Yokomizo Shinya, Maci Megi, Stafford April M, Miller Morgan R, Perle Stephen James, Takahashi Shusaku, Brown-Harding Heather, Liang Linda, Lovely Alex, Algamal Moustafa, Gillani Rebecca L, Zwang Theodore J, Richardson Douglas, Naegele Janice R, Vogt Daniel, Kastanenka Ksenia V
Department of Neurology, MassGeneral Institute of Neurodegenerative Diseases, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.
Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.
bioRxiv. 2025 May 31:2025.05.31.656412. doi: 10.1101/2025.05.31.656412.
In addition to dementia, Alzheimer's patients suffer from sleep impairments and aberrations in sleep-dependent brain rhythms. Deficits in inhibitory GABAergic interneuron function disrupt one of those rhythms, slow oscillation in particular, and actively contribute to Alzheimer's progression. We tested the degree to which transplantation of healthy donor interneuron progenitors would restore slow oscillation rhythm in young APP mice. We harvested medial ganglionic eminence (MGE) progenitors from mouse embryos and transplanted them into host APP mutant cortices. 3D light-sheet and structured illumination microscopy revealed that transplanted MGE progenitors survived and matured into healthy interneurons. multiphoton calcium imaging and voltage-sensitive dye imaging showed functional integration and slow oscillation rescue in absence or presence of optogenetic stimulation. Our work provides proof-of-concept evidence that stem cell therapy may serve as a viable strategy to rescue functional impairments in cortical circuits of APP mice and potentially those of Alzheimer's patients.
除了痴呆症,阿尔茨海默病患者还存在睡眠障碍以及与睡眠相关的脑节律异常。抑制性γ-氨基丁酸能中间神经元功能缺陷会破坏其中一种节律,尤其是慢振荡,并积极促进阿尔茨海默病的进展。我们测试了移植健康供体中间神经元祖细胞能在多大程度上恢复年轻APP小鼠的慢振荡节律。我们从小鼠胚胎中获取内侧神经节隆起(MGE)祖细胞,并将其移植到宿主APP突变体皮质中。三维光片和结构照明显微镜显示,移植的MGE祖细胞存活并成熟为健康的中间神经元。多光子钙成像和电压敏感染料成像显示,在有无光遗传学刺激的情况下,均有功能整合和慢振荡恢复。我们的工作提供了概念验证证据,表明干细胞疗法可能是挽救APP小鼠皮质回路功能障碍以及潜在地挽救阿尔茨海默病患者皮质回路功能障碍的可行策略。