Establishment and characterization of murine bone marrow-derived spontaneously immortalized cell lines and clones expressing properties of normal macrophages

Keyphrases

• Jerusalem 100%
• Macrophages 100%
• Lipopolysaccharide 100%
• L-cells 100%
• Cell-conditioned Medium 100%
• Murine Bone Marrow 100%
• Cell Clones 100%
• Bone Marrow Macrophages 100%
• Bone Marrow-derived 100%
• Immortalized Cell Lines 100%
• Soft Agar 66%
• Liquid Medium 66%
• Zymosan 66%
• Lymphokines 66%
• Culture Dish 66%
• Interleukin-1β 33%
• Surface Antigen 33%
• Tumor 33%
• Proliferative Activity 33%
• Lysozyme 33%
• Tumor Necrosis Factor-α 33%
• Bone Marrow Cells 33%
• Fc Receptor 33%
• First Month 33%
• Syngeneic 33%
• M-function 33%
• Slow Growth 33%
• Antigen Expression 33%
• Subcutaneous Injection 33%
• Exponential Growth Phase 33%
• Homogeneous Population 33%
• Female Mice 33%
• Cell Ingrowth 33%
• Killing Bacteria 33%
• CSF-1 33%
• Respiratory Burst 33%
• Complete Expression 33%
• Tumoricidal Activity 33%
• Cloning Efficiency 33%
• Murine Bone Marrow Cells 33%
• Tissue Culture Plastic 33%
• Continuous Cultivation 33%
• Non-activated 33%
• Nonspecific Esterases 33%

Immunology and Microbiology

• Macrophage 100%
• Cell Clone 100%
• Spontaneously Immortalized Cell Line 100%
• Agar 40%
• Bone Marrow Cell 40%
• Lymphokine 40%
• Maturation 20%
• Cell Population 20%
• Cell Line 20%
• Interleukin 1 20%
• Tumor Necrosis Factor 20%
• Fc Receptor 20%
• Ingestion 20%
• Tissue Culture 20%
• Antigen Expression 20%
• Colony Stimulating Factor 20%
• Respiratory Burst 20%
• Membrane Antigen 20%
• Syngenic 20%
• Antineoplastic Activity 20%
• Staining 20%
• Ia Antigen 20%
• Lysozyme 20%
• Bacterium 20%