TY - JOUR
T1 - Astrocytic-neuronal crosstalk
T2 - Implications for neuroprotection from brain injury
AU - Barreto, George E.
AU - Gonzalez, Janneth
AU - Torres, Yolima
AU - Morales, L.
N1 - Copyright © 2011 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
PY - 2011/10
Y1 - 2011/10
N2 - The older neurocentric view of the central nervous system (CNS) has changed radically with the growing understanding of the many essential functions of astrocytes. Advances in our understanding of astrocytes include new observations about their structure, organization, function and supportive actions to other cells. Although the contribution of astrocytes to the process of brain injury has not been clearly defined, it is thought that their ability to provide support to neurons after cerebral damage is critical. Astrocytes play a fundamental role in the pathogenesis of brain injury-associated neuronal death, and this secondary injury is primarily a consequence of the failure of astrocytes to support the essential metabolic needs of neurons. These needs include K + buffering, glutamate clearance, brain antioxidant defense, close metabolic coupling with neurons, and the modulation of neuronal excitability. In this review, we will focus on astrocytic activities that can both protect and endanger neurons, and discuss how manipulating these functions provides a novel and important strategy to enhance neuronal survival and improve the outcome following brain injury.
AB - The older neurocentric view of the central nervous system (CNS) has changed radically with the growing understanding of the many essential functions of astrocytes. Advances in our understanding of astrocytes include new observations about their structure, organization, function and supportive actions to other cells. Although the contribution of astrocytes to the process of brain injury has not been clearly defined, it is thought that their ability to provide support to neurons after cerebral damage is critical. Astrocytes play a fundamental role in the pathogenesis of brain injury-associated neuronal death, and this secondary injury is primarily a consequence of the failure of astrocytes to support the essential metabolic needs of neurons. These needs include K + buffering, glutamate clearance, brain antioxidant defense, close metabolic coupling with neurons, and the modulation of neuronal excitability. In this review, we will focus on astrocytic activities that can both protect and endanger neurons, and discuss how manipulating these functions provides a novel and important strategy to enhance neuronal survival and improve the outcome following brain injury.
KW - Astrocytes
KW - Brain injury
KW - Inflammation
KW - Neurons
KW - Neuroprotection
UR - http://www.scopus.com/inward/record.url?scp=80052361500&partnerID=8YFLogxK
U2 - 10.1016/j.neures.2011.06.004
DO - 10.1016/j.neures.2011.06.004
M3 - Review article
C2 - 21693140
AN - SCOPUS:80052361500
SN - 0168-0102
VL - 71
SP - 107
EP - 113
JO - Neuroscience Research
JF - Neuroscience Research
IS - 2
ER -