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Loss of surface fibronectin after infection of cultured cells by HSV-1 and 2

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Summary

Fibronection is lost from the surface of HSV infected cells during cell rounding. In order to investigate also the fate of fibronection during the process of HSV-induced cell-fusion, BHK, Vero as well as primary or secondary rabbit kidney cells were infected with HSV-1 strains producing cell-fusion. By immunofluorescence and immunoelectron microscopy a considerable loss of fibronectin after HSV infection could be demonstrated leaving only irregular clumps of fibronectin containing virus particles on the cell surface. Decrease and disarrangement of fibronectin was similar during cell rounding and cell fusion. Loss of Fibronectin was closely connected with the two types of the cytopathic effect (CPE) and could not be prevented by protease inhibitors. The immediate-early protein 175K is essential for induction of CPE and loss of fibronectin. The damage to the cell membrane during HSV infection shows certain analogous mechanisms with events induced by Cytochalasin B and might be explained by the loss of hypothetical fibronectin receptors.

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References

  1. Mullins, D. E., Rohrlich, S. T.: The role of proteinases in cellular invasiveness. BBA695, 177–214 (1983).

    Google Scholar 

  2. Dienes, H. P., Müller, S., Falke, D.: The influence of replicating HSV on the microfilaments of cells. (In preparation.)

  3. Dargan, D., Subak-Sharpe, J. H.: Ultrastructural Characterization of Herpes simplex Virus Type 1 (Strain 17) Temperature-sensitive mutants. J. gen. Virol.64, 1311–1326 (1983).

    Google Scholar 

  4. Dienes, H. P., Ramadori, G., Falke, D., Thoenes, W.: Electron microscopic observations on primary hepatocyte cultures infected with Herpes simplex virus types 1 und 2. Virchows Arch. (Cell Pathol.)46, 321–332 (1984).

    Google Scholar 

  5. Dierich, M. P., Landen, B., Schulz, Th., Falke, D.: Protease activity on the surface of HSV-infected cells. J. gen. Virol.45, 241–244 (1979).

    Google Scholar 

  6. Geiger, B.: Membrane-Cytoskeleton Interaction. BBA737, 305–341 (1983).

    Google Scholar 

  7. Goertz, J., Brake, B., Härle-Grupp, V., Falke, D.: Replication of HSV-1 in murine peritoneal macrophages: Comparison of various virus strains with different properties. Arch. Virol.79, 173–187 (1984).

    Google Scholar 

  8. Heeg, U., Haase, W., Brauer, D., Falke, D.: Microtubules and microfilaments in HSV-infected rabbit kidney cells. Arch. Virol.70, 233–246 (1981).

    Google Scholar 

  9. Heeg, U., Hiller, G., Härle-Grupp, V., Falke, D.: The cytoskeleton of HSV-infected cells. Herpes viruses, Cold Spring Harbor 31. 8.–5. 9. 1982, p. 100 (1982).

  10. Heeg, U., Hiller, G., Härle-Grupp, V., Falke, D.: Alterations of the cycloskeleton after infection with HSV. Workshop of Section Virology of Deutsche Ges. f. Hyg. and Microbiol., Würzburg 13.–17. März, Zbl. Bakt. I Orig.A 255, 171 (1983).

    Google Scholar 

  11. Howett, M. K., High, C. S., Rapp, F.: Production of plasminogen activator by cells transformed by herpes viruses. Cancer Res.38, 1075–1078 (1978).

    Google Scholar 

  12. Hynes, R. O.: Cell surface proteins and malignant transformation. BBA458, 73–107 (1976).

    Google Scholar 

  13. Julkuinen, J., Hautanen, A., Keski-Oja, J.: Interaction of viral envelope glycoproteins with Fibronectin. Infect. Immun.40, 876–881 (1982).

    Google Scholar 

  14. Kleinman, H. K., Martin, G. R., Fishman, P. H.: Ganglioside inhibition of fibronectin-mediated cell-adhesion to collagen. Proc. Natl. Acad. Sci. U.S.A.76, 3367–3371 (1979).

    Google Scholar 

  15. Kurkinen, M., Wartiovaara, J., Vaheri, A.: Cytochalasin B releases a major surface-associated glycoprotein, Fibronection, from cultured fibroblasts. Exp. Cell Res.111, 127–137 (1978).

    Google Scholar 

  16. Norrild, B., Virtanen, I., Lehto, V.-P., Pedersen, B.: Accumulation of Herpes simplex type 1 glycoprotein D in adhesion areas of infected cells. J. gen. Virol.64, 2499–2503 (1983).

    Google Scholar 

  17. Podleski, T. R., Greenberg, J., Schlessinger, J., Yamada, K. M.: Fibronectin delays the fusion of L6 myoblasts. Exp. Cell Res.122, 317–326 (1979).

    Google Scholar 

  18. Richter, I. E., Falke, D.: Scanning Electron Microscope Observations on the Inhibition of Herpes-induced giant cell formation by Cpd 48/80 and Cytochalasin B. Eur. Journ. Path.9, 59–73 (1974).

    Google Scholar 

  19. Stanislawski, L.: Attachment of Rous Sarcoma Virus to the Fibroncetin matrix of infected chick embryo fibroblasts. J. Ultrastruc. Res.82, 134–142 (1983).

    Google Scholar 

  20. Vaheri, A., Kurkinen, M., Lehto, V.-P., Linder, E., Timpl, R.: Codistribution of pericellular matrix proteins in cultured fibroblasts and loss in transformation: fibronectin and Procollagen. Proc. Natl. Acad. Sci. U.S.A.75, 4944–4948 (1978).

    Google Scholar 

  21. Vaheri, A., Mosher, D. F.: High Molecular weight, cell surface-associated glycoprotein (Fibronectin) lost in malignant transformation. BBA516, 1–25 (1978).

    Google Scholar 

  22. Vartio, T., Vaheri, A.: Fibronectin: Chains of domains with diversified functions. TIBS8, 442–444 (1983).

    Google Scholar 

  23. Weber, K., Rathke, P. C., Osborn, M., Franke, W. W.: Distribution of actin and tubulin in cells and in glycerinated cell models after treatment with cytochalasin B (CB). Exp. Cell Res.101, 285–297 (1976).

    Google Scholar 

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Dienes, H.P., Knoblich, A. & Falke, D. Loss of surface fibronectin after infection of cultured cells by HSV-1 and 2. Archives of Virology 86, 223–237 (1985). https://doi.org/10.1007/BF01309827

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  • DOI: https://doi.org/10.1007/BF01309827

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