Evidence map›Paper›PMID 31042061›Full record

ArticleAmerican journal of physiology. Renal physiology2019

Characterizing novel olfactory receptors expressed in the murine renal cortex.

Victoria L Halperin Kuhns, Jason Sanchez, Dylan C Sarver, Zoya Khalil, Premraj Rajkumar, Kieren A Marr, Jennifer L Pluznick

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  17. Landscape of GPCR expression along the mouse nephron.American journal of physiology. Renal physiology · 2021
    Article
  18. Kidney physiology: our future is now.American journal of physiology. Renal physiology · 2021
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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

7 authors at 2 institutions in 1 country.

Victoria L Halperin KuhnsDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Jason SanchezDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Dylan C SarverDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Zoya KhalilDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Premraj RajkumarDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Kieren A MarrTransplant and Oncology Infectious Diseases, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Jennifer L PluznickDepartment of Physiology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

Uncovering the Functional Role of Olfr78 in Blood Pressure RegulationR01DK107726 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PLUZNICK, JENNIFER L · 2016 to 2020
$1.8M
Renal Olfactory Receptor 90: ligands, localization and functionF31DK104454 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI HALPERIN KUHNS, VICTORIA · 2015 to 2017
$129k
NIDDK NIH HHS F31 DK104454NIDDK NIH HHS R01 DK107726
6 · The paper itself

Abstract

The kidney uses specialized G protein-coupled receptors, including olfactory receptors (ORs), to act as sensors of molecules and metabolites. In the present study, we cloned and studied seven renal ORs, which we previously found to be expressed in the murine renal cortex. As most ORs are orphan receptors, our goal was to identify ligands for these ORs in the hope that this will guide future research into their functional roles. We identified novel ligands for two ORs: Olfr558 and Olfr90. For Olfr558, we confirmed activation by previously reported ligands and identified 16 additional carboxylic acids that activated this OR. The strongest activation of Olfr558 was produced by butyric, cyclobutanecarboxylic, isovaleric, 2-methylvaleric, 3-methylvaleric, 4-methylvaleric, and valeric acids. The primary in vivo source of both butyric and isovaleric acids is gut microbial metabolism. We also identified 14 novel ligands that activated Olfr90, the strongest of which were 2-methyl-4-propyl-1,3-oxathiane, 1-octen-3-ol, 2-octanol, and 3-octanol. Interestingly, 8 of these 14 ligands are of fungal origin. We also investigated the tissue distribution of these receptors and found that they are each found in a subset of "nonsensory" tissues. Finally, we examined the putative human orthologs of Olfr558 and Olfr90 and found that the human ortholog of Olfr558 (OR51E1) has a similar ligand profile, indicating that the role of this OR is likely evolutionarily conserved. In summary, we examined seven novel renal ORs and identified new ligands for Olfr558 and Olfr90, which imply that both of these receptors serve to detect metabolites produced by microorganisms.

Indexed as

AnimalsCarboxylic AcidsGastrointestinal MicrobiomeHumansKidney CortexLigandsMice, Inbred C57BLProtein TransportReceptors, G-Protein-CoupledReceptors, OdorantSignal TransductionTissue DistributionCarboxylic AcidsLigandsOlfr558 protein, mouseOlfr90 protein, mouseReceptors, G-Protein-CoupledReceptors, OdorantG protein-coupled receptorsmicrobiotaOlfr558Olfr90OR51E1

Identifiers

PMID31042061
PMCPMC6692720
OpenAlexW2942828241

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.