Evidence map›Paper›PMID 39207915›Full record

ArticleeLife2024

PKR activation-induced mitochondrial dysfunction in HIV-transgenic mice with nephropathy.

Teruhiko Yoshida, Khun Zaw Latt, Avi Z Rosenberg, Briana A Santo, Komuraiah Myakala, Yu Ishimoto, Yongmei Zhao, Shashi Shrivastav, Bryce A Jones, Xiaoping Yang and 7 more

Abstract read
In one paragraph

Article in eLife, 2024. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. NAD deficiency contributes to progressive kidney disease in HIV-nephropathy mice.American journal of physiology. Renal physiology · 2024
    Article
  4. 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

17 authors.

Teruhiko Yoshida *Kidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.ORCID https://orcid.org/0000-0002-2049-7347
Khun Zaw Latt *Kidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.
Avi Z RosenbergDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, United States.
Briana A SantoDepartment of Pathology and Anatomical Sciences, Jacobs School of Medicine & Biomedical Sciences, University at Buffalo, Buffalo, United States.
Komuraiah MyakalaDepartment of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, United States.ORCID https://orcid.org/0000-0003-3233-047X
Yu IshimotoPolycystic Kidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.
Yongmei ZhaoFrederick National Laboratory for Cancer Research, NCI, NIH, Frederick, United States.
Shashi ShrivastavKidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.
Bryce A JonesDepartment of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, United States.
Xiaoping YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, United States.ORCID https://orcid.org/0000-0003-1263-2710
Xiaoxin X WangDepartment of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, United States.
Vincent M TutinoDepartment of Pathology and Anatomical Sciences, Jacobs School of Medicine & Biomedical Sciences, University at Buffalo, Buffalo, United States.
Pinaki SarderDepartment of Pathology and Anatomical Sciences, Jacobs School of Medicine & Biomedical Sciences, University at Buffalo, Buffalo, United States.
Moshe LeviDepartment of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, United States.ORCID https://orcid.org/0000-0001-6403-2261
Koji OkamotoKidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.
Cheryl A WinklerFrederick National Laboratory for Cancer Research, NCI, NIH, Frederick, United States.
Jeffrey B KoppKidney Disease Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, United States.

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Focal segmental glomerulosclerosis: HIV-associated nephropathyZIADK043411 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI HEYMANN, JURGEN · 2009 to 2024
$7.3M
Computational Imaging of Renal Structures for Diagnosing DiabeticNephropathyR01DK114485 · NIDDK · UNIVERSITY OF FLORIDA · PI Michael Thomas Eadon, Avi Z Rosenberg · 2018 to 2026
$4.7M
Obeticholic acid as a novel treatment for Alport syndromeF30DK129003 · NIDDK · GEORGETOWN UNIVERSITY · PI JONES, BRYCE ALAN · 2021 to 2024
$187k
Intramural NIH HHS ZIA DK043411NCI NIH HHS 75N91019D00024NIDDK NIH HHS F30 DK129003NIDDK NIH HHS R01 DK114485NIDDK NIH HHS ZIADK043411
6 · The paper itself

Abstract

HIV disease remains prevalent in the USA and chronic kidney disease remains a major cause of morbidity in HIV-1-positive patients. Host double-stranded RNA (dsRNA)-activated protein kinase (PKR) is a sensor for viral dsRNA, including HIV-1. We show that PKR inhibition by compound C16 ameliorates the HIV-associated nephropathy (HIVAN) kidney phenotype in the Tg26 transgenic mouse model, with reversal of mitochondrial dysfunction. Combined analysis of single-nucleus RNA-seq and bulk RNA-seq data revealed that oxidative phosphorylation was one of the most downregulated pathways and identified signal transducer and activator of transcription (STAT3) as a potential mediating factor. We identified in Tg26 mice a novel proximal tubular cell cluster enriched in mitochondrial transcripts. Podocytes showed high levels of HIV-1 gene expression and dysregulation of cytoskeleton-related genes, and these cells dedifferentiated. In injured proximal tubules, cell-cell interaction analysis indicated activation of the pro-fibrogenic PKR-STAT3-platelet-derived growth factor (PDGF)-D pathway. These findings suggest that PKR inhibition and mitochondrial rescue are potential novel therapeutic approaches for HIVAN.

Indexed as

AIDS-Associated NephropathyeIF-2 KinaseMice, TransgenicMitochondriaAnimalsDisease Models, AnimalHIV-1HumansMicePodocytesSTAT3 Transcription FactoreIF-2 Kinaseprotein kinase R, mouseSTAT3 Transcription FactorHIVHIV-associated nephropathymedicinemitochondriamouseprotein kinase RRNA-seqsingle-nucleus RNA-seq

Identifiers

PMID39207915
PMCPMC11361708

What Socratic holds

Textmetadata
LicenceCC0
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 Socratic graph.