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小胶质细胞通过磷脂酰肌醇3激酶信号介导的神经炎症导致认知功能障碍。

Microglia-Mediated Neuroinflammation Through Phosphatidylinositol 3-Kinase Signaling Causes Cognitive Dysfunction.

作者信息

Maziz Mohammad Nazmul Hasan, Chakravarthi Srikumar, Aung Thidar, Htoo Phone Myint, Shwe Wana Hla, Gupalo Sergey, Udayah Manglesh Waran, Singh Hardev, Kabir Mohammed Shahjahan, Thangarajan Rajesh, Kodali Maheedhar

机构信息

School of Medicine, Perdana University, Damansara Heights, Kuala Lumpur 50490, Malaysia.

Faculty of Medicine, Nursing and Health Sciences, SEGi University, Kota Damansara Campus, Petaling Jaya 47810, Selangor, Malaysia.

出版信息

Int J Mol Sci. 2025 Jul 25;26(15):7212. doi: 10.3390/ijms26157212.

Abstract

Microglia, as the immune guardians of the central nervous system (CNS), have the ability to maintain neural homeostasis, respond to environmental changes, and remodel the synaptic landscape. However, persistent microglial activation can lead to chronic neuroinflammation, which can alter neuronal signaling pathways, resulting in accelerated cognitive decline. Phosphoinositol 3-kinase (PI3K) has emerged as a critical driver, connecting inflammation to neurodegeneration, serving as the nexus of numerous intracellular processes that govern microglial activation. This review focuses on the relationship between PI3K signaling and microglial activation, which might lead to cognitive impairment, inflammation, or even neurodegeneration. The review delves into the components of the PI3K signaling cascade, isoforms, and receptors of PI3K, as well as the downstream effects of PI3K signaling, including its effectors such as protein kinase B (Akt) and mammalian target of rapamycin (mTOR) and the negative regulator phosphatase and tensin homolog (PTEN). Experiments have shown that the overproduction of certain cytokines, coupled with abnormal oxidative stress, is a consequence of poor PI3K regulation, resulting in excessive synapse pruning and, consequently, impacting learning and memory functions. The review also highlights the implications of autonomously activated microglia exhibiting M1/M2 polarization driven by PI3K on hippocampal, cortical, and subcortical circuits. Conclusions from behavioral studies, electrophysiology, and neuroimaging linking cognitive performance and PI3K activity were evaluated, along with new approaches to therapy using selective inhibitors or gene editing. The review concludes by highlighting important knowledge gaps, including the specific effects of different isoforms, the risks associated with long-term pathway modulation, and the limitations of translational potential, underscoring the crucial role of PI3K in mitigating cognitive impairment driven by neuroinflammation.

摘要

小胶质细胞作为中枢神经系统(CNS)的免疫卫士,具有维持神经稳态、响应环境变化以及重塑突触格局的能力。然而,小胶质细胞的持续激活会导致慢性神经炎症,进而改变神经元信号通路,加速认知衰退。磷酸肌醇3激酶(PI3K)已成为将炎症与神经退行性变联系起来的关键驱动因素,是众多调控小胶质细胞激活的细胞内过程的枢纽。本综述聚焦于PI3K信号传导与小胶质细胞激活之间的关系,这可能导致认知障碍、炎症甚至神经退行性变。该综述深入探讨了PI3K信号级联的组成部分、PI3K的亚型和受体,以及PI3K信号的下游效应,包括其效应分子如蛋白激酶B(Akt)和雷帕霉素哺乳动物靶蛋白(mTOR)以及负调节因子磷酸酶和张力蛋白同源物(PTEN)。实验表明,某些细胞因子的过度产生,加上异常的氧化应激,是PI3K调控不佳的结果,导致过度的突触修剪,进而影响学习和记忆功能。该综述还强调了由PI3K驱动的自主激活的小胶质细胞表现出M1/M2极化对海马、皮质和皮质下回路的影响。评估了将认知表现与PI3K活性联系起来的行为研究、电生理学和神经影像学的结论,以及使用选择性抑制剂或基因编辑的新治疗方法。综述最后强调了重要的知识空白,包括不同亚型的具体作用、长期通路调节相关的风险以及转化潜力的局限性,强调了PI3K在减轻神经炎症驱动的认知障碍中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bb/12346505/1e63a0c5e010/ijms-26-07212-g001.jpg

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