Li Wei-Wu, Yang Hsueh-Hui, Chiou Tzyy-Wen, Woon Peng-Yeong, Xu Yue-Xuan, Tjandra Cynthia, Wijaya Ivan, Harn Horng-Jyh, Lin Shinn-Zong
Bioinnovation Center, Buddhist Tzu Chi Medical Foundation, Hualien 97002, Taiwan.
Department of Medical Research, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien 97002, Taiwan.
Int J Mol Sci. 2025 Apr 4;26(7):3382. doi: 10.3390/ijms26073382.
Adipose-derived mesenchymal stem cells (ADSCs) have exhibited promising therapeutic potential in Alzheimer's disease (AD), although the underlying mechanisms remain poorly understood. Previously established Alzheimer's disease neuron models derived from Ts21-induced pluripotent stem cells (Ts21-iPSCs) have been shown to exhibit progressive amyloid beta accumulation during neuronal differentiation. In this study, we employed a Transwell co-culture system to investigate the interaction between neurons derived from Ts21-iPSCs and ADSCs. Our findings revealed that co-culture with ADSCs significantly enhanced the survival rate of AD neurons. Proteomics analysis identified significant upregulation of left-right determination factor 2 (LEFTY2) protein in the co-culture medium. Supplementation with 2 nM LEFTY2 markedly improved the survival and growth of AD neurons. Furthermore, LEFTY2 effectively downregulates the expression of apolipoprotein E4 and amyloid beta 1-42, along with attenuating phosphorylated tau231 levels in AD neurons. These results suggest the potential of LEFTY2 as a promising therapeutic candidate for Alzheimer's disease.
脂肪来源的间充质干细胞(ADSCs)在阿尔茨海默病(AD)中已展现出有前景的治疗潜力,尽管其潜在机制仍知之甚少。先前建立的源自21号染色体三体诱导多能干细胞(Ts21-iPSCs)的阿尔茨海默病神经元模型已被证明在神经元分化过程中会出现渐进性淀粉样β蛋白积累。在本研究中,我们采用Transwell共培养系统来研究源自Ts21-iPSCs的神经元与ADSCs之间的相互作用。我们的研究结果表明,与ADSCs共培养显著提高了AD神经元的存活率。蛋白质组学分析确定了共培养基中左右决定因子2(LEFTY2)蛋白的显著上调。补充2 nM LEFTY2可显著改善AD神经元的存活和生长。此外,LEFTY2有效下调载脂蛋白E4和淀粉样β蛋白1-42的表达,并降低AD神经元中磷酸化tau231的水平。这些结果表明LEFTY2作为阿尔茨海默病有前景的治疗候选物的潜力。