Wen Wei, Prada Adriana M, Turrigiano Gina G
Department of Biology, Brandeis University, Waltham, MA 02453, USA.
bioRxiv. 2025 Feb 19:2024.06.01.596982. doi: 10.1101/2024.06.01.596982.
Neocortical circuits use synaptic and intrinsic forms of homeostatic plasticity to stabilize key features of network activity, but whether these different homeostatic mechanisms act redundantly, or can be independently recruited to stabilize different network features, is unknown. Here we used pharmacological and genetic perturbations both and to determine whether synaptic scaling and intrinsic homeostatic plasticity (IHP) are arranged and recruited in a hierarchical or modular manner within L2/3 pyramidal neurons in rodent V1. Surprisingly, although the expression of synaptic scaling and IHP was dependent on overlapping signaling pathways, they could be independently recruited by manipulating spiking activity or NMDAR signaling, respectively. Further, we found that changes in visual experience that affect NMDAR activation but not mean firing selectively trigger IHP, without recruiting synaptic scaling. These findings support a modular model in which synaptic and intrinsic homeostatic plasticity respond to and stabilize distinct aspects of network activity.
新皮质回路利用突触和内在形式的稳态可塑性来稳定网络活动的关键特征,但这些不同的稳态机制是冗余作用,还是可被独立募集以稳定不同的网络特征,目前尚不清楚。在这里,我们使用药理学和遗传学扰动来确定突触缩放和内在稳态可塑性(IHP)在啮齿动物初级视觉皮层(V1)的第2/3层锥体神经元内是以分层还是模块化方式排列和募集的。令人惊讶的是,虽然突触缩放和IHP的表达依赖于重叠的信号通路,但它们可以分别通过操纵放电活动或NMDAR信号通路而被独立募集。此外,我们发现影响NMDAR激活但不影响平均放电的视觉经验变化会选择性地触发IHP,而不会募集突触缩放。这些发现支持了一种模块化模型,其中突触和内在稳态可塑性对网络活动的不同方面做出反应并使其稳定。