神经保护
程序性细胞死亡
吞噬作用
神经毒性
神经科学
小胶质细胞
神经退行性变
神经元
转基因小鼠
自噬
生物
细胞生物学
转基因
细胞凋亡
医学
病理
免疫学
炎症
毒性
生物化学
内科学
基因
疾病
作者
Trevor Balena,Kevin J. Staley
标识
DOI:10.1177/10738584241282632
摘要
Fatally injured neurons may necrose and rupture immediately, or they may initiate a programmed cell death pathway and then wait for microglial phagocytosis. Biochemical and histopathologic assays of neuronal death assess the numbers of neurons awaiting phagocytosis at a particular time point after injury. This number varies with the fraction of neurons that have necrosed vs initiated programmed cell death, the time elapsed since injury, the rate of phagocytosis, and the assay’s ability to detect neurons at different stages of programmed cell death. Many of these variables can be altered by putatively neurotoxic and neuroprotective interventions independent of the effects on neuronal death. This complicates analyses of neurotoxicity and neuroprotection and has likely contributed to difficulties with clinical translation of neuroprotective strategies after brain injury. Time-resolved assays of neuronal health, such as ongoing expression of transgenic fluorescent proteins, are a useful means of avoiding these problems.
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