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NK sensitivity, H-2 expression and metastatic potential: analysis of H-2Dk gene transfected fibrosarcoma cells.

Abstract
We have used the 3-Methylcholanthrene induced T-10 fibrosarcoma tumour cell system (H-2b xH-2k)F1 to elucidate the possible correlation between metastatic potential, expression of individual H-2 antigens and susceptibility to NK cells. Transfection of the non-metastatic and NK sensitive IC9 cells (Db+, Dk-, Kb-, Kk-) with the H-2Dk gene, altered the metastatic phenotype of the parental cells, yet had no effect on the susceptibility of these tumour cells to lysis by NK and did not elicit a specific CTL response in syngeneic hosts. Variants of the metastatic and NK resistant IE7 clone (Db+, Dk+, Kb-, Kk-), lacking H-2Dk, were selected by treatment with monoclonal anti H-2Dk antibodies and complement. These variants were sensitive to NK and poorly or non metastatic. Retransfection of 'Dk' 'loss' variants with the H-2Dk gene, resulted in the isolation of several clones expressing a wide range of metastatic phenotypes but maintained sensitivity to NK. These results indicate that the H-2D region of the MHC and or closely linked genes may be involved in the complex interrelationship between target susceptibility to NK and metastasis.
AuthorsJ Gopas, B Rager-Zisman, I Har-Vardi, G J Hammerling, M Bar-Eli, S Segal
JournalJournal of immunogenetics (J Immunogenet) 1989 Aug-Oct Vol. 16 Issue 4-5 Pg. 305-13 ISSN: 0305-1811 [Print] England
PMID2639905 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Monoclonal
  • H-2 Antigens
  • Histocompatibility Antigen H-2D
  • Methylcholanthrene
  • Complement System Proteins
Topics
  • Animals
  • Antibodies, Monoclonal
  • Complement System Proteins
  • Cytotoxicity, Immunologic (immunology)
  • Fibrosarcoma (chemically induced, genetics, immunology, secondary)
  • H-2 Antigens (genetics, immunology)
  • Histocompatibility Antigen H-2D
  • Killer Cells, Natural (immunology)
  • Methylcholanthrene
  • Mice
  • Mice, Inbred BALB C
  • Phenotype
  • Transfection

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