Physiological and pathological roles of tissue plasminogen activator and its inhibitor neuroserpin in the nervous system

被引:34
|
作者
Lee, Tet Woo [1 ,2 ]
Tsang, Vicky W. K. [1 ,2 ]
Birch, Nigel P. [1 ,2 ,3 ]
机构
[1] Univ Auckland, Sch Biol Sci, Auckland 1142, New Zealand
[2] Univ Auckland, Ctr Brain Res, Auckland 1142, New Zealand
[3] Brain Res New Zealand, Rangahau Roro Aotearoa, Auckland, New Zealand
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2015年 / 9卷
关键词
serine protease; serpin; neuronal migration; neurite growth; synaptic plasticity; neurodegeneration and neuroprotection; Alzheimer's disease; neurovascular unit; SERINE-PROTEASE INHIBITOR; LONG-TERM POTENTIATION; BLOOD-BRAIN-BARRIER; PROGRESSIVE MYOCLONUS EPILEPSY; CULTURED HIPPOCAMPAL-NEURONS; ACTIVITY-DEPENDENT RELEASE; RECEPTOR-RELATED PROTEIN; D-ASPARTATE RECEPTORS; MICE LACKING; GENE-EXPRESSION;
D O I
10.3389/fncel.2015.00396
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although its roles in the vascular space are most well-known, tissue plasminogen activator (tPA) is widely expressed in the developing and adult nervous system, where its activity is believed to be regulated by neuroserpin, a predominantly brain-specific member of the serpin family of protease inhibitors. In the normal physiological state, tPA has been shown to play roles in the development and plasticity of the nervous system. Ischemic damage, however, may lead to excess tPA activity in the brain and this is believed to contribute to neurodegeneration. In this article, we briefly review the physiological and pathological roles of tPA in the nervous system, which includes neuronal migration, axonal growth, synaptic plasticity, neuroprotection and neurodegeneration, as well as a contribution to neurological disease. We summarize tPA's multiple mechanisms of action and also highlight the contributions of the inhibitor neuroserpin to these processes.
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页数:9
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