Evidence map›Paper›PMID 24101515›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice.

William C Wetsel, Ramona M Rodriguiz, Johann Guillemot, Estelle Rousselet, Rachid Essalmani, Il Hwan Kim, Jesse C Bryant, Jadwiga Marcinkiewicz, Roxane Desjardins, Robert Day and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 84 citations in OpenAlex.

  1. Microglial dectin-1/Frontiers in immunology · 2026
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  8. Can PCSK7 be A New Pharmaceutical Target?Journal of atherosclerosis and thrombosis · 2022
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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

13 authors at 6 institutions in 5 countries.

William C WetselDepartments of Psychiatry and Behavioral Sciences, Cell Biology, and Neurobiology, Mouse Behavioral and Neuroendocrine Analysis Core Facility, Duke University Medical Center, Durham, NC 27710.
Ramona M Rodriguiz
Johann Guillemot
Estelle Rousselet
Rachid Essalmani
Il Hwan Kim
Jesse C Bryant
Jadwiga Marcinkiewicz
Roxane Desjardins
Robert Day
Daniel B Constam
Annik Prat
Nabil G Seidah
Université de Montréal · CADuke University · USUniversité de Sherbrooke · CADuke Medical Center · USDuke University Hospital · USÉcole Polytechnique Fédérale de Lausanne · CH

Funding

Screening CoreU19MH082441 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CARON, MARC G., ROTH, BRYAN L. · 2007 to 2016
$15.2M
CIHR CTP-82946CIHR MOP-36496NIMH NIH HHS MH082441NIMH NIH HHS U19 MH082441
6 · The paper itself

Abstract

PC7 belongs to the proprotein convertase family, whose members are implicated in the cleavage of secretory precursors. The in vivo function of PC7 is unknown. Herein, we find that the precursor proBDNF is processed into mature BDNF in COS-1 cells coexpressing proBDNF with either PC7 or Furin. Conversely, the processing of proBDNF into BDNF is markedly reduced in the absence of either Furin or PC7 in mouse primary hepatocytes. In vivo we observe that BDNF and PC7 mRNAs are colocalized in mouse hippocampus and amygdala and that mature BDNF protein levels are reduced in these brain areas in PC7 KO mice but not in the hippocampus of PC1/3 KO mice. Various behavioral tests reveal that in PC7 KO mice spatial memory is intact and plasticity of responding is mildly abnormal. Episodic and emotional memories are severely impaired, but both are rescued with the tyrosine receptor kinase B agonist 7,8-dihydroxyflavone. Altogether, these results support an in vivo role for PC7 in the regulation of certain types of cognitive performance, in part via proBDNF processing. Because polymorphic variants of human PC7 are being characterized, it will be important in future studies to determine their effects on additional physiological and behavioral processes.

Indexed as

AmygdalaAnimalsBlotting, WesternBrain-Derived Neurotrophic FactorCells, CulturedChlorocebus aethiopsCOS CellsFemaleFlavanonesGene ExpressionHEK293 CellsHepatocytesHippocampusHumansIn Situ HybridizationMale7,8-dihydroxyflavanoneBrain-Derived Neurotrophic FactorFlavanonesPcsk7 protein, mouseProtein PrecursorsRNA, MessengerSubtilisinsBDNF processingbrain phenotypesfear conditioninggene knockoutPC7 substrates

Identifiers

PMID24101515
PMCPMC3808632
OpenAlexW2130834237

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.