Evidence map›Paper›PMID 23977027›Full record

ArticlePloS one2013

Disruption in connexin-based communication is associated with intracellular Ca²⁺ signal alterations in astrocytes from Niemann-Pick type C mice.

Pablo J Sáez, Juan A Orellana, Natalia Vega-Riveros, Vania A Figueroa, Diego E Hernández, Juan F Castro, Andrés D Klein, Jean X Jiang, Silvana Zanlungo, Juan C Sáez

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

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  19. Lysosomal Storage Diseases-Regulating Neurodegeneration.Journal of experimental neuroscience · 2015
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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

10 authors at 2 institutions in 2 countries.

Pablo J SáezDepartamento de Fisiología, Pontificia Universidad Católica de Chile, Santiago, Chile.
Juan A Orellana
Natalia Vega-Riveros
Vania A Figueroa
Diego E Hernández
Juan F Castro
Andrés D Klein
Jean X Jiang
Silvana Zanlungo
Juan C Sáez
Pontificia Universidad Católica de Chile · CLThe University of Texas Health Science Center at San Antonio · US

Funding

Intercellular Communication in the Eye LensR01EY012085 · NEI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jean X Jiang · 2003 to 2026
$8.4M
INTERCELLULAR COMMUNICATION IN THE EYE LENSR29EY012085 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI JIANG, JEAN X · 1998 to 2002
$312k
NEI NIH HHS R01 EY012085NEI NIH HHS R29 EY012085
6 · The paper itself

Abstract

Reduced astrocytic gap junctional communication and enhanced hemichannel activity were recently shown to increase astroglial and neuronal vulnerability to neuroinflammation. Moreover, increasing evidence suggests that neuroinflammation plays a pivotal role in the development of Niemann-Pick type C (NPC) disease, an autosomal lethal neurodegenerative disorder that is mainly caused by mutations in the NPC1 gene. Therefore, we investigated whether the lack of NPC1 expression in murine astrocytes affects the functional state of gap junction channels and hemichannels. Cultured cortical astrocytes of NPC1 knock-out mice (Npc1⁻/⁻) showed reduced intercellular communication via gap junctions and increased hemichannel activity. Similarly, astrocytes of newborn Npc1⁻/⁻ hippocampal slices presented high hemichannel activity, which was completely abrogated by connexin 43 hemichannel blockers and was resistant to inhibitors of pannexin 1 hemichannels. Npc1⁻/⁻ astrocytes also showed more intracellular Ca²⁺ signal oscillations mediated by functional connexin 43 hemichannels and P2Y₁ receptors. Therefore, Npc1⁻/⁻ astrocytes present features of connexin based channels compatible with those of reactive astrocytes and hemichannels might be a novel therapeutic target to reduce neuroinflammation in NPC disease.

Indexed as

Adenosine DiphosphateAnimalsAnimals, NewbornAntibodiesAstrocytesCalciumCalcium SignalingCell CommunicationCells, CulturedConnexin 43ConnexinsDisease Models, AnimalGap JunctionsGene DeletionGene Expression RegulationHippocampusAdenosine DiphosphateAntibodiesCalciumConnexin 43ConnexinsIntracellular Signaling Peptides and ProteinsN(6)-methyl-2'-deoxyadenosine 3',5'-diphosphateNerve Tissue ProteinsNiemann-Pick C1 ProteinNpc1 protein, mousePanx1 protein, mouseProteinsReceptors, Purinergic P2Y1

Identifiers

PMID23977027
PMCPMC3744576
OpenAlexW1971705886

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.