Physiological and pathological functions of neuroserpin: Regulation of cellular responses through multiple mechanisms

被引:30
作者
Lee, Tet Woo [1 ,2 ]
Tsang, Vicky W. K. [1 ,2 ]
Loef, Evert Jan [1 ,2 ,3 ]
Birch, Nigel P. [1 ,2 ,4 ]
机构
[1] Univ Auckland, Sch Biol Sci, Level 2,Thomas Bldg,3a Symonds, Auckland 1010, New Zealand
[2] Univ Auckland, Ctr Brain Res, Auckland, New Zealand
[3] Univ Auckland, Maurice Wilkins Ctr Mol Biodiscovery, Auckland, New Zealand
[4] Rangahau Roro Aotearoa, Brain Res New Zealand, Auckland, New Zealand
关键词
Protease inhibitor; Tissue plasminogen activator; Synaptic plasticity; Neuroprotection; Alzheimer's disease; Brain cancer; TISSUE-PLASMINOGEN ACTIVATOR; SERINE-PROTEASE INHIBITOR; NERVE GROWTH-FACTOR; RETICULUM-ASSOCIATED DEGRADATION; RECEPTOR-RELATED PROTEIN; BLOOD-BRAIN-BARRIER; ENDOPLASMIC-RETICULUM; ALZHEIMERS-DISEASE; DEMENTIA FENIB; MUTANT NEUROSERPIN;
D O I
10.1016/j.semcdb.2016.09.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is 27 years since neuroserpin was first discovered in the nervous system and identified as a member of the serpin superfamily. Since that time potential roles for this serine protease inhibitor have been identified in neuronal and non-neuronal systems. Many are linked to inhibition of neuroserpin's principal enzyme target, tissue plasminogen activator (tPA), although some have been suggested to involve alternate non-inhibitory mechanisms. This review focuses mainly on the inhibitory roles of neuroserpin and discusses the evidence supporting tPA as the physiological target. While the major sites of neuroserpin expression are neural, endocrine and immune tissues, most progress on characterizing functional roles for neuroserpin have been in the brain. Roles in emotional behaviour, synaptic plasticity and neuroprotection in stroke and excitotoxicity models are discussed. Current knowledge on three neurological diseases associated with neuroserpin mutation or activity, Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB), Alzheimer's disease and brain metastasis is presented. Finally, we consider mechanistic studies that have revealed a distinct inhibitory mechanism for neuroserpin and its possible implications for neuroserpin function. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:152 / 159
页数:8
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