Department of Anatomy and Cell Biology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, Ontario, Canada.
J Neurophysiol. 2023 Apr 1;129(4):937-947. doi: 10.1152/jn.00029.2022. Epub 2023 Mar 22.
Disruptions in the gene are known to cause language impairments and symptoms associated with autism spectrum disorder (ASD). Importantly, knocking out this gene in rodents results in ASD-like symptoms that include auditory processing deficits. This study used in vitro patch-clamp electrophysiology to examine developmental alterations in auditory cortex pyramidal neurons of rats, hypothesizing that is essential for maintaining intrinsic neuronal properties and synaptic wiring in the developing auditory cortex. Whole cell patch-clamp recordings were conducted in wildtype and littermates at three postnatal age ranges (-, -, and -). Consistent changes across age were seen in all measures of intrinsic membrane properties and spontaneous synaptic input. Intrinsic cell properties such as action potential half-widths, rheobase, and action-potential firing frequencies were different between wildtype and rats predominantly during the juvenile stage (-), whereas adult rats showed higher frequencies of spontaneous and mini postsynaptic currents (sPSCs; mPSCs), with lower sPSC amplitudes. These results indicate that intrinsic cell properties are altered in rats during the juvenile age, leading to a hyperexcitable phenotype during this stage of synaptic remodeling and refinement. Although intrinsic properties eventually normalize by reaching adulthood, changes in synaptic input, potentially caused by the differences in intrinsic membrane properties, seem to manifest in the adult age and are presumably responsible for the hyperreactive behavioral phenotype. In conjunction with a previous study, the present results also indicate a large influence of breeding scheme, i.e., pre- or postnatal environment, on the impact of on cellular physiology. This study shows that neurons in the auditory cortex of knockout rats are hyperexcitable only during the juvenile age, whereas resulting changes in synaptic input persist in the adult. In conjunction with a previous study, the present results indicate that it is not the genes alone, but also the influence of pre- and postnatal environment, that shape neuronal function, highlighting the importance of early intervention in neurodevelopmental disorders.
该基因的突变已知会导致语言障碍和自闭症谱系障碍(ASD)的相关症状。重要的是,敲除啮齿动物中的这种基因会导致类似 ASD 的症状,包括听觉处理缺陷。本研究使用体外膜片钳电生理学技术,研究了大鼠听觉皮层锥体神经元的发育变化,假设 对于维持发育中的听觉皮层的内在神经元特性和突触连接至关重要。在三个出生后年龄范围(-、-和-)的野生型和 同窝仔鼠中进行全细胞膜片钳记录。在所有内在膜特性和自发性突触输入的测量中,均观察到跨年龄的一致变化。动作电位半宽度、阈强度和动作电位放电频率等内在细胞特性在野生型和 大鼠之间存在差异,主要发生在幼年阶段(-),而成年 大鼠表现出更高频率的自发性和微小突触后电流(sPSCs;mPSCs),sPSC 幅度较低。这些结果表明,内在细胞特性在 大鼠中在幼年时期发生改变,导致在这个突触重塑和细化的阶段表现出过度兴奋的表型。尽管内在特性最终通过成年期达到正常化,但由于内在膜特性的差异引起的突触输入变化似乎在成年期表现出来,并且可能是导致过度活跃的行为表型的原因。与之前的研究相结合,本研究结果还表明,繁殖方案(即产前或产后环境)对 对细胞生理学的影响有很大影响。本研究表明,只有在幼年时期, 敲除大鼠听觉皮层中的神经元才会过度兴奋,而突触输入的变化在成年期仍然存在。与之前的研究相结合,本研究结果表明,影响神经元功能的不仅是基因,还有产前和产后环境的影响,这突出了早期干预神经发育障碍的重要性。