Chicken Embryo Fibroblast Viability and Trans-Differentiation Potential for Cultured Meat Production Across Passagesopen access
- Authors
- Kim, So-Hee; Kim, Chan-Jin; Lee, Eun-Yeong; Hwang, Young-Hwa; Joo, Seon-Tea
- Issue Date
- Oct-2024
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- chicken embryo fibroblast; cultured fat; cultured meat; adipogenic trans-differentiation; adipocyte; primary fibroblast; passage
- Citation
- Cells, v.13, no.20
- Indexed
- SCIE
SCOPUS
- Journal Title
- Cells
- Volume
- 13
- Number
- 20
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74765
- DOI
- 10.3390/cells13201734
- ISSN
- 2073-4409
2073-4409
- Abstract
- This 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.
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