Published 1987 | Version v1
Report

C-reactive protein interaction with macrophages: in vitro induction of tumor cytotoxicity, and characterization of C-reactive protein binding to macrophages

Description

The ability of C-reactive protein (CRP) to activate macrophages to tumoricidal state was examined. CRP was able to activate macrophages to kill tumor cells. The activation was shown to be due to CRP and not to low levels of other activators present in the CRP preparations, since specific removal of CRP led to abrogation of the CRP mediated activation of macrophages. The role of lipopolysaccharide (LPS) as a contaminating activator was eliminated by showing the ability of CRP preparations to activate macrophages from LPS non-responsive strains of mice, and to activate macrophages under conditions which specifically inactivated or removed the contaminating LPS. In order to exclude the possibility of indirect activation of macrophages by other cells present in the peritoneal exudate cell population, effect of CRP on pure macrophages was examined. Bone marrow derived macrophages as well as well as macrophage cell lines exhibited a significant increase in their capacity to kill tumor cells after treatment with CRP. The nature of CRP and macrophage interaction was examined using radioiodinated CRP. Labelled CRP bound specifically to macrophages and macrophage cell lines

Availability note (English)

University Microfilms Order No. 88-04,130.

Additional details

Publishing Information

Imprint Pagination
186 p.

INIS

Country of Publication
United States
Country of Input or Organization
United States
INIS RN
20048629
Subject category
S60: APPLIED LIFE SCIENCES;
Resource subtype / Literary indicator
Thesis, Non-conventional Literature
Descriptors DEI
BIOCHEMICAL REACTION KINETICS; CELL KILLING; IN VITRO; IODINE ISOTOPES; MACROPHAGES; MICE; PROTEINS; RECEPTORS; TRACER TECHNIQUES; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; ANIMALS; CONNECTIVE TISSUE CELLS; ISOTOPE APPLICATIONS; KINETICS; MAMMALS; ORGANIC COMPOUNDS; PHAGOCYTES; REACTION KINETICS; RODENTS; SOMATIC CELLS; VERTEBRATES