脂肪生成
细胞生物学
细胞分化
化学
油酸
脂滴
生物化学
转录因子
脂肪组织
脂质代谢
信号转导
油红O
基因表达调控
形态发生
生物
转铁蛋白
基因表达
再生医学
转铁蛋白受体
脂肪生成
间充质干细胞
细胞内
作者
Zhou Fu,Yingying Li,S. Wang,Shilei Li,Duo Tang,Xiang Guo,Yu Qi,Pengfei Zhao,Wenting Liu,Chen Guo,Yeting Shen,Feng Yang
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2026-04-13
卷期号:15 (8): 684-684
标识
DOI:10.3390/cells15080684
摘要
Cultured meat represents an emerging frontier in cellular agriculture, garnering increasing interest due to its potential benefits regarding sustainability, animal welfare, and food safety. However, its development is hampered by challenges in flavor modulation and sensory quality, primarily due to the limited biosynthesis of fat-derived flavor compounds. Although adipose tissue engineering has been extensively studied, its industrial-scale production is hampered by serum dependency and low differentiation efficiency. Therefore, the establishment of serum-free, efficient strategies for regulating lipid synthesis is urgently needed. In this study, we developed a serum-free adipogenic induction system and investigated its underlying regulatory mechanisms. We demonstrated that Serum-Free Differentiation Medium 1 (SFM-1) initiated the differentiation program and induced intracellular lipid deposition in preadipocytes (~10% by Day 8). Serum-free differentiation medium 2 (SFM-2), which supplied oleic acid (OA) as a lipid substrate and signaling activator, markedly enhanced lipid droplet accumulation and differentiation efficiency. Ultimately, serum-free differentiation medium 3 (SFM-3), leveraging the synergistic action of oleic acid (OA) and transferrin (TRF), successfully activates the expression of SEPTIN4, which in turn regulates a core adipogenic network-including the master transcription factors PPARγ and CEBPα, as well as downstream functional genes. Mechanistically, the OA/TRF combination in SFM-3 upregulates SEPTIN4, unveiling a previously unrecognized regulatory axis that activates the PPARγ signaling pathway, thereby synchronizing the proliferation and differentiation of precursors and guiding them from initiation to functional maturity. Our study presents a chemically defined, scalable platform for the serum-free adipogenic differentiation of porcine adipocytes, offering a promising strategy for the controllable production of fat components in cultured meat and supporting its industrialization.
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