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International journal of cancer1975; 15(2); 171-179; doi: 10.1002/ijc.2910150202

Transformation of horse skin cells by type-C sarcoma viruses.

Abstract: A horse skin cell line (E. Derm, NBL-6, CCL-57) was susceptible to focus formation by the Kirsten mouse sarcoma virus, feline sarcoma virus (ST stain) and the MSV pseudotypes with woolly monkey, gibbon monkey, RD-114, AT-124, baboon placenta and murine xenotropic (BALB/c 3T3 and C57L/JD) type-C viruses. Foci were detected within 5 days after infection and the transformed cells continued to produce infectious virus and group-specific antigen of their respective type-C leukemia viruses. The transformation efficiency of various type-C sarcoma viruses in horse cells was also very high.
Publication Date: 1975-02-15 PubMed ID: 165152DOI: 10.1002/ijc.2910150202Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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The research explores how horse skin cells can be influenced by different kind of type-C sarcoma viruses, which can cause foci formation, and continue to produce infectious virus and antigen related to the specific type-C leukemia viruses used for infection.

Objective

The primary objective of this research was to examine the potential vulnerability of a horse skin cell line to focus formation initiated by various type-C sarcoma viruses. The viruses used in the study include: Kirsten mouse sarcoma virus, feline sarcoma virus, and multiple MSV pseudotypes.

Method

  • The study used a specific horse skin cell line identified as E. Derm, NBL-6, CCL-57.
  • These cells were exposed to the different mentioned viruses, showcasing their susceptibility to focus formation by each virus.
  • The researchers monitored the cells for a period of five days following the infection.

Results

  • The researchers found that foci, which are clusters of cellular transformation usually indicative of cancerous cells, were detected within this five-day period.
  • The transformed cells then continued to produce infectious virus and group-specific antigen related to their respective type-C leukemia viruses. The production of these antigens signifies that the cells were effectively transformed by the viruses into leukemia cells.
  • The research also showcased that the transformation efficiency of the various type-C sarcoma viruses in the horse cells was notably high.

Conclusion

The results of this investigation underline the significant susceptibility of the horse skin cells to various type-C sarcoma viruses. It also demonstrates the potential these viruses can have on inducing focus formation, cell transformation, and the subsequent production of infectious virus and group-specific antigens, suggesting that the cells have become a source of ongoing viral reproduction and spreading. As such, the implications of these findings towards understanding horse health and developing preventative strategies against these viruses are quite vast and noteworthy.

Cite This Article

APA
Rhim JS, Ro HS, Kim EB, Gilden RV, Huebner RJ. (1975). Transformation of horse skin cells by type-C sarcoma viruses. Int J Cancer, 15(2), 171-179. https://doi.org/10.1002/ijc.2910150202

Publication

ISSN: 0020-7136
NlmUniqueID: 0042124
Country: United States
Language: English
Volume: 15
Issue: 2
Pages: 171-179

Researcher Affiliations

Rhim, J S
    Ro, H S
      Kim, E B
        Gilden, R V
          Huebner, R J

            MeSH Terms

            • Animals
            • Antibodies, Neoplasm
            • Antigens, Neoplasm
            • Cell Line
            • Cell Transformation, Neoplastic
            • Complement Fixation Tests
            • Culture Media
            • Dogs
            • Gammaretrovirus / immunology
            • Haplorhini
            • Horses
            • Immune Sera
            • Mice
            • Mice, Inbred BALB C
            • Mice, Inbred C57BL
            • Moloney murine leukemia virus / immunology
            • Papio
            • Retroviridae / immunology
            • Sarcoma, Experimental / immunology
            • Skin / cytology
            • Virus Replication

            Citations

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