Human mast cell tryptase activates single-chain urinary-type plasminogen activator (pro-urokinase)

J Biol Chem. 1994 Apr 1;269(13):9416-9.

Abstract

Human lung mast cell tryptase is a trypsin-like serine proteinase that is stored in mast cell granules and released by activated mast cells. Here we report that mast cell tryptase is a potent activator of single-chain urinary-type plasminogen activator (scu-PA, or prourokinase), the zymogen form of urinary-type plasminogen activator (u-PA). Activation was complete within 75 min using an enzyme:substrate molar ratio of 1:50 and was accompanied by cleavage of scu-PA at Lys158-Ile159, generating active two-chain u-PA. The reaction was dependent on enzyme concentration and obeyed Michaelis-Menten kinetics. Kinetic constants calculated for scu-PA activation by mast cell tryptase are Km = 34 microM, Vmax = 3.6 pmol of u-PA/min, and kcat = 0.08 s-1. These data suggest that tryptase from tumor-associated mast cells may participate in the activation of scu-PA.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Chymases
  • Enzyme Activation
  • Humans
  • Isoleucine
  • Kinetics
  • Lung / enzymology*
  • Lysine
  • Mast Cells / enzymology
  • Molecular Sequence Data
  • Protein Processing, Post-Translational*
  • Recombinant Proteins / metabolism
  • Serine Endopeptidases / isolation & purification
  • Serine Endopeptidases / metabolism*
  • Substrate Specificity
  • Tryptases
  • Urokinase-Type Plasminogen Activator / metabolism*

Substances

  • Recombinant Proteins
  • Isoleucine
  • Serine Endopeptidases
  • chymase 2
  • Chymases
  • Tryptases
  • Urokinase-Type Plasminogen Activator
  • Lysine
  • saruplase