Involvement of astrocytes in purine-mediated reparative processes in the brain

被引:197
作者
Ciccarelli, R
Ballerini, P
Sabatino, G
Rathbone, MP
D'Onofrio, M
Caciagli, F
Di Iorio, P
机构
[1] Dept Biomed Sci, Pharmacol Sect, I-66013 Chieti, Italy
[2] Univ G dAnnunzio, Sch Med, Sect Neonatol, Dept Med & Ageing Sci, Chieti, Italy
[3] McMaster Univ, Dept Med, Hamilton, ON L8S 4L8, Canada
[4] Neuromed Inst, Pozzilli, Italy
关键词
astrocytes; purines; brain repair; neuroprotection;
D O I
10.1016/S0736-5748(00)00084-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Astrocytes are involved in multiple blain functions in physiological conditions, participating in neuronal development, synaptic activity and homeostatic control of the extracellular environment. They also actively participate in the processes triggered by brain injuries, aimed at limiting and repairing blain damages. Purines may play a significant role in the pathophysiology of numerous acute and chronic disorders of the central nervous system (CNS). Astrocytes are the main source of cerebral purines. They release either adenine-based purines, e.g. adenosine and adenosine triphosphate. or guanine-based purines, e.g. guanosine and guanosine triphosphate. in physiological conditions and release even more of these purines in pathological conditions. Astrocytes express several receptor subtypes of P1 and P2 types for adenine-based purines. Receptors for guanine-based purines are being characterised. Specific ecto-enzymes such as nucleotidases, adenosine deaminase and, likely, purine nucleoside phosphorylase, metabolise both adenine- and guanine-based purines after release from astrocytes. This regulates the effects of nucleotides and nucleosides by reducing their interaction with specific membrane binding sites. Adenine-based nucleotides stimulate astrocyte proliferation by a P2-mediated increase in intracellular [Ca2+] and isoprenylated proteins. Adenosine also, via A(2) receptors, may stimulate astrocyte proliferation, but mostly, via A(1) and/or A(3) receptors, inhibits astrocyte proliferation, thus controlling the excessive reactive astrogliosis triggered by P2 receptors. The activation of A(2) receptors also stimulates astrocytes to produce trophic factors, such as nerve growth factor, S100 beta protein and transforming growth factor beta, which contribute to protect neurons against injuries. Guanosine stimulates the output of adenine-based purines from astrocytes and in addition it directly triggers these cells to proliferate and to produce large amount of neuroprotective factors. These data indicate that adenine- and guanine-based purines released in large amounts from injured or dying cells of CNS may act as: signals to initiate brain repair mechanisms widely involving astrocytes. (C) 2001 ISDN. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:395 / 414
页数:20
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