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dc.contributor.authorKojima, Hidenobuen
dc.contributor.authorYasuchika, Kentaroen
dc.contributor.authorFukumitsu, Kenen
dc.contributor.authorIshii, Takamichien
dc.contributor.authorOgiso, Satoshien
dc.contributor.authorMiyauchi, Yuyaen
dc.contributor.authorYamaoka, Ryoyaen
dc.contributor.authorKawai, Takayukien
dc.contributor.authorKatayama, Hokahiroen
dc.contributor.authorYoshitoshi-Uebayashi, Elena Yukieen
dc.contributor.authorKita, Sadahikoen
dc.contributor.authorYasuda, Katsutaroen
dc.contributor.authorSasaki, Naoyaen
dc.contributor.authorKomori, Junjien
dc.contributor.authorUemoto, Shinjien
dc.date.accessioned2025-06-17T06:21:33Z-
dc.date.available2025-06-17T06:21:33Z-
dc.date.issued2018-06-
dc.identifier.urihttp://hdl.handle.net/2433/294708-
dc.description.abstractTissue decellularization produces a three-dimensional scaffold that can be used to fabricate functional liver grafts following recellularization. Inappropriate cell distribution and clotting during blood perfusion hinder the practical use of recellularized livers. Here we aimed to establish a seeding method for the optimal distribution of parenchymal and endothelial cells, and to evaluate the effect of liver sinusoidal endothelial cells (LSECs) in the decellularized liver. Primary rat hepatocytes and LSECs were seeded into decellularized whole-liver scaffolds via the biliary duct and portal vein, respectively. Biliary duct seeding provided appropriate hepatocyte distribution into the parenchymal space, and portal vein–seeded LSECs simultaneously lined the portal lumen, thereby maintaining function and morphology. Hepatocytes co-seeded with LSECs retained their function compared with those seeded alone. Platelet deposition was significantly decreased and hepatocyte viability was maintained in the co-seeded group after extracorporeal blood perfusion. In conclusion, our seeding method provided optimal cell distribution into the parenchyma and vasculature according to the three-dimensional structure of the decellularized liver. LSECs maintained hepatic function, and supported hepatocyte viability under blood perfusion in the engineered liver graft owing to their antithrombogenicity. This recellularization procedure could help produce practical liver grafts with blood perfusion.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2018 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved. Published by Elsevier Inc.en
dc.rightsThis manuscript version is made available under the CC-BY-NC-ND 4.0 license.en
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectanimal models: murineen
dc.subjectartificial organs/support devicesen
dc.subjectbasic (laboratory) research/scienceen
dc.subjectcellular biologyen
dc.subjectliver transplantation/hepatologyen
dc.subjecttissue/organ engineeringen
dc.titleEstablishment of practical recellularized liver graft for blood perfusion using primary rat hepatocytes and liver sinusoidal endothelial cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleAmerican Journal of Transplantationen
dc.identifier.volume18-
dc.identifier.issue6-
dc.identifier.spage1351-
dc.identifier.epage1359-
dc.relation.doi10.1111/ajt.14666-
dc.textversionpublisher-
dc.identifier.pmid29338127-
dcterms.accessRightsopen access-
dc.identifier.pissn1600-6135-
dc.identifier.eissn1600-6143-
出現コレクション:学術雑誌掲載論文等

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