Murphy Ashley R, Franco Rose Ann, Allenby Mark C
School of Chemical Engineering, Faculty of Engineering, Architecture and Information Technology, The University of Queensland, St Lucia, 4072, Australia.
Small. 2025 Aug;21(32):e2501834. doi: 10.1002/smll.202501834. Epub 2025 Jun 17.
In vitro co-culture processes supporting simultaneous formation of vessel networks alongside differentiation toward mature parenchymal tissue have numerous clinical and agricultural applications but remain unrealized due to contrasting culture requirements. Of specific interest is lab-grown vascularized adipose tissue to study diabetes, obesity, metabolic syndrome, and cardiovascular diseases, and to advance cultivated meat technologies. A microfluidic 3D hydrogel culture device capable of supporting live-imaging of fluorescent reporter cell lines and generating counter-current gradients of vasculogenic and adipogenic growth factors is reported. For the first time, experimental conditions capable of reproducibly forming diverse microvascular networks from telomerase immortalized endothelial and mesenchymal stem cells in both 2D and 3D hydrogel-embedded cultures are reported. This novel microfluidic culture design demonstrates the generation of growth factor environments which support the 3D co-formation of integrated robust microvascular networks and lipid-producing adipocytes after 31-days gradient culture. Microvascular networks substantially support parenchymal stromal cell differentiation to mature adipose tissue (67.4% lipid coverage), unachieved in avascular cultures (1.86% lipid coverage). It is attempted to validate the co-culture model by applying inhibitors of vessel-mediated lipogenesis (spermidine and VO-OHpic), which are demonstrated to be ineffective in this novel human preclinical model.
支持血管网络与向成熟实质组织分化同时形成的体外共培养过程具有众多临床和农业应用,但由于培养要求相互矛盾,这些应用尚未实现。特别令人感兴趣的是实验室培养的血管化脂肪组织,用于研究糖尿病、肥胖症、代谢综合征和心血管疾病,并推动人造肉技术的发展。本文报道了一种微流控3D水凝胶培养装置,该装置能够支持荧光报告细胞系的实时成像,并能产生血管生成和成脂生长因子的逆流梯度。首次报道了在二维和三维水凝胶包埋培养中,能够从端粒酶永生化内皮细胞和间充质干细胞可重复形成多种微血管网络的实验条件。这种新颖的微流控培养设计表明,在31天的梯度培养后,生长因子环境的产生支持了整合的强大微血管网络和产脂脂肪细胞的三维共形成。微血管网络极大地支持实质基质细胞分化为成熟脂肪组织(脂质覆盖率67.4%),而在无血管培养中无法实现(脂质覆盖率1.86%)。尝试通过应用血管介导的脂肪生成抑制剂(亚精胺和VO-OHpic)来验证共培养模型,但结果表明这些抑制剂在这种新型人类临床前模型中无效。