Goswami Apeksha Bharatgiri, Rybchyn Mark S, Walsh W R, le Coutre Johannes
School of Chemical Engineering, University of New South Wales, Sydney, New South Wales, Sydney, Australia.
School of Clinical Medicine, University of New South Wales, Sydney, New South Wales, 2052, Australia.
Heliyon. 2024 Sep 17;10(18):e38006. doi: 10.1016/j.heliyon.2024.e38006. eCollection 2024 Sep 30.
Cellular Agriculture (CellAg) is an attractive concept for innovative technology with the intent to provide food and nutrition complementary to existing supply streams. The past decade has seen considerable progress in the field with advancement of cellular technology that delivers the initial building blocks for meaningful implementation. The availability of natural cell-based material that can serve as nutrient-filled source for human consumption at low cost is a critical challenge for the emerging cellular agriculture industry. Therefore, here the isolation of bovine myofibroblasts of the Black Angus breed has been pursued and accomplished together with its characterisation by using RNA sequencing and proteomics through western blotting. To transition CellAg from a concept to a game changing technology for the industry, multiple challenges need to be overcome. The field requires powerful initial material, i.e., dedicated cells that can proliferate and differentiate robustly at scale. The methodology described allows for the production of healthy cells, which have been unequivocally characterized as clonal representatives of a stable myofibroblast cell line using transcriptomics and proteomics validation. Stringent and rigorous live cell monitoring of a nascent cell line derived from healthy muscle tissue allowed for stable cell growth. In this research article, a simple and precise methodology is presented for creating a bovine myofibroblast cell line (). Our work puts forward a low-tech use of materials and expertise that is devoid of transgenic approaches, thus creating a reliable approach for lab-scale research.
细胞农业(CellAg)是一个具有吸引力的创新技术概念,旨在提供与现有供应渠道互补的食品和营养。在过去十年中,随着细胞技术的进步,该领域取得了显著进展,为有意义的实施提供了初步的基础要素。对于新兴的细胞农业产业来说,能否以低成本获得可作为人类食用的富含营养的天然细胞基材料是一项关键挑战。因此,本文开展了黑安格斯牛成肌纤维细胞的分离工作,并通过RNA测序和蛋白质印迹法进行蛋白质组学分析对其进行了表征。为了将细胞农业从一个概念转变为该行业的变革性技术,需要克服多重挑战。该领域需要强大的起始材料,即能够大规模强劲增殖和分化的特定细胞。本文所述方法能够生产出健康细胞,通过转录组学和蛋白质组学验证,这些细胞已被明确表征为稳定的成肌纤维细胞系的克隆代表。对源自健康肌肉组织的新生细胞系进行严格且精确的活细胞监测,确保了细胞的稳定生长。在这篇研究文章中,提出了一种简单精确的方法来创建牛成肌纤维细胞系()。我们的工作提出了一种无需转基因方法的低技术材料和专业知识的应用,从而为实验室规模的研究创造了一种可靠的方法。