Characterization of a membrane tyrosine phosphatase in AR42J cells: regulation by somatostatin

Am J Physiol. 1992 Jun;262(6 Pt 1):G1007-14. doi: 10.1152/ajpgi.1992.262.6.G1007.

Abstract

A phosphotyrosyl protein phosphatase (PTPase) activity has been characterized in the plasma membranes of confluent AR42J pancreatic tumor cells using 32P-labeled poly(Glu, Tyr) as substrate. Membrane PTPase activity exhibited an apparent Michaelis constant of 3 microM and an apparent maximal velocity of 0.9 nmol.min-1.mg-1. It was inhibited by orthovanadate, zinc, poly(Glu,Tyr) and was stimulated by EDTA and dithiothreitol. Gel filtration of solubilized plasma membranes gave a peak of enzyme activity at a relative molecular weight of 70,000. Plasma membrane PTPase activity was changed during AR42J cell growth. At the beginning of culture, the control PTPase activity was minimal. Over the 5 days of culture, PTPase activity increased to reach a maximum (3.5-fold over control activity) preceding confluency by 2 days. Then the high level of PTPase activity was sustained until confluency. Incubation of the cells with the stable somatostatin analogue SMS 201-995 (SMS) resulted in a rapid and transient activation of crude membrane PTPase activity. Activation reached a maximum level within 5 min of addition and return to control levels within 20 min. The effect of SMS was dose dependent with half-maximal and maximal activation occurring at 6 pM and 0.1 nM SMS respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Membrane / enzymology*
  • Chlorides / pharmacology
  • Chromatography, Gel
  • Enzyme Stability
  • Hydrogen-Ion Concentration
  • Intercellular Signaling Peptides and Proteins
  • Kinetics
  • Octreotide / pharmacology*
  • Pancreatic Neoplasms
  • Peptides / pharmacology
  • Protein Tyrosine Phosphatases / isolation & purification
  • Protein Tyrosine Phosphatases / metabolism*
  • Somatostatin / physiology*
  • Vanadates / pharmacology
  • Zinc / pharmacology
  • Zinc Compounds*

Substances

  • Chlorides
  • Intercellular Signaling Peptides and Proteins
  • Peptides
  • Zinc Compounds
  • L-glutamic acid-L-tyrosine copolymer
  • Vanadates
  • Somatostatin
  • zinc chloride
  • Protein Tyrosine Phosphatases
  • Zinc
  • Octreotide