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Psychiatric Implications of Genetic Variations in Oligodendrocytes: Insights from hiPSC Models
by
Pullano, Ilaria
, Monaco, Francesco
, Di Stefano, Valeria
, Steardo, Luca
, D’Angelo, Martina
in
Abnormalities
/ Biomarkers
/ Bipolar disorder
/ Brain
/ Brain research
/ Cell culture
/ Cell cycle
/ Development and progression
/ Gene expression
/ Genetic aspects
/ Genetic diversity
/ Genetic variation
/ Glial cells
/ Glial stem cells
/ Health aspects
/ Interneurons
/ Localization
/ Magnetic resonance imaging
/ Major depressive disorder
/ Mental depression
/ Mental disorders
/ Mutation
/ Myelination
/ Neural networks
/ neurodevelopment
/ Neuronal-glial interactions
/ Neurons
/ neuron–glia interaction
/ Neuroplasticity
/ oligodendrocyte precursor cells
/ Oligodendrocytes
/ Oligodendroglia
/ Parvalbumin
/ Pathogenesis
/ Pathology
/ Pathophysiology
/ Patients
/ Proteins
/ psychiatric disorders
/ Psychiatric research
/ Review
/ Risk factors
/ Schizophrenia
/ Synaptic plasticity
/ Therapeutic applications
/ Transcriptomics
2025
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Psychiatric Implications of Genetic Variations in Oligodendrocytes: Insights from hiPSC Models
by
Pullano, Ilaria
, Monaco, Francesco
, Di Stefano, Valeria
, Steardo, Luca
, D’Angelo, Martina
in
Abnormalities
/ Biomarkers
/ Bipolar disorder
/ Brain
/ Brain research
/ Cell culture
/ Cell cycle
/ Development and progression
/ Gene expression
/ Genetic aspects
/ Genetic diversity
/ Genetic variation
/ Glial cells
/ Glial stem cells
/ Health aspects
/ Interneurons
/ Localization
/ Magnetic resonance imaging
/ Major depressive disorder
/ Mental depression
/ Mental disorders
/ Mutation
/ Myelination
/ Neural networks
/ neurodevelopment
/ Neuronal-glial interactions
/ Neurons
/ neuron–glia interaction
/ Neuroplasticity
/ oligodendrocyte precursor cells
/ Oligodendrocytes
/ Oligodendroglia
/ Parvalbumin
/ Pathogenesis
/ Pathology
/ Pathophysiology
/ Patients
/ Proteins
/ psychiatric disorders
/ Psychiatric research
/ Review
/ Risk factors
/ Schizophrenia
/ Synaptic plasticity
/ Therapeutic applications
/ Transcriptomics
2025
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Do you wish to request the book?
Psychiatric Implications of Genetic Variations in Oligodendrocytes: Insights from hiPSC Models
by
Pullano, Ilaria
, Monaco, Francesco
, Di Stefano, Valeria
, Steardo, Luca
, D’Angelo, Martina
in
Abnormalities
/ Biomarkers
/ Bipolar disorder
/ Brain
/ Brain research
/ Cell culture
/ Cell cycle
/ Development and progression
/ Gene expression
/ Genetic aspects
/ Genetic diversity
/ Genetic variation
/ Glial cells
/ Glial stem cells
/ Health aspects
/ Interneurons
/ Localization
/ Magnetic resonance imaging
/ Major depressive disorder
/ Mental depression
/ Mental disorders
/ Mutation
/ Myelination
/ Neural networks
/ neurodevelopment
/ Neuronal-glial interactions
/ Neurons
/ neuron–glia interaction
/ Neuroplasticity
/ oligodendrocyte precursor cells
/ Oligodendrocytes
/ Oligodendroglia
/ Parvalbumin
/ Pathogenesis
/ Pathology
/ Pathophysiology
/ Patients
/ Proteins
/ psychiatric disorders
/ Psychiatric research
/ Review
/ Risk factors
/ Schizophrenia
/ Synaptic plasticity
/ Therapeutic applications
/ Transcriptomics
2025
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Psychiatric Implications of Genetic Variations in Oligodendrocytes: Insights from hiPSC Models
Journal Article
Psychiatric Implications of Genetic Variations in Oligodendrocytes: Insights from hiPSC Models
2025
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Overview
Oligodendrocyte precursor cells (OPCs) are a dynamic and heterogeneous population of glial cells essential for brain development and myelination. Beyond their well-established role in oligodendrogenesis, emerging evidence suggests that OPCs contribute to synaptic regulation, neuronal communication, and brain plasticity. Recent studies have increasingly implicated OPC dysfunction in the pathophysiology of psychiatric disorders, particularly schizophrenia (SCZ), bipolar disorder (BD), and major depressive disorder (MDD). This narrative review integrates clinical, genetic, transcriptomic, and histological findings to examine the role of OPC alterations in mental illnesses. In SCZ, OPC abnormalities predominantly affect myelination, but recent data also suggest deficits in non-canonical functions, including neuron–OPC communication. Findings in BD largely mirror those in SCZ, implying shared OPC-related mechanisms across these disorders. In contrast, OPC involvement in MDD appears more complex, with evidence supporting both myelination deficits and non-canonical dysfunctions, such as impaired neuro–glial interactions and perineuronal network alterations. The developmental timing of OPC dysfunction may represent a common denominator underlying psychiatric disorders, as early-life stress and neurodevelopmental disturbances have been linked to OPC impairments. Moreover, given the shared developmental origins of OPCs and parvalbumin-positive interneurons, disruptions in their mutual interactions may contribute to broader neural network dysregulation. Despite these insights, the field remains in its infancy. Future studies integrating independent human cohorts with robust preclinical models are needed to clarify the extent of OPC involvement in psychiatric pathophysiology. Understanding OPC dysfunction may reveal novel biomarkers and open new avenues for individualized therapeutic interventions and preventive strategies in mental health.
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