ATP released in the extracellular space by neuronal injury can influence neighboring neurons via activation of purinergic receptors, In vitro data suggest the involvement of ATP and purinergic receptors as trophic agents in different biological events such as neuritogenesis and cell survival. Recently, in vitro studies has demonstrated modifications in the glial expression of ionotropic purinergic receptors after CNS lesions. In the present study, we investigated the effects of CNS lesion on the neuronal expression of P2X(1) and P2X(2) receptor subunits by immunohistochemistry and western blotting techniques. In the precerebellar structures of normal animals the expression of P2X(1) and P2X(2) was lower than previously reported. P2X(1) immunostaining was confined only to fibers, while P2X(2) immunostaining demonstrated a neuronal expression. After unilateral cerebellar lesion (hemicerebellectomy) axotomized precerebellar neurons underwent marked cell loss however, some precerebellar neurons did not degenerate. Seven to 35 dabs after hemicerebellectomy, a transient, time-dependent, marked increase in the number of immunopositive P2X(1) and P2X(2) neurons was observed in the precerebellar nuclei of the experimental side. An even distribution of immunopositive neurons was present in almost all precerebellar nuclei examined, except for the inferior olive. In this latter structure, differences in the distribution or immunopositive neurons were evident among the subnuclei. Up-regulation of immunoreactivity over relatively long time periods. distribution selectivity and absence of degenerating morphological features in immunopositive neurons suggest that purinergic receptors may have a role in mediating the survival of neuronal responses to axotomy. The present findings are the first report in the CNS of P2X(1) and P2X(2) receptor subunit involvement in neuronal reaction to axotomy. They provide in vivo evidence of a correlation between purinergic receptor subunit up-regulation and survival of injured neurons, (C) 2002 IBRO. Published by Elsevier Science Ltd. All rights reserved.
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Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, EnglandKings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
Bradbury, EJ
;
Burnstock, G
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机构:Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
Burnstock, G
;
McMahon, SB
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机构:Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
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UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England
Dunn, PM
;
Zhong, Y
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UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England
Zhong, Y
;
Burnstock, G
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UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England
机构:
Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, EnglandKings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
Bradbury, EJ
;
Burnstock, G
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机构:Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
Burnstock, G
;
McMahon, SB
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机构:Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, London SE1 7EH, England
机构:
UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England
Dunn, PM
;
Zhong, Y
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h-index: 0
机构:
UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England
Zhong, Y
;
Burnstock, G
论文数: 0引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, EnglandUCL Royal Free & Univ Coll, Sch Med, Auton Neurosci Inst, London NW3 2PF, England