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The plasminogen activation system and the regulation of catecholaminergic function
- Source :
- Journal of Biomedicine and Biotechnology. Sept-Oct, 2012
- Publication Year :
- 2012
-
Abstract
- The local environment of neurosecretory cells contains the major components of the plasminogen activation system, including the plasminogen activators, tissue plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA), as well as binding sites for t-PA, the receptor for u-PA (uPAR), and also the plasminogen activator inhibitor, PAI-1. Furthermore, these cells express specific binding sites for plasminogen, which is available in the circulation and in interstitial fluid. Colocalization of plasminogen and its activators on cell surfaces provides a mechanism for promoting local plasminogen activation. Plasmin is retained on the cell surface where it is protected from its inhibitor, [α.sub.2]-antiplasmin. In neurosecretory cells, localized plasmin activity provides a mechanism for extracellular processing of secreted hormones. Neurotransmitter release from catecholaminergic cells is negatively regulated by cleavage products formed by plasmin-mediated proteolysis. Recently, we have identified a major plasminogen receptor, Plg-[R.sub.KT]. We have found that Plg-[R.sub.KT] is highly expressed in chromaffin cells of the adrenal medulla as well as in other catecholaminergic cells and tissues. Plg-[R.sub.KT]-dependent plasminogen activation plays a key role in regulating catecholaminergic neurosecretory cell function.<br />1. Introduction Chromaffin cells of the adrenal medulla and other neurosecretory cells contain specific binding sites for plasminogen [1, 2], which is available at high concentration in the circulation and [...]
- Subjects :
- Thrombolytic drugs
Biotechnology industry
High technology industry
Subjects
Details
- Language :
- English
- ISSN :
- 11107243
- Database :
- Gale General OneFile
- Journal :
- Journal of Biomedicine and Biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.339000222
- Full Text :
- https://doi.org/10.1155/2012/721657