NR8383大鼠肺泡巨噬细胞

产品介绍

目录号 Serial	GNR 9
标识符 Identifier	CSTR:19375.09.3101RATGNR9
描述 Description	NR8383 (正常大鼠，1983年8月3日)来源于肺灌洗时的正常大鼠肺泡巨噬细胞。细胞在gerbil肺细胞连续培养液存在下培养了大约8-9个月。随后，不再需要外源生长因子。通过有限稀释法从单个细胞克隆并亚克隆NR8383细胞，并三次用软琼脂亚克隆。细胞表现出巨噬细胞的特性，吞噬酵母多糖和铜绿，非特异性脂酶活性，Fc受体，氧化降解；分泌IL-1, TNF beta和IL-6，可重复地响应外源生长因子。 NR8383细胞响应博莱霉素，分泌TGF beta前体。在博莱霉素刺激下，TGF beta mRNA表达也上升。细胞对内毒素敏感。 1-10 钠克/毫升的LPS水平抑制增生达50%。即使达到0.001毫克/毫升的水平，LPS抑制还是无毒且在后续过程中可逆的。 NR8383细胞株提供了高响应的肺泡巨噬细胞的均一来源，可以用于体外研究巨响细胞相关活性。此细胞半悬浮生长。在本库通过支原体检测。
动物种别 Organism	大鼠
性别 Gender	***
组织来源 Tissue and Cell Type	肺；巨噬细胞；肺泡
形态 Morphology	巨噬细胞，半悬浮或悬浮生长并部分聚团
培养基和添加剂 Complete Growth Medium and Culture Conditions	F-12K Nutrient Mixture (gibco by life technologies 21127-022)，80%；优质胎牛血清，20%。气相：空气，95%；二氧化碳，5%。温度：37摄氏度。
供应限制 Permits and Restrictions	A。仅供研究之用。
REFERENCE	Hidalgo HA , et al. Pneumocystis carinii induces an oxidative burst in alveolar macrophages. Infect. Immun. 60: 1-7, 1992. PubMed: 1729174Helmke RJ , et al. A continuous alveolar macrophage cell line: comparisons with freshly derived alveolar macrophages. In Vitro Cell. Dev. Biol. 25: 44-48, 1989. PubMed: 2914814Helmke RJ , et al. From growth factor dependence to growth factor responsiveness: the genesis of an alveolar macrophage cell line. In Vitro Cell. Dev. Biol. 23: 567-574, 1987. PubMed: 3497918Limper AH , Standing JE . Vitronectin interacts with Candida albicans and augments organism attachment to the NR8383 macrophage cell line. Immunol. Lett. 42: 139-144, 1994.PubMed: 7534269Hidalgo HA , et al. The effects of cyclosporine and dexamethasone on an alveolar macrophage cell line (NR8383). Transplantation 53: 620-623, 1992. PubMed: 1549855Denholm EM , Rollins SM . Expression and secretion of transforming growth factor-beta by bleomycin-stimulated rat alveolar macrophages. Am. J. Physiol. 264: L36-L42, 1993. PubMed: 7679254Krieg DP , et al. Resistance of mucoid Pseudomonas aeruginosa to nonopsonic phagocytosis by alveolar macrophages in vitro. Infect. Immun. 56: 3173-3169, 1988. PubMed: 3141284Sherman MP , et al. Pyrrolidine dithiocarbamate inhibits induction of nitric oxide synthase activity in rat alveolar macrophages. Biochem. Biophys. Res. Commun. 191: 1301-1308, 1993. PubMed: 7682068Griscavage JM , et al. Inducible nitric oxide synthase from a rat alveolar macrophage cell line is inhibited by nitric oxide. J. Immunol. 151: 6329-6337, 1993. PubMed: 7504017Henderson SA , et al. Nitric oxide reduces early growth response-1 gene expression in rat lung macrophages treated with interferon-gamma and lipopolysaccharide. J. Biol. Chem. 269: 25239-25242, 1994. PubMed: 7523382Huang S , et al. Rat KC cDNA cloning and mRNA expression in lung macrophages and fibroblasts. Biochem. Biophys. Res. Commun. 184: 922-929, 1992. PubMed: 1374243 Hay, R. J., Caputo, J. L, and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC. Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227. 1988. Fleming, D.O., Richardson, J. H., TuIis, J.J. and Vesley, D.,(1995) Laboratory Safety: Principles and Practice. Secondedition, ASM press, Washington, DC. Centers for Disease Control (1993), Biosafety inMicrobiological and Biomedical Laboratories Human HealthService Publication No. (CDC) 93-8395. U.S. Dept. of Health and Human Services; 3rd Edition U.S. Government Printing Office Washington D.C.

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