[Frontiers in Bioscience 11, 33-45, January 1, 2006]

Neuroserpin

Giovanna Galliciotti and Peter Sonderegger

Institute of Biochemistry, University of Zurich, Switzerland

TABLE OF CONTENTS

1. Abstract
2. Early phase of the characterization of neuroserpin
2.1. Isolation and initial characterization of neuroserpin
2.2. The neuroserpin gene
2.3. The neuroserpin mRNA
2.4. Structural aspects of neuroserpin
3. Expression of neuroserpin
3.1. Regulation of neuroserpin expression
3.2. Expression of neuroserpin during development
3.3. Expression of neuroserpin in the adult
3.4. Investigation of neuroserpin expression using DNA microarray analysis
4. Physiological function of neuroserpin
4.1. In vitro complex formation
4.2. Neuroserpin function in the neuroendocrine tissue
4.3. Role of neuroserpin in the regulation of the emotional state
4.4. Role in synaptic plasticity
4.5. Neuroserpin catabolism
5. Pathological functions of neuroserpin
5.1. Neuroprotective role of neuroserpin in stroke
5.2. Neuroprotective role of neuroserpin in seizures
5.3. Is neuroserpin a cancer-associated gene?
5.4. Familial encephalopathy with neuroserpin inclusion bodies
5.4.1. Inclusion body distribution
5.4.2. Characterization of the accumulated neuroserpin
5.4.3. Mechanism of polymerization
5.4.4. Comparison of the four variants
5.4.5. Is the absence of neuroserpin or its accumulation responsible for the neurodegeneration?
6. References

1. ABSTRACT

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.