Evidence map›Paper›PMID 36480070›Full record

ArticlePflugers Archiv : European journal of physiology2023

Localization of natriuretic peptide receptors A, B, and C in healthy and diseased mouse kidneys.

Elena-Sofia Heinl, Katharina Anna-Elisabeth Broeker, Claudia Lehrmann, Rosmarie Heydn, Katharina Krieger, Katharina Ortmaier, Philipp Tauber, Frank Schweda

Open access · hybridAbstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Renal Tubule Cell-SpecificHypertension (Dallas, Tex. : 1979) · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Deletion of ATAmerican journal of physiology. Renal physiology · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. 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

8 authors at 1 institution in 1 country.

Elena-Sofia HeinlInstitute for Physiology, University Regensburg, Regensburg, Germany. Elena.Heinl@ur.de.
Katharina Anna-Elisabeth BroekerInstitute for Physiology, University Regensburg, Regensburg, Germany.
Claudia LehrmannInstitute for Physiology, University Regensburg, Regensburg, Germany.
Rosmarie HeydnInstitute for Physiology, University Regensburg, Regensburg, Germany.
Katharina KriegerInstitute for Physiology, University Regensburg, Regensburg, Germany.
Katharina OrtmaierInstitute for Physiology, University Regensburg, Regensburg, Germany.
Philipp TauberInstitute for Physiology, University Regensburg, Regensburg, Germany.
Frank SchwedaInstitute for Physiology, University Regensburg, Regensburg, Germany. frank.schweda@ukr.de.
University of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The natriuretic peptides (NPs) ANP (atrial natriuretic peptide) and BNP (B-type natriuretic peptide) mediate their widespread effects by activating the natriuretic peptide receptor-A (NPR-A), while C-type natriuretic peptide (CNP) acts via natriuretic peptide receptor-B (NPR-B). NPs are removed from the circulation by internalization via the natriuretic peptide clearance receptor natriuretic peptide receptor-C (NPR-C). In addition to their well-known functions, for instance on blood pressure, all three NPs confer significant cardioprotection and renoprotection. Since neither the NP-mediated renal functions nor the renal target cells of renoprotection are completely understood, we performed systematic localization studies of NP receptors using in situ hybridization (RNAscope) in mouse kidneys. NPR-A mRNA is highly expressed in glomeruli (mainly podocytes), renal arterioles, endothelial cells of peritubular capillaries, and PDGFR-receptor β positive (PDGFR-β) interstitial cells. No NPR-A mRNA was detected by RNAscope in the tubular system. In contrast, NPR-B expression is highest in proximal tubules. NPR-C is located in glomeruli (mainly podocytes), in endothelial cells and PDGFR-β positive cells. To test for a possible regulation of NPRs in kidney diseases, their distribution was studied in adenine nephropathy. Signal intensity of NPR-A and NPR-B mRNA was reduced while their spatial distribution was unaltered compared with healthy kidneys. In contrast, NPR-C mRNA signal was markedly enhanced in cell clusters of myofibroblasts in fibrotic areas of adenine kidneys. In conclusion, the primary renal targets of ANP and BNP are glomerular, vascular, and interstitial cells but not the tubular compartment, while the CNP receptor NPR-B is highly expressed in proximal tubules. Further studies are needed to clarify the function and interplay of this specific receptor expression pattern.

Indexed as

Endothelial CellsNatriuretic PeptidesAnimalsAtrial Natriuretic FactorKidneyMiceNatriuretic Peptide, BrainReceptors, PeptideRNA, MessengerVasodilator AgentsAtrial Natriuretic FactorNatriuretic Peptide, BrainNatriuretic PeptidesReceptors, PeptideRNA, MessengerVasodilator AgentsANPBNPCNPNatriuretic peptideNatriuretic peptide receptorNephroprotection

Identifiers

PMID36480070
PMCPMC9908653
OpenAlexW4310948908

What OpenQuestion holds

Textmetadata
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.