Evidence map›Paper›PMID 18601530›Full record

ArticleJournal of biomedical optics

Rab4 and Rab11 coordinately regulate the recycling of angiotensin II type I receptor as demonstrated by fluorescence resonance energy transfer microscopy.

Hewang Li, Hui-Fang Li, Robin A Felder, Ammasi Periasamy, Pedro A Jose

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biomedical optics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  6. The Endolysosomal System: The Acid Test for SARS-CoV-2.International journal of molecular sciences · 2022
    Review
  7. Dopamine DHypertension research : official journal of the Japanese Society of Hypertension · 2021
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  15. Article
  16. Postendocytic Sorting of Adrenergic and Opioid Receptors: New Mechanisms and Functions.Progress in molecular biology and translational science · 2015
    Review
  17. Article
  18. Article
  19. Förster resonance energy transfer microscopy and spectroscopy for localizing protein-protein interactions in living cells.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2013
    Review
  20. Novel role of sorting nexin 5 in renal D(1) dopamine receptor trafficking and function: implications for hypertension.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    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

5 authors at 3 institutions in 1 country.

Hewang LiGeorgetown University Medical Center, Department of Pediatrics, Washington, DC 20057, USA.
Hui-Fang Li
Robin A Felder
Ammasi Periasamy
Pedro A Jose
Georgetown University Medical Center · USUniversity of Virginia · USGeorgetown University · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Spatiotemporal transregulation of D1-like angiotensin receptors in genetically...P01HL074940 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CAREY, ROBERT MUNSON · 2004 to 2020
$31.8M
Renal Vascular Oxidative Stress in HypertensionP01HL068686 · NHLBI · GEORGETOWN UNIVERSITY · PI JOSE, PEDRO A., SANDBERG, KATHRYN L · 2001 to 2017
$28.8M
RENAL DOPAMINE-1 RECEPTOR DEFECT IN HYPERTENSIONR01DK039308 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI JOSE, PEDRO A. · 1987 to 2020
$7.4M
STRUCTURAL AND FUNCTIONAL DEVELOPMENT OF THE KIDNEYP50DK052612 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GOMEZ, ROBERTO ARIEL · 1997 to 2006
$6.8M
Renal Dopamine Receptor & RegulationR37HL023081 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI JOSE, PEDRO A. · 2007 to 2016
$4.3M
RENAL DOPAMINE RECEPTOR REGULATION AND FUNCTIONR01HL023081 · NHLBI · GEORGETOWN UNIVERSITY · PI JOSE, PEDRO A. · 1985 to 2006
$2.4M
FLUORESCENCE IMAGING OF LIVE CELLS AND TISSUESS10RR015768 · NCRR · GEORGETOWN UNIVERSITY · PI MUELLER, SUSETTE C · 2001 to 2001
$221k
NCI NIH HHS 2P30-CA-51008NCI NIH HHS P30 CA051008NCRR NIH HHS 1S10RR15768-01NHLBI NIH HHS HL074940-01NHLBI NIH HHS HL23081NHLBI NIH HHS HL68686NHLBI NIH HHS P01 HL068686NHLBI NIH HHS P01 HL074940NHLBI NIH HHS R01 HL023081NHLBI NIH HHS R37 HL023081NIDDK NIH HHS DK39308NIDDK NIH HHS DK52612NIDDK NIH HHS P50 DK052612NIDDK NIH HHS R01 DK039308
6 · The paper itself

Abstract

The recycling of G-protein-coupled receptors (GPCR) to the cell surface after internalization plays an important role in the regulation of overall GPCR activity. The angiotensin II type I receptor (AT1R) belongs to class B GPCRs that recycle slowly back to the cell surface. Previous studies have proposed that Rab11 controls the recycling of AT1R; however, recent reports show that Rab4, a rapid recycling regulator, co-localizes also with internalized AT1R. Different from the subcellular co-localization provided by fluorescence microscopy, fluorescence resonance energy transfer (FRET) microscopy provided the spatial relationship of AT1R with Rab4 and Rab11 in the nanometer-range proximity during the entire course of AT1R recycling. During the early recycling stage, internalized AT1Rs were mainly associated with Rab4 in the cytoplasm. During the mid-recycling stage, AT1Rs were associated with both Rab4 and Rab11 in the perinuclear compartments. However, during the late-recycling stage, AT1Rs were mainly associated with Rab11, both in the perinuclear compartments and the plasma membrane. Co-immunoprecipitation data confirmed these dynamic associations, which were disrupted by silencing of either the Rab4 or Rab11 gene. Based on these observations, we propose a Rab4 and Rab11 coordinated model for AT1R recycling.

Indexed as

Cell LineFluorescence Resonance Energy TransferGene Expression RegulationGTP-Binding ProteinsHumansKidneyMicroscopy, Fluorescencerab4 GTP-Binding ProteinsReceptor, Angiotensin, Type 1GTP-Binding Proteinsrab4 GTP-Binding ProteinsReceptor, Angiotensin, Type 1Wdr44 protein, rat

Identifiers

PMID18601530
PMCPMC3731076
OpenAlexW2095095044

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.