Neuron-glia communication: metallothionein expression is specifically up-regulated by astrocytes in response to neuronal injury

被引:64
作者
Chung, RS
Adlard, PA
Dittmann, J
Vickers, JC
Chuah, MI
West, AK
机构
[1] Univ Tasmania, Sch Med, NeuroRepair Grp, Hobart, Tas 7001, Australia
[2] Univ Calif Irvine, Inst Brain Aging & Dementia, Gillespie Neurosci Res Facil, Irvine, CA USA
关键词
brain injury; metallothionein; neuronal injury;
D O I
10.1046/j.1471-4159.2003.02193.x
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
Recent data suggests that metallothioneins (MTs) are major neuroprotective proteins within the CNS. In this regard, we have recently demonstrated that MT-IIA (the major human MT-I/-II isoform) promotes neural recovery following focal cortical brain injury. To further investigate the role of MTs in cortical brain injury, MT-I/-II expression was examined in several different experimental models of cortical neuron injury. While MT-I/-II immunoreactivity was not detectable in the uninjured rat neocortex, by 4 days, following a focal cortical brain injury, MT-I/-II was found in astrocytes aligned along the injury site. At latter time points, astrocytes, at a distance up to several hundred microns from the original injury tract, were MT-I/-II immunoreactive. Induced MT-I/-II was found both within the cell body and processes. Using a cortical neuron/astrocyte co-culture model, we observed a similar MT-I/-II response following in vitro injury. Intriguingly, scratch wound injury in pure astrocyte cultures resulted in no change in MT-I/-II expression. This suggests that MT induction was specifically elicited by neuronal injury. Based upon recent reports indicating that MT-I/-II are major neuroprotective proteins within the brain, our results provide further evidence that MT-I/-II plays an important role in the cellular response to neuronal injury.
引用
收藏
页码:454 / 461
页数:8
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