Deciphering the Iron Side of Stroke: Neurodegeneration at the Crossroads Between Iron Dyshomeostasis, Excitotoxicity, and Ferroptosis
Por:
DeGregorio-Rocasolano, N, Marti-Sistac, O and Gasull, T
Publicada:
19 feb 2019
Ahead of Print:
19 feb 2019
Categoría:
Neuroscience (miscellaneous)
Resumen:
In general, iron represents a double-edged sword in metabolism in most tissues, especially in the brain. Although the high metabolic demands of brain cells require iron as a redox-active metal for ATP-producing enzymes, the brain is highly vulnerable to the devastating consequences of excessive iron-induced oxidative stress and, as recently found, to ferroptosis as well. The blood-brain barrier (BBB) protects the brain from fluctuations in systemic iron. Under pathological conditions, especially in acute brain pathologies such as stroke, the BBB is disrupted, and iron pools from the blood gain sudden access to the brain parenchyma, which is crucial in mediating strokeinduced neurodegeneration. Each brain cell type reacts with changes in their expression of proteins involved in iron uptake, efflux, storage, and mobilization to preserve its internal iron homeostasis, with specific organelles such as mitochondria showing specialized responses. However, during ischemia, neurons are challenged with excess extracellular glutamate in the presence of high levels of extracellular iron; this causes glutamate receptor overactivation that boosts neuronal iron uptake and a subsequent overproduction of membrane peroxides. This glutamate-driven neuronal death can be attenuated by iron-chelating compounds or free radical scavenger molecules. Moreover, vascular wall rupture in hemorrhagic stroke results in the accumulation and lysis of iron-rich red blood cells at the brain parenchyma and the subsequent presence of hemoglobin and heme iron at the extracellular milieu, thereby contributing to ironinduced lipid peroxidation and cell death. This review summarizes recent progresses made in understanding the ferroptosis component underlying both ischemic and hemorrhagic stroke subtypes.
Filiaciones:
:
Germans Trias & Pujol Res Inst IGTP, Dept Neurosci, Cellular & Mol Neurobiol Res Grp, Badalona, Spain
Marti-Sistac, O:
Germans Trias & Pujol Res Inst IGTP, Dept Neurosci, Cellular & Mol Neurobiol Res Grp, Badalona, Spain
Univ Autonoma Barcelona, Dept Cellular Biol Physiol & Immunol, Bellaterra, Spain
:
Germans Trias & Pujol Res Inst IGTP, Dept Neurosci, Cellular & Mol Neurobiol Res Grp, Badalona, Spain
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