Neuronal Death: Is There a Role for Astrocytes?

被引:0
作者
Maria Teresa Tacconi
机构
[1] Istituto di Ricerche Farmacologiche Mario Negri,Unit of Biomembranes, Laboratory of Enzyme Biochemistry
来源
Neurochemical Research | 1998年 / 23卷
关键词
Astroglia; neurodegeneration; ischemia; metabolic encephalopathies;
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学科分类号
摘要
Astrocytes are ubiquitous in the brain and have multiple functions. It is becoming increasingly clear that they play an important role in monitoring the neuromicroenvironment in CNS and in information processing or signaling in the nervous system in normal conditions and respond to CNS injuries in a gradual and varied way. It is still debated whether such reactions are beneficial or detrimental. It was believed that reactive astrogliosis observed in most neurological disorders may regulate the removal of toxic compounds produced by damaged neurons and support neuronal growth by releasing trophic factors. However it was also suggested that astrocytes contribute to a decline of neurologic function, for example by accumulation and release of excitotoxic aminoacids after ischemia and oxidative stress, formation of epileptogenic scars in response to CNS injury and metabolism of protoxins to potent toxins. In a number of metabolic diseases astrocytes, not neurons, may be the primary target. The astrocyte's role in normal and pathological conditions will be discussed in the light of recent information about their metabolism, receptor distribution and release.
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页码:759 / 765
页数:6
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  • [21] Giaume C.(1988)Fatty acid transport through the blood-brain barrier J. Neurochem. 50 639-643
  • [22] Premont J.(1996)Entry of polyunsaturated fatty acids into the brain: evidence that high-density lipoprotein-induced methylation of phosphatidylethanolamine and phospholipase A2 are involved Biochem. J. 316 805-811
  • [23] Chiu S. Y.(1991)Astrocytes, not neurons, produce docosahexaenoic acid (22:6w-3) and arachidonic acid (20:4w-6) J. Neurochem. 56 518-524
  • [24] Kriegler S.(1979)Neuron-glia interactions Neurosci. Res. Progr. Bull. 17 1-239
  • [25] Norenberg M. D.(1983)Functional interactions between neurons and astrocytes. II. Potassium homeostasis at the cellular level Progr. Neurobiol. 20 133-183
  • [26] Landis D. M. D.(1993)Cytokine production by human fetal microglia and astrocytes J. Immunol. 150 2659-2667
  • [27] Schipper H. M.(1995)Tumor necrosis factor alfa and interleukin-1 alfa enhance glucose utilization by astrocytes: involvement of phospholipase A Mol. Pharmacol. 48 550-558
  • [28] Eddleston M.(1992)Induction of nitric oxide synthase in glial cells J. Neurochem. 59 897-905
  • [29] Mucke L(1996)Astrocytes and Bergmann glia as an important site of nitric oxide synthase I Glia 16 165-173
  • [30] Vernadakis A.(1995)Differential regulation by cytokines of human astrocyte nitric oxide production Glia 15 491-494