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[A new antigen induced by oncornavirus D in mouse fibroblast culture]

Voprosy Virusologii
|September 1, 1976
PubMed

Insights

Oncornavirus D infection of mouse cells creates a new antigen, distinct from viral or cell components. This induced antigen

Area of Science:

  • Virology and Immunology
  • Cell Biology
  • Oncornavirus Research

Background:

  • Oncornaviruses are known to interact with host cells.
  • Cellular responses to viral infections can involve the expression of new antigens.
  • Previous studies have identified new antigens in human cell lines infected with certain viruses.

Purpose of the Study:

  • To investigate the induction of new antigens in mouse fibroblast cultures following oncornavirus D inoculation.
  • To characterize the properties of the induced antigen.
  • To compare the induced antigen with antigens found in human cell lines.

Main Methods:

  • Complement fixation test (CFT) and immunofluorescence were used to detect and characterize the antigen.
  • Mouse fibroblast cultures were inoculated with oncornavirus D.
  • Oncornavirus was inactivated by heating or neutralized by antiserum to assess antigen induction specificity.
  • Physico-chemical and immunological properties of the induced antigen were analyzed.

Main Results:

  • Oncornavirus D inoculation induced a new antigen in mouse fibroblast cultures.
  • The induced antigen differed from the virus and original host cell antigens.
  • Antigen accumulation was observed during the cultivation of infected cells.
  • Inactivated or neutralized oncornavirus did not induce the antigen.
  • The induced antigen exhibited identical physico-chemical and immunological properties to those found in human cell lines (J-96, HeLa, HEp-2).

Conclusions:

  • Oncornavirus D actively induces a specific new antigen in mouse fibroblast cells.
  • The induction of this antigen is dependent on the infectivity of the oncornavirus.
  • The newly induced antigen in mouse cells shares characteristics with similar antigens in human cell lines, suggesting conserved mechanisms across species.

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