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Macrophage cell line

Fiirvonen M.-R., Nevalainen, A., N, Monkkonen, J., and Savolainen, K. (1997). Streptomyces spores trom mouldy houses induce nitric acid, TTNFa and 11,-6 secretion from R.AW264.7 macrophage cell line without causing subsequent cell death. Environ. Toxicol. Pharmacol. 4, 57-63. [Pg.344]

McDevitt, TM, Tchao, R, Harrison, EH, and Morel, DW, 2005. Carotenoids normally present in serum inhibit proliferation and induce differentiation of a human monocyte/macrophage cell line (U937). J Nutr 135, 160-164. [Pg.347]

Sakata K, Hirose Y, Qiao Z, Tanaka T and Mori H. 2003. Inhibition of inducible isoforms of cyclooxygenase and nitric oxide synthase by flavonoid hesperidin in mouse macrophage cell line. Cancer Lett 199(2)439-145. [Pg.174]

Ichikawa, D. et al., Effect of various catechins on the IL-12p40 production by murine peritoneal macrophages and a macrophage cell line, J774.1, Biol Pharm Bull, 27, 1353, 2004. [Pg.202]

Z. Z., Morris, S. M., )r., Coinduction of nitric oxide synthase and argininosuccinate synthetase in a murine macrophage cell line. Implications for regulation of nitric oxide production,/. Biol. Chem. 269 (1994), p. 1257-12561... [Pg.278]

Kobuchi H, Droy-Lefaix MT, Christen Y, Packer L. (1997). Ginkgo biloba extract (EGb 761) inhibitory effect on nitric oxide production in the macrophage cell line RAW 264.7. Biochem Pharmacol. 53(6) 897-903. [Pg.478]

Andersen O. 1983. Effects of coal combustion products and metal compounds on sister chromatid exchange (SCE) in a macrophage cell line. Environ Health Perspect 47 239-253. [Pg.223]

Tumor necrosis factor inhibition. Ethanol (95%) extract of the rhizome, in cell culture at a concentration of 100 pg/mL, was inactive on macrophage cell line RAW 264.7 vs EPS induction of TNF-az° zp Tumor promotion inhibition. Ethyl acetate and methanol extracts of the dried rhizome, in cell culture at a concentration of 50 pg/mL, produced weak activity on G3H/ lOTl/2 cells vs tetradecanoyl phorbol acetate-induced acetate phospholipid synthesis. The hexane extract was inactiveZ . Ethanol (95%) and petroleum ether extracts of the dried rhizome, in cell culture at a concentration of 160 and 80 pg/mL, re-... [Pg.542]

Analysis by SDS-polyacrylamide gel electrophoresis of purified NOS from isolated HC from rats injected with killed Corynebacterium parvum (H), and from the murine macrophage cell line RAW 264-7 (M) (courtesy of D. Stuehr, The Cleveland Clinic, Cleveland, OH) which was exposed to LPS and IFNy. Crude cytosols were separated using ion exchange and affinity 2 5 -ADP Sepharose chromatography. Last step by gel filtration is equivalent to separation by molecular weight. [Pg.226]

Previous studies on the effects of N=0 production on the alloimmune response utilized bulk populations of responder and stimulator cells. In order to more clearly define the circumstances that induce -N=0 synthesis in allogeneic macrophage-lymphocyte cocultures, mouse splenocyte populations were depleted of accessory cells (>90% Thy 1.2+) and cultured with mitomycin-C-treated macrophage cell lines, as the alloantigen presenting cells. The P388D1 (H2 ) and RAW 264.7 (H2 ) macrophage lines were selected because... [Pg.245]

CTM = cytotoxic activity against mouse macrophage cell line (RAW 264.7) [167] ... [Pg.231]

Nham, S. U., and Fuller, G. M. (1986). Effect of fibrinogen degradation products on production of hepatocyte stimulating factor by a macrophage cell line (P388D1). Thromb. Res. 44, 467-475. [Pg.293]

Recently, Tan et al. (Tan et ah, 2007) demonstrated that activation of (32-adrenoreceptors in the macrophage cell line (RAW264.7) in the absence of inflammatory stimulus increased the transcription and protein synthesis of IL-1 (3 and IL-6. This increase was not reduced by neither a PKA nor a NF-kB inhibitor, but was dependent on p38 and p42/44 MAPK activation, which in turn, activated activating transcription factor (ATF)l and ATF2. [Pg.29]

Brown SW, Meyers RT, Brennan KM, Rumble JM, Narasimhachari N, Perozzi EF, Ryan JJ, Stewart JK, Fischer-Stenger K (2003) Catecholamines in a macrophage cell line. J. [Pg.35]

Channon, J. Y., and Leslie, C. C. 1990. A calcium-dependent mechanism for associating a soluble arachidonoyl-hydrolyzing phospholipase A2 with membrane in the macrophage cell line RAW 264.7. J. Biol Chem. 265 5409-5413. [Pg.371]

Fig. 14.2 Cytokine responses to a human macrophage cell line (MonoMac 6) exposed to liposomal formulations of GLA. Liposomes contained the lipids indicated on the x-axis, cholesterol, and GLA. Adjuvant concentration was serially diluted by factors of 5 for each group, from left to right. LPS is the positive control. Variations in adjuvant activity are apparent depending on the phospholipid composition of the liposomes... Fig. 14.2 Cytokine responses to a human macrophage cell line (MonoMac 6) exposed to liposomal formulations of GLA. Liposomes contained the lipids indicated on the x-axis, cholesterol, and GLA. Adjuvant concentration was serially diluted by factors of 5 for each group, from left to right. LPS is the positive control. Variations in adjuvant activity are apparent depending on the phospholipid composition of the liposomes...

See other pages where Macrophage cell line is mentioned: [Pg.193]    [Pg.136]    [Pg.163]    [Pg.370]    [Pg.9]    [Pg.12]    [Pg.41]    [Pg.270]    [Pg.90]    [Pg.124]    [Pg.122]    [Pg.88]    [Pg.164]    [Pg.196]    [Pg.44]    [Pg.66]    [Pg.29]    [Pg.206]    [Pg.287]    [Pg.195]    [Pg.205]    [Pg.180]    [Pg.535]    [Pg.470]    [Pg.470]    [Pg.87]    [Pg.81]    [Pg.47]    [Pg.49]    [Pg.391]    [Pg.140]    [Pg.161]   
See also in sourсe #XX -- [ Pg.438 ]




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