Functional and Biochemical Properties of Rat Kupffer Cells and Peritoneal Macrophages

Functional and biochemical techniques were used to further characterize heterogeneity between rat Kupffer cells and peritoneal macrophages. Both macrophage cell types were found to phagocytize antibody coated sheep red blood cells in a time‐dependent manner. However, Kupffer cells were two to three times more phagocytic than were peritoneal macrophages. In contrast, the peritoneal cells released significantly more superoxide anion in response to the complement cleavage product, C5a and the phorbol ester tumor promoter, 12‐0‐tetradecanoyl‐phorbol‐13‐acetate, and produced more hydrogen peroxide than did the liver macrophages. Both cell types responded chemotactically to C5a. These results suggest that macrophages may develop specialized functions depending on the needs of their local environment. Using one and two dimensional SDS‐polyacrylamide gel electrophoresis, we also compared the production of newly synthesized proteins by Kupffer cells and peritoneal macrophages. In general, the macrophages were found to produce similar types and numbers of proteins with some exceptions. These included proteins that were unique to peritoneal macrophages and other proteins observed only in Kupffer cells. The production of these proteins in liver macrophages did not appear to correlate with levels of functional activation, but may be more related to the tissue origin of the cells.

[1]  D. Laskin,et al.  Differential sensitivity of tumor targets to liver macrophage-mediated cytotoxicity. , 1987, Cancer research.

[2]  S. Russell,et al.  Protein Phenotypes of Mouse Macrophages Activated In Vivo for Tumor Cell Killing , 1987, Journal of leukocyte biology.

[3]  R. Johnston,et al.  Macrophage membrane proteins: possible role in the regulation of priming for enhanced respiratory burst activity. , 1986, Cellular immunology.

[4]  D. Laskin,et al.  Potential role of activated macrophages in acetaminophen hepatotoxicity. I. Isolation and characterization of activated macrophages from rat liver. , 1986, Toxicology and applied pharmacology.

[5]  S. Russell,et al.  Protein changes associated with stages of activation of mouse macrophages for tumor cell killing. , 1986, Journal of immunology.

[6]  D. Laskin,et al.  Accumulation of Activated Mononuclear Phagocytes in the Liver Following Lipopolysaccharide Treatment of Rats , 1986, Journal of leukocyte biology.

[7]  T. Hamilton,et al.  Effects of bacterial lipopolysaccharide on protein synthesis in murine peritoneal macrophages: Relationship to activation for macrophage tumoricidal function , 1986, Journal of cellular physiology.

[8]  K. Renton,et al.  Kupffer cell factor mediated depression of hepatic parenchymal cell cytochrome P-450. , 1986, Biochemical pharmacology.

[9]  C. Tannenbaum,et al.  LPS regulation of specific protein synthesis in murine peritoneal macrophages. , 1986, Journal of immunology.

[10]  F. Cerra,et al.  Macrophage-mediated modulation of hepatic function in multiple-system failure. , 1985, The Journal of surgical research.

[11]  R. Steinman,et al.  Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates , 1985, The Journal of experimental medicine.

[12]  D. Laskin,et al.  Stimulation of human neutrophilic granulocyte chemotaxis by monoclonal antibodies. , 1985, Journal of immunology.

[13]  T. Matsuzaki,et al.  Oxygen radical production by peritoneal macrophages and Kupffer cells elicited with Lactobacillus casei , 1984, Infection and immunity.

[14]  G. Kaplan,et al.  Heterogeneity in surface glycoproteins of mouse peritoneal macrophage populations. , 1981, Experimental cell research.

[15]  R. N. Macsween,et al.  Heterogeneity of rat peritoneal and alveolar macrophage populations: characterization of their surface antigens by antisera. , 1981, British journal of experimental pathology.

[16]  R. Carchman,et al.  Modulation of phagocytosis by tumor promoters and epidermal growth factor in normal and transformed macrophages. , 1980, Cancer research.

[17]  R. Crofton,et al.  The origin, kinetics, and characteristics of the kupffer cells in the normal steady state , 1978, The Journal of experimental medicine.

[18]  Howard M. Goodman,et al.  High resolution two-dimensional electrophoresis of basic as well as acidic proteins , 1977, Cell.

[19]  J. Zawacki,et al.  Glycosidases of rat Kupffer cells, hepatocytes and peritoneal macrophages. , 1975, Biochimica et biophysica acta.

[20]  P. O’Farrell High resolution two-dimensional electrophoresis of proteins. , 1975, The Journal of biological chemistry.

[21]  R. D. Martínez,et al.  A study of the specificity of alveolar macrophage antigen(s). , 1973, Immunology.

[22]  E. Pollock,et al.  Distribution of a macrophage-specific antigen. , 1972, Cellular immunology.

[23]  I. Montfort,et al.  Two Antigenically Different Types of Macrophages , 1971, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[24]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[25]  P. Ward CHEMOTAXIS OF MONONUCLEAR CELLS , 1968, The Journal of experimental medicine.

[26]  R. Snyderman,et al.  Chemotactic and Anaphylatoxic Fragment Cleaved from the Fifth Component of Guinea Pig Complement , 1968, Science.

[27]  S. Boyden THE CHEMOTACTIC EFFECT OF MIXTURES OF ANTIBODY AND ANTIGEN ON POLYMORPHONUCLEAR LEUCOCYTES , 1962, The Journal of experimental medicine.

[28]  T. Hamilton,et al.  The cell biology of macrophage activation. , 1984, Annual review of immunology.