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P2X4 receptors expressed on microglial cells in post-ischemic inflammation of brain ischemic injury
Rui-Dong Cheng1, Jing-Jing Ren2, Yan-Yan Zhang3
1Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China.
Abstract:
Post-ischemic inflammation is an essential step in the progression of brain ischemia injury. P2X4 receptors are the predominant purinergic P2X receptor subtypes expressed on immune and neural cells. The subtype traffic between intracellular compartments and the plasma membrane form protein interactions with each other to regulate ATP-dependent signaling. The P2X4 receptors expressed on microglial cells have been reported to be involved in the inflammatory response of many central nervous system diseases. However, the mechanism that activates microglial cells and the role of P2X4 receptor expressed in microglial cells in the ischemic brain remains to be clarified. Here we provide a review for understanding and exploring converging lines of evidence for involvement of P2X4 receptors expressed on microglial cells in the post-ischemic inflammation in the brain ischemic injury.
Insights
Post-ischemic inflammation involves P2X4 receptors on microglial cells. This review explores their role in brain injury progression and inflammation, clarifying their activation mechanisms.
Area of Science:
- Neuroscience
- Immunology
- Cell Biology
Background:
- Post-ischemic inflammation is critical in brain ischemia injury progression.
- P2X4 receptors are key purinergic receptors on immune and neural cells, regulating ATP signaling.
- Microglial P2X4 receptors are implicated in central nervous system inflammatory diseases.
Purpose of the Study:
- To review and explore evidence for P2X4 receptor involvement in microglial cells during brain ischemia.
- To clarify the mechanisms of microglial activation and the role of P2X4 receptors in ischemic brain inflammation.
Main Methods:
- Literature review of existing research on P2X4 receptors and brain ischemia.
- Analysis of studies investigating microglial cell activation and inflammatory responses.
- Synthesis of evidence regarding P2X4 receptor function in post-ischemic inflammation.
Main Results:
- P2X4 receptors are predominantly expressed on microglial cells in the brain.
- These receptors traffic between intracellular compartments and the plasma membrane, interacting with other proteins.
- Evidence suggests a significant role for microglial P2X4 receptors in post-ischemic inflammation.
Conclusions:
- P2X4 receptors on microglial cells are crucial mediators of inflammation in brain ischemia.
- Further research is needed to fully elucidate microglial activation pathways and P2X4 receptor function in ischemic injury.
- Targeting microglial P2X4 receptors may offer therapeutic strategies for brain ischemia.
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