Neuroserpin

被引:42
作者
Galliciotti, G [1 ]
Sonderegger, P [1 ]
机构
[1] Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
serpin; serine protease inhibitor; familial encephalopathy with neuroserpin inclusion bodies; FENIB; neurodegeneration; conformational disease; neural plasticity; review;
D O I
10.2741/1778
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
Neuroserpin is a member of the serpin family of serine protease inhibitors. Tissue distribution analysis reveals a predominantly neuronal expression during the late stages of neurogenesis and, in the adult brain, in areas where synaptic changes are associated with learning and memory ( synaptic plasticity). In vitro studies revealed complex formation between neuroserpin and different serine proteases, i. e. tPA, uPA, and plasmin. The neuroserpin- target complex has so far not been characterized in vivo. However, some investigations help to understand the functional role of this serpin. Neuroserpin was shown to be involved in the regulation of the morphology of neuroendocrine cells in culture, possibly by modulating the degradation of the extracellular matrix by proteolytic enzymes such as tPA. Moreover, a role of neuroserpin in mood regulation has been deduced from the over- and underexpression of neuroserpin in genetically modified mice, which showed increased anxiety and novelty- induced hypo- locomotion. In pathological conditions of the central nervous system ( i. e. stroke and seizures), neuroserpin plays a neuroprotective role, probably by blocking the deleterious effects of tPA. A familial form of a neurodegenerative disease, termed familial encephalopathy with neuroserpin inclusion bodies, is caused by point mutations in the neuroserpin gene. This condition is characterized by the intracellular polymerization and accumulation of mutated neuroserpin, leading to neuronal death and dementia.
引用
收藏
页码:33 / 45
页数:13
相关论文
共 67 条
[1]   Acyl-enzyme complexes between tissue-type plasminogen activator and neuroserpin are short-lived in vitro [J].
Barker-Carlson, K ;
Lawrence, DA ;
Schwartz, BS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :46852-46857
[2]   Neuroserpin Portland (Ser52Arg) is trapped as an inactive intermediate that rapidly forms polymers - Implications for the epilepsy seen in the dementia FENIB [J].
Belorgey, D ;
Sharp, LK ;
Crowther, DC ;
Onda, M ;
Johansson, J ;
Lomas, DA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (16) :3360-3367
[3]   Mutant neuroserpin (S49P) that causes familial encephalopathy with neuroserpin inclusion bodies is a poor proteinase inhibitor and readily forms polymers in vitro [J].
Belorgey, D ;
Crowther, DC ;
Mahadeva, R ;
Lomas, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (19) :17367-17373
[4]   Structure of the mouse gene for the serine protease inhibitor neuroserpin (PI12) [J].
Berger, P ;
Kozlov, SV ;
Krueger, SR ;
Sonderegger, P .
GENE, 1998, 214 (1-2) :25-33
[5]   Neuronal depolarization enhances the transcription of the neuronal serine protease inhibitor neuroserpin [J].
Berger, P ;
Kozlov, SV ;
Cinelli, P ;
Krüger, SR ;
Vogt, L ;
Sonderegger, P .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1999, 14 (06) :455-467
[6]   Cognitive deficits associated with a recently reported familial neurodegenerative disease - Familial encephalopathy with neuroserpin inclusion bodies [J].
Bradshaw, CB ;
Davis, RL ;
Shrimpton, AE ;
Holohan, PD ;
Rea, CB ;
Fieglin, D ;
Kent, P ;
Collins, GH .
ARCHIVES OF NEUROLOGY, 2001, 58 (09) :1429-1434
[7]   Gene induction and categorical reprogramming during in vitro human endometrial fibroblast decidualization [J].
Brar, AK ;
Handwerger, S ;
Kessler, CA ;
Aronow, BJ .
PHYSIOLOGICAL GENOMICS, 2001, 7 (02) :135-148
[8]   Crystal structure of neuroserpin:: a neuronal serpin involved in a conformational disease [J].
Briand, C ;
Kozlov, SV ;
Sonderegger, P ;
Grütter, MG .
FEBS LETTERS, 2001, 505 (01) :18-22
[9]  
Chang WSW, 2000, GENE CHROMOSOME CANC, V29, P240
[10]   Mice deficient for testis-brain RNA-binding protein exhibit a coordinate loss of TRAX, reduced fertility, altered gene expression in the brain, and behavioral changes [J].
Chennathukuzhi, V ;
Stein, JM ;
Abel, T ;
Donlon, S ;
Yang, SC ;
Miller, JP ;
Allman, DM ;
Simmons, RA ;
Hecht, NB .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (18) :6419-6434