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Chicken Embryo Fibroblast Viability and Trans-Differentiation Potential for Cultured Meat Production Across Passages

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dc.contributor.authorKim, So-Hee-
dc.contributor.authorKim, Chan-Jin-
dc.contributor.authorLee, Eun-Yeong-
dc.contributor.authorHwang, Young-Hwa-
dc.contributor.authorJoo, Seon-Tea-
dc.date.accessioned2024-12-03T08:00:45Z-
dc.date.available2024-12-03T08:00:45Z-
dc.date.issued2024-10-
dc.identifier.issn2073-4409-
dc.identifier.issn2073-4409-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/74765-
dc.description.abstractThis study was conducted to analyze the viability of primary chicken embryo fibroblasts and the efficiency of adipogenic trans-differentiation for cultured meat production. In isolating chicken embryo fibroblasts (CEFs) from a heterogeneous cell pool containing chicken satellite cells (CSCs), over 90% of CEFs expressed CD29 and vimentin. The analysis of the proliferative capabilities of CEFs revealed no significant differences in EdU-positive cells (%), cumulative cell number, doubling time, and growth rate from passage 1 to passage 9 (p > 0.05). This indicates that CEFs can be isolated by 2 h of pre-plating and survive stably up to passage 9, and that primary fibroblasts can serve as a valuable cell source for the cultured meat industry. Adipogenic trans-differentiation was induced up to passage 9 of CEFs. As passages increased, lipid accumulation and adipocyte size significantly decreased (p < 0.05). The reduced differentiation rate of primary CEFs with increasing passages poses a major challenge to the cost and efficiency of cultured meat production. Thus, effective cell management and the maintenance of cellular characteristics for a long time are crucial for ensuring stable and efficient cultured fat production in the cultured meat industry.-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleChicken Embryo Fibroblast Viability and Trans-Differentiation Potential for Cultured Meat Production Across Passages-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/cells13201734-
dc.identifier.scopusid2-s2.0-85207360229-
dc.identifier.wosid001342656300001-
dc.identifier.bibliographicCitationCells, v.13, no.20-
dc.citation.titleCells-
dc.citation.volume13-
dc.citation.number20-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusPROLIFERATOR-ACTIVATED RECEPTOR-
dc.subject.keywordPlusSATELLITE CELLS-
dc.subject.keywordPlusADIPOCYTE DIFFERENTIATION-
dc.subject.keywordPlusTRANSDIFFERENTIATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGAMMA-
dc.subject.keywordPlusPAX7-
dc.subject.keywordAuthorchicken embryo fibroblast-
dc.subject.keywordAuthorcultured fat-
dc.subject.keywordAuthorcultured meat-
dc.subject.keywordAuthoradipogenic trans-differentiation-
dc.subject.keywordAuthoradipocyte-
dc.subject.keywordAuthorprimary fibroblast-
dc.subject.keywordAuthorpassage-
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