Whitehouse Chloe, Bravington Ellie, Patir Anirudh, Wei Wei, Brownlees Janet, He Yufang, Corbett Nicola
MSD (UK) Limited, 120 Moorgate, London EC2M 6UR, UK.
Merck & Co., Inc., Rahway, NJ 07065, USA.
Bioengineering (Basel). 2025 Feb 28;12(3):245. doi: 10.3390/bioengineering12030245.
Here, we present a novel 3D bioprinted model of the forebrain cortex designed to quantify neurite outgrowth across a hydrogel bridge. To validate this model, we cultured Alzheimer's disease (AD) forebrain cortical populations derived from human iPSCs carrying APP (amyloid precursor protein) mutations (K670M/N671L + V717F). Neurite and synapse formation were significantly impaired in 3D AD mutant cultures compared to controls, but this was not replicated in 2D, highlighting deficits in these traditional 2D cell culture models. To investigate the mechanisms underlying impaired neurite outgrowth in 3D and 2D models of AD, we assessed amyloid-β dysfunction, mitochondrial health, and oxidative stress in both conditions. In the 3D model, APP mutant cultures exhibited reduced mitochondrial membrane potential and fragmented networks, indicating dysfunction and potential cellular energy deficits. Additionally, elevated oxidative stress and proteostasis disruption were identified in the 3D AD models as indicators of cellular damage, which may be limiting neurite extension. Furthermore, transcriptomic (bulk RNA-Seq) analysis revealed distinct differences in gene expression pathways between 2D and 3D models of AD, suggesting alternate underlying mechanisms of disease pathology between the culture conditions. This study demonstrates the functionality of this novel 3D bioprinted model for quantifying neurite connectivity and identifying underlying disease mechanisms.
在此,我们展示了一种新型的前脑皮质3D生物打印模型,该模型旨在量化穿过水凝胶桥的神经突生长。为了验证该模型,我们培养了源自携带APP(淀粉样前体蛋白)突变(K670M/N671L + V717F)的人诱导多能干细胞的阿尔茨海默病(AD)前脑皮质细胞群体。与对照相比,3D AD突变体培养物中的神经突和突触形成明显受损,但在2D培养中未观察到这种情况,这突出了这些传统2D细胞培养模型的缺陷。为了研究AD的3D和2D模型中神经突生长受损的潜在机制,我们在两种条件下评估了淀粉样β蛋白功能障碍、线粒体健康状况和氧化应激。在3D模型中,APP突变体培养物表现出线粒体膜电位降低和网络碎片化,表明功能障碍和潜在的细胞能量不足。此外,在3D AD模型中发现氧化应激升高和蛋白质稳态破坏是细胞损伤的指标,这可能限制了神经突的延伸。此外,转录组学(批量RNA测序)分析揭示了AD的2D和3D模型之间基因表达途径的明显差异,表明不同培养条件下疾病病理的潜在机制不同。这项研究证明了这种新型3D生物打印模型在量化神经突连接性和识别潜在疾病机制方面的功能。