Liu Qingying, Xie Lianghua, Chen Wei
Department of Traditional Chinese Medicine, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China.
Department of Food Science and Nutrition, College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058, China.
J Agric Food Chem. 2025 Jan 22;73(3):2008-2018. doi: 10.1021/acs.jafc.4c09215. Epub 2025 Jan 8.
Cultured meat is an emerging technology with the potential to meet future protein demands while addressing the challenges associated with traditional livestock farming. The production of cultured meat requires efficient, animal component-free systems for muscle stem cell (MuSC) expansion. Fibroblast growth factor 1 (FGF1) is a critical growth factor that regulates the MuSC function. In this study, we established an efficient method for the soluble expression and purification of recombinant porcine FGF1 (rpFGF1) in , achieving a yield of 48 mg of purified protein per liter of culture. Treatment with rpFGF1 significantly enhanced the proliferation of porcine MuSC under serum-free conditions. Furthermore, rpFGF1 induced mitochondrial fission and mitophagy by activating the ERK-dependent phosphorylation of DRP1 at Ser616, resulting in improved mitochondrial function and proliferation capacity in porcine MuSC. These findings highlight the potential of rpFGF1 in the development of serum-free media for scalable and sustainable cultured meat production.
cultured meat is an emerging technology with the potential to meet future protein demands while addressing the challenges associated with traditional livestock farming. The production of cultured meat requires efficient, animal component-free systems for muscle stem cell (MuSC) expansion. Fibroblast growth factor 1 (FGF1) is a critical growth factor that regulates the MuSC function. In this study, we established an efficient method for the soluble expression and purification of recombinant porcine FGF1 (rpFGF1) in, achieving a yield of 48 mg of purified protein per liter of culture. Treatment with rpFGF1 significantly enhanced the proliferation of porcine MuSC under serum-free conditions. Furthermore, rpFGF1 induced mitochondrial fission and mitophagy by activating the ERK-dependent phosphorylation of DRP1 at Ser616, resulting in improved mitochondrial function and proliferation capacity in porcine MuSC. These findings highlight the potential of rpFGF1 in the development of serum-free media for scalable and sustainable cultured meat production.
培养肉是一项新兴技术,有潜力满足未来的蛋白质需求,同时应对传统畜牧业带来的挑战。培养肉的生产需要高效的、无动物成分系统来扩增肌肉干细胞(MuSC)。成纤维细胞生长因子1(FGF1)是调节MuSC功能的关键生长因子。在本研究中我们建立了一种在大肠杆菌中可溶性表达和纯化重组猪FGF1(rpFGF1)的有效方法,每升培养物可获得48毫克纯化蛋白。在无血清条件下,rpFGF1处理显著增强了猪MuSC的增殖。此外,rpFGF1通过激活DRP1在Ser616位点的ERK依赖性磷酸化诱导线粒体分裂和线粒体自噬,从而改善了猪MuSC的线粒体功能和增殖能力。这些发现突出了rpFGF1在开发用于规模化和可持续培养肉生产的无血清培养基方面的潜力。