Production of fibronectin by normal and malignant human mammary epithelial cells.

The production and retention of fibronectin by primary cultures of cells derived from the human breast has been analyzed. Two examples of each of the following cell types were examined: (a) normal epithelium from milk; (b) metastatic breast cancer cells in pleural effusions; (c) fibroblasts; (d) tissue macrophages of milk. Cell-associated fibronectin could be detected by indirect immunofluorescent staining on normal and malignant mammary epithelium and on mammary fibroblasts, but not on milk macrophages. Immune precipitation followed by gel electrophoresis of 35S-labeled cell lysates and conditioned medium confirmed that fibronectin was indeed synthesized by both types of epithelial cells and by fibroblasts, but not by macrophages, and that much of the protein was released into the medium. Quantitative analysis with radioimmune assay of the fibronectin on cells and in media showed that both normal and malignant epithelial cells synthesized levels of protein comparable to that produced by fibroblasts, but only a small fraction (less than 10%) of the material synthesized was retained by the cells. Growth on collagen-coated plastic increased the percentage of fibronectin retained by normal and malignant epithelium but did not affect retention by fibroblasts.

[1]  I. Fentiman,et al.  Cholera toxin and analogues of cyclic AMP stimulate the growth of cultured human mammary epithelial cells , 1980, Journal of cellular physiology.

[2]  P. Furmanski,et al.  Absence of fibronectin and presence of plasminogen activator in both normal and malignant human mammary epithelial cells in culture , 1980, The Journal of cell biology.

[3]  K. von Figura,et al.  Primary cultures of rat hepatocytes synthesize fibronectin. , 1979, Biochemical and biophysical research communications.

[4]  J. Riggs,et al.  Production of fibronectin by human epithelial cells in culture. , 1979, Cancer research.

[5]  N. Hogg,et al.  Characterization of human breast milk macrophages cytostatic for human cell lines. , 1979, Journal of immunology.

[6]  J. Keski‐Oja,et al.  Rapid release of fibronectin from human lung fibroblasts by biologically active phorbol esters , 1979, International journal of cancer.

[7]  Kenneth M. Yamada,et al.  Enhanced cellular fibronectin accumulation in chondrocytes treated with vitamin A , 1979, Cell.

[8]  T. Ji,et al.  Cross-linking of fibronectin to sulfated proteoglycans at the cell surface , 1979, Cell.

[9]  M. Bernfield,et al.  Collagen reduces glycosaminoglycan degradation by cultured mammary epithelial cells: possible mechanism for basal lamina formation. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Foidart,et al.  Dexamethasone-induced accumulation of a fibronectin and collagen extracellular matrix in transformed human cells , 1979, Nature.

[11]  J. Riggs,et al.  Properties of epithelial cells cultured from human carcinomas and nonmalignant tissues. , 1979, Journal of supramolecular structure.

[12]  K. Isselbacher,et al.  Fibronectin synthesis by epithelial crypt cells of rat small intestine. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Kenneth M. Yamada,et al.  Fibronectins—adhesive glycoproteins of cell surface and blood , 1978, Nature.

[14]  D. Mosher,et al.  High molecular weight, cell surface-associated glycoprotein (fibronectin) lost in maglinant transformation , 1978 .

[15]  E. Engvall,et al.  Interaction of fibronectin with antibodies and collagen in radioimmunoassay. , 1978, Biochimica et biophysica acta.

[16]  E. Macarak,et al.  Synthesis of cold-insoluble globulin by cultured calf endothelial cells. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Vaheri,et al.  Appearance of fibronectin during differentiation of mouse teratocarcinoma in vitro , 1978, Nature.

[18]  G. Wendelschafer‐Crabb,et al.  Immunocytochemical localization of fibronectin (LETS protein) on the surface of L6 myoblasts: light and electron microscopic studies , 1978, Cell.

[19]  D. Mosher,et al.  High molecular weight, cell surface-associated glycoprotein (fibronectin) lost in malignant transformation. , 1978, Biochimica et biophysica acta.

[20]  A. Vaheri,et al.  Cytochalasin B releases a major surface-associated glycoprotein, fibronectin, from cultured fibroblasts. , 1978, Experimental cell research.

[21]  J. Taylor‐Papadimitriou,et al.  Growth requirements of human mammary epithelial cells in culture , 1977, International journal of cancer.

[22]  T. Sun,et al.  Control of a cell surface major glycoprotein by epidermal growth factor. , 1977, Science.

[23]  E. Engvall,et al.  Binding of soluble form of fibroblast surface protein, fibronectin, to collagen , 1977, International journal of cancer.

[24]  J. Taylor‐Papadimitriou,et al.  Some properties of cells cultured from early-lactation human milk. , 1977, Journal of the National Cancer Institute.

[25]  C. Marshall,et al.  Markers of neoplastic transformation in epithelial cell lines derived from human carcinomas. , 1977, Journal of the National Cancer Institute.

[26]  R. Hynes,et al.  Restoration of normal morphology, adhesion and cytoskeleton in transformed cells by addition of a transformation-sensitive surface protein , 1977, Cell.

[27]  N. Maitland,et al.  Detection of the large external transformation-sensitive protein on some epithelial cells. , 1977, Experimental cell research.

[28]  J. McDougall,et al.  Correlation between tumor induction and the large external transformation sensitive protein on the cell surface. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[29]  E. Pearlstein Plasma membrane glycoprotein which mediates adhesion of fibroblasts to collagen , 1976, Nature.

[30]  R. Hynes Cell surface proteins and malignant transformation. , 1976, Biochimica et biophysica acta.

[31]  G. Nicolson Trans-membrane control of the receptors on normal and tumor cells. II. Surface changes associated with transformation and malignancy. , 1976, Biochimica et biophysica acta.

[32]  G. Nicolson Transmembrane control of the receptors on normal and tumor cells. I. Cytoplasmic influence over surface components. , 1976, Biochimica et biophysica acta.

[33]  I. Pastan,et al.  Cell surface protein partially restores morphology, adhesiveness, and contact inhibition of movement to transformed fibroblasts. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[34]  S W Kessler,et al.  Rapid isolation of antigens from cells with a staphylococcal protein A-antibody adsorbent: parameters of the interaction of antibody-antigen complexes with protein A. , 1975, Journal of immunology.

[35]  P. Branton,et al.  The chick fibroblast cell surface after transformation by Rous sarcoma virus. , 1975, Cold Spring Harbor symposia on quantitative biology.

[36]  R. Klebe,et al.  Isolation of a collagen-dependent cell attachment factor , 1974, Nature.

[37]  E. Ruoslahti,et al.  Disappearance of a major cell‐type specific surface glycoprotein antigen (SF) after transformation of fibroblasts by rous sarcoma virus , 1974, International journal of cancer.

[38]  C. Gahmberg,et al.  Changes in a surface-labelled galactoprotein and in glycolipid concentrations in cells transformed by a temperature-sensitive polyoma virus mutant , 1974, Nature.

[39]  N. Hogg A comparison of membrane proteins of normal and transformed cells by lactoperoxidase labeling. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[40]  R. Hynes Alteration of cell-surface proteins by viral transformation and by proteolysis. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Buehring Gc Culture of human mammary epithelial cells: keeping abreast with a new method. , 1972 .

[42]  G. Buehring Culture of human mammary epithelial cells: keeping abreast with a new method. , 1972, Journal of the National Cancer Institute.

[43]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[44]  H. Gaylord,et al.  AMERICAN ASSOCIATION FOR CANCER RESEARCH. , 1913, California state journal of medicine.