Human keratinocytes and monocytes release factors which regulate the synthesis of major acute phase plasma proteins in hepatic cells from man, rat, and mouse

• Published in: The Journal of biological chemistry 1984-06, Vol.259 (11), p.7331-7342
• Main Authors: Baumann, H, Jahreis, G P, Sauder, D N, Koj, A
• Format: Article
• Language: English
• Subjects: Acute-Phase Proteins; Animals; Biological and medical sciences; Blood Proteins - biosynthesis; Carcinoma, Hepatocellular - metabolism; Carcinoma, Squamous Cell - metabolism; Culture Media; Dexamethasone - pharmacology; Epidermis - metabolism; Female; Fundamental and applied biological sciences. Psychology; Humans; Immunoelectrophoresis, Two-Dimensional; Inflammation; Liver - metabolism; Liver Neoplasms; Male; Mice; Mice, Inbred C57BL; Molecular and cellular biology; Monocytes - metabolism; Rats; Rats, Inbred BUF; Thymus Gland - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)39876-9

Human keratinocytes and activated monocytes produces factors which can stimulate the proliferation of thymocytes. The same activity has also been implicated in regulating the expression of plasma proteins in liver cells during the acute phase reaction. To assess whether factors produced by such cells can directly influence liver cells to change the production of acute phase plasma proteins, we studied in tissue culture the response pattern of hepatic cells from three species: human hepatoma cells ( HepG2 cells), and primary cultures of rat and mouse hepatocytes. Conditioned media from the squamous carcinoma COLO-16 cells, normal epidermal cells, and activated peripheral monocytes were able to stimulate the synthesis of specific acute phase plasma proteins: alpha 1-antichymotrypsin in HepG -2 cells, alpha 1-antichymotrypsin, alpha 1-acid glycoprotein, alpha 1-acute phase protein, and alpha 2-macroglobulin in rat hepatocytes, and alpha 1-acid glycoprotein, haptoglobin, and hemopexin in mouse hepatocytes. Only in rat cells, dexamethasone was found to have further enhancing effect. The increased production of plasma proteins could be explained by an elevated level of functional mRNA. Comparing thymocyte-stimulating activities with the effects on plasma protein production, we found some difference both between the conditioned media of epidermal cells and monocytes, and between the responses of the three hepatic cell systems. Furthermore, gel chromatography of conditioned media resulted in partial separation of activities regulating liver cells and thymocytes. Since there is no strict correlation between thymocyte- and hepatocyte-stimulating activities, the presence of different sets of specific factors is assumed.