Cell surface changes in mouse peritoneal macrophages after induction with proteose peptone or thioglycollate
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
114430
Knihovny.cz E-resources
- MeSH
- Ascitic Fluid cytology MeSH
- Cell Adhesion drug effects MeSH
- Genotype MeSH
- Glutaral pharmacology MeSH
- Histocompatibility Antigens analysis MeSH
- Mice, Inbred Strains MeSH
- Caseins pharmacology MeSH
- Colchicine pharmacology MeSH
- Culture Media MeSH
- Macrophages immunology radiation effects MeSH
- Mice MeSH
- Peptide Fragments pharmacology MeSH
- Thioglycolates pharmacology MeSH
- Rosette Formation * MeSH
- Gamma Rays MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Glutaral MeSH
- Histocompatibility Antigens MeSH
- Caseins MeSH
- Colchicine MeSH
- Culture Media MeSH
- Peptide Fragments MeSH
- Thioglycolates MeSH
Some five to six per cent of mouse PEC spontaneously form rosettes with SRBC. This weak intercellular interaction is most likely mediated by a "receptor" for SRBC located on the surface of peritoneal macrophages. Manifestation of the receptor is influenced by the genetic background and the H-2 haplotype of PEC donors; a high proportion of RFC is associated with the H-2s haplotype. PEC derived from intact mice markedly differ in morphological and functional characteristics from those of PP- or TG-pretreated donors. Formation of rosettes by induced macrophages depends on the time interval between stimulation and PEC harvesting and on the type of the inducing agent; it is also radiosensitive and more responsive to the action of colchicine. TG-induced macrophages have a significantly reduced capacity to bind syngeneic lymphoid cells. The difference in adhesivity between intact and stimulated PEC can be abolished by glutaraldehyde prefixation. In vivo induction results in modified morphological and functional properties of macrophages, including transformation of their cell surface.
Phagocytosis of protamine-heparin aggregates by mouse peritoneal exudate cells