallipattu · 2017 to 2026
$3.5M
Mechanisms mediating podocyte-parietal epithelial cell crosstalk in proliferative glomerulopathiesR01DK121846 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI HE, JOHN CIJIANG, MALLIPATTU, SANDEEP K · 2020 to 2024
$2.7M
BLRD VA I01 BX003698Center for Integrated Healthcare, U.S. Department of Veterans Affairs (VISN 2 Center for Integrated Healthcare) 1I01BX005300NIDDK NIH HHS R01 DK112984NIDDK NIH HHS R01 DK121846U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK112984U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK121846U.S. Department of Veterans Affairs (Department of Veterans Affairs) 1I01BX003698
6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is the main cause of chronic kidney disease worldwide. While injury to the podocytes, visceral epithelial cells that comprise the glomerular filtration barrier, drives albuminuria, proximal tubule (PT) dysfunction is the critical mediator of DKD progression. Here, we report that the podocyte-specific induction of human KLF6, a zinc-finger binding transcription factor, attenuates podocyte loss, PT dysfunction, and eventual interstitial fibrosis in a male murine model of DKD. Utilizing combination of snRNA-seq, snATAC-seq, and tandem mass spectrometry, we demonstrate that podocyte-specific KLF6 triggers the release of secretory ApoJ to activate calcium/calmodulin dependent protein kinase 1D (CaMK1D) signaling in neighboring PT cells. CaMK1D is enriched in the first segment of the PT, proximal to the podocytes, and is critical to attenuating mitochondrial fission and restoring mitochondrial function under diabetic conditions. Targeting podocyte-PT signaling by enhancing ApoJ-CaMK1D might be a key therapeutic strategy in attenuating the progression of DKD.

Indexed as

Diabetic NephropathiesKidney Tubules, ProximalKruppel-Like Factor 6PodocytesSignal TransductionAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 1Disease Models, AnimalHumansMaleMiceMice, Inbred C57BLCalcium-Calmodulin-Dependent Protein Kinase Type 1KLF6 protein, humanKruppel-Like Factor 6

Identifiers

PMID39271683
PMCPMC11399446

What OpenQuestion holds

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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.