Evidence map›Paper›PMID 24412205›Full record

ArticleCurrent biology : CB2014

Intercellular transfer of GPRC5B via exosomes drives HGF-mediated outward growth.

Sang-Ho Kwon, Kathleen D Liu, Keith E Mostov

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Location bias: A "Hidden Variable" in GPCR pharmacology.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Review
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  5. Article
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  7. Article
  8. Pharmacology of T2R Mediated Host-Microbe Interactions.Handbook of experimental pharmacology · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. COVID-19 diagnostic testing: Technology perspective.Clinical and translational medicine · 2020
    Article
  14. Exosomes in Sepsis.Frontiers in immunology · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Sang-Ho KwonDepartment of Anatomy, University of California, San Francisco, San Francisco, CA 94143, USA.
Kathleen D LiuDepartment of Medicine, Division of Nephrology, University of California, San Francisco, San Francisco, CA 94143, USA.
Keith E MostovDepartment of Anatomy, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Biochemistry and Biophysics, and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: keith.mostov@ucsf.edu.
University of California, San Francisco · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Sulfs and Injury Repair in Mucosal EpitheliaP01AI053194 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOSTOV, KEITH E · 2002 to 2012
$13.4M
TRAINING PROGRAM IN PEDIATRIC GASTROENTEROLOGY/NUTRITIONT32DK007762 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI James Bayrer · 1998 to 2026
$7.3M
Recovery from acute kidney injuryR01DK074398 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOSTOV, KEITH E · 2007 to 2015
$3.0M
Control of Epithelial PolarityR01DK091530 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOSTOV, KEITH E · 2011 to 2015
$1.7M
Transcriptional profiling of 2.5 dimensional MDCK tubulogenesisF32DK082115 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWON, KENNETH · 2009 to 2010
$109k
NIAID NIH HHS AI53194NIAID NIH HHS P01 AI053194NIDDK NIH HHS DK074398NIDDK NIH HHS DK082115NIDDK NIH HHS DK091530NIDDK NIH HHS F32 DK082115NIDDK NIH HHS P30 DK026743NIDDK NIH HHS R01 DK074398NIDDK NIH HHS R01 DK091530NIDDK NIH HHS T32 DK007762
6 · The paper itself

Abstract

How cells communicate during development and regeneration is a critical question. One mechanism of intercellular communication is via exosomes, extracellular vesicles that originate by the fusion of multivesicular endosomes with the plasma membrane [1-8]. To model exosome-based intercellular communication, we used Madin-Darby canine kidney (MDCK) cell cysts grown in 3D gels of extracellular matrix, which form tubules in response to hepatocyte growth factor (HGF). We report that GPRC5B, an orphan G protein coupled receptor, is in exosomes produced by HGF-treated cysts and released into the cyst lumen. Exosomal GPRC5B is taken up by nearby cells and together with HGF promotes extracellular signal-regulated kinase 1/2 (ERK1/2) activation and tubulogenesis, even under conditions where tubulogenesis would otherwise not occur. Recovery from injury, such as acute kidney injury (AKI), often recapitulates developmental processes. Here, we show that GPRC5B is elevated in urinary exosomes from patients with AKI. Our results elucidate how GPRC5B is carried by exosomes and augments HGF-induced morphogenesis. The unexpected role of exosomes in transporting GPRC5B between cells during morphogenesis and the ability of GPRC5B to predict the disease state of AKI elucidate a novel mechanism for intercellular communication during development and repair.

Indexed as

AnimalsCell EnlargementDogsExosomesHepatocyte Growth FactorIntracellular SpaceMadin Darby Canine Kidney CellsProtein TransportReceptors, G-Protein-CoupledHepatocyte Growth FactorReceptors, G-Protein-Coupled

Identifiers

PMID24412205
PMCPMC3938203
OpenAlexW2071651622

What OpenQuestion holds

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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.