TRANSFERRIN-BOUND IRON;
DIVALENT METAL TRANSPORTER-1;
RAT-BRAIN;
MOLECULAR-MECHANISMS;
REGULATORY PROTEINS;
CEREBROSPINAL-FLUID;
PARKINSONS-DISEASE;
PHOSPHOLIPASE A(2);
ALZHEIMER-DISEASE;
ION TRANSPORTER;
D O I:
10.4155/FMC.09.140
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Trace metals, such as iron, copper, zinc, manganese and cobalt, are essential cofactors for many cellular enzymes. Extensive research on iron, the most abundant transition metal in biology, has contributed to an increased understanding of the molecular machinery involved in maintaining its homeostasis in mammalian peripheral tissues. However, the cellular and intercellular iron-transport mechanisms in the CNS are still poorly understood. Accumulating evidence suggests that impaired iron metabolism is an initial cause of neurodegeneration and several common genetic and sporadic neurodegenerative disorders have been proposed as being associated with dysregulated CNS iron homeostasis. This review aims to provide a summary of the molecular mechanisms of brain iron transport. Our discussion is focused on iron transport across endothelial cells of the blood brain barrier and within the neuro- and glial-vascular units of the brain, with the aim of revealing novel therapeutic targets for neurodegenerative and CNS disorders.
机构:
Univ Vita Salute San Raffaele, Sch Med, I-20132 Milan, Italy
Ist Sci San Raffaele, Div Neurosci, I-20132 Milan, ItalyUniv Vita Salute San Raffaele, Sch Med, I-20132 Milan, Italy
Levi, Sonia
Tiranti, Valeria
论文数: 0引用数: 0
h-index: 0
机构:
Fdn IRCCS Ist Neurol Carlo Besta, I-20126 Milan, ItalyUniv Vita Salute San Raffaele, Sch Med, I-20132 Milan, Italy