IMR Press / FBL / Volume 13 / Issue 5 / DOI: 10.2741/2818

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
Mosaic serine proteases in the mammalian central nervous system
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1 Department of Neurobiology and Anatomy, Kochi Medical School, Oko-cho, Nankoku 783-8505, Japan
2 Department of Cell Biology, Research Institute for Geriatrics, Kyoto Medical School, Kyoto 602-8566, Japan
3 Department of Neurology and Gerontology, Research Institute for Geriatrics, Kyoto Medical School, Kyoto 602-8566, Japan
4 Cell Biology and Protein Engineering, Environmental Systems Science, Doshisha University, Kyotanabe, Kyoto 610- 0394, Japan

*Author to whom correspondence should be addressed.

Front. Biosci. (Landmark Ed) 2008, 13(5), 1991–2000; https://doi.org/10.2741/2818
Published: 1 January 2008
Abstract

We review the structure and function of three kinds of mosaic serine proteases expressed in the mammalian central nervous system (CNS). Mosaic serine proteases have several domains in the proenzyme fragment, which modulate proteolytic function, and a protease domain at the C-terminus. Spinesin/TMPRSS5 is a transmembrane serine protease whose presynaptic distribution on motor neurons in the spinal cord suggests that it is significant for neuronal plasticity. Cell type-specific alternative splicing gives this protease diverse functions by modulating its intracellular localization. Motopsin/PRSS12 is a mosaic protease, and loss of its function causes mental retardation. Recent reports indicate the significance of this protease for cognitive function. We mention the fibrinolytic protease, tissue plasminogen activator (tPA), which has physiological and pathological functions in the CNS.

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