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Neuroglia in Neurologic and Psychiatric Disorders. Part II / edited by Alexei Verkhratsky [and three others].
- Format:
- Book
- Series:
- Handbook of clinical neurology ; Volume 210.
- Handbook of Clinical Neurology Series ; Volume 210
- Language:
- English
- Subjects (All):
- Nervous system--Diseases.
- Nervous system.
- Neuroglia.
- Physical Description:
- 1 online resource (916 pages)
- Edition:
- First edition.
- Place of Publication:
- Amsterdam, Netherlands : Elsevier B.V., [2025]
- Summary:
- Neuroglia in Neurologic and Psychiatric Disorders, Part II discusses glia relative to neurologic and psychiatric disorders, emphasizing cross-disease-glial cell dysfunctions.Driven by advances in genetics, transcriptomics, electrophysiologic and imaging techniques, as well as by the increase in knowledge on neuropathologic features and underlying.
- Contents:
- Front Cover
- Neuroglia in Neurologic and Psychiatric Disorders, Part II
- Copyright
- Handbook of Clinical Neurology 3rd Series
- Foreword
- Preface
- Contributors
- Contents
- Part I: Glia in neurological disorders
- Chapter 1: General pathophysiology of neuroglia
- Neuroglia in Neuropathology: Historic Prelude
- Principles of Pathophysiology of Neuroglia
- Conclusions
- References
- Chapter 2: Neuroglia in neurodegeneration: Alzheimer, Parkinson, and Huntington disease
- Introduction: The Rise of Neurodegenerative Diseases
- Neuroglia in Alzheimer Disease
- Brief overview of AD pathogenesis and clinical presentation
- AD mouse models
- FAD-linked mutations recapitulate selected features of human pathology
- Are existing mouse models useful to study neuroglial AD-related pathology?
- Human iPSC-derived astrocytes in AD research
- Astrocytes in AD
- Morphologic changes: Reactivity and atrophy
- Functional significance of astrocytic changes in AD: Homeostatic failure and glial paralysis
- Calcium signaling in AD astrocytes
- Microglia in AD
- Oligodendrocytes in AD
- Myelin breakdown in AD
- Oligodendroglia malfunction in AD
- White matter abnormalities
- Neuroglia in PD
- Brief overview of PD pathogenesis and clinical picture
- PD animal models
- Chemical PD models
- Genetic models of PD
- iPSC-derived astrocytes in PD research
- Astrocytes in PD
- Microglia in PD
- Oligodendrocytes and myelin in PD
- Neuroglia in Huntington Disease
- Brief overview of HD pathogenesis and clinical picture
- HD animal models
- Neurotoxin-mediated striatal lesions
- Mouse HD models
- Astrocytes in HD
- Morphologic changes of astrocytes in HD
- Alterations of neurotransmitter homeostasis and K+ buffering
- Reduced BDNF release by HD astrocytes
- Microglia in HD
- Oligodendrocytes and myelin in HD
- Astrotaupathies.
- Conclusions
- Conflict of interest
- Funding
- Chapter 3: Neuroglia in neurodegeneration: Amyotrophic lateral sclerosis and frontotemporal dementia
- Introduction
- Amyotrophic lateral sclerosis
- Frontotemporal dementia
- Animal Models of ALS and FTD
- SOD1 rodent models of ALS
- TDP-43 rodent models of ALS and FTD
- Chromosome 9 open reading frame 72 (C9ORF72) mutant models of ALS and FTD
- TBK1 mutant models of ALS and FTD
- OPTN mutant models of ALS and FTD
- Glial Involvement in ALS/FTD: In Human Evidence
- Glial histopathology in ALS and FTD: Postmortem evidence
- In vivo imaging of glia in ALS and FTD
- The Role of Glia in ALS and FTD
- Astrocytes in ALS and FTD
- Microglia in ALS and FTD
- Oligodendrocytes in ALS and FTD
- Glia-immunity cross talk
- Glial Biomarkers in CSF and Blood
- Glial-Based Clinical Trials in ALS and FTD
- Chapter 4: Neuroglia in epilepsy
- Epilepsy
- Glia
- Astroglia
- Astroglia and the BBB in epilepsy
- The blood-brain barrier
- BBB perturbations
- Astroglial contribution to BBB perturbations
- Cellular and molecular changes to astroglia in epilepsy
- Astroglial contribution to water and K+ homeostasis
- Astroglial contribution to glutamate metabolism
- Glutamate transporters
- Glutamate receptors
- Glutamine synthetase
- Astroglial contribution to adenosine metabolism
- Astroglial gap junctions
- Astroglial contribution to immune and inflammatory functions in the context of epilepsy
- Astroglia act as antigen presenting cells in cerebral innate immunity
- Astroglia modulate cerebral adaptive immunity through cytokine and chemokine secretion
- Microglia
- Oligodendroglia
- Demyelination and epilepsy
- Cellular and molecular changes to oligodendroglia in epilepsy
- Potential Glial Therapeutic Targets
- References.
- Chapter 5: Neuroglia pathology in genetic and epigenetic disorders of the central nervous system
- MicroRNAs of Individual Glial Cells
- Examples of Genetic/Metabolic Diseases in Which Glial Cells Are Altered
- Agenesis of the corpus callosum
- Alexander disease
- Rett syndrome
- Fragile-X syndrome
- Aicardi-Goutières syndrome
- Down syndrome
- Fetal alcohol spectrum disorder
- Other Neuropathological Features That Involve Glial Cells
- Satellitosis
- α-B-crystallin as a glial marker of epileptic foci
- Loss of subpial granular glial layer of Brun
- Fetal astrocytic synthesis of keratan sulfate to guide axonal projections and insulate fascicles
- Acknowledgments
- Ethics committee approval
- Disclosures
- Chapter 6: Neuroglia in stroke
- Historic Prelude: From Hippocratic Apoplexy to Stroke
- Stroke: General Remarks
- Loss of Ion, Water, and Metabolic Homeostasis in the Ischemic Core and Penumbra
- Astrocytes in Stroke: Neuroprotection and Reactive Astrogliosis
- Astrocytic protection of neurons
- Astrocytic perilesional limitans border formation around fibrotic scar tissue
- Neuroglia and Brain-Wide Poststroke Pathology
- Oligodendrocytes and White Matter Stroke
- Microglia in Stroke
- Chapter 7: Unraveling the complexity of microglial responses in traumatic brain and spinal cord injury
- Origin and Function of Microglia
- Microglia in the Injured CNS: Primed for Immune Dysfunction and Chronic Neuroinflammation
- Identification of Novel Microglial Phenotypic States in CNS Injury States
- Microglia as a Therapeutic Target in TBI
- Could Microglial Elimination or Forced Turnover in the Injured Brain be Neuroprotective for TBI?
- Understanding Microglia Responses in Large Animal Models of TBI.
- Microglia in Human TBI: What Is the Current Evidence of Their Phenotypic and Functional Roles?
- The Therapeutic Potential of Targeting Microglia Responses in SCI
- Conclusion
- Chapter 8: Astrocytes and microglia in multiple sclerosis and neuromyelitis optica
- Historic Prelude
- Overview of Multiple Sclerosis and Neuromyelitis Optica
- Overview of Neuroglia in the Context of MS and NMO
- Microglia in Multiple Sclerosis
- Microglial phenotypes
- Microglia contribution to pathogenesis of multiple sclerosis
- Astrocytes in Multiple Sclerosis
- Cross Talk Between Astrocytes and Microglia
- Neurodegeneration as a Feature of MS: Role for Neuroglia
- Neuroglia as a Therapeutic Target in Multiple Sclerosis
- Targeting microglia
- Targeting astrocytes
- Neuroglia in NMO
- Astrocytes
- Interaction of microglia and astrocytes with immune cells
- Interaction of microglia and astrocytes with brain resident cells
- Neuroglia as a Therapeutic Target in NMO
- Chapter 9: Neuroglia in autoimmune encephalitis
- Autoimmune GFAP astrocytopathy
- Oligodendrocytes
- MOG ab-associated AE
- Conclusions and Future Perspectives
- Chapter 10: Neuroglia in leukodystrophies
- Astroglial Leukodystrophies
- Vanishing white matter disease
- Histopathologic features of VWM astrocytes
- Relating astrocytic malfunction to the pathologies of other cells
- Megalencephalic leukoencephalopathy with subcortical cysts
- Loss of function of astrocytes in MLC
- Effects of MLC1/GlialCAM mutations on astrocyte function
- Role of astrocyte malfunction in oligodendrocytes and myelin pathology in MLC
- Aicardi-Goutières syndrome.
- Genetic Etiology, Molecular Pathogenesis, and Genotype-Phenotype Correlation
- Oligodendroglial Leukodystrophies
- Krabbe disease or globoid cell leukodystrophy
- Adult-onset autosomal dominant leukodystrophy
- Metachromatic leukodystrophy
- Canavan disease
- Pelizaeus-Merzbacher disease
- Hypomyelination with atrophy of basal ganglia and cerebellum
- Microglial Leukodystrophies
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy or Nasu-Hakola disease
- Hereditary adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- Acknowledgment
- Chapter 11: Reciprocal interactions between glioma and tissue-resident cells fueling tumor progression
- TAM-Glioma Cell Interactions
- Soluble Factors Mediating TAM-Glioma Cross Talk
- Chemokines
- Cytokines
- Neurotrophic factors
- miRNAs
- Oncometabolite D-2HG
- Modulation of the extracellular matrix
- Contributions of TAM-Glioma Interactions for Tumor Behavior
- Impact of glioma cells on TAM spatial organization
- Impact of glioma cells on TAM polarization
- Glioma cells drive the metabolic reprogramming of TAMs
- Impact of TAMs on tumor growth
- Impact of TAMs on tumor migration and invasion
- Neuron-Glioma Interactions
- Neuronal activity promotes tumor growth while glioma cells affect local neuronal network activities
- Synaptic influences on glioma cells
- Glutamatergic signaling and glioma excitatory drive
- GABAergic signaling and chloride regulation in gliomas
- Concluding remarks
- Chapter 12: Neuroglia in hepatic encephalopathy
- Hepatic Encephalopathy: Basic Information
- Types of HE
- Causes
- Symptoms
- Experimental Models
- Alzheimer II Astrocytes: The Response of Astrocytes to Chronic HE
- Metabolic Remodeling of Astrocytes at the Onset of ALF.
- Astrocytic Impact on the Excitation/Inhibition Balance.
- Notes:
- Includes bibliographical references and index.
- Description based on publisher supplied metadata and other sources.
- Description based on print version record.
- ISBN:
- 9780443191039
- 0443191034
- 9780443191022
- 0443191026
- OCLC:
- 1513305873
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