Division of Life Science, The Hong Kong University of Science and Technology, China.
Molecular Neuroscience Center, The Hong Kong University of Science and Technology, China.
FEBS J. 2022 Apr;289(8):2202-2218. doi: 10.1111/febs.15878. Epub 2021 May 10.
In the adult hippocampus, synaptic plasticity is important for information processing, learning, and memory encoding. Astrocytes, the most common glial cells, play a pivotal role in the regulation of hippocampal synaptic plasticity. While astrocytes were initially described as a homogenous cell population, emerging evidence indicates that in the adult hippocampus, astrocytes are highly heterogeneous and can differentially respond to changes in neuronal activity in a subregion-dependent manner to actively modulate synaptic plasticity. In this review, we summarize how local neuronal activity changes regulate the interactions between astrocytes and synapses, either by modulating the secretion of gliotransmitters and synaptogenic proteins or via contact-mediated signaling pathways. In turn, these specific responses induced in astrocytes mediate the interactions between astrocytes and neurons, thus shaping synaptic communication in the adult hippocampus. Importantly, the activation of astrocytic signaling is required for memory performance including memory acquisition and recall. Meanwhile, the dysregulation of this signaling can cause hippocampal circuit dysfunction in pathological conditions, resulting in cognitive impairment and neurodegeneration. Indeed, reactive astrocytes, which have dysregulated signaling associated with memory, are induced in the brains of patients with Alzheimer's disease (AD) and transgenic mouse model of AD. Emerging technologies that can precisely manipulate and monitor astrocytic signaling in vivo enable the examination of the specific actions of astrocytes in response to neuronal activity changes as well as how they modulate synaptic connections and circuit activity. Such findings will clarify the roles of astrocytes in hippocampal synaptic plasticity and memory in health and disease.
在成年海马体中,突触可塑性对于信息处理、学习和记忆编码至关重要。星形胶质细胞是最常见的神经胶质细胞,在调节海马体突触可塑性方面发挥着关键作用。尽管星形胶质细胞最初被描述为均质细胞群体,但新出现的证据表明,在成年海马体中,星形胶质细胞高度异质,能够以亚区依赖的方式对神经元活动的变化做出不同的反应,从而主动调节突触可塑性。在这篇综述中,我们总结了局部神经元活动变化如何调节星形胶质细胞和突触之间的相互作用,这种调节既可以通过调节神经递质和突触发生蛋白的分泌来实现,也可以通过接触介导的信号通路来实现。反过来,星形胶质细胞中诱导的这些特定反应介导了星形胶质细胞和神经元之间的相互作用,从而塑造了成年海马体中的突触通讯。重要的是,星形胶质细胞信号的激活对于包括记忆获取和回忆在内的记忆表现是必需的。同时,这种信号的失调会导致病理性条件下海马体回路功能障碍,从而导致认知障碍和神经退行性变。事实上,阿尔茨海默病(AD)患者和 AD 转基因小鼠模型的大脑中存在与记忆相关的信号失调的反应性星形胶质细胞。新兴的技术可以精确地在体内操纵和监测星形胶质细胞信号,从而可以检查星形胶质细胞对神经元活动变化的反应以及它们如何调节突触连接和电路活动的具体作用。这些发现将阐明星形胶质细胞在健康和疾病状态下海马体突触可塑性和记忆中的作用。