Decline in Constitutive Proliferative Activity in the Zebrafish Retina with Ageing

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Bioloxía Funcionales_ES
dc.contributor.authorHernández Núñez, Ismael
dc.contributor.authorQuelle Regaldie, Ana
dc.contributor.authorSánchez Piñón, Laura
dc.contributor.authorAdrio Fondevila, Fátima
dc.contributor.authorCandal Suárez, Eva María
dc.contributor.authorBarreiro Iglesias, Antón
dc.date.accessioned2024-01-24T14:12:01Z
dc.date.available2024-01-24T14:12:01Z
dc.date.issued2021
dc.descriptionSupplementary Materials The following are available online at https://www.mdpi.com/article/10.3390/ijms222111715/s1. Table S1: Studies demonstrating the presence of proliferating cells in the juvenile/adult retina of different teleost species. File S1: Mean ± S.E.M. data and data on statistical multiple comparisons related to graphs shown in Figure 2; File S2: Mean ± S.E.M. data and data on statistical multiple comparisons related to graphs shown in Figure 3.es_ES
dc.description.abstractIt is largely assumed that the teleost retina shows continuous and active proliferative and neurogenic activity throughout life. However, when delving into the teleost literature, one finds that assumptions about a highly active and continuous proliferation in the adult retina are based on studies in which proliferation was not quantified in a comparative way at the different life stages or was mainly studied in juveniles/young adults. Here, we performed a systematic and comparative study of the constitutive proliferative activity of the retina from early developing (2 days post-fertilisation) to aged (up to 3–4 years post-fertilisation) zebrafish. The mitotic activity and cell cycle progression were analysed by using immunofluorescence against pH3 and PCNA, respectively. We observed a decline in the cell proliferation in the retina with ageing despite the occurrence of a wave of secondary proliferation during sexual maturation. During this wave of secondary proliferation, the distribution of proliferating and mitotic cells changes from the inner to the outer nuclear layer in the central retina. Importantly, in aged zebrafish, there is a virtual disappearance of mitotic activity. Our results showing a decline in the proliferative activity of the zebrafish retina with ageing are of crucial importance since it is generally assumed that the fish retina has continuous proliferative activity throughout life.es_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipThis research was funded by Ministerio de Economía Industria y Competitividad (to E.C.), grant number BFU-2017-89861-P; Ministerio de Ciencia e Innovación-Agencia Estatal de Investigación (to A.B.-I.), grant number PID2020-115121GB-I00; Xunta de Galicia (to E.C.), grant number ED431C 2021/18; Xunta de Galicia (to I.H.-N.), grant number ED 481 A2018 216. “The APC was funded by the Xunta de Galicia”. Grants were partially financed by the European Social Fund.es_ES
dc.identifier.citationHernández-Núñez, I.; Quelle-Regaldie, A.; Sánchez, L.; Adrio, F.; Candal, E.; Barreiro-Iglesias, A. Decline in Constitutive Proliferative Activity in the Zebrafish Retina with Ageing. Int. J. Mol. Sci. 2021, 22, 11715es_ES
dc.identifier.doi10.3390/ijms222111715
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10347/31976
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ijms222111715es_ES
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY)es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectRetinaes_ES
dc.subjectZebrafishes_ES
dc.subjectProliferationes_ES
dc.subjectSecondary neurogenesises_ES
dc.subjectPCNAes_ES
dc.subjectpH3es_ES
dc.subjectAgeinges_ES
dc.titleDecline in Constitutive Proliferative Activity in the Zebrafish Retina with Ageinges_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery017b2725-d3de-40d7-8859-18c50f038d1d

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