Evidence map›Paper›PMID 33858824›Full record

ArticleDiabetes2021

Diabetic Kidney Disease Alters the Transcriptome and Function of Human Adipose-Derived Mesenchymal Stromal Cells but Maintains Immunomodulatory and Paracrine Activities Important for Renal Repair.

LaTonya J Hickson, Alfonso Eirin, Sabena M Conley, Timucin Taner, Xiaohui Bian, Ahmed Saad, Sandra M Herrmann, Ramila A Mehta, Travis J McKenzie, Todd A Kellogg and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Mitigation of Ferroptosis in Diabetic Kidney Disease Through Mesenchymal Stem Cell Intervention via the Smad2/3/METTL3/S1PR1 Axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Exosomes in Diabetic Kidney Disease.Kidney diseases (Basel, Switzerland) · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. hucMSC-sEVs-Derived 14-3-3Oxidative medicine and cellular longevity · 2022
    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 at 4 institutions in 3 countries.

LaTonya J HicksonDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN hickson.latonya@mayo.edu.ORCID 0000-0002-7485-336X
Alfonso EirinDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Sabena M ConleyDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Timucin TanerDepartment of Surgery, Mayo Clinic, Rochester, MN.
Xiaohui BianDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Ahmed SaadDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Sandra M HerrmannDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Ramila A MehtaDivision of Clinical Trials and Biostatistics, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
Travis J McKenzieDepartment of Surgery, Mayo Clinic, Rochester, MN.
Todd A KelloggDepartment of Surgery, Mayo Clinic, Rochester, MN.
James L KirklandDivision of Geriatric Medicine and Gerontology, Department of Medicine, Mayo Clinic, Rochester, MN.
Tamar TchkoniaDivision of Geriatric Medicine and Gerontology, Department of Medicine, Mayo Clinic, Rochester, MN.
Ishran M SaadiqDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Hui TangDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Kyra L JordanDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Xiangyang ZhuDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Mathew D GriffinRegenerative Medicine Institute (REMEDI) at CÚRAM SFI Centre for Research in Medical Devices, School of Medicine, National University of Ireland Galway, Galway, Ireland.
Andrew D RuleDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Andre J van WijnenOrthopedic Surgery, Mayo Clinic, Rochester, MN.
Stephen C TextorDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Lilach O LermanDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN.
Mayo Clinic · USMayo Clinic in Arizona · USMayo Clinic in Florida · USOllscoil na Gaillimhe – University of Galway · IE

Funding

Mayo Clinic Center for Clinical and Translational Science (CCaTS UL1 Supplement - Dr. Timothy Curry)UL1TR002377 · NCATS · MAYO CLINIC ROCHESTER · PI VESNA D GAROVIC · 2017 to 2026
$78.4M
Coordinating and Bioinformatics Unit for the MMPC/DiaCompU24DK076169 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2006 to 2018
$42.4M
Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
Coordinating Unit for DiaCompU24DK115255 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2017 to 2020
$11.6M
Effect of Aging on Preadipocyte DifferentiationR37AG013925 · NIA · MAYO CLINIC ROCHESTER · PI KIRKLAND, JAMES L. · 2016 to 2025
$6.6M
Effect of Aging on Preadipocyte DifferentiationR01AG013925 · NIA · MAYO CLINIC ROCHESTER · PI KIRKLAND, JAMES L. · 1997 to 2012
$3.7M
KIDNEY DISEASES RESEARCH TRAINING PROGRAMT32DK007013 · NIDDK · MAYO CLINIC ROCHESTER · PI LIESKE, JOHN C · 1986 to 2023
$3.7M
Hypoxia and inflammatory injury in human renovascular hypertensionR01DK100081 · NIDDK · MAYO CLINIC ROCHESTER · PI LERMAN, LILACH O, TEXTOR, STEPHEN C · 2014 to 2018
$2.8M
Obesity-induced mesenchymal stem cell senescenceR01DK120292 · NIDDK · MAYO CLINIC ROCHESTER · PI LERMAN, LILACH O · 2019 to 2022
$2.6M
Quantitative magnetization transfer MRI for evaluation of renal fibrosisR01DK122734 · NIDDK · MAYO CLINIC ROCHESTER · PI LERMAN, LILACH O · 2020 to 2023
$2.2M
Mesenchymal stem cell senescence in diabetic nephropathy (K23 COVID Admin Supplement)K23DK109134 · NIDDK · MAYO CLINIC ROCHESTER · PI HICKSON, LATONYA J · 2016 to 2021
$1.0M
NCATS NIH HHS UL1 TR000135NCATS NIH HHS UL1 TR002377NIA NIH HHS P01 AG062413NIA NIH HHS R01 AG013925NIA NIH HHS R21 AG062104NIA NIH HHS R37 AG013925NIDDK NIH HHS K08 DK106427NIDDK NIH HHS K08 DK118120NIDDK NIH HHS K23 DK109134NIDDK NIH HHS R01 DK100081NIDDK NIH HHS R01 DK120292NIDDK NIH HHS R01 DK122734NIDDK NIH HHS R03 DK123492NIDDK NIH HHS T32 DK007013NIDDK NIH HHS U24 DK076169NIDDK NIH HHS U24 DK115255
6 · The paper itself

Abstract

Mesenchymal stem/stromal cells (MSCs) facilitate repair in experimental diabetic kidney disease (DKD). However, the hyperglycemic and uremic milieu may diminish regenerative capacity of patient-derived therapy. We hypothesized that DKD reduces human MSC paracrine function. Adipose-derived MSC from 38 participants with DKD and 16 control subjects were assessed for cell surface markers, trilineage differentiation, RNA sequencing (RNA-seq), in vitro function (coculture or conditioned medium experiments with T cells and human kidney cells [HK-2]), secretome profile, and cellular senescence abundance. The direction of association between MSC function and patient characteristics were also tested. RNA-seq analysis identified 353 differentially expressed genes and downregulation of several immunomodulatory genes/pathways in DKD-MSC versus Control-MSC. DKD-MSC phenotype, differentiation, and tube formation capacity were preserved, but migration was reduced. DKD-MSC with and without interferon-γ priming inhibited T-cell proliferation greater than Control-MSC. DKD-MSC medium contained higher levels of anti-inflammatory cytokines (indoleamine 2,3-deoxygenase 1 and prostaglandin-E2) and prorepair factors (hepatocyte growth factor and stromal cell-derived factor 1) but lower IL-6 versus control-MSC medium. DKD-MSC medium protected high glucose plus transforming growth factor-β-exposed HK-2 cells by reducing apoptotic, fibrotic, and inflammatory marker expression. Few DKD-MSC functions were affected by patient characteristics, including age, sex, BMI, hemoglobin A

Indexed as

ImmunomodulationTranscriptomeAdipose TissueApoptosisCells, CulturedCellular SenescenceDiabetic NephropathiesHumansLymphocyte ActivationMesenchymal Stem CellsT-Lymphocytes

Identifiers

PMID33858824
PMCPMC8336004
OpenAlexW3152927336

What Socratic holds

Textmetadata
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.