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dc.contributor.authorGhazizadeh, Zaniar
dc.contributor.authorZhu, Jiajun
dc.contributor.authorFattahi, Faranak
dc.contributor.authorTang, Alice
dc.contributor.authorSun, Xiaolu
dc.contributor.authorAmin, Sadaf
dc.contributor.authorTsai, Su-Yi
dc.contributor.authorKhalaj, Mona
dc.contributor.authorZhou, Ting
dc.contributor.authorSamuel, Ryan M.
dc.contributor.authorZhang, Tuo
dc.contributor.authorOrtega, Francis A.
dc.contributor.authorGordillo, Miriam
dc.contributor.authorMoroziewicz, Dorota
dc.contributor.authorPaull, Daniel
dc.contributor.authorNoggle, Scott A.
dc.contributor.authorXiang, Jenny Zhaoying
dc.contributor.authorStuder, Lorenz
dc.contributor.authorChristini, David J.
dc.contributor.authorPitt, Geoffrey S.
dc.contributor.authorEvans, Todd
dc.contributor.authorChen, Shuibing
dc.date.accessioned2024-11-04T18:51:10Z
dc.date.available2024-11-04T18:51:10Z
dc.date.issued2022-04-15
dc.identifier.citationGhazizadeh Z, Zhu J, Fattahi F, Tang A, Sun X, Amin S, Tsai SY, Khalaj M, Zhou T, Samuel RM, Zhang T, Ortega FA, Gordillo M, Moroziewicz D; NYSCF Global Stem Cell Array® Team; Paull D, Noggle SA, Xiang JZ, Studer L, Christini DJ, Pitt GS, Evans T, Chen S. A dual SHOX2:GFP; MYH6:mCherry knockin hESC reporter line for derivation of human SAN-like cells. iScience. 2022 Mar 25;25(4):104153. doi: 10.1016/j.isci.2022.104153. PMID: 35434558; PMCID: PMC9010642.en_US
dc.identifier.issn2589-0042
dc.identifier.doi10.1016/j.isci.2022.104153
dc.identifier.pmid35434558
dc.identifier.piiS2589004222004230
dc.identifier.urihttp://hdl.handle.net/20.500.12648/15755
dc.description.abstractThe sinoatrial node (SAN) is the primary pacemaker of the heart. The human SAN is poorly understood due to limited primary tissue access and limitations in robust in vitro derivation methods. We developed a dual SHOX2:GFP; MYH6:mCherry knockin human embryonic stem cell (hESC) reporter line, which allows the identification and purification of SAN-like cells. Using this line, we performed several rounds of chemical screens and developed an efficient strategy to generate and purify hESC-derived SAN-like cells (hESC-SAN). The derived hESC-SAN cells display molecular and electrophysiological characteristics of bona fide nodal cells, which allowed exploration of their transcriptional profile at single-cell level. In sum, our dual reporter system facilitated an effective strategy for deriving human SAN-like cells, which can potentially be used for future disease modeling and drug discovery.en_US
dc.description.sponsorshipAmerican Heart Association Incen_US
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.relation.urlhttps://www.cell.com/iscience/fulltext/S2589-0042(22)00423-0en_US
dc.rights© 2022 The Authors.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://www.elsevier.com/tdm/userlicense/1.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectbiological sciencesen_US
dc.subjectmethodology in biological sciencesen_US
dc.subjectstem cells researchen_US
dc.titleA dual SHOX2:GFP; MYH6:mCherry knockin hESC reporter line for derivation of human SAN-like cellsen_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleiScienceen_US
dc.source.volume25
dc.source.issue4
dc.source.beginpage104153
dc.description.versionVoRen_US
refterms.dateFOA2024-11-04T18:51:11Z
dc.description.institutionSUNY Downstateen_US
dc.description.departmentPhysiology and Pharmacologyen_US
dc.description.degreelevelN/Aen_US
dc.identifier.issue4en_US


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