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Culturing Microglia from the Neonatal and Adult Central Nervous System
Published on: August 9, 2013
TRPM2 Channel in Microglia as a New Player in Neuroinflammation Associated With a Spectrum of Central Nervous System
Philippa Malko1, Sharifah A Syed Mortadza1,2, Joseph McWilliam1
1School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom.
Abstract:
Microglial cells in the central nervous system (CNS) are crucial in maintaining a healthy environment for neurons to function properly. However, aberrant microglial cell activation can lead to excessive generation of neurotoxic proinflammatory mediators and neuroinflammation, which represents a contributing factor in a wide spectrum of CNS pathologies, including ischemic stroke, traumatic brain damage, Alzheimer's disease, Parkinson's disease, multiple sclerosis, psychiatric disorders, autism spectrum disorders, and chronic neuropathic pain. Oxidative stress is a salient and common feature of these conditions and has been strongly implicated in microglial cell activation and neuroinflammation. The transient receptor potential melastatin-related 2 (TRPM2) channel, an oxidative stress-sensitive calcium-permeable cationic channel, is highly expressed in microglial cells. In this review, we examine the recent studies that provide evidence to support an important role for the TRPM2 channel, particularly TRPM2-mediated Ca2+ signaling, in mediating microglial cell activation, generation of proinflammatory mediators and neuroinflammation, which are of relevance to CNS pathologies. These findings lead to a growing interest in the TRPM2 channel, a new player in neuroinflammation, as a novel therapeutic target for CNS diseases.
Insights
The transient receptor potential melastatin-related 2 (TRPM2) channel in microglial cells drives neuroinflammation and CNS diseases. Targeting TRPM2 offers a new therapeutic strategy for neurological disorders.
Area of Science:
- Neuroscience
- Immunology
- Cell Biology
Background:
- Microglial cells are vital for CNS health but can cause neuroinflammation when activated.
- Neuroinflammation is linked to various CNS pathologies like stroke, Alzheimer's, and Parkinson's.
- Oxidative stress is a common factor in these diseases and microglial activation.
Purpose of the Study:
- To review the role of the TRPM2 channel in microglial activation and neuroinflammation.
- To explore TRPM2 as a potential therapeutic target for CNS diseases.
Main Methods:
- Review of recent studies on TRPM2 channel function in microglial cells.
- Analysis of TRPM2-mediated calcium signaling in neuroinflammation.
- Examination of TRPM2's involvement in CNS pathologies.
Main Results:
- TRPM2 channels are highly expressed in microglial cells and are sensitive to oxidative stress.
- TRPM2-mediated calcium signaling is crucial for microglial activation.
- This activation leads to the production of neurotoxic proinflammatory mediators.
Conclusions:
- TRPM2 channel activity significantly contributes to neuroinflammation in CNS diseases.
- TRPM2 represents a promising novel therapeutic target for treating neurological disorders.
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