Evidence map›Paper›PMID 37474759›Full record

ArticleNature chemical biology2024

Cardiac contraction and relaxation are regulated by distinct subcellular cAMP pools.

Ting-Yu Lin, Quynh N Mai, Hao Zhang, Emily Wilson, Huan-Chieh Chien, Sook Wah Yee, Kathleen M Giacomini, Jeffrey E Olgin, Roshanak Irannejad

Open access · hybridAbstract read
In one paragraph

Article in Nature chemical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  6. G-protein regulatory network governs receptor internalization dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  8. A BBB-permeable βScience advances · 2026
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  9. Review
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  11. β-Adrenergic Receptors: Not Always Outside-In.Physiology (Bethesda, Md.) · 2026
    Review
  12. Article
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  15. 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

9 authors at 1 institution in 1 country.

Ting-Yu Lin *Cardiovascular Research Institute, University of California, San Francisco, CA, USA.
Quynh N Mai *Cardiovascular Research Institute, University of California, San Francisco, CA, USA.
Hao ZhangCardiovascular Research Institute, University of California, San Francisco, CA, USA.
Emily WilsonCardiovascular Research Institute, University of California, San Francisco, CA, USA.
Huan-Chieh ChienDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, California, CA, USA.
Sook Wah YeeDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, California, CA, USA.
Kathleen M GiacominiDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, California, CA, USA.
Jeffrey E OlginCardiovascular Research Institute, University of California, San Francisco, CA, USA.
Roshanak IrannejadCardiovascular Research Institute, University of California, San Francisco, CA, USA. roshanak.irannejad@ucsf.edu.ORCID 0000-0001-8702-2285
University of California, San Francisco · US

Funding

MOLECULAR AND CELLULAR BASIS OF CARDIOVASCULAR DISEASET32HL007731 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian L Black · 1992 to 2026
$12.4M
INVESTIGATION OF A NEWLY DISCOVERED ORGANELLE-BASED SIGNALING PARADIGMR35GM133521 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Roshanak Irannejad · 2019 to 2026
$3.3M
Equipment Supplement NOT-GM-24-021R01GM139875 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GIACOMINI, KATHLEEN M · 2021 to 2024
$1.9M
NHLBI NIH HHS T32 HL007731NIGMS NIH HHS R01 GM139875NIGMS NIH HHS R35 GM133521
6 · The paper itself

Abstract

Cells interpret a variety of signals through G-protein-coupled receptors (GPCRs) and stimulate the generation of second messengers such as cyclic adenosine monophosphate (cAMP). A long-standing puzzle is deciphering how GPCRs elicit different physiological responses despite generating similar levels of cAMP. We previously showed that some GPCRs generate cAMP from both the plasma membrane and the Golgi apparatus. Here we demonstrate that cardiomyocytes distinguish between subcellular cAMP inputs to elicit different physiological outputs. We show that generating cAMP from the Golgi leads to the regulation of a specific protein kinase A (PKA) target that increases the rate of cardiomyocyte relaxation. In contrast, cAMP generation from the plasma membrane activates a different PKA target that increases contractile force. We further validated the physiological consequences of these observations in intact zebrafish and mice. Thus, we demonstrate that the same GPCR acting through the same second messenger regulates cardiac contraction and relaxation dependent on its subcellular location.

Indexed as

Signal TransductionZebrafishAnimalsCyclic AMPMiceMyocytes, CardiacReceptors, G-Protein-CoupledSecond Messenger SystemsCyclic AMPReceptors, G-Protein-Coupled

Identifiers

PMID37474759
PMCPMC10746541
OpenAlexW4384923389

What OpenQuestion holds

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LicenceCC BY
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.