Protein A-activated rat splenic lymphocyte proliferation involves tyrosine kinase-phospholipase C-protein kinase C pathway

Immunopharmacol Immunotoxicol. 2000 Feb;22(1):75-90. doi: 10.3109/08923970009016407.

Abstract

Protein A (PA) of Staphylococcus aureus was long been known for its affinity towards the Fc domain of immunoglobulin G. It is now well established that PA is a potent biological response modifier showing simultaneously antitumor, antitoxic, and anticarcinogenic properties. This bacterial protein was also observed to stimulate production of cytokines. But the molecular mechanism(s) of immunocyte activation by PA still remained essentially unknown. In this report, we demonstrate a hitherto undescribed role of PA as a signal inducer in rat splenic lymphocytes. Our studies describe that PA induces transition of G0/G1 to S and G2/M phases of cell cycle, thus ultimately stimulating splenic lymphocyte proliferation. It has also been revealed that PA binds to rat splenic lymphocytes in a dose dependent manner and stimulates proliferation via tyrosine kinase-phospholipase C (PLC)-Ca2+-dependent protein kinase C (PKC) pathway. These observations will be of valid help in correlating the immunostimulatory activities of PA with the molecular mechanism(s) of its action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Flow Cytometry
  • Lymphocyte Activation / drug effects
  • Lymphocytes / drug effects*
  • Lymphocytes / metabolism
  • Phosphorylation
  • Protein Kinase C / physiology*
  • Protein-Tyrosine Kinases / physiology*
  • Rats
  • Signal Transduction / drug effects
  • Spleen / cytology*
  • Spleen / drug effects
  • Staphylococcal Protein A / metabolism
  • Staphylococcal Protein A / pharmacology*
  • Type C Phospholipases / physiology*

Substances

  • Staphylococcal Protein A
  • Protein-Tyrosine Kinases
  • Protein Kinase C
  • Type C Phospholipases