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TREM1-Microglia crosstalk: Neurocognitive disorders
Huashan Li1, Wanqiu Yu2, Xue Zheng3
1Department of Anesthesiology, Affiliated Hospital of Zunyi Medical University, Zunyi 563003, China; Department of Anesthesiology, Zunyi Maternal And Child Health Care Hospital, Zunyi 563000, China.
Triggering receptor expressed on myeloid cells 1 (TREM1) on microglia drives inflammation in neurocognitive disorders. Upregulation of TREM1 exacerbates microglial activation, contributing to cognitive impairment.
Area of Science:
- Neuroscience
- Immunology
- Pathology
Background:
- Neurocognitive Disorders (NCDs) impair cognitive functions like memory and learning.
- Microglial inflammatory activation in the hippocampus is implicated in NCD pathogenesis.
- Pattern-recognition receptors on microglia play a role in CNS inflammation.
Purpose of the Study:
- To review the role of Triggering Receptor Expressed on Myeloid cells 1 (TREM1) in neurocognitive disorders.
- To elucidate TREM1's function in microglial activation and inflammation within the CNS.
Main Methods:
- Literature review of studies on TREM1, microglia, and neurocognitive disorders.
- Analysis of TREM1 expression and function in response to CNS injury and inflammation.
Main Results:
- TREM1 is upregulated on microglia during CNS injury and inflammation.
- TREM1 amplifies inflammatory responses, promoting microglial activation.
- Upregulated TREM1 contributes to the development of neurocognitive disorders.
Conclusions:
- TREM1 is a critical receptor in microglia-mediated inflammation.
- Targeting TREM1 may offer a therapeutic strategy for neurocognitive disorders.
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