Evidence map›Paper›PMID 42640497›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2026

Altered Pannexin2 Expression in Retinal Degeneration: Insights from the P23H Mouse Model of Retinis Pigmentosa.

Mateo Ruiz-Conca, Enola Missonnier, Estela Tébar-Garcerán, Marta Estalrich-Soliveres, Oksana Kutsyr, Eva Tudurí, Lorena Vidal-Gil, Natalia Martínez-Gil, Laura Fernández-Sánchez, Victoria Maneu

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Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 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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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

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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

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5 · Who and what money

Authors and funding

10 authors.

Mateo Ruiz-ConcaDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0001-7092-7993
Enola MissonnierDepartment of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0009-0001-6795-9430
Estela Tébar-GarceránDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0009-0004-3361-3265
Marta Estalrich-SoliveresDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0009-0006-6537-2587
Oksana KutsyrCellSight Ocular Stem Cell and Regeneration Program, Department of Ophthalmology, Sue Anschutz-Rodgers Eye Center, School of Medicine, University of Colorado, Aurora, CO, USA.ORCID http://orcid.org/0000-0002-1173-6916
Eva TuduríDepartment of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0001-8999-2605
Lorena Vidal-GilDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0002-4709-7175
Natalia Martínez-GilDepartment of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0001-8882-5602
Laura Fernández-SánchezDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain.ORCID http://orcid.org/0000-0002-3629-0156
Victoria ManeuDepartment of Optics, Pharmacology and Anatomy, University of Alicante, Alicante, Spain. vmaneu@ua.es.ORCID http://orcid.org/0000-0002-5265-1361

Funding

Horizon 2020 HORIZON MSCA 2021-DN-01-01_RETORNA 101073316Universidad de Alicante REDSALUD25-03Universidad de Alicante UAFPU23-04
6 · The paper itself

Abstract

Pannexins are large channels involved in purinergic signaling within the nervous system. However, their role in human disease and their therapeutic potential remain poorly understood, particularly for Pannexin-2 (Panx2). The aim of this study was to investigate whether Panx2 is associated with retinal neurodegenerative diseases. Using immunohistochemistry and flow cytometry, we analyzed Panx2 expression in the retina of the P23H mouse model of retinitis pigmentosa and in control C57BL/6J mice. We observed that healthy retinas contained a small population of Panx2-positive cells. In contrast, the Panx2 positive population was increased in the retinas of P23H retina, particulary at advanced stages of the disease. Panx2 was found to co-occur with the purinergic receptors P2X7R but not with P2X4R. This result was further supported by the reanalysis of RNA-seq data from GEO functional genomics data repository, which indicated an increased Panx2 mRNA expression in P23H mice at intermediate stages of the disease, compared with control animals. Together, these findings suggest that Panx2 expression is altered during retinal degeneration in the P23H model and may be associated with purinergic signaling pathways involved in disease progression. These results raise interesting questions for further investigation regarding the role of Panx2 in retinal degeneration.

Indexed as

ConnexinsNerve Tissue ProteinsRetinal DegenerationRetinitis PigmentosaAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLReceptors, Purinergic P2X7ConnexinsNerve Tissue ProteinsPanx2 protein, mouseReceptors, Purinergic P2X7DegenerationP2X4RP2X7RPannexinPanx2Retina

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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.