Brain iron toxicity: Differential responses of astrocytes, neurons, and endothelial cells

被引:181
作者
Gaasch, Julie A.
Lockman, Paul R.
Geldenhuys, Werner J.
Allen, David D.
Van der Schyf, Cornelis J.
机构
[1] Northeastern Ohio Univ Coll Med & Pharm, Dept Pharmaceut Sci, Rootstown, OH 44272 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Sch Pharm, Dept Pharmaceut Sci, Amarillo, TX 79106 USA
关键词
brain iron toxicity; toxic mechanisms; neurodegeneration; neuron; astrocyte; endothelial cell;
D O I
10.1007/s11064-007-9290-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Iron accumulation or iron overload in brain is commonly associated with neurodegenerative disorders such as Parkinson's and Alzheimer's diseases, and also plays a role in cellular damage following hemorrhagic stroke and traumatic brain injury. Despite the brain's highly regulated system for iron utilization and metabolism, these disorders often present following disruptions within iron metabolic pathways. Such dysregulation allows saturation of proteins involved in iron transport and storage, and may cause an increase in free ferrous iron within brain leading to oxidative damage. Not only do astrocytes, neurons, and brain endothelial cells serve unique purposes within the brain, but their individual cell types are equipped with distinct protective mechanisms against iron-induced injury. This review evaluates iron metabolism within the brain under homeostatic and pathological conditions and focuses on the mechanism(s) of brain cellular iron toxicity and differential responses of astrocytes, neurons, and brain vascular endothelial cells to excessive free iron.
引用
收藏
页码:1196 / 1208
页数:13
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