Evidence map›Paper›PMID 19535568›Full record

ArticleAmerican journal of physiology. Renal physiology2009

The long-term label retaining population of the renal papilla arises through divergent regional growth of the kidney.

Derek C Adams, Leif Oxburgh

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Cellular plasticity in kidney injury and repair.Nature reviews. Nephrology · 2017
    Review
  7. LGR4 is required for sequential molar development.Biochemistry and biophysics reports · 2016
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. The bigger the better: determining nephron size in kidney.Pediatric nephrology (Berlin, Germany) · 2014
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Characterization and fate of telomerase-expressing epithelia during kidney repair.Journal of the American Society of Nephrology : JASN · 2011
    Article
  18. Repair of injured proximal tubule does not involve specialized progenitors.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  19. 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

2 authors at 1 institution in 1 country.

Derek C AdamsCenter for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, ME 04074, USA.
Leif Oxburgh
Maine Medical Center Research Institute · US

Funding

WNT SIGNALING IN PREIMPLANTATION EMBRYOP20RR018789 · NCRR · MAINE MEDICAL CENTER · PI WANG, ZACK Z. · 2003 to 2011
$18.9M
NCRR NIH HHS 2P20RR18789-06
6 · The paper itself

Abstract

Long-term pulse chase experiments previously identified a sizable population of BrdU-retaining cells within the renal papilla. The origin of these cells has been unclear, and in this work we test the hypothesis that they become quiescent early during the course of kidney development and organ growth. Indeed, we find that BrdU-retaining cells of the papilla can be labeled only by pulsing with BrdU from embryonic (E) day 11.25 to postnatal (P) day 7, the approximate period of kidney development in the mouse. BrdU signal in the cortex and outer medulla is rapidly diluted by cellular proliferation during embryonic development and juvenile growth, whereas cells within the papilla differentiate and exit the cell cycle during organogenesis. Indeed, by E17.5, little or no active proliferation can be seen in the distal papilla, indicating maturation of this structure in a distal-to-proximal manner during organogenesis. We conclude that BrdU-retaining cells of the papilla represent a population of cells that quiesce during embryonic development and localize within a region of the kidney that matures early. We therefore propose that selective papillary retention of BrdU arises through a combination of regionalized slowing of, and exit from, the cell cycle within the papilla during the period of ongoing kidney development, and extensive proliferative growth of the juvenile kidney resulting in dilution of BrdU below the detection level in extra-papillary regions.

Indexed as

Cell ProliferationAnimalsAnimals, NewbornBromodeoxyuridineCell CycleCell DifferentiationFemaleGestational AgeInjections, IntraperitonealKidney CortexKidney MedullaMiceMice, Inbred ICRPregnancyStaining and LabelingBromodeoxyuridine

Identifiers

PMID19535568
PMCPMC2739716
OpenAlexW2062654058

What OpenQuestion 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 OpenQuestion graph.