José Duarte Dias, João Filipe Viana, Luís Samuel Alves, Alexandra Veiga, Bruna Matos, João Luís Machado, João Filipe Oliveira
{"title":"星战:星形胶质细胞代谢谷氨酸受体 5 的回归。","authors":"José Duarte Dias, João Filipe Viana, Luís Samuel Alves, Alexandra Veiga, Bruna Matos, João Luís Machado, João Filipe Oliveira","doi":"10.1113/JP288403","DOIUrl":null,"url":null,"abstract":"<p><p>In the brain, astrocytes express glutamate receptors to detect glutamatergic signalling at synapses. Numerous studies have been conducted to characterize the types and levels of receptor expression, their physiological properties and functional roles. The metabotropic glutamate receptor 5 (mGluR5) is particularly noteworthy. Although it is described as the only classical excitatory metabotropic receptor expressed by astrocytes, recent studies indicate that its expression levels are lower in adulthood compared to the postnatal period. Nevertheless, mGluR5 activation in adulthood remains sufficient to induce robust astrocytic activity. To resolve these seemingly contradictory findings, we review the current understanding of the physiology of astrocytic mGluR5, its expression level variations throughout life, activation consequences and functional roles. In summary, astrocytes maintain sufficient functional levels of mGluR5 throughout life, activation of which triggers Ca<sup>2+</sup> activity. This activation triggers intracellular processes to modulate synaptic and circuit function, which is relevant due to the extensive glutamatergic signalling in the brain. Moreover, most studies on mGluR5 activation in astrocytes have been conducted using cultured astrocytes or acute brain slices from young rodents. Therefore, further research is needed to investigate the roles of mGluR5 in adulthood, not only in synaptic function but also in behavioural processing. Understanding the regulation of mGluR5 expression levels, physiological properties and functional consequences during adulthood is crucial for fully understanding glutamatergic signalling in brain circuits and its role in the pathophysiology of various neurobiological diseases.</p>","PeriodicalId":50088,"journal":{"name":"Journal of Physiology-London","volume":" ","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"AstroWars: the return of the astrocytic metabotropic glutamate receptor 5.\",\"authors\":\"José Duarte Dias, João Filipe Viana, Luís Samuel Alves, Alexandra Veiga, Bruna Matos, João Luís Machado, João Filipe Oliveira\",\"doi\":\"10.1113/JP288403\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In the brain, astrocytes express glutamate receptors to detect glutamatergic signalling at synapses. Numerous studies have been conducted to characterize the types and levels of receptor expression, their physiological properties and functional roles. The metabotropic glutamate receptor 5 (mGluR5) is particularly noteworthy. Although it is described as the only classical excitatory metabotropic receptor expressed by astrocytes, recent studies indicate that its expression levels are lower in adulthood compared to the postnatal period. Nevertheless, mGluR5 activation in adulthood remains sufficient to induce robust astrocytic activity. To resolve these seemingly contradictory findings, we review the current understanding of the physiology of astrocytic mGluR5, its expression level variations throughout life, activation consequences and functional roles. In summary, astrocytes maintain sufficient functional levels of mGluR5 throughout life, activation of which triggers Ca<sup>2+</sup> activity. This activation triggers intracellular processes to modulate synaptic and circuit function, which is relevant due to the extensive glutamatergic signalling in the brain. Moreover, most studies on mGluR5 activation in astrocytes have been conducted using cultured astrocytes or acute brain slices from young rodents. Therefore, further research is needed to investigate the roles of mGluR5 in adulthood, not only in synaptic function but also in behavioural processing. Understanding the regulation of mGluR5 expression levels, physiological properties and functional consequences during adulthood is crucial for fully understanding glutamatergic signalling in brain circuits and its role in the pathophysiology of various neurobiological diseases.</p>\",\"PeriodicalId\":50088,\"journal\":{\"name\":\"Journal of Physiology-London\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-04-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Physiology-London\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1113/JP288403\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Physiology-London","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1113/JP288403","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
AstroWars: the return of the astrocytic metabotropic glutamate receptor 5.
In the brain, astrocytes express glutamate receptors to detect glutamatergic signalling at synapses. Numerous studies have been conducted to characterize the types and levels of receptor expression, their physiological properties and functional roles. The metabotropic glutamate receptor 5 (mGluR5) is particularly noteworthy. Although it is described as the only classical excitatory metabotropic receptor expressed by astrocytes, recent studies indicate that its expression levels are lower in adulthood compared to the postnatal period. Nevertheless, mGluR5 activation in adulthood remains sufficient to induce robust astrocytic activity. To resolve these seemingly contradictory findings, we review the current understanding of the physiology of astrocytic mGluR5, its expression level variations throughout life, activation consequences and functional roles. In summary, astrocytes maintain sufficient functional levels of mGluR5 throughout life, activation of which triggers Ca2+ activity. This activation triggers intracellular processes to modulate synaptic and circuit function, which is relevant due to the extensive glutamatergic signalling in the brain. Moreover, most studies on mGluR5 activation in astrocytes have been conducted using cultured astrocytes or acute brain slices from young rodents. Therefore, further research is needed to investigate the roles of mGluR5 in adulthood, not only in synaptic function but also in behavioural processing. Understanding the regulation of mGluR5 expression levels, physiological properties and functional consequences during adulthood is crucial for fully understanding glutamatergic signalling in brain circuits and its role in the pathophysiology of various neurobiological diseases.
期刊介绍:
The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew.
The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.