Oligodendrocytes as A New Therapeutic Target in Schizophrenia: From Histopathological Findings to Neuron-Oligodendrocyte Interaction

Autor: Mikael Simons, Ludovico Cantuti-Castelvetri, Florian Raabe, Moritz J. Rossner, Andrea Schmitt, Lenka Slapakova, Peter Falkai
Jazyk: angličtina
Rok vydání: 2019
Předmět:
cognition
0301 basic medicine
drug therapy [Cognitive Dysfunction]
Postmortem studies
Interneuron
pathology [Cognitive Dysfunction]
drug therapy [Schizophrenia]
oligodendrocytes
drug effects [Oligodendroglia]
Review
interneuron
Disease
Biology
metabolism [Oligodendroglia]
03 medical and health sciences
Myelin
metabolism [Cognitive Dysfunction]
0302 clinical medicine
ddc:570
medicine
Animals
Humans
drug effects [Neurons]
pathology [Neurons]
Cognitive Dysfunction
Induced pluripotent stem cell
pathology [Schizophrenia]
Neurons
treatment
Cognition
Cell Differentiation
General Medicine
Oligodendrocyte
schizophrenia
myelin
Oligodendroglia
030104 developmental biology
medicine.anatomical_structure
metabolism [Neurons]
pathology [Oligodendroglia]
metabolism [Schizophrenia]
Neuron
pluripotent stem cells
Neuroscience
030217 neurology & neurosurgery
Zdroj: Cells 8(12), 1496-(2019). doi:10.3390/cells8121496
Cells
DOI: 10.3390/cells8121496
Popis: Imaging and postmortem studies have revealed disturbed oligodendroglia-related processes in patients with schizophrenia and provided much evidence for disturbed myelination, irregular gene expression, and altered numbers of oligodendrocytes in the brains of schizophrenia patients. Oligodendrocyte deficits in schizophrenia might be a result of failed maturation and disturbed regeneration and may underlie the cognitive deficits of the disease, which are strongly associated with impaired long-term outcome. Cognition depends on the coordinated activity of neurons and interneurons and intact connectivity. Oligodendrocyte precursors form a synaptic network with parvalbuminergic interneurons, and disturbed crosstalk between these cells may be a cellular basis of pathology in schizophrenia. However, very little is known about the exact axon-glial cellular and molecular processes that may be disturbed in schizophrenia. Until now, investigations were restricted to peripheral tissues, such as blood, correlative imaging studies, genetics, and molecular and histological analyses of postmortem brain samples. The advent of human-induced pluripotent stem cells (hiPSCs) will enable functional analysis in patient-derived living cells and holds great potential for understanding the molecular mechanisms of disturbed oligodendroglial function in schizophrenia. Targeting such mechanisms may contribute to new treatment strategies for previously treatment-resistant cognitive symptoms.
Databáze: OpenAIRE