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A murine macrophage cell line, immortalized by v-raf and v-myc oncogenes, exhibits normal macrophage functions
E Blasi1, D Radzioch, S K Durum
1Laboratory of Molecular Immunoregulation, National Cancer Institute, Frederick.
Abstract:
In vitro immortalized cell lines with the morphology and phenotype of mature macrophages (M phi) have been generated by infecting freshly isolated bone marrow cells from C3H/HeJ mice with a recombinant retrovirus carrying v-raf and v-myc oncogenes. All of the clones obtained had M phi-like phenotypes, and one such clone, GG2EE, has been compared to normal M phi to ascertain the effects of immortalization on the expression of the biological functions of the lines. GG2EE cells expressed cytotoxic activity against L5178Y, P815 or RL male 1 target cells in response to stimulation with interferon-gamma (IFN-gamma) and heat-killed Listeria monocytogenes; in contrast, they failed to kill YAC-1 target cells. GG2EE cells did not constitutively express I-A or I-E antigens; nevertheless, I region-coded antigens could be induced by IFN-gamma treatment. GG2EE cells produced interleukin 1 upon stimulation with a T cell-derived lymphokine; they were weakly phagocytic, yet became highly phagocytic following IFN-gamma treatment. Since c-fos mRNA is augmented in peritoneal exudate M phi by protein kinase C activators but not by IFN-gamma, we evaluated the effects of calcium ionophore, phorbol myristate acetate, L-alpha-1-oleoyl-2-acetoyl-sn-3 glycerol (OAG) and IFN-gamma on the levels of c-fos mRNA in GG2EE cells. We found that calcium ionophore, PMA and OAG stimulation enhanced the expression of c-fos mRNA, but IFN-gamma treatment did not. The kinetics of c-fos induction in GG2EE cells were also comparable to those observed in peritoneal exudate M phi. Overall, the GG2EE cell line has the same biological properties as normal tissue M phi. Because it is capable of both constitutive and inducible M phi-like functions, this cell line provides a valuable tool for studying the molecular mechanisms controlling induction and/or expression of biological activities in M phi. It is striking that a cell line immortalized in vitro by two oncogenes, v-raf and v-myc, behaves, according to the criteria mentioned above, like a normal M phi population.
Insights
Researchers immortalized mouse macrophages (M phi) using oncogenes, creating the GG2EE cell line. This cell line retains key biological functions of normal macrophages, making it a valuable tool for studying macrophage activity.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- In vitro immortalized cell lines are crucial for studying cellular functions.
- Macrophages (M phi) play vital roles in immunity and inflammation.
- Understanding macrophage biology requires reliable experimental models.
Purpose of the Study:
- To generate and characterize an immortalized macrophage cell line.
- To compare the biological functions of the immortalized cell line (GG2EE) with normal macrophages.
- To assess the utility of the GG2EE cell line for studying macrophage molecular mechanisms.
Main Methods:
- Bone marrow cells from C3H/HeJ mice were infected with a retrovirus carrying v-raf and v-myc oncogenes.
- Immortalized clones were selected, and the GG2EE clone was extensively characterized.
- Functional assays included cytotoxicity, antigen expression, cytokine production, phagocytosis, and c-fos mRNA induction.
Main Results:
- The GG2EE cell line exhibited M phi-like morphology and phenotype.
- GG2EE cells showed inducible cytotoxic activity, antigen expression (I-A, I-E), and interleukin-1 production.
- Phagocytic capacity and c-fos mRNA induction kinetics in GG2EE cells mirrored those of normal macrophages.
Conclusions:
- The immortalized GG2EE cell line accurately recapitulates the biological functions of normal macrophages.
- GG2EE cells serve as a valuable model for investigating the molecular regulation of macrophage activities.
- Oncogene-induced immortalization can yield cell lines that retain critical normal cell functions.