Evidence map›Paper›PMID 20861083›Full record

ArticleAmerican journal of physiology. Renal physiology2011

P2X7 receptors mediate deleterious renal epithelial-fibroblast cross talk.

Murugavel Ponnusamy, Li Ma, Rujun Gong, Maoyin Pang, Y Eugene Chin, Shougang Zhuang

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. P2X7 Receptors: An Untapped Target for the Management of Cardiovascular Disease.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Review
  5. Review
  6. Review
  7. Article
  8. The dark side of extracellular ATP in kidney diseases.Journal of the American Society of Nephrology : JASN · 2015
    Review
  9. P2X7 receptor inhibition protects against ischemic acute kidney injury in mice.American journal of physiology. Cell physiology · 2015
    Article
  10. Exaggerated renal fibrosis in P2X4 receptor-deficient mice following unilateral ureteric obstruction.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2014
    Article
  11. Review
  12. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Murugavel PonnusamyDepartment of Medicine, Rhode Island Hospital and Warren Alpert Medical School of Brown University, Middle House 301, 593 Eddy St., Providence, RI 02903, USA.
Li Ma
Rujun Gong
Maoyin Pang
Y Eugene Chin
Shougang Zhuang
Brown University · US

Funding

Histone deacetylases as novel therapeutic targets for kidney fibrosisR01DK085065 · NIDDK · RHODE ISLAND HOSPITAL · PI ZHUANG, SHOUGANG · 2010 to 2017
$2.8M
Dedifferentiation Following Renal Cell InjuryR01DK071997 · NIDDK · RHODE ISLAND HOSPITAL · PI ZHUANG, SHOUGANG · 2006 to 2009
$1.1M
NIDDK NIH HHS DK-071997NIDDK NIH HHS R01 DK085065
6 · The paper itself

Abstract

Peritubular fibroblasts in the kidney are the major erythropoietin-producing cells and also contribute to renal repair following acute kidney injury (AKI). Although few fibroblasts were observed in the interstitium adjacent to damaged tubular epithelium in the early phase of AKI, the underlying mechanism by which their numbers were reduced remains unknown. In this study, we tested the hypothesis that damaged renal epithelial cells directly induce renal interstitial fibroblast death by releasing intracellular ATP and activating purinergic signaling. Exposure of a cultured rat renal interstitial fibroblast cell line (NRK-49F) to necrotic renal proximal tubular cells (RPTC) lysate or supernatant induced NRK-49F cell death by apoptosis and necrosis. Depletion of ATP with apyrase or inhibition of the P2X purinergic receptor with pyridoxal phosphate-6-azophenyl-2',4'-disulfonic acid blocked the deleterious effect of necrotic RPTC supernatant. The P2X7 receptor, an ATP-sensitive purinergic receptor, was not detected in cultured NRK-49F cells but was inducible by necrotic RPTC supernatant. Treatment with A438079, a highly selective P2X7 receptor inhibitor, or knockdown of the P2X7 receptor with small interference RNA diminished renal fibroblast death induced by necrotic RPTC supernatant. Conversely, overexpression of the P2X7 receptor potentiated this response. Collectively, these findings provide strong evidence that damaged renal epithelial cells can directly induce the death of renal interstitial fibroblasts by ATP activation of the P2X7 receptor.

Indexed as

Acute Kidney InjuryAdenosine TriphosphateAnimalsApoptosisCells, CulturedCoculture TechniquesFibroblastsKidneyKidney Tubules, ProximalNecrosisPurinergic P2X Receptor AntagonistsPyridinesRatsReceptors, Purinergic P2X7Signal TransductionTetrazoles3-(5-(2,3-dichlorophenyl)-1H-tetrazol-1-yl)methylpyridineAdenosine TriphosphatePurinergic P2X Receptor AntagonistsPyridinesReceptors, Purinergic P2X7TetrazolesTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID20861083
PMCPMC3023231
OpenAlexW2102155201

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.