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Generation of Human Neurons and Oligodendrocytes from Pluripotent Stem Cells for Modeling Neuron-Oligodendrocyte Interactions
Published on: November 9, 2020
Varicella zoster virus (VZV)-human neuron interaction.
Nicholas L Baird1, Xiaoli Yu, Randall J Cohrs
1Departments of Neurology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Varicella zoster virus (VZV) establishes lifelong latency in neurons. Understanding VZV-neuron interactions is key to preventing reactivation, which causes shingles and neurological complications.
Area of Science:
- Virology
- Neuroscience
- Immunology
Background:
- Varicella zoster virus (VZV) is a human herpesvirus causing chickenpox and shingles.
- VZV establishes lifelong latency in ganglionic neurons.
- Reactivation of VZV leads to neurological and ocular complications, but triggers remain unknown.
Purpose of the Study:
- To investigate the VZV-neuron interaction during latency and reactivation.
- To identify molecular triggers for VZV reactivation.
- To develop in vitro systems for studying VZV latency and reactivation.
Main Methods:
- Infection of human neurons in SCID mice.
- Infection of human stem cells, including induced pluripotent stem cells.
- Infection of human neural progenitor tissue-like assemblies.
- Analysis of VZV-infected, terminally differentiated human neurons.
Main Results:
- VZV infection of human neurons and stem cells can be established without cytopathic effects.
- Recent studies show promise in modeling VZV infection in vitro.
- Further analysis of pure, differentiated neurons is needed to understand reactivation.
Conclusions:
- Current in vitro systems are advancing the study of VZV latency and reactivation.
- Understanding the VZV-neuron interaction is crucial for preventing shingles and associated neurological disorders.
- Further research using advanced neuronal models is required to elucidate VZV reactivation mechanisms.
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