Evidence map›Paper›PMID 34913963›Full record

ArticleThe Journal of cell biology2022

Engineered synaptic tools reveal localized cAMP signaling in synapse assembly.

Richard Sando, Milan Lyndie Ho, Xinran Liu, Thomas C Südhof

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Synaptic Gα12/13 signaling establishes hippocampal PV inhibitory circuits.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Article
  10. Essential Role of Latrophilin-1 Adhesion GPCR Nanoclusters in Inhibitory Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Cell Adhesion Molecule Signaling at the Synapse: Beyond the Scaffold.Cold Spring Harbor perspectives in biology · 2024
    Review
  12. Review
  13. 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

4 authors at 2 institutions in 1 country.

Richard SandoDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0002-1797-2346
Milan Lyndie HoDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA.
Xinran LiuDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT.ORCID 0000-0002-1586-2151
Thomas C SüdhofDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0003-3361-9275
Howard Hughes Medical Institute · USYale University · US

Funding

Latrophilin Function in Synapse FormationR01MH126929 · NIMH · STANFORD UNIVERSITY · PI Thomas C. Sudhof · 2021 to 2026
$4.3M
Investigating how signaling via adhesion GPCR Latrophilins regulates synapse formation and specificity in the hippocampusK99MH117235 · NIMH · STANFORD UNIVERSITY · PI SANDO, RICHARD CHESLOCK · 2018 to 2019
$222k
NIH HHS K99-MH117235NIMH NIH HHS K99 MH117235NIMH NIH HHS R01 MH126929
6 · The paper itself

Abstract

The physiological mechanisms driving synapse formation are elusive. Although numerous signals are known to regulate synapses, it remains unclear which signaling mechanisms organize initial synapse assembly. Here, we describe new tools, referred to as "SynTAMs" for synaptic targeting molecules, that enable localized perturbations of cAMP signaling in developing postsynaptic specializations. We show that locally restricted suppression of postsynaptic cAMP levels or of cAMP-dependent protein-kinase activity severely impairs excitatory synapse formation without affecting neuronal maturation, dendritic arborization, or inhibitory synapse formation. In vivo, suppression of postsynaptic cAMP signaling in CA1 neurons prevented formation of both Schaffer-collateral and entorhinal-CA1/temporoammonic-path synapses, suggesting a general principle. Retrograde trans-synaptic rabies virus tracing revealed that postsynaptic cAMP signaling is required for continuous replacement of synapses throughout life. Given that postsynaptic latrophilin adhesion-GPCRs drive synapse formation and produce cAMP, we suggest that spatially restricted postsynaptic cAMP signals organize assembly of postsynaptic specializations during synapse formation.

Indexed as

Genetic EngineeringSignal TransductionAnimalsCyclic AMPHippocampusMiceMice, Inbred C57BLSingle-Domain AntibodiesSynapsesCyclic AMPSingle-Domain Antibodies

Identifiers

PMID34913963
PMCPMC8685283
OpenAlexW4200272347

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.