Department of Biosciences, School of Life and Health Sciences, Aston University, Birmingham, UK.
Department of Chemical Engineering, University of Birmingham, Birmingham, UK.
Biotechnol Bioeng. 2020 Oct;117(10):3029-3039. doi: 10.1002/bit.27469. Epub 2020 Jul 23.
Traditional farm-based products based on livestock are one of the main contributors to greenhouse gas emissions. Cultivated meat is an alternative that mimics animal meat, being produced in a bioreactor under controlled conditions rather than through the slaughtering of animals. The first step in the production of cultivated meat is the generation of sufficient reserves of starting cells. In this study, bovine adipose-derived stem cells (bASCs) were used as starting cells due to their ability to differentiate towards both fat and muscle, two cell types found in meat. A bioprocess for the expansion of these cells on microcarriers in spinner flasks was developed. Different cell seeding densities (1,500, 3,000, and 6,000 cells/cm ) and feeding strategies (80%, 65%, 50%, and combined 80%/50% medium exchanges) were investigated. Cell characterization was assessed pre- and postbioprocessing to ensure that bioprocessing did not negatively affect bASC quality. The best growth was obtained with the lowest cell seeding density (1,500 cells/cm ) with an 80% medium exchange performed (p < .0001) which yielded a 28-fold expansion. The ability to differentiate towards adipogenic, osteogenic, and chondrogenic lineages was retained postbioprocessing and no significant difference (p > .5) was found in clonogenicity pre- or postbioprocessing in any of the feeding regimes tested.
传统的基于牲畜的农场产品是温室气体排放的主要贡献者之一。养殖肉是一种替代动物肉的方法,它是在生物反应器中在受控条件下生产的,而不是通过屠宰动物来生产。培养肉生产的第一步是产生足够的起始细胞储备。在这项研究中,由于牛脂肪来源的干细胞(bASC)能够向脂肪和肌肉两种类型的细胞分化,因此将其用作起始细胞,而肌肉是肉中的两种类型的细胞。开发了一种在旋转瓶中的微载体上扩增这些细胞的生物工艺。研究了不同的细胞接种密度(1,500、3,000 和 6,000 个细胞/cm )和喂养策略(80%、65%、50%和 80%/50%的组合培养基交换)。在生物处理前后对细胞进行了表征,以确保生物处理不会对 bASC 质量产生负面影响。以最低的细胞接种密度(1,500 个细胞/cm )和 80%的培养基交换获得最佳生长(p < 0.0001),其扩增倍数达到 28 倍。在生物处理后保留了向脂肪生成、成骨和软骨谱系分化的能力,并且在任何测试的喂养方案中,在生物处理前后,克隆形成能力都没有显著差异(p > 0.5)。