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Pretreatment with recombinant human interleukin 2 (rhIL-2) Up-regulates PCNA-positive cells after partial hepatectomy in rat liver

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dc.contributor.authorJeon, Miae-
dc.contributor.authorKwon, Hyun Jung-
dc.contributor.authorKim, Yong Hyun-
dc.contributor.authorHan, Kook-Il-
dc.contributor.authorNam, Kung-Woo-
dc.contributor.authorBaik, Yeongjun-
dc.contributor.authorLee, Sunghee-
dc.contributor.authorKim, Wan-Jong-
dc.contributor.authorHan, Man-Deuk-
dc.date.accessioned2021-08-11T23:25:37Z-
dc.date.available2021-08-11T23:25:37Z-
dc.date.issued2014-02-
dc.identifier.issn1226-8372-
dc.identifier.issn1976-3816-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/12450-
dc.description.abstractWe prepared recombinant human interleukin-2 (rhIL-2) and studied its pretreated influence on liver regeneration and the blood profile in partially (67%) hepatectomized (PH) male Sprague-Dawley rats. Rats were injected in the tail vein with rhIL-2 three times per day for 3 consecutive days and 67% underwent a partial hepatectomy (PH). Five days after the PH, liver tissue and blood samples were analyzed for liver regeneration and hematological changes. The weight of the liver in the rhIL-2 pretreated groups increased in a dose-dependent manner; with the highest treatment (24 x 10(4) IU/kg), the maximum liver weight of 88.6% was exhibited. The control group showed a gradual increase to 76.3% of the original liver weight. A histological analysis of the liver showed an increase in proliferating cell nuclear antigen (PCNA)-positive cells in rhIL-2 pretreated rat livers. The rate of hepatocyte proliferation also increased significantly in primary cultured rat liver cells following rhIL-2 treatment. These results suggest that pretreatment with rhIL-2 may play adjuvant roles in liver regeneration after PH.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisher한국생물공학회-
dc.titlePretreatment with recombinant human interleukin 2 (rhIL-2) Up-regulates PCNA-positive cells after partial hepatectomy in rat liver-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s12257-013-0667-8-
dc.identifier.scopusid2-s2.0-84896985748-
dc.identifier.wosid000333012300006-
dc.identifier.bibliographicCitationBiotechnology and Bioprocess Engineering, v.19, no.1, pp 43 - 51-
dc.citation.titleBiotechnology and Bioprocess Engineering-
dc.citation.volume19-
dc.citation.number1-
dc.citation.startPage43-
dc.citation.endPage51-
dc.type.docTypeArticle-
dc.identifier.kciidART001855702-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusIL-2-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusMUSCLE-
dc.subject.keywordAuthorrhIL-2-
dc.subject.keywordAuthorpartial hepatectomy (PH)-
dc.subject.keywordAuthorPCNA-
dc.subject.keywordAuthorimmunohistochemistry-
dc.subject.keywordAuthorliver regeneration-
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