Expression of functional cell surface C1-inactivator by U937 cells

Clin Immunol Immunopathol. 1988 Dec;49(3):463-77. doi: 10.1016/0090-1229(88)90133-x.

Abstract

We have previously shown that the human monocyte-like cell line U937 synthesizes C1-INA and expresses cell surface C1-INA. In this report we provide evidence that this surface-expressed C1-INA is functionally active. Intact U937 cells demonstrated functional C1-INA activity in a hemolytic assay. This activity was blocked when the cells were incubated with monospecific antibody to C1-INA, and was not detectable in cell-free supernatants of U937 cells. SDS-PAGE analysis of radiolabeled U937 cell surface proteins purified by anti-C1-INA affinity chromatography revealed two distinct bands. One protein had a Mr of 105 kDa identical to plasma C1-INA, and the second had a Mr of 200 kDa. We were unable to determine the identity of the 200 kDa protein by Western blotting with anti-C1-INA. However, the possibility exists that this 200 kDa molecule may represent a C1-INA receptor, a dimeric form of C1-INA, or an unrelated cell surface protein with affinity for C1-INA. Furthermore, we show that treatment of U937 cells with phorbol ester resulted in an increase in the percentage of cells expressing surface C1-INA. These results suggest that U937 cells express functional cell surface C1-INA, which could function in vivo to protect these human tumor cells from lysis by host complement.

Publication types

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

MeSH terms

  • Blotting, Western
  • Cell Line
  • Cell-Free System
  • Complement C1 Inactivator Proteins / immunology
  • Complement C1 Inactivator Proteins / isolation & purification*
  • Complement C1 Inactivator Proteins / physiology
  • Complement C4 / analysis
  • Detergents
  • Electrophoresis, Polyacrylamide Gel
  • Hemolysis
  • Humans
  • Immunoglobulin G / physiology
  • Membrane Proteins / immunology
  • Membrane Proteins / isolation & purification*
  • Membrane Proteins / physiology
  • Monocytes / analysis*
  • Neutralization Tests
  • Tetradecanoylphorbol Acetate

Substances

  • Complement C1 Inactivator Proteins
  • Complement C4
  • Detergents
  • Immunoglobulin G
  • Membrane Proteins
  • Tetradecanoylphorbol Acetate