Evidence map›Paper›PMID 42794472›Full record

ArticleInternational journal of molecular sciences2026

Spatio-Temporal Expression Patterns of Connexins 43 and 30 in Hippocampal Astrocytes During Postnatal Development.

Alejandro Uribe-Arias, Jérôme Ribot, Pascal Ezan, Philippe Mailly, Nathalie Rouach

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Alejandro Uribe-AriasCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, PSL-Neuro, 75005 Paris, France.ORCID 0000-0003-2082-9126
Jérôme RibotCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, PSL-Neuro, 75005 Paris, France.
Pascal EzanCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, PSL-Neuro, 75005 Paris, France.
Philippe MaillyCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, PSL-Neuro, 75005 Paris, France.
Nathalie RouachCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, PSL-Neuro, 75005 Paris, France.ORCID 0000-0002-5574-888X

Funding

Agence Nationale de la Recherche ANR-10-IDEX-0001Agence Nationale de la Recherche ANR-24-CHBS-0007Doctoral school parisFondation pour la Recherche Médicale
6 · The paper itself

Abstract

Astrocytes are extensively interconnected via gap junction channels formed primarily by connexin 43 (Cx43) and connexin 30 (Cx30), two proteins that play central roles in intercellular signaling and homeostatic regulation in the brain. Although the functional properties of these connexins have been widely investigated, their spatial organization within astrocytes and its evolution during postnatal development remain poorly characterized. Here, we combined confocal and stimulated emission depletion (STED) super-resolution microscopy to examine the expression, distribution and colocalization of Cx43 and Cx30 immunoreactive puncta in hippocampal astrocytes from postnatal day 15 to adulthood. Quantitative analyses revealed a progressive increase in the number of both Cx43 and Cx30 puncta during development, whereas puncta size remained largely unchanged. Although connexin puncta appeared more distally distributed in mature astrocytes, this shift was fully accounted for by the growth of astrocytes during development. In addition, colocalization between Cx43 and Cx30 increased during maturation, reaching a stable level after postnatal day 30. Finally, STED super-resolution imaging revealed a diversity of connexin arrangements, including isolated puncta as well as complex assemblies composed of multiple neighboring connexin clusters. Together, these findings provide a quantitative characterization of the developmental remodeling of astroglial connexins and identify structural features that may contribute to the maturation of astrocytic networks.

Indexed as

AstrocytesConnexin 30Connexin 43ConnexinsHippocampusAnimalsGap JunctionsGene Expression Regulation, DevelopmentalNeurodevelopmentRatsConnexin 30Connexin 43Connexinsastrocyteconnexindevelopmentsuper-resolution imaging

Identifiers

PMID42794472
PMCPMC13607773

What OpenQuestion holds

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Registered trials

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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.