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 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 KT. We have found that Plg- R KT is highly expressed in chromaffin cells of the adrenal medulla as well as in other catecholaminergic cells and tissues. Plg- R KT -dependent plasminogen activation plays a key role in regulating catecholaminergic neurosecretory cell function. © 2012 Hongdong Bai et al.
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CITATION STYLE
Bai, H., Nangia, S., & Parmer, R. J. (2012). The plasminogen activation system and the regulation of catecholaminergic function. Journal of Biomedicine and Biotechnology. https://doi.org/10.1155/2012/721657
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