Please use this identifier to cite or link to this item: https://doi.org/10.1242/bio.052027
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dc.titleReissner fibre-induced urotensin signalling from cerebrospinal fluid-contacting neurons prevents scoliosis of the vertebrate spine
dc.contributor.authorLu, H.
dc.contributor.authorShagirova, A.
dc.contributor.authorGoggi, J.L.
dc.contributor.authorYeo, H.L.
dc.contributor.authorRoy, S.
dc.date.accessioned2021-08-23T03:12:23Z
dc.date.available2021-08-23T03:12:23Z
dc.date.issued2020-05-14
dc.identifier.citationLu, H., Shagirova, A., Goggi, J.L., Yeo, H.L., Roy, S. (2020-05-14). Reissner fibre-induced urotensin signalling from cerebrospinal fluid-contacting neurons prevents scoliosis of the vertebrate spine. Biology Open 9 (5) : bio052027. ScholarBank@NUS Repository. https://doi.org/10.1242/bio.052027
dc.identifier.issn20466390
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/198590
dc.description.abstractReissner fibre (RF), discovered by the 19th-century German anatomist Ernst Reissner, is a filamentous structure present in cerebrospinal fluid (CSF). RF forms by aggregation of a glycoprotein called SCO-spondin (Sspo), but its function has remained enigmatic. Recent studies have shown that zebrafish sspo mutants develop a curved embryonic body axis. Zebrafish embryos with impaired cilia motility also develop curved bodies, which arises from failure of expression of urotensin related peptide (urp) genes in CSFcontacting neurons (CSF-cNs), impairing downstream signalling in trunk muscles. Here, we show that sspo mutants can survive into adulthood, but display severe curvatures of the vertebral column, resembling the common human spine disorder idiopathic scoliosis (IS). sspo mutants also exhibit significant reduction of urp gene expression from CSF-cNs. Consistent with epinephrine in CSF being bound by RF and required for urp expression, treating sspo mutants with this catecholamine rescued expression of the urp genes and axial defects. More strikingly, providing Urp2, specifically in the CSFcNs, rescued body curvature of sspo homozygotes during larval stages as well as in the adult. These findings bridge existing gaps in our knowledge between cilia motility, RF, Urp signalling and spine deformities, and suggest that targeting the Urotensin pathway could provide novel therapeutic avenues for IS. © 2020. Published by The Company of Biologists Ltd.
dc.publisherCompany of Biologists Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.subjectCerebrospinal fluid
dc.subjectCerebrospinal fluid-contacting neurons
dc.subjectCilia
dc.subjectReissner fibre
dc.subjectSlow-twitch muscle
dc.subjectUrotensin-related peptide
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1242/bio.052027
dc.description.sourcetitleBiology Open
dc.description.volume9
dc.description.issue5
dc.description.pagebio052027
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