Monoclonal (MAb 362.50) and polyclonal (anti-gp 105-2) antibodies have been used to examine the expression by transplantable (THC) and primary (PHC) hepatocellular carcinomas of a 105 kd rat hepatocyte cell adhesion molecule designated cell-CAM 105. Two-dimensional gel analysis of components immunoprecipitated with MAb 362.50 or anti-gp 105-2 antibodies from detergent extracts of cells surface labeled with 125I showed that cell-CAM 105 from three different THC exhibited a more basic pI than its counterpart from normal rat hepatocytes. Immunoprecipitation of detergent extracts from radioiodinated hepatocytes with anti-THC antisera raised in rabbits by four immunizations with THC cells showed that six THC lines which were negative when stained by indirect immunofluorescence with MAb 362.50 expressed sufficient levels of cell-CAM 105 to induce precipitating antibodies. In contrast, antisera collected after eight immunizations with THC 253.1 and THC 252.2, showed no detectable reactivity with cell-CAM 105 suggesting that these THC lines had completely lost the expression of this molecule. Immunofluorescence analysis of normal rat tissues indicated that cell-CAM 105 was also present in the brush border of the small intestine and a subset of tubules in the kidney, raising the possibility that THC cells were expressing an isoform normally found in nonhepatic tissues. However, cell-CAM 105 isolated from kidney showed a mobility on two-dimensional gels that was distinct from both the THC and hepatocyte forms of this molecule. Indirect immunofluorescence analysis of PHC induced by ethionine in a choline-deficient diet or by the Solt/Farber protocol showed that 52% and 65% of the persistent hepatic nodules induced by ethionine in a choline-deficient diet and by the Solt/Farber protocol, respectively, were unreactive with MAb 362.50. Immunoprecipitation analysis of PHC induced by ethionine or diethylnitrosamine and choline-deficient diet showed that one of four PHC was expressing an altered form of cell-CAM 105 with the more basic pI characteristic of the THC form of this molecule. Taken together, these results suggest that quantitative and qualitative changes in the expression of cell-CAM 105 may constitute an important step in the acquisition of the malignant phenotype.
Download full-text PDF |
Source |
---|
Eur J Clin Invest
December 2024
Department of Medicine, Masonic Cancer Center, University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
Background: In addition to the long-known antibacterial actions of neutrophils, neutrophils are recognized to have a variety of other effects and are functionally diverse. Neutrophils can either stimulate or inhibit B cells and T cells, regulate NK development and activity, augment or direct the resolution of inflammation, act as myeloid-derived suppressor cells, modulate tumour growth and metastasis and trigger autoimmune diseases. CEACAMs 1, 3, 6 and 8 are expressed on human neutrophils.
View Article and Find Full Text PDFEur J Clin Invest
December 2024
Institute of Immunology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany.
Background: CEACAM1 in leukocytes controls cell activation during inflammation. This and its expression in epithelial cells led to frequent independent appropriation of CEACAM1 as receptor by pathogens in humans and other species to gain host access and to downregulate its immune response. As a countermeasure, decoy receptors with CEACAM1-like pathogen-binding domains evolved.
View Article and Find Full Text PDFEur J Clin Invest
December 2024
Department of Surgery, University of California Los Angeles, Los Angeles, California, USA.
Background: Alternative splicing is a fundamental mechanism in the post-transcriptional regulation of genes. The multifunctional transmembrane glycoprotein receptor carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) undergoes extensive alternative splicing to allow for tunable functions in cell signalling, adhesion and modulation of immune and metabolic responses. Splice isoforms that differ in their ectodomain and short or long cytoplasmic tail (CEACAM1-S/CEACAM1-L) have distinct functional roles.
View Article and Find Full Text PDFEur J Clin Invest
December 2024
Division of Gastroenterology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Eur J Clin Invest
December 2024
Institute of Anatomy and Cell Biology, University of Wuerzburg, Wuerzburg, Germany.
The Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1, also CD66a), a transmembrane glycoprotein of the immunoglobulin superfamily, is a pivotal mediator of various physiological and pathological processes, including oncologic disorders. However, its precise role in tumorigenicity is contradictory discussed by several clinical studies. This review aims to elucidate the clinical significance of CEACAM1 in different cancer entities focusing on tumour formation, progression and metastasis as well as on CEACAM1-mediated treatment resistance.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!