Skip to main content

Advertisement

Log in

Alteration of nuclear lamina protein in human fibroblasts infected with cytomegalovirus (HCMV)

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

Immunoblotting with monoclonal as well as polyclonal lamin antibodies revealed that nuclear lamina proteins of human foreskin fibroblasts (HFF) were differentially affected after infection with human cytomegalovirus (HCMV). Lamin A immunoreactivity was progressively lost during the course of the infectious cycle whereas that of lamin C was comparatively stable. This process was not observed in herpes simplex virus-infected HFF. On the other hand, noninfected arrested HFF stimulated by serum to enter S-phase also exhibited loss of lamin A immunoreactivity. Selective in vivo proteolysis of lamin A is suggested as the possible underlying mechanism.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Albrecht TH, Cavallo T, Cole NL, Graves K (1980) Cytomegalovirus: Development and progression of cytopathic effects in human cell culture. Lab Invest 42: 1–7

    Google Scholar 

  2. Benko D, Haltiwanger R, Hart G, Gibson W (1988) Virion basic phosphoprotein from human cytomegalovirus contains O-linked N-acetylglucosamine. Proc Natl Acad Sci USA 85: 2573–2577

    Google Scholar 

  3. Bibor-Hardy V, Suh M, Pouchelet M, Simard R (1982) Modifications of the nuclear envelope of BHK cells after infection with herpes simplex virus type 1. J Gen Virol 63: 81–94

    Google Scholar 

  4. Britt W, Vugler L, Stephens E (1988) Induction of complement-dependent and -independent neutralizing antibodies by recombinant-derived human cytomegalovirus gp 55–116 (gB). J Virol 62: 3309–3318

    Google Scholar 

  5. Davis L, Blobel G (1987) Nuclear pore complex contains a family of glycoproteins that includes p 62: glycosylation through a previously unidentified cellular pathway. Proc Natl Acad Sci USA 84: 7552–7556

    Google Scholar 

  6. Gerace L, Blobel G (1980) The nuclear envelope lamina is reversibly depolymerized during mitosis. Cell 19: 277–287

    Google Scholar 

  7. Hart G, Holt G, Haltiwanger R (1988) Nuclear and cytoplasmic glycosylation: novel saccharide linkages in unexpected places. TIBS 13: 380–384

    Google Scholar 

  8. Hirai K, Watanabe Y (1976) Induction of alpha-type DNA polymerase in human cytomegalovirus-infected Wi-38 cells. Biochim Biophys Acta 447: 328–339

    Google Scholar 

  9. Högner D (1986) Produktion monoklonaler Antikörper gegen Lamine und andere karyophile Proteine und Charakterisierung der Antigene. PhD Thesis, University of Giessen, Giessen, Federal Republic of Germany

    Google Scholar 

  10. Jahn G, Kouzarides T, Mach M, Scholl B-C, Plachter B, Traupe B, Preddie E, Satchwell S, Fleckenstein B, Barrell B (1987) Map position and nucleotide sequence of the gene for the large structural phosphoprotein of human cytomegalovirus. J Virol 61: 1358–1367

    Google Scholar 

  11. Kaiser CJ, Radsak K (1987) Inhibition by monensin of human cytomegalovirus DNA replication. Arch Virol 94: 229–245

    Google Scholar 

  12. Kari B, Lussenhop N, Goertz R, Wabuke-Bunoti M, Radeke R, Gehrz R (1986) Characterization of monoclonal antibodies reactive to several biochemically distinct human cytomegalovirus glycoprotein complexes. J Virol 60: 345–352

    Google Scholar 

  13. Lin J-C, Pagano J (1986) Sequential detection of different antigens induced by Epstein-Barr virus and herpes simplex virus in the same Western blot by using dual antibody probes. J Virol 59: 522–524

    Google Scholar 

  14. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265–275

    Google Scholar 

  15. Musiani M, Zerbini M (1984) Influence of cell cycle on the efficiency of transfection with purified human cytomegalovirus DNA. Arch Virol 78: 287–292

    Google Scholar 

  16. Newport J, Forbes D (1987) The nucleus: structure, function, and dynamics. Ann Rev Biochem 56: 535–565

    Google Scholar 

  17. Ottaviano Y, Gerace L (1985) Phosphorylation of the nuclear lamins during interphase and mitosis. J Biol Chem 260: 624–632

    Google Scholar 

  18. Paine P, Moore L, Horowitz S (1975) Nuclear envelope permeability. Nature 254: 109–114

    Google Scholar 

  19. Radsak K, Kaiser CJ, Haustein D, Rapp F (1988) Polypeptide synthesis in human fibroblasts infected with DNA-negative mutants of cytomegalovirus. Intervirology 29: 101–107

    Google Scholar 

  20. Radsak K, Wiegandt H, Unterdörfer U, Wagner C, Kaiser CJ (1985) Sodium butyrate selectively inhibits host cell glycoprotein synthesis in human fibroblasts infected with cytomegalovirus. Biosci Rep 5: 589–599

    Google Scholar 

  21. Severi B, Landini M, Govoni E (1988) Human cytomegalovirus morphogenesis: an ultrastructural study of the late cytoplasmic phases. Arch Virol 98: 51–64

    Google Scholar 

  22. Smith J (1980) An additional role for the outer nuclear membrane in the morphogenesis of herpes simplex virus. Intervirology 13: 312–316

    Google Scholar 

  23. Weiland F, Keil G, Reddehase M, Koszinowski U (1986) Studies on the morphogenesis of murine cytomegalovirus. Intervirology 26: 192–201

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Radsak, K., Schneider, D., Jost, E. et al. Alteration of nuclear lamina protein in human fibroblasts infected with cytomegalovirus (HCMV). Archives of Virology 105, 103–112 (1989). https://doi.org/10.1007/BF01311120

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01311120

Keywords

Navigation