Inhibiting JNK and PI3K-Akt signaling pathways altered spontaneous network bursts and developmental trajectories of neuronal networks.

IF 3.8
Xiaoli Jia, Qiuyan Zhu, Hailin Lu, Zhihong Zhou, Tahir Ali, Shupeng Li, Jinxing Feng
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Abstract

Objective.Spontaneous network bursts (NBs) are critical for neuronal circuit development, influencing synaptogenesis and functional organization. While JNK and PI3K-Akt signaling pathways are known to regulate synaptic plasticity, their specific roles in governing NBs dynamics and functional network organization remain poorly understood. This study investigates the roles of JNK and PI3K-Akt signaling in regulating spontaneous NBs dynamics and network organization in cultured neuronal networks.Approach.Using longitudinal microelectrode array (MEA) recordings from cultured cortical neurons (DIV14-49), we pharmacologically inhibited JNK (SP600125, JNK-IN-8) and PI3K-Akt (LY294002, GDC-0941) pathways. We quantitatively analyzed NBs profiles (maximum firing rate/MFR, burst length/BL, rising phase/RP) and functional network properties (modularity, betweenness centrality) during development.Main results.JNK inhibition increased MFR but reduced RP and FP, and decreased betweenness centrality and network modularity, particularly in DIV21. PI3K-Akt inhibition caused delayed effects: decreased MFR at DIV49 with increased RP, while enhancing network modularity. Developmental analysis revealed a transition from core-node-driven NBs (strong MFR-betweenness and BL-betweenness correlation at DIV14) to modularly organized NBs (strong BL-modularity and MFR-modularity correlation at DIV49), with pathway inhibitors differentially altering these relationships.Significance.Our findings demonstrate that JNK and PI3K-Akt pathways play distinct temporal roles in regulating NBs dynamics and network organization. JNK signaling is crucial for maintaining early core-node functionality, whereas PI3K-Akt signaling promotes the development of mature modular architecture. Our findings enhance the understanding of how molecular signaling influences neuronal network dynamics, contributing to a broader framework for studying neurodevelopmental principles.

抑制JNK和PI3K-Akt信号通路改变了神经网络的自发网络爆发和发育轨迹。
目的:自发网络爆发(NBs)是神经回路发育的关键,影响突触发生和功能组织。虽然已知JNK和PI3K-Akt信号通路调节突触可塑性,但它们在调控NBs动力学和功能网络组织中的具体作用仍知之甚少。本研究探讨了JNK和PI3K-Akt信号在调节神经网络自发NBs动态和网络组织中的作用。方法:利用培养皮层神经元(DIV14-49)的纵向微电极阵列(MEA)记录,我们从药理学上抑制了JNK (SP600125, JNK- in -8)和PI3K-Akt (LY294002, GDC-0941)通路。我们定量分析了NBs谱(最大发射速率/MFR、爆发长度/BL、上升相/RP)和功能网络特性(模块化、中间中心性)。主要结果:JNK抑制增加了MFR,降低了RP和FP,降低了中间中心性和网络模块化,特别是在DIV21中。PI3K-Akt抑制导致延迟效应:DIV49的MFR降低,RP增加,同时增强网络模块化。发育分析揭示了从核心节点驱动的NBs (DIV14处强mfr -间性和bl -间性相关)到模块化组织的NBs (DIV49处强bl -模块化和mfr -模块化相关)的转变,途径抑制剂不同程度地改变了这些关系。意义:我们的研究结果表明,JNK和PI3K-Akt通路在调节NBs动态和网络组织方面发挥了不同的时间作用。JNK信号对于维持早期核心节点功能至关重要,而PI3K-Akt信号则促进成熟模块化架构的发展。我们的发现增强了对分子信号如何影响神经网络动力学的理解,有助于研究神经发育原理的更广泛框架。 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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