Evidence map›Paper›PMID 14724236›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

PSD93 regulates synaptic stability at neuronal cholinergic synapses.

Michael J Parker, Shengli Zhao, David S Bredt, Joshua R Sanes, Guoping Feng

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Article
  6. Review
  7. Article
  8. ACh Transfers: Homeostatic Plasticity of Cholinergic Synapses.Cellular and molecular neurobiology · 2023
    Review
  9. Article
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  11. Article
  12. Article
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  19. Review
  20. Article

1 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Michael J ParkerDepartment of Neurobiology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Shengli Zhao
David S Bredt
Joshua R Sanes
Guoping Feng
Duke University · USDuke University Hospital · USUniversity of California, San Francisco · USWashington University in St. Louis · US

Funding

SYNAPTIC REGULATION OF NITRIC OXIDER01NS036017 · NINDS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BREDT, DAVID S · 1997 to 2005
$1.8M
Formation of Neuronal Cholinergic SynapsesR01NS042609 · NINDS · DUKE UNIVERSITY · PI FENG, GUOPING · 2002 to 2006
$1.7M
NINDS NIH HHS NS036017NINDS NIH HHS R01 NS036017NINDS NIH HHS R01 NS042609NINDS NIH HHS R01 NS42609
6 · The paper itself

Abstract

Neuronal cholinergic synapses play important roles in both the PNS and CNS. However, the mechanisms that regulate the formation, maturation, and stability of neuronal cholinergic synapses are poorly understood. In this study, we use the readily accessible mouse superior cervical ganglion (SCG) and submandibular ganglion (SMG) to examine the assembly of the postsynaptic complex of neuronal cholinergic synapses. We find that novel splicing forms of PSD93 (postsynaptic density 93) are expressed in SCG. By immunostaining, we show that PSD93 proteins precisely colocalize with neuronal nicotinic acetylcholine receptors (nAChRs) at synapses of the SCG and SMG. Subcellular fractionation demonstrates that PSD93 is enriched in the PSD fraction of SCG, and coimmunoprecipitation shows that PSD93 and neuronal nAChRs form a complex in vivo. Furthermore, two additional components of the well characterized glutamatergic postsynaptic complex, GKAP/SAPAP (guanylate kinase domain-associated protein/synapse-associated protein-associated protein) and Shank/ProSAP family proteins, are also present at neuronal cholinergic synapses. To assess the function of this protein complex at neuronal cholinergic synapses in vivo, we examined ganglia in mice that lack PSD93. We find that neuronal cholinergic synapses form properly in PSD93 null mice. After denervation, however, synaptic clusters of nAChRs disassemble much faster in mice lacking PSD93 than those in wild-type mice. These results demonstrate that PSD93 is a key component of the postsynaptic scaffold at neuronal cholinergic synapses and plays an important role in synaptic stability. In addition, these results suggest that the mechanism of postsynaptic scaffolding is conserved between neuronal cholinergic and glutamatergic synapses.

Indexed as

Alternative SplicingAmino Acid SequenceAnimalsMacromolecular SubstancesMiceMice, KnockoutMolecular Sequence DataNerve Tissue ProteinsNeuronsRatsReceptors, CholinergicSequence AlignmentSynapsesMacromolecular SubstancesNerve Tissue Proteinspostsynaptic density proteinsReceptors, Cholinergic

Identifiers

PMID14724236
PMCPMC6729987
OpenAlexW1995184912

What OpenQuestion holds

Textmetadata
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.