Evidence map›Paper›PMID 26120499›Full record

ArticleCurrent pathobiology reports2015

Kidney Regeneration: Lessons from Development.

Takuto Chiba, Neil Hukriede, Mark P de Caestecker

Abstract read
In one paragraph

Article in Current pathobiology reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Formation of the glomerular microvasculature is regulated by VEGFR-3.American journal of physiology. Renal physiology · 2023
    Article
  4. Early activation of fibroblasts is required for kidney repair and regeneration after injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  5. Article
  6. Article
  7. Does Renal Repair Recapitulate Kidney Development?Journal of the American Society of Nephrology : JASN · 2017
    Review
  8. 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

3 authors.

Takuto ChibaDepartment of Medicine, Division of Nephrology, Vanderbilt University ; Department of Cell and Developmental Biology, Vanderbilt University.
Neil HukriedeDepartment of Developmental Biology, University of Pittsburgh.
Mark P de CaesteckerDepartment of Medicine, Division of Nephrology, Vanderbilt University ; Department of Cell and Developmental Biology, Vanderbilt University.

Funding

Single Nephron and MetabolomicsP30DK079307 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2008 to 2022
$13.4M
Regulation of Renal Progenitor Cells in Regenerating KidneysR01DK069403 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUKRIEDE, NEIL A · 2006 to 2020
$4.8M
Utilizing Small Molecule Screens to Delineate Embryonic Signaling MechanismsR01HD053287 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUKRIEDE, NEIL A, TSANG, MICHAEL WAIKOK · 2007 to 2016
$3.1M
Small Molecule-Mediated Augmentation of Kidney RegenerationRC4DK090770 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUKRIEDE, NEIL A · 2010 to 2010
$2.8M
BMP Signaling and Pulmonary VasoreactivityR01HL093057 · NHLBI · VANDERBILT UNIVERSITY · PI DE CAESTECKER, MARK P. · 2010 to 2013
$1.5M
NHLBI NIH HHS R01 HL093057NICHD NIH HHS R01 HD053287NIDDK NIH HHS P30 DK079307NIDDK NIH HHS R01 DK069403NIDDK NIH HHS RC4 DK090770
6 · The paper itself

Abstract

A number of genes involved in kidney development are reactivated in the adult after acute kidney injury (AKI). This has led to the belief that tissue repair mechanisms recapitulate pathways involved in embryonic development after AKI. We will discuss evidence to support this hypothesis by comparing the mechanisms of development with common pathways known to regulate post-AKI repair, or that we identified as cell-specific candidates based on public datasets from recent AKI translational profiling studies. We will argue that while many of these developmental pathways are reactivated after AKI, this is not associated with general cellular reprogramming to an embryonic state. We will show that reactivation of these developmental genes is often associated with expression in cells that are not normally involved in mediating parallel responses in the embryo, and that depending on the cellular context, these responses can have beneficial or detrimental effects on injury and repair after AKI.

Indexed as

Acute kidney injuryembryonic developmentendothelial cellsfibroblastsischemia reperfusionmacrophagesregenerationtissue repairtranslational profilingtubular epithelial cellsvascular pericytes

Identifiers

PMID26120499
PMCPMC4477536

What OpenQuestion holds

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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.