小胶质细胞
神经炎症
医学
神经科学
神经影像学
疾病
机制(生物学)
可药性
生物信息学
炎症
精神科
免疫学
心理学
生物
病理
哲学
认识论
生物化学
基因
作者
Jatia Mills,Liliana Ladner,Eman Soliman,John Leonard,Paul D. Morton,Michelle H. Theus
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2022-10-25
卷期号:11 (21): 3364-3364
被引量:4
标识
DOI:10.3390/cells11213364
摘要
Neurological disorders are highly prevalent and often lead to chronic debilitating disease. Neuroinflammation is a major driver across the spectrum of disorders, and microglia are key mediators of this response, gaining wide acceptance as a druggable cell target. Moreover, clinical providers have limited ability to objectively quantify patient-specific changes in microglia status, which can be a predictor of illness and recovery. This necessitates the development of diagnostic biomarkers and imaging techniques to monitor microglia-mediated neuroinflammation in coordination with neurological outcomes. New insights into the polarization status of microglia have shed light on the regulation of disease progression and helped identify a modifiable target for therapeutics. Thus, the detection and monitoring of microglia activation through the inclusion of diagnostic biomarkers and imaging techniques will provide clinical tools to aid our understanding of the neurologic sequelae and improve long-term clinical care for patients. Recent achievements demonstrated by pre-clinical studies, using novel depletion and cell-targeted approaches as well as single-cell RNAseq, underscore the mechanistic players that coordinate microglial activation status and offer a future avenue for therapeutic intervention.
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