Evidence map›Paper›PMID 26081073›Full record

ArticleAging2015

Interstitial pericytes decrease in aged mouse kidneys.

Ania Stefanska, Diana Eng, Natalya Kaverina, Jeremy S Duffield, Jeffrey W Pippin, Peter Rabinovitch, Stuart J Shankland

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

  1. Pericytes in tissue fibrosis.American journal of physiology. Cell physiology · 2025
    Review
  2. Review
  3. Article
  4. Review
  5. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  6. Review
  7. Pressure-Natriuresis Response Is Diminished in Old Age.Frontiers in cardiovascular medicine · 2022
    Article
  8. Article
  9. Article
  10. Pericyte migration and proliferation are tightly synchronized to endothelial cell sprouting dynamics.Integrative biology : quantitative biosciences from nano to macro · 2021
    Article
  11. Article
  12. Red Carrot Cells CulturedFrontiers in bioengineering and biotechnology · 2020
    Article
  13. The pericyte microenvironment during vascular development.Microcirculation (New York, N.Y. : 1994) · 2019
    Review
  14. Article
  15. Article
  16. Microvascular bioengineering: a focus on pericytes.Journal of biological engineering · 2019
    Review
  17. Review
  18. Review
  19. Mechanisms of altered renal sodium handling in age-related hypertension.American journal of physiology. Renal physiology · 2018
    Review
  20. Establishment and characterization of an embryonic pericyte cell line.Microcirculation (New York, N.Y. : 1994) · 2018
    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

7 authors at 2 institutions in 1 country.

Ania StefanskaDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
Diana EngDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
Natalya KaverinaDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
Jeremy S DuffieldDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
Jeffrey W PippinDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
Peter RabinovitchDepartment of Pathology, University of Washington, Seattle, WA 98195, USA.
Stuart J ShanklandDivision of Nephrology, Department of Medicine, University of Washington, Seattle, WA 98104, USA.
University of Washington · USBiogen (United States) · US

Funding

University of Washington Nathan Shock Center of Excellence in the Basic Biology of AgingP30AG013280 · NIA · UNIVERSITY OF WASHINGTON · PI Michael MacCoss · 1995 to 2026
$27.1M
Juxta-glomerular cells serve as glomerular epithelial cell progenitors in glomerular diseaseR01DK097598 · NIDDK · UNIVERSITY OF WASHINGTON · PI SHANKLAND, STUART JAMES, WESSELY, OLIVER · 2014 to 2022
$5.2M
CELL CYCLE PROTEINS AND GLOMERULAR APOPTOSISR01DK056799 · NIDDK · UNIVERSITY OF WASHINGTON · PI SHANKLAND, STUART JAMES · 2000 to 2014
$3.6M
Cardiomyocyte mitochondria and mtROS in cardiac aging, hypertrophy and failureR01HL101186 · NHLBI · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 2010 to 2013
$2.5M
Pericyte-endothelial cross talk in vascular stability after kidney injuryR01DK093493 · NIDDK · UNIVERSITY OF WASHINGTON · PI SHANKLAND, STUART JAMES · 2012 to 2016
$2.5M
The importance of mTOR signaling in cardiac aging and lifespan in mammalsR01AG038550 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 2010 to 2014
$1.5M
Kidney Progenitor Cells in DiseaseR24DK094768 · NIDDK · UNIVERSITY OF WASHINGTON · PI GROSS, KENNETH W, PRUITT, STEVEN C · 2012 to 2012
$533k
NHLBI NIH HHS R01 HL101186NIA NIH HHS P30 AG013280NIA NIH HHS R01 AG038550NIDDK NIH HHS R01 5R01DK056799-10NIDDK NIH HHS R01 DK056799NIDDK NIH HHS R01 DK093493NIDDK NIH HHS R01 DK093493-02NIDDK NIH HHS R01 DK097598NIDDK NIH HHS R01 DK097598-01NIDDK NIH HHS R24 DK094768NIDDK NIH HHS R24 DK094768-01
6 · The paper itself

Abstract

With increasing age, the kidney undergoes characteristic changes in the glomerular and tubulo-interstitial compartments, which are ultimately accompanied by reduced kidney function. Studies have shown age-related loss of peritubular vessels. Normal peritubular vessel tone, function and survival depend on neighboring pericytes. Pericyte detachment leads to vascular damage, which can be accompanied by their differentiation to fibroblasts and myofibroblasts, a state that favors matrix production. To better understand the fate of pericytes in the aged kidney, 27 month-old mice were studied. Compared to 3 month-old young adult mice, aged kidneys showed a substantial decrease in capillaries, identified by CD31 staining, in both cortex and medulla. This was accompanied by a marked decrease in surrounding NG2+ / PDGFRβ+ pericytes. This decrease was more pronounced in the medulla. Capillaries devoid of pericytes were typically dilated in aged mice. Aged kidneys were also characterized by interstitial fibrosis due to increased collagen-I and -III staining. This was accompanied by an increase in the number of pericytes that acquired a pro-fibrotic phenotype, identified by increased PDGFRβ+ / αSMA+ staining. These findings are consistent with the decline in kidney interstitial pericytes as a critical step in the development of changes to the peritubular vasculature with aging, and accompanying fibrosis.

Indexed as

AgingAnimalsAntigensCapillariesChondroitin Sulfate Proteoglycan 4FemaleGene Expression RegulationKidneyMiceMice, Inbred C57BLPericytesProteoglycansReceptor, Platelet-Derived Growth Factor betaRenal InsufficiencyAntigensChondroitin Sulfate Proteoglycan 4ProteoglycansReceptor, Platelet-Derived Growth Factor betaendotheliumnephropathyNG2PDGFβ-receptortubulo-interstitial fibrosis

Identifiers

PMID26081073
PMCPMC4505164
OpenAlexW1491097444

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.