Gabriel George C, Yagi Hisato, Tan Tuantuan, Bais Abha, Glennon Benjamin J, Stapleton Margaret C, Huang Lihua, Reynolds William T, Shaffer Marla G, Ganapathiraju Madhavi, Simon Dennis, Panigrahy Ashok, Wu Yijen L, Lo Cecilia W
Department of Pediatrics and Department of Developmental Biology, University of Pittsburgh, Pittsburgh, USA.
Chinese University of Hong Kong, Hong Kong, China.
Nat Commun. 2025 Jan 7;16(1):469. doi: 10.1038/s41467-024-55741-6.
Hypoplastic left heart syndrome (HLHS) is a severe congenital heart disease associated with microcephaly and poor neurodevelopmental outcomes. Here we show that the Ohia HLHS mouse model, with mutations in Sap130, a chromatin modifier, and Pcdha9, a cell adhesion protein, also exhibits microcephaly associated with mitotic block and increased apoptosis leading to impaired cortical neurogenesis. Transcriptome profiling, DNA methylation, and Sap130 ChIPseq analyses all demonstrate dysregulation of genes associated with autism and cognitive impairment. This includes perturbation of REST transcriptional regulation of neurogenesis, disruption of CREB signaling regulating synaptic plasticity, and defects in neurovascular coupling mediating cerebral blood flow. Adult mice harboring either the Pcdha9 mutation, which show normal brain anatomy, or forebrain-specific Sap130 deletion via Emx1-Cre, which show microcephaly, both demonstrate learning and memory deficits and autism-like behavior. These findings provide mechanistic insights indicating the adverse neurodevelopment in HLHS may involve cell autonomous/nonautonomous defects and epigenetic dysregulation.
左心发育不全综合征(HLHS)是一种严重的先天性心脏病,与小头畸形和不良的神经发育结局相关。我们在此表明,Ohia HLHS小鼠模型中,染色质修饰因子Sap130和细胞粘附蛋白Pcdha9发生突变,也表现出与有丝分裂阻滞和凋亡增加相关的小头畸形,导致皮质神经发生受损。转录组分析、DNA甲基化分析和Sap130染色质免疫沉淀测序(ChIPseq)分析均表明,与自闭症和认知障碍相关的基因存在失调。这包括神经发生的REST转录调控受到干扰、调节突触可塑性的CREB信号传导中断,以及介导脑血流量的神经血管耦合缺陷。携带Pcdha9突变(脑解剖结构正常)的成年小鼠,或通过Emx1-Cre进行前脑特异性Sap130缺失(表现出小头畸形)的成年小鼠,均表现出学习和记忆缺陷以及自闭症样行为。这些发现提供了机制上的见解,表明HLHS中不良的神经发育可能涉及细胞自主/非自主缺陷和表观遗传失调。