Alexei Verkhratsky和Arthur M.Butt的《神经胶质细胞:功能和病理学》。

IF 5.6 2区 医学 Q1 PHYSIOLOGY Acta Physiologica Pub Date : 2023-08-22 DOI:10.1111/apha.14033
Tibor Harkany, Tomas Hökfelt
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We could not be more wrong and on an arduous journey to fundamentally misinterpret brain operations if holding onto these views. It is time to acknowledge the contribution of other cell types, cumulatively termed “neuroglia,” with astroglia, oligodendroglia, and microglia being present in the central nervous system alone. Adding Schwann cells, satellite glia, enteric glia, and glial cells of sensory organs to this list is a thrilling reminder that an amazing variety of glial cell types not only exists at around 1:1 ratio but works in unison in the human nervous systems to allow it to reach its computational, intellectual, and emotional power that makes us unique.</p><p>“Would you know a renown ‘glioscientist’ as if a neuroscientist?” For many, this could be an unexpectedly challenging question still. Here, we introduce <b>Alexei Verkhratsky</b> and <b>Arthur M. Butt</b> as two of the most eminent glia biologists of our time whose new book, titled “<b>Neuroglia: Function and Pathology</b>” is a wonderfully illustrated, comprehensive, thematic, and insightful account of the vast knowledge that has accumulated on glial cells of both the central and peripheral nervous systems over the past ~150 years. This book, the newest in a series of compendia on glial cells,<span><sup>1-4</sup></span> is educational for it systematically summarizing the origins, development, anatomy, molecular make-up, membrane biophysics, cellular interactions, and functions in relation to nerve cells and the broader brain homeostasis of each major glial cell type. Yet, it is an enticing read that also answers many unexpected questions ranging from the history of neuroscience (e.g., “do you know who coined the word astrocyte?”) to debunking some of the most pressing dogmas, like the number of neurons versus other cells in the brain. To this point, and using even evolutionary biology, a ~ 1:1 neuron: astrocyte ratio is formulated, which could work well if one considers that each neuron could have its “personal” caretaker, which supports, interacts, facilitates, removes waste, and even protects against disease and demise.</p><p><b>Neuroglia: Function and Pathology</b> starts with a historical account of discoveries that shaped this field, continues with the in-depth narration of neuroglia physiology, and seamlessly flows to the detailed description of the defining roles of neuroglia in brain diseases. Its part on physiology embraces all types of glia, be these either central or peripheral, and provides an exciting picture of these highly heterogeneous cells in form and function: It goes on to highlight that the ability of constant change amongst glia provides the basis of lifelong adaptation of the nervous system. On astrocytes, we learn that learning, memory, or neural plasticity, phenomena that are commonly assigned to neurons, simply cannot take place without them. Likewise, it is sobering to realize that neurons are incapable of producing their acting tools, the two major amino acid neurotransmitters (whether glutamate or GABA) without astrocytes supplying them with glutamine, the obligatory precursor of both chemical messengers. Similarly, astrocytes support synaptogenesis and synapse integrity. When this function fails, synaptic plasticity is eliminated. On microglia, the concept of synapse turnover is exemplified, which is the dynamic cycle of synapses being born, maintained if used, and then removed. If synaptic pruning by microglia is affected, then the neurocircuits neither develop nor function properly. Instead, the brain consumes massive amounts of excess energy, the production of which is inevitably associated with oxidative stress. And astrocytes are the foremost cell type to protect against oxidative stress by producing the bulk of glutathione, its scavenger.</p><p>Glutamate, however powerful as an excitatory neurotransmitter, is even more powerful as a natural poison that kills by producing a state of excitotoxicity for neurons. It is therefore not entirely unexpected that silencing glutamate clearance by astrocytes effectively tarnishes the brain. This and many similar fundamental homeostatic actions make neuroglia central to neuropathology: every disease is a homeostatic challenge. When homeostatic cells of the nervous system cannot meet a challenge, then the nervous system cannot survive. Despite the “neurocentric” views of modern-day neurology, this book reinforces the observation that neuroglia defines neuronal survival, neuronal protection, postlesion regeneration, and tissue rehabilitation. In other words, <i>Verkratsky</i> and <i>Butt</i> make it plain obvious that neuroglia defines the resilience of the nervous system. Accordingly, the decline of neuroglia accompanies aging, thus opening the gate for neurodegeneration, which limits cognitive longevity. It is commendable, therefore, that the second part of <b>Neuroglia: Function and Pathology</b> provides breathtaking insights into brain diseases, be these sporadic or inherited in origin, and includes pathological aging/neurodegeneration, mental illnesses, neurodevelopmental disorders, toxic encephalopathies, pain, viral infections, and cancer, to contextualize all that is said about the anatomy and function of glial cells populating the brain, as well as the peripheral nervous system.</p><p>This new book shall undoubtedly find its way onto the bookshelves of the researchers working on glia biology because of its attention to detail, and depth of insight. 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We could not be more wrong and on an arduous journey to fundamentally misinterpret brain operations if holding onto these views. It is time to acknowledge the contribution of other cell types, cumulatively termed “neuroglia,” with astroglia, oligodendroglia, and microglia being present in the central nervous system alone. Adding Schwann cells, satellite glia, enteric glia, and glial cells of sensory organs to this list is a thrilling reminder that an amazing variety of glial cell types not only exists at around 1:1 ratio but works in unison in the human nervous systems to allow it to reach its computational, intellectual, and emotional power that makes us unique.</p><p>“Would you know a renown ‘glioscientist’ as if a neuroscientist?” For many, this could be an unexpectedly challenging question still. Here, we introduce <b>Alexei Verkhratsky</b> and <b>Arthur M. Butt</b> as two of the most eminent glia biologists of our time whose new book, titled “<b>Neuroglia: Function and Pathology</b>” is a wonderfully illustrated, comprehensive, thematic, and insightful account of the vast knowledge that has accumulated on glial cells of both the central and peripheral nervous systems over the past ~150 years. This book, the newest in a series of compendia on glial cells,<span><sup>1-4</sup></span> is educational for it systematically summarizing the origins, development, anatomy, molecular make-up, membrane biophysics, cellular interactions, and functions in relation to nerve cells and the broader brain homeostasis of each major glial cell type. Yet, it is an enticing read that also answers many unexpected questions ranging from the history of neuroscience (e.g., “do you know who coined the word astrocyte?”) to debunking some of the most pressing dogmas, like the number of neurons versus other cells in the brain. To this point, and using even evolutionary biology, a ~ 1:1 neuron: astrocyte ratio is formulated, which could work well if one considers that each neuron could have its “personal” caretaker, which supports, interacts, facilitates, removes waste, and even protects against disease and demise.</p><p><b>Neuroglia: Function and Pathology</b> starts with a historical account of discoveries that shaped this field, continues with the in-depth narration of neuroglia physiology, and seamlessly flows to the detailed description of the defining roles of neuroglia in brain diseases. Its part on physiology embraces all types of glia, be these either central or peripheral, and provides an exciting picture of these highly heterogeneous cells in form and function: It goes on to highlight that the ability of constant change amongst glia provides the basis of lifelong adaptation of the nervous system. 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引用次数: 0

摘要

“神经胶质细胞在大脑中支持神经元”是神经科学家定期向未来几代神经生物学家讲授的老生常谈之一。在神经科学主题课程中,对神经胶质生理学和病理生物学的详细见解通常被忽视。事实上,神经科学领域的经典偏见来自于“neuro”这个词本身。一般的想法认为,当一个人可以操纵特定的神经元亚型,这些神经元亚型可能是由几个分子的信号以毫秒级的化学精度或光来区分的,并从实验生物体(无论是无脊椎动物还是脊椎动物)那里得到行为反应时,那么仅神经元就足以组织大脑的输出。如果我们坚持这些观点,我们就大错特错了,从根本上误解了大脑的运作,这是一段艰难的旅程。是时候承认其他细胞类型的贡献了,它们累积起来被称为“神经胶质细胞”,星形胶质细胞、少突胶质细胞和小胶质细胞仅存在于中枢神经系统中。将雪旺细胞、卫星神经胶质细胞、肠神经胶质细胞和感觉器官的神经胶质细胞添加到这个列表中,这令人兴奋地提醒我们,各种各样的神经胶质细胞类型不仅以1:1的比例存在,而且在人类神经系统中协同工作,使其达到其计算、智力和情感的能力,使我们与众不同。“你会把一个著名的‘神经胶质科学家’当作一个神经科学家来认识吗?”对许多人来说,这可能仍然是一个出乎意料的具有挑战性的问题。在这里,我们介绍Alexei Verkhratsky和Arthur M. Butt这两位当代最杰出的神经胶质生物学家,他们的新书《神经胶质细胞:功能和病理学》对过去150年来中枢和周围神经系统胶质细胞积累的大量知识进行了精彩的阐述、全面、主题和深刻的描述。这本书,最新的一系列纲目胶质细胞,1-4是有教育意义的,它系统地总结了起源,发展,解剖,分子组成,膜生物物理学,细胞相互作用,以及与神经细胞和每一个主要胶质细胞类型的更广泛的大脑稳态相关的功能。然而,这本书也回答了许多意想不到的问题,从神经科学的历史(例如,“你知道谁创造了星形胶质细胞这个词吗?”)到揭露一些最紧迫的教条,比如神经元的数量与大脑中其他细胞的数量之比。在这一点上,甚至使用进化生物学,一个约1:1的神经元:星形胶质细胞的比例被制定出来,如果一个人考虑到每个神经元都有它的“个人”看护人,它可以支持,相互作用,促进,清除废物,甚至保护免受疾病和死亡。《神经胶质:功能与病理学》从塑造这一领域的发现的历史叙述开始,继续深入叙述神经胶质生理学,并无缝地流向神经胶质在脑部疾病中的定义角色的详细描述。它在生理学上的作用涵盖了所有类型的胶质细胞,无论是中枢的还是外周的,并提供了这些高度异质细胞在形式和功能上的令人兴奋的画面:它继续强调胶质细胞之间不断变化的能力为神经系统的终身适应提供了基础。在星形胶质细胞上,我们了解到学习、记忆或神经可塑性,这些通常被分配给神经元的现象,如果没有它们就不可能发生。同样,我们清醒地认识到,如果没有星形胶质细胞为神经元提供谷氨酰胺(这两种化学信使的必要前体),神经元就无法产生它们的作用工具,即两种主要的氨基酸神经递质(无论是谷氨酸还是GABA)。同样,星形胶质细胞支持突触发生和突触完整性。当这个功能失效时,突触的可塑性就被消除了。在小胶质细胞中,突触更替的概念得到了例证,这是突触诞生、使用时维持、然后移除的动态循环。如果小胶质细胞的突触修剪受到影响,那么神经回路既不能发育也不能正常运作。相反,大脑消耗了大量多余的能量,这些能量的产生不可避免地与氧化应激有关。星形胶质细胞是最重要的细胞类型,通过产生大量的谷胱甘肽(它的清道夫)来防止氧化应激。谷氨酸,作为一种兴奋性神经递质,它是一种更强大的天然毒药,通过对神经元产生兴奋性毒性状态而杀死细胞。因此,星形胶质细胞对谷氨酸清除的沉默有效地玷污了大脑,这并不完全出乎意料。这和许多类似的基本内平衡作用使神经胶质细胞成为神经病理学的中心:每一种疾病都是对内平衡的挑战。
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Neuroglia: Function and Pathology by Alexei Verkhratsky and Arthur M. Butt

“Glial cells are in the brain to support neurons” is one of the commonplaces taught at regular lectures by neuroscientists to future generations of neurobiologists. Never mind that detailed insights into glial physiology and pathobiology are usually neglected in thematic neuroscience curricula. Indeed, the classic bias in the field of neuroscience comes from the term “neuro” itself. General thinking dictates that when one can manipulate specific subtypes of neurons distinguished by a signature of probably a handful of molecules at millisecond precision chemically or by light, and receive a behavioral response from the experimental organism, be this invertebrate or vertebrate, then neurons alone shall be sufficient to organize the brain's output. We could not be more wrong and on an arduous journey to fundamentally misinterpret brain operations if holding onto these views. It is time to acknowledge the contribution of other cell types, cumulatively termed “neuroglia,” with astroglia, oligodendroglia, and microglia being present in the central nervous system alone. Adding Schwann cells, satellite glia, enteric glia, and glial cells of sensory organs to this list is a thrilling reminder that an amazing variety of glial cell types not only exists at around 1:1 ratio but works in unison in the human nervous systems to allow it to reach its computational, intellectual, and emotional power that makes us unique.

“Would you know a renown ‘glioscientist’ as if a neuroscientist?” For many, this could be an unexpectedly challenging question still. Here, we introduce Alexei Verkhratsky and Arthur M. Butt as two of the most eminent glia biologists of our time whose new book, titled “Neuroglia: Function and Pathology” is a wonderfully illustrated, comprehensive, thematic, and insightful account of the vast knowledge that has accumulated on glial cells of both the central and peripheral nervous systems over the past ~150 years. This book, the newest in a series of compendia on glial cells,1-4 is educational for it systematically summarizing the origins, development, anatomy, molecular make-up, membrane biophysics, cellular interactions, and functions in relation to nerve cells and the broader brain homeostasis of each major glial cell type. Yet, it is an enticing read that also answers many unexpected questions ranging from the history of neuroscience (e.g., “do you know who coined the word astrocyte?”) to debunking some of the most pressing dogmas, like the number of neurons versus other cells in the brain. To this point, and using even evolutionary biology, a ~ 1:1 neuron: astrocyte ratio is formulated, which could work well if one considers that each neuron could have its “personal” caretaker, which supports, interacts, facilitates, removes waste, and even protects against disease and demise.

Neuroglia: Function and Pathology starts with a historical account of discoveries that shaped this field, continues with the in-depth narration of neuroglia physiology, and seamlessly flows to the detailed description of the defining roles of neuroglia in brain diseases. Its part on physiology embraces all types of glia, be these either central or peripheral, and provides an exciting picture of these highly heterogeneous cells in form and function: It goes on to highlight that the ability of constant change amongst glia provides the basis of lifelong adaptation of the nervous system. On astrocytes, we learn that learning, memory, or neural plasticity, phenomena that are commonly assigned to neurons, simply cannot take place without them. Likewise, it is sobering to realize that neurons are incapable of producing their acting tools, the two major amino acid neurotransmitters (whether glutamate or GABA) without astrocytes supplying them with glutamine, the obligatory precursor of both chemical messengers. Similarly, astrocytes support synaptogenesis and synapse integrity. When this function fails, synaptic plasticity is eliminated. On microglia, the concept of synapse turnover is exemplified, which is the dynamic cycle of synapses being born, maintained if used, and then removed. If synaptic pruning by microglia is affected, then the neurocircuits neither develop nor function properly. Instead, the brain consumes massive amounts of excess energy, the production of which is inevitably associated with oxidative stress. And astrocytes are the foremost cell type to protect against oxidative stress by producing the bulk of glutathione, its scavenger.

Glutamate, however powerful as an excitatory neurotransmitter, is even more powerful as a natural poison that kills by producing a state of excitotoxicity for neurons. It is therefore not entirely unexpected that silencing glutamate clearance by astrocytes effectively tarnishes the brain. This and many similar fundamental homeostatic actions make neuroglia central to neuropathology: every disease is a homeostatic challenge. When homeostatic cells of the nervous system cannot meet a challenge, then the nervous system cannot survive. Despite the “neurocentric” views of modern-day neurology, this book reinforces the observation that neuroglia defines neuronal survival, neuronal protection, postlesion regeneration, and tissue rehabilitation. In other words, Verkratsky and Butt make it plain obvious that neuroglia defines the resilience of the nervous system. Accordingly, the decline of neuroglia accompanies aging, thus opening the gate for neurodegeneration, which limits cognitive longevity. It is commendable, therefore, that the second part of Neuroglia: Function and Pathology provides breathtaking insights into brain diseases, be these sporadic or inherited in origin, and includes pathological aging/neurodegeneration, mental illnesses, neurodevelopmental disorders, toxic encephalopathies, pain, viral infections, and cancer, to contextualize all that is said about the anatomy and function of glial cells populating the brain, as well as the peripheral nervous system.

This new book shall undoubtedly find its way onto the bookshelves of the researchers working on glia biology because of its attention to detail, and depth of insight. But it shall equally be sought after by students of all ages because of it being an entertaining read and an educational summary of digestible bouts of information for anyone who needs to look up a specific feature of a certain glial cell type. In the age of Google, this book will still stand firm because of its completeness, conceptualization, and being exceptionally well-referenced for all its facts and figures. Therefore, and regardless of using its paper print or online document version, we will certainly be among those relying on its vast content for our own work until the next iteration1-3 will come about.

Tibor Harkany and Tomas Hökfelt co-wrote this editorial.

This work was supported by the Swedish Research Council (2020-01688, T.Hö.; 2018-02838; T.Ha.); The Arvid Carlsson Foundation (T.Hö.), the Swedish Brain Foundation (Hjärnfonden, FO2020-0178, T.Ha.), the Novo Nordisk Foundation (NNF20OC0053667, T.Ha.), and the European Research Council (FOODFORLIFE, ERC-2020-AdG-101021016; T.Ha.).

There is no conflict of interest.

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来源期刊
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
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Correction to "Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease". Issue Information Impaired suppression of fatty acid release by insulin is a strong predictor of reduced whole-body insulin-mediated glucose uptake and skeletal muscle insulin receptor activation. Differential production of mitochondrial reactive oxygen species between mouse (Mus musculus) and crucian carp (Carassius carassius) A quantitative analysis of bestrophin 1 cellular localization in mouse cerebral cortex.
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