Evidence map›Paper›PMID 29196502›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2018

Identifying the localization and exploring a functional role for Gprc5c in the kidney.

Premraj Rajkumar, Boyoung Cha, Jianyi Yin, Lois J Arend, Teodor G Păunescu, Yoshio Hirabayashi, Mark Donowitz, Jennifer L Pluznick

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. GPR39 activation inhibits AQP2 trafficking and alters cytoskeletal organization.American journal of physiology. Cell physiology · 2026
    Article
  3. Renal Ghrelin-Family GPR39 Receptor and Urinary Concentrating Ability.Journal of the American Society of Nephrology : JASN · 2025
    Article
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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

8 authors at 4 institutions in 2 countries.

Premraj RajkumarDepartment of Physiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Boyoung ChaDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jianyi YinDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Lois J ArendDepartment of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Teodor G PăunescuDivision of Nephrology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Yoshio HirabayashiLaboratory for Molecular Membrane Neuroscience, RIKEN Brain Science Institute, Saitama, Japan.
Mark DonowitzDepartment of Physiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jennifer L PluznickDepartment of Physiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USHarvard University · USJohns Hopkins Medicine · USRIKEN Center for Brain Science · JP

Funding

Translational Research Enhancement CoreP30DK089502 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ZACHOS, NICHOLAS CONSTANTINE · 2011 to 2020
$12.0M
Translational Approaches to Develop Drug Therapy for DiarrheaR24DK099803 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI DONOWITZ, MARK · 2014 to 2019
$8.9M
Olfactory Proteins in the Kidney and Regulation of Glomerular Filtration RateR00DK081610 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PLUZNICK, JENNIFER L · 2010 to 2012
$760k
NIDDK NIH HHS P30 DK089502NIDDK NIH HHS R00 DK081610NIDDK NIH HHS R24 DK099803
6 · The paper itself

Abstract

The investigation of orphan GPCRs (GPRs) has the potential to uncover novel insights into whole animal physiology. In this study, our goal was to determine the renal localization of Gprc5c, a receptor that we previously reported to be highly expressed in murine whole kidney, and to examine physiologic parameters in Gprc5c knockout (KO) mice to gain insight into function. Gprc5c localized to the apical membrane of renal proximal tubules (PTs) in mice, rats, and humans. With the comparison of Gprc5c wild-type (WT) and KO mice, we found that Gprc5c KO mice have altered acid-base homeostasis. Specifically, Gprc5c KO mice have lower blood pH and higher urine pH compared with WT mice, with a reduced level of titratable acids in their urine. In an in vitro GPCR internalization assay, we observed that Gprc5c internalization (an index of activation) was triggered by alkaline extracellular pH. Furthermore, with the use of an in vitro BCECF assay, we observed that Gprc5c increases Na

Indexed as

AcidsAlkaliesAnimalsHEK293 CellsHumansKidney Tubules, ProximalMiceMice, Inbred C57BLProtein TransportReceptors, G-Protein-CoupledSodium-Hydrogen Exchanger 3Water-Electrolyte BalanceAcidsAlkaliesGPRC5C protein, mouseReceptors, G-Protein-CoupledSlc9a3 protein, mouseSodium-Hydrogen Exchanger 3NHE3pH regulationproximal tubule

Identifiers

PMID29196502
PMCPMC5893170
OpenAlexW2775648663

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.