Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-020-75683-5
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dc.titleRed-COLA1: a human fibroblast reporter cell line for type I collagen transcription
dc.contributor.authorWong, H.H.
dc.contributor.authorSeet, S.H.
dc.contributor.authorBascom, C.C.
dc.contributor.authorIsfort, R.J.
dc.contributor.authorBard, F.
dc.date.accessioned2021-08-25T14:05:08Z
dc.date.available2021-08-25T14:05:08Z
dc.date.issued2020
dc.identifier.citationWong, H.H., Seet, S.H., Bascom, C.C., Isfort, R.J., Bard, F. (2020). Red-COLA1: a human fibroblast reporter cell line for type I collagen transcription. Scientific Reports 10 (1) : 19723. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-020-75683-5
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/199292
dc.description.abstractType I collagen is a key protein of most connective tissue and its up-regulation is required for wound healing but is also involved in fibrosis. Control of expression of this collagen remains poorly understood apart from Transforming Growth Factor beta (TGF-?1)-mediated induction. To generate a sensitive, practical, robust, image-based high-throughput-compatible reporter system, we genetically inserted a short-lived fluorescence reporter downstream of the endogenous type I collagen (COL1A1) promoter in skin fibroblasts. Using a variety of controls, we demonstrate that the cell line faithfully reports changes in type I collagen expression with at least threefold enhanced sensitivity compared to endogenous collagen monitoring. We use this assay to test the potency of anti-fibrotic compounds and screen siRNAs for regulators of TGF-?1-induced type I collagen expression. We propose our reporter cell line, Red-COLA1, as a new efficient tool to study type I collagen transcriptional regulation. © 2020, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1038/s41598-020-75683-5
dc.description.sourcetitleScientific Reports
dc.description.volume10
dc.description.issue1
dc.description.page19723
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