Adenosine signaling and function in glial cells

被引:230
作者
Boison, D. [1 ]
Chen, J-F [2 ]
Fredholm, B. B. [3 ]
机构
[1] Robert Stone Dow Neurobiol Labs, Portland, OR 97232 USA
[2] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
[3] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
关键词
astrocyte; adenosine receptor; adenosine kinase; epilepsy; excitotoxicity; neurodegeneration; TRAUMATIC BRAIN-INJURY; RAT CEREBRAL-CORTEX; AMINO-ACID RELEASE; EQUILIBRATIVE NUCLEOSIDE TRANSPORTER; A(2A) RECEPTOR ANTAGONISTS; CULTURED MOUSE ASTROCYTES; TRANSIENT FOCAL ISCHEMIA; ACTIVATED PROTEIN-KINASE; TEMPORAL-LOBE EPILEPSY; CENTRAL-NERVOUS-SYSTEM;
D O I
10.1038/cdd.2009.131
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
Despite major advances in a variety of neuroscientific research fields, the majority of neurodegenerative and neurological diseases are poorly controlled by currently available drugs, which are largely based on a neurocentric drug design. Research from the past 5 years has established a central role of glia to determine how neurons function and, consequently, glial dysfunction is implicated in almost every neurodegenerative and neurological disease. Glial cells are key regulators of the brain's endogenous neuroprotectant and anticonvulsant adenosine. This review will summarize how glial cells contribute to adenosine homeostasis and how glial adenosine receptors affect glial function. We will then move on to discuss how glial cells interact with neurons and the vasculature, and outline new methods to study glial function. We will discuss how glial control of adenosine function affects neuronal cell death, and its implications for epilepsy, traumatic brain injury, ischemia, and Parkinson's disease. Eventually, glial adenosine-modulating drug targets might be an attractive alternative for the treatment of neurodegenerative diseases. There are, however, several major open questions that remain to be tackled. Cell Death and Differentiation (2010) 17, 1071-1082; doi:10.1038/cdd.2009.131; published online 18 September 2009
引用
收藏
页码:1071 / 1082
页数:12
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