Evidence map›Paper›PMID 30628061›Full record

ArticleThe Journal of comparative neurology2019

Selective Cre-mediated gene deletion identifies connexin 43 as the main connexin channel supporting olfactory ensheathing cell networks.

Ana Paula Piantanida, Luis Ernesto Acosta, Lucila Brocardo, Claudia Capurro, Charles A Greer, Lorena Rela

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. AMPA Receptor-Mediated CaFrontiers in cellular neuroscience · 2019
    Article
  5. 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

6 authors at 2 institutions in 2 countries.

Ana Paula PiantanidaCONICET, Instituto de Fisiología y Biofísica Bernardo Houssay (IFIBIO), Neurociencia de Sistemas, Buenos Aires, Argentina.
Luis Ernesto AcostaCONICET, Instituto de Fisiología y Biofísica Bernardo Houssay (IFIBIO), Neurociencia de Sistemas, Buenos Aires, Argentina.
Lucila BrocardoCONICET, Instituto de Fisiología y Biofísica Bernardo Houssay (IFIBIO), Neurociencia de Sistemas, Buenos Aires, Argentina.
Claudia CapurroCONICET, Instituto de Fisiología y Biofísica Bernardo Houssay (IFIBIO), Neurociencia de Sistemas, Buenos Aires, Argentina.
Charles A GreerDepartment of Neuroscience, Yale University School of Medicine, New Haven, Connecticut.
Lorena RelaCONICET, Instituto de Fisiología y Biofísica Bernardo Houssay (IFIBIO), Neurociencia de Sistemas, Buenos Aires, Argentina.ORCID 0000-0001-5109-7170
Consejo Nacional de Investigaciones Científicas y Técnicas · ARYale University · US

Funding

Piriform cortex: sequential developmental eventsR01DC013791 · NIDCD · YALE UNIVERSITY · PI Charles A Greer · 2015 to 2026
$3.9M
The Glomerular ConnectomeR21DC015438 · NIDCD · YALE UNIVERSITY · PI GREER, CHARLES A · 2016 to 2017
$461k
DENGUE FEVER AND OTHER INFECTIONS IN THE AIDS ERAF06TW002009 · FIC · UNIVERSITY OF WASHINGTON · PI FOY, HJORDIS M · 1994 to 1994
–
RETINOIDS AND CANCERF15TW000332 · FIC · U.S. FOGARTY INTERNATIONAL CENTER · PI NORUM, KAARE REIDAR · 1989 to 1994
–
NIDCD NIH HHS R01 DC013791NIDCD NIH HHS R21 DC015438
6 · The paper itself

Abstract

Many functions of glial cells depend on the formation of selective glial networks mediated by gap junctions formed by members of the connexin family. Olfactory ensheathing cells (OECs) are specialized glia associated with olfactory sensory neuron axons. Like other glia, they form selective networks, however, the connexins that support OEC connectivity in vivo have not been identified. We used an in vivo mouse model to selectively delete candidate connexin genes with temporal control from OECs and address the physiological consequences. Using this model, we effectively abolished the expression of connexin 43 (Cx43) in OECs in both juvenile and adult mice. Cx43-deleted OECs exhibited features consistent with the loss of gap junctions including reduced membrane conductance, largely reduced sensitivity to the gap junction blocker meclofenamic acid and loss of dye coupling. This indicates that Cx43, a typically astrocytic connexin, is the main connexin forming functional channels in OECs. Despite these changes in functional properties, the deletion of Cx43 deletion did not alter the density of OECs. The strategy used here may prove useful to delete other candidate genes to better understand the functional roles of OECs in vivo.

Indexed as

Gene Knockout TechniquesAgingAnimalsConnexin 43Crosses, GeneticFemaleGap JunctionsGenes, ReporterGenes, SyntheticIntegrasesMaleMeclofenamic AcidMiceMice, KnockoutMyelin Proteolipid ProteinNeurogliaConnexin 43Cre recombinaseGJA1 protein, mouseIntegrasesMeclofenamic AcidMyelin Proteolipid ProteinPlp1 protein, mouseTamoxifenconnexin 43Cre recombinasegap junctionsolfactory ensheathing cellsproteolipid proteinRRID:AB_10000325RRID:AB_141596RRID:AB_2110187RRID:AB_2533973RRID:AB_2533979RRID:AB_2576217RRID:AB_561049RRID:IMSR_JAX:005975RRID:IMSR_JAX:007914RRID:IMSR_JAX:008039

Identifiers

PMID30628061
PMCPMC6401266
OpenAlexW2911223764

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.