类有机物
自闭症
诱导多能干细胞
神经干细胞
表型
基因敲除
胚胎干细胞
医学
癌症研究
生物
细胞生物学
干细胞
遗传学
细胞培养
基因
精神科
作者
Xiao Han,Yuanlin He,Yuanhao Wang,Wenzhu Hu,Chu Chu,Lei Huang,Yuan Hong,Lu Han,Shouxin Zhang,Yao Gao,Lin Yuan,Hongxia Ma,Hongbing Shen,Xiaoyan Ke,Yan Liu,Zhibin Hu
标识
DOI:10.1002/advs.202406849
摘要
Abstract Autism spectrum disorder (ASD), which is caused by heterogeneous genetic and environmental factors, is characterized by diverse clinical phenotypes linked to distinct pathological mechanisms. ASD individuals with a shared clinical phenotype might contribute to revealing the molecular mechanism underlying ASD progression. Here, it is generated induced pluripotent stem cell (iPSC)‐derived cerebral organoids from normocephalic individuals with ASD in a prospective birth cohort with a shared clinical diagnosis. Multiple cell lines and time series scRNA‐seq combined with a histomorphological analysis revealed premature neural differentiation of neural stem cells (NSCs) and decreased expression of Fatty acid binding protein 7 (FABP7) in ASD organoids. It is subsequently revealed alterations in the phosphorylation levels of Mitogen‐Activated Protein Kinase Kinase 1/2 (MEK1/2), which are downstream of FABP7, and the regulation of the FABP7/MEK pathway reversed improper neural differentiation in the ASD organoids. Moreover, both Fabp7‐knockdown and MEK2‐overexpressing mice exhibited repetitive stereotyped behaviors and social defects relevant to autism. This study reveals the role of the FABP7/MEK pathway in abnormal NSC differentiation in normocephalic individuals with ASD, which might provide a promising therapeutic target for ASD treatment.
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