Application | Comment | Organism |
---|---|---|
drug development | neutrophils are good candidates to be the main source of metalloproteinase-9 following t-PA stroke treatment and in consequence, are partially responsible for thrombolysis-related brain bleedings. Combined therapy of t-PA with a metalloproteinase-9 or a neutrophil degranulation inhibitor may improve safety and efficacy of thrombolytic therapy in the acute phase of stroke | synthetic construct |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
synthetic construct | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | t-PA treatment promotes metalloproteinase-9, metalloproteinase-8, and tissue inhibitor metalloproteinase-2 release from human neutrophils ex vivo within 10 and 30 min. t-PA treatment also promotes metalloproteinase-9 release in formyl peptide-preactivated neutrophils. t-PA treatment stimulates neutrophil degranulation | synthetic construct | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
t-PA | - |
synthetic construct |
Tissue plasminogen activator | - |
synthetic construct |