190 related articles for article (PubMed ID: 2509612)
1. Role of C5a in the induction of tumoricidal activity in C3H/HeJ (Lpsd) and C3H/OuJ (Lpsn) macrophages.
Hogan MM; Yancey KB; Vogel SN
J Leukoc Biol; 1989 Dec; 46(6):565-70. PubMed ID: 2509612
[TBL] [Abstract][Full Text] [Related]
2. Production of tumor necrosis factor by rIFN-gamma-primed C3H/HeJ (Lpsd) macrophages requires the presence of lipid A-associated proteins.
Hogan MM; Vogel SN
J Immunol; 1988 Dec; 141(12):4196-202. PubMed ID: 3143760
[TBL] [Abstract][Full Text] [Related]
3. Lipid A-associated proteins provide an alternate "second signal" in the activation of recombinant interferon-gamma-primed, C3H/HeJ macrophages to a fully tumoricidal state.
Hogan MM; Vogel SN
J Immunol; 1987 Dec; 139(11):3697-702. PubMed ID: 3119714
[TBL] [Abstract][Full Text] [Related]
4. Bone marrow progenitors cultured in the presence of granulocyte-macrophage colony-stimulating factor versus macrophage colony-stimulating factor differentiate into macrophages with distinct tumoricidal capacities.
Falk LA; Hogan MM; Vogel SN
J Leukoc Biol; 1988 May; 43(5):471-6. PubMed ID: 3131473
[TBL] [Abstract][Full Text] [Related]
5. Inhibition of macrophage tumoricidal activity by glucocorticoids.
Hogan MM; Vogel SN
J Immunol; 1988 Jan; 140(2):513-9. PubMed ID: 3121748
[TBL] [Abstract][Full Text] [Related]
6. Taxol provides a second signal for murine macrophage tumoricidal activity.
Manthey CL; Perera PY; Salkowski CA; Vogel SN
J Immunol; 1994 Jan; 152(2):825-31. PubMed ID: 7506736
[TBL] [Abstract][Full Text] [Related]
7. Restoration of lipopolysaccharide-mediated cytotoxic macrophage induction in C3H/HeJ mice by interferon-gamma or a calcium ionophore.
Akagawa KS; Kamoshita K; Onodera S; Tokunaga T
Jpn J Cancer Res; 1987 Mar; 78(3):279-87. PubMed ID: 3106284
[TBL] [Abstract][Full Text] [Related]
8. Role of macrophage lipids in regulating tumoricidal activity. II. Internal genetic and external physiologic regulatory factors controlling macrophage tumor cytotoxicity also control characteristic lipid changes associated with tumoricidal cells.
Schlager SI; Meltzer MS
Cell Immunol; 1983 Aug; 80(1):10-9. PubMed ID: 6872005
[TBL] [Abstract][Full Text] [Related]
9. Macrophages from endotoxin-hyporesponsive (Lpsd) C3H/HeJ mice are permissive for vesicular stomatitis virus because of reduced levels of endogenous interferon: possible mechanism for natural resistance to virus infection.
Vogel SN; Fertsch D
J Virol; 1987 Mar; 61(3):812-8. PubMed ID: 2433468
[TBL] [Abstract][Full Text] [Related]
10. Establishment of murine macrophage hybridoma clones capable of acquiring tumoricidal activity upon activation with recombinant interferon-gamma and lipopolysaccharide.
Kiyotaki C; Katagiri T; Tatsumi Y; Fujiwara H; Hamaoka T
J Cancer Res Clin Oncol; 1987; 113(4):383-6. PubMed ID: 3110175
[TBL] [Abstract][Full Text] [Related]
11. Identification and characterization of monoclonal antibodies specific for macrophages at intermediate stages in the tumoricidal activation pathway.
Paulnock DM; Lambert LE
J Immunol; 1990 Jan; 144(2):765-73. PubMed ID: 2104906
[TBL] [Abstract][Full Text] [Related]
12. Activation of C3H/HeJ macrophage tumoricidal activity and cytokine release by R-chemotype lipopolysaccharide preparations. Differential effects of IFN-gamma.
Flebbe LM; Chapes SK; Morrison DC
J Immunol; 1990 Sep; 145(5):1505-11. PubMed ID: 2117032
[TBL] [Abstract][Full Text] [Related]
13. Protein tyrosine kinase inhibitors decrease induction of nitric oxide synthase activity in lipopolysaccharide-responsive and lipopolysaccharide-nonresponsive murine macrophages.
Dong Z; Qi X; Xie K; Fidler IJ
J Immunol; 1993 Sep; 151(5):2717-24. PubMed ID: 7689614
[TBL] [Abstract][Full Text] [Related]
14. Detection and analysis of the 80-kd lipopolysaccharide receptor in macrophages derived from Lpsn and Lpsd mice.
Perera PY; Chan TY; Morrison DC; Vogel SN
J Leukoc Biol; 1992 May; 51(5):501-6. PubMed ID: 1376353
[TBL] [Abstract][Full Text] [Related]
15. The activation of tumoricidal properties in macrophages of endotoxin responder and nonresponder mice by liposome-encapsulated immunomodulators.
Fogler WE; Talmadge JE; Fidler IJ
J Reticuloendothel Soc; 1983 Mar; 33(3):165-74. PubMed ID: 6834360
[TBL] [Abstract][Full Text] [Related]
16. Synergistic interactions between IFN-gamma and IFN-beta in priming murine macrophages for tumor cell killing.
Pace JL
J Leukoc Biol; 1988 Dec; 44(6):514-20. PubMed ID: 3142957
[TBL] [Abstract][Full Text] [Related]
17. Regulation of murine macrophage function by IL-4: IL-4 and IFN-gamma differentially regulate macrophage tumoricidal activation.
Suk K; Somers SD; Erickson KL
Immunology; 1993 Dec; 80(4):617-24. PubMed ID: 8307612
[TBL] [Abstract][Full Text] [Related]
18. The correlation between specific protein synthesis and tumoricidal function in murine peritoneal macrophages.
Tannenbaum CS; Largen MT
Cell Immunol; 1990 Nov; 131(1):52-66. PubMed ID: 2121374
[TBL] [Abstract][Full Text] [Related]
19. Tumor cell killing and cytostasis by C3H/HeJ macrophages activated in vitro by lipid A-associated protein and interferon gamma.
Chapes SK; Killion JW; Morrison DC
J Leukoc Biol; 1988 Mar; 43(3):232-7. PubMed ID: 3125294
[TBL] [Abstract][Full Text] [Related]
20. Induction of IFN-gamma in macrophages by lipopolysaccharide.
Fultz MJ; Barber SA; Dieffenbach CW; Vogel SN
Int Immunol; 1993 Nov; 5(11):1383-92. PubMed ID: 8260452
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
