Evidence map›Paper›PMID 29231251›Full record

ArticleJournal of cellular biochemistry2018

Mechanoactivation of the angiotensin II type 1 receptor induces β-arrestin-biased signaling through Gα

Jialu Wang, Kenji Hanada, Clarice Gareri, Howard A Rockman

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. The role of mechanosignaling in the control of myocardial mass.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Insights Into the Role of Angiotensin-II ATHypertension (Dallas, Tex. : 1979) · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Mechanosignals in abdominal aortic aneurysms.Frontiers in cardiovascular medicine · 2022
    Review
  18. Central regulation of body fluid homeostasis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Jialu WangDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina.
Kenji HanadaDepartment of Medicine, Duke University Medical Center, Durham, North Carolina.
Clarice GareriDepartment of Medicine, Duke University Medical Center, Durham, North Carolina.
Howard A RockmanDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina.ORCID 0000-0003-2921-1584
Duke Medical Center · USDuke University · US

Funding

Regulation of Beta-Adrenergic Receptor Signaling by S-NitrosylationP01HL075443 · NHLBI · DUKE UNIVERSITY · PI STAMLER, JONATHAN S. · 2004 to 2019
$26.1M
MECHANISMS OF MALADAPTATION IN HEART FAILURER01HL056687 · NHLBI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI Howard A Rockman · 1996 to 2026
$12.3M
NHLBI NIH HHS P01 HL075443NHLBI NIH HHS R01 HL056687
6 · The paper itself

Abstract

Ligand activation of the angiotensin II type 1 receptor (AT1R), a member of the G protein-coupled receptor (GPCR) family, stimulates intracellular signaling to mediate a variety of physiological responses. The AT1R is also known to be a mechanical sensor. When activated by mechanical stretch, the AT1R can signal via the multifunctional adaptor protein β-arrestin, rather than through classical heterotrimeric G protein pathways. To date, the AT1R conformation induced by membrane stretch in the absence of ligand was thought to be the same as that induced by β-arrestin-biased agonists, which selectively engage β-arrestin thereby preventing G protein coupling. Here, we show that in contrast to the β-arrestin-biased agonists TRV120023 and TRV120026, membrane stretch uniquely promotes the coupling of the inhibitory G protein (Gα

Indexed as

beta-ArrestinsGTP-Binding Protein alpha Subunits, Gi-GoHEK293 CellsHumansImmunoprecipitationMicroscopy, ConfocalOligopeptidesReceptor, Angiotensin, Type 1Signal Transductionbeta-ArrestinsGTP-Binding Protein alpha Subunits, Gi-GoOligopeptidesReceptor, Angiotensin, Type 1sarcosine-arginyl-valyl-tyrosyl-lysyl-histidyl-prolyl-alanineangiotensin IIG proteinmechanotransductionβ-arrestin

Identifiers

PMID29231251
PMCPMC5826900
OpenAlexW2773978638

What OpenQuestion holds

Textmetadata
LicenceTDM
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.