Abstract / Description of output
Unlike other serine proteases that are zymogens, the single-chain form of tissue plasminogen activator (sc-tPA) exhibits an intrinsic activity similar to that of its cleaved two-chain form (tc-tPA), especially in the presence of fibrin. In the central nervous system tPA controls brain functions and dysfunctions through its proteolytic activity. We demonstrated here, both in vitro and in vivo, that the intrinsic activity of sc-tPA selectively modulates N-methyl-D-aspartate receptor (NMDAR) signaling as compared with tc-tPA. Thus, sc-tPA enhances NMDAR-mediated calcium influx, Erk(½) activation and neurotoxicity in cultured cortical neurons, excitotoxicity in the striatum and NMDAR-dependent long-term potentiation in the hippocampal CA-1 network. As the first demonstration of a differential function for sc-tPA and tc-tPA, this finding opens a new area of investigations on tPA functions in the absence of its allosteric regulator, fibrin.
Original language | English |
---|---|
Pages (from-to) | 1983-91 |
Number of pages | 9 |
Journal | Cell Death & Differentiation (CDD) |
Volume | 19 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2012 |
Keywords / Materials (for Non-textual outputs)
- Animals
- Calcium/metabolism
- Cells, Cultured
- Humans
- Mice
- Mitogen-Activated Protein Kinase 1/metabolism
- Mitogen-Activated Protein Kinase 3/metabolism
- N-Methylaspartate/toxicity
- Neurons/drug effects
- Receptors, N-Methyl-D-Aspartate/metabolism
- Recombinant Proteins/genetics
- Signal Transduction/drug effects
- Tissue Plasminogen Activator/genetics