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.
|
Authors | J Gopas, B Rager-Zisman, I Har-Vardi, G J Hammerling, M Bar-Eli, S Segal |
Journal | Journal of immunogenetics
(J Immunogenet)
1989 Aug-Oct
Vol. 16
Issue 4-5
Pg. 305-13
ISSN: 0305-1811 [Print] England |
PMID | 2639905
(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
|