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Combinations of Growth Factors Enhance the Potency of Islets In Vitro

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dc.contributor.authorLim, Jong Yeon-
dc.contributor.authorMin, Byoung Hoon-
dc.contributor.authorKim, Byoung Geun-
dc.contributor.authorShin, Jun-Seop-
dc.contributor.authorPark, Chang Sook-
dc.contributor.authorYoon, Tai Wook-
dc.contributor.authorHan, Sung Sik-
dc.date.accessioned2021-09-08T17:43:14Z-
dc.date.available2021-09-08T17:43:14Z-
dc.date.issued2009-05-
dc.identifier.issn0885-3177-
dc.identifier.issn1536-4828-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120176-
dc.description.abstractObjectives: Recent studies have demonstrated the impressive expansion of A cells in vitro. But unfortunately, expanded A cells do not function in the same way as fully differentiated A cells. Therefore, we developed a condition that would allow islet cells to proliferate while maintaining their endocrine function. Methods: We tested the different use of growth factors in a different culture period. And we tested the possibility of adult islets, which expanded during a short period, as a clinical source of islet cells by comparing the efficiency of transplantation of cultured islets with that of fresh islets. Results: The islets showed a time-dependent increase in proliferative activity, reaching 32.2% on day 5. After 5 days of culture, the efficiency of transplantation of cultured islets was increased (2-fold) in comparison to that of noncultured islets. Moreover, islet transplantation immediately induced normoglycemia at a level equal to native islets. Conclusions: These findings suggest that adult A cells have the potential to proliferate while maintaining their endocrine function, which can be improved through careful regulation of proliferation and differentiation.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.titleCombinations of Growth Factors Enhance the Potency of Islets In Vitro-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1097/MPA.0b013e318197a62e-
dc.identifier.scopusid2-s2.0-66149112524-
dc.identifier.wosid000265659600015-
dc.identifier.bibliographicCitationPANCREAS, v.38, no.4, pp 447 - 453-
dc.citation.titlePANCREAS-
dc.citation.volume38-
dc.citation.number4-
dc.citation.startPage447-
dc.citation.endPage453-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusPANCREATIC BETA-CELLS-
dc.subject.keywordPlusENDOCRINE PROGENITOR CELLS-
dc.subject.keywordPlusINSULIN-SECRETION-
dc.subject.keywordPlusRAT PANCREAS-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusMASS-
dc.subject.keywordAuthorislet-
dc.subject.keywordAuthorgrowth factor-
dc.subject.keywordAuthorproliferation-
dc.subject.keywordAuthordifferentiation-
dc.subject.keywordAuthortransplantation-
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