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Revisiting in vivo staining with alizarin red S - a valuable approach to analyse zebrafish skeletal mineralization during development and regeneration

dc.contributor.authorBensimon-Brito, A.
dc.contributor.authorCardeira, J.
dc.contributor.authorDionísio, Gisela
dc.contributor.authorHuysseune, A.
dc.contributor.authorCancela, M. L.
dc.contributor.authorWitten, P. E.
dc.date.accessioned2020-01-19T19:13:49Z
dc.date.available2020-01-19T19:13:49Z
dc.date.issued2016
dc.description.abstractBackground: The correct evaluation of mineralization is fundamental for the study of skeletal development, maintenance, and regeneration. Current methods to visualize mineralized tissue in zebrafish rely on: 1) fixed specimens; 2) radiographic and μCT techniques, that are ultimately limited in resolution; or 3) vital stains with fluorochromes that are indistinguishable from the signal of green fluorescent protein (GFP)-labelled cells. Alizarin compounds, either in the form of alizarin red S (ARS) or alizarin complexone (ALC), have long been used to stain the mineralized skeleton in fixed specimens from all vertebrate groups. Recent works have used ARS vital staining in zebrafish and medaka, yet not based on consistent protocols. There is a fundamental concern on whether ARS vital staining, achieved by adding ARS to the water, can affect bone formation in juvenile and adult zebrafish, as ARS has been shown to inhibit skeletal growth and mineralization in mammals. Results: Here we present a protocol for vital staining of mineralized structures in zebrafish with a low ARS concentration that does not affect bone mineralization, even after repetitive ARS staining events, as confirmed by careful imaging under fluorescent light. Early and late stages of bone development are equally unaffected by this vital staining protocol. From all tested concentrations, 0.01 % ARS yielded correct detection of bone calcium deposits without inducing additional stress to fish. Conclusions: The proposed ARS vital staining protocol can be combined with GFP fluorescence associated with skeletal tissues and thus represents a powerful tool for in vivo monitoring of mineralized structures. We provide examples from wild type and transgenic GFP-expressing zebrafish, for endoskeletal development and dermal fin ray regeneration.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1186/s12861-016-0102-4pt_PT
dc.identifier.issn1471-213X
dc.identifier.urihttp://hdl.handle.net/10451/41090
dc.language.isoengpt_PT
dc.publisherBMCpt_PT
dc.relation.publisherversionhttps://bmcdevbiol.biomedcentral.com/articles/10.1186/s12861-016-0102-4pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectVertebral columnpt_PT
dc.subjectCaudal finpt_PT
dc.subjectMineral appositionpt_PT
dc.subjectBonept_PT
dc.subjectFluorescence imagingpt_PT
dc.subjectCalciumpt_PT
dc.subjectHydroxyapatitept_PT
dc.subjectAlizarin red Spt_PT
dc.titleRevisiting in vivo staining with alizarin red S - a valuable approach to analyse zebrafish skeletal mineralization during development and regenerationpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.startPage2pt_PT
oaire.citation.titleBMC Developmental Biologypt_PT
oaire.citation.volume16pt_PT
person.familyNameDionísio
person.givenNameGisela
person.identifier.ciencia-id321D-EE64-25CD
person.identifier.orcid0000-0001-8891-9908
person.identifier.scopus-author-id15833954700
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationd02e3d2c-6519-42dd-bbf5-d1eed97f1aa8
relation.isAuthorOfPublication.latestForDiscoveryd02e3d2c-6519-42dd-bbf5-d1eed97f1aa8

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