Evidence map›Paper›PMID 19558670›Full record

ArticleFibrogenesis & tissue repair2009

Possible mechanisms of kidney repair.

Paola Romagnani, Raghu Kalluri

Open access · hybridAbstract read
In one paragraph

Article in Fibrogenesis & tissue repair, 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
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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Renal Interstitial Platelet-Derived Growth Factor Receptor-Journal of the American Society of Nephrology : JASN · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. New tides: using zebrafish to study renal regeneration.Translational research : the journal of laboratory and clinical medicine · 2014
    Review
  12. Can kidney regeneration be visualized?Nephron. Experimental nephrology · 2014
    Review
  13. Aquaporin 11 insufficiency modulates kidney susceptibility to oxidative stress.American journal of physiology. Renal physiology · 2013
    Article
  14. Histone deacetylase inhibitor enhances recovery after AKI.Journal of the American Society of Nephrology : JASN · 2013
    Article
  15. Renal stem cells: fact or science fiction?The Biochemical journal · 2012
    Review
  16. The Role of PEC Progenitors in ADPKD Progression.International journal of stem cells · 2012
    Article
  17. Article
  18. Zebrafish kidney development: basic science to translational research.Birth defects research. Part C, Embryo today : reviews · 2011
    Review
  19. 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

2 authors at 2 institutions in 2 countries.

Paola RomagnaniExcellence Centre for Research, Transfer and High Education DENOthe, University of Florence, Florence, Italy. p.romagnani@dfc.unifi.it
Raghu Kalluri
Beth Israel Deaconess Medical Center · USUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In most adult epithelia the process of replacing damaged or dead cells is maintained through the presence of stem/progenitor cells, which allow epithelial tissues to be repaired following injury. Existing evidence strongly supports the presence of stem cells in the adult kidney. Indeed, recent findings provide evidence in favour of a role for intrinsic renal cells and against a physiological role for bone marrow-derived stem cells in the regeneration of renal epithelial cells. In addition, recent studies have identified a subset of CD24+CD133+ renal progenitors within the Bowman's capsule of adult human kidney, which provides regenerative potential for injured renal epithelial cells. Intriguingly, CD24+CD133+ renal progenitors also represent common progenitors of tubular cells and podocytes during renal development. Chronic injury causes dysfunction of the tubular epithelial cells, which triggers the release of fibrogenic cytokines and recruitment of inflammatory cells to injured kidneys. The rapid interposition of scar tissue probably confers a survival advantage by preventing infectious microorganisms from invading the wound, but prevents subsequent tissue regeneration. However, the existence of renal epithelial progenitors in the kidney suggests a possible explanation for the regression of renal lesions which has been observed in experimental animals and even in humans. Thus, manipulation of the wound repair process in order to shift it towards regeneration will probably require the ability to slow the rapid fibrotic response so that renal progenitor cells can allow tissue regeneration rather than scar formation.

Identifiers

PMID19558670
PMCPMC2711960
OpenAlexW1996045954

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.