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dc.contributor.authorYun, Dae Hee
dc.contributor.authorPark, Young-Gyun
dc.contributor.authorCho, Jae Hun
dc.contributor.authorKamentsky, Lee
dc.contributor.authorEvans, Nicholas B
dc.contributor.authorDiNapoli, Nicholas
dc.contributor.authorXie, Katherine
dc.contributor.authorChoi, Seo Woo
dc.contributor.authorAlbanese, Alexandre
dc.contributor.authorTian, Yuxuan
dc.contributor.authorSohn, Chang Ho
dc.contributor.authorZhang, Qiangge
dc.contributor.authorKim, Minyoung E
dc.contributor.authorSwaney, Justin
dc.contributor.authorGuan, Webster
dc.contributor.authorPark, Juhyuk
dc.contributor.authorDrummond, Gabi
dc.contributor.authorChoi, Heejin
dc.contributor.authorRuelas, Luzdary
dc.contributor.authorFeng, Guoping
dc.contributor.authorChung, Kwanghun
dc.date.accessioned2025-02-05T19:44:58Z
dc.date.available2025-02-05T19:44:58Z
dc.date.issued2025-01-24
dc.identifier.urihttps://hdl.handle.net/1721.1/158176
dc.description.abstractExtending single-cell analysis to intact tissues while maintaining organ-scale spatial information poses a major challenge due to unequal chemical processing of densely packed cells. Here we introduce Continuous Redispersion of Volumetric Equilibrium (CuRVE) in nanoporous matrices, a framework to address this challenge. CuRVE ensures uniform processing of all cells in organ-scale tissues by perpetually maintaining dynamic equilibrium of the tissue's gradually shifting chemical environment. The tissue chemical reaction environment changes at a continuous, slow rate, allowing redispersion of unevenly distributed chemicals and preserving chemical equilibrium tissue wide at any given moment. We implemented CuRVE to immunologically label whole mouse and rat brains and marmoset and human tissue blocks within 1 day. We discovered highly variable regionalized reduction of parvalbumin immunoreactive cells in wild-type adult mice, a phenotype missed by the commonly used genetic labeling. We envision that our platform will advance volumetric single-cell processing and analysis, facilitating comprehensive single-cell level investigations within their spatial context in organ-scale tissues.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41587-024-02533-4en_US
dc.rightsCreative Commons Attribution-Noncommercial-ShareAlikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceAuthoren_US
dc.titleUniform volumetric single-cell processing for organ-scale molecular phenotypingen_US
dc.typeArticleen_US
dc.identifier.citationYun, D.H., Park, YG., Cho, J.H. et al. Uniform volumetric single-cell processing for organ-scale molecular phenotyping. Nat Biotechnol (2025).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentPicower Institute for Learning and Memoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.relation.journalNature Biotechnologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2025-02-05T19:28:06Z
dspace.orderedauthorsYun, DH; Park, Y-G; Cho, JH; Kamentsky, L; Evans, NB; DiNapoli, N; Xie, K; Choi, SW; Albanese, A; Tian, Y; Sohn, CH; Zhang, Q; Kim, ME; Swaney, J; Guan, W; Park, J; Drummond, G; Choi, H; Ruelas, L; Feng, G; Chung, Ken_US
dspace.date.submission2025-02-05T19:28:14Z
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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