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培养的大鼠库普弗细胞对脂多糖的反应。

Response of cultured rat Kupffer cells to lipopolysaccharide.

作者信息

Van Bossuyt H, Desmaretz C, Rombaut B, Wisse E

机构信息

Laboratory for Cell Biology and Histology, Free University of Brussels, Belgium.

出版信息

Arch Toxicol. 1988;62(4):316-24. doi: 10.1007/BF00332494.

DOI:10.1007/BF00332494
PMID:3240096
Abstract

The effects of Salmonella abortus equi lipopolysaccharides (LPS) on pure cultures of rat Kupffer cells (Kc) were studied. In vitro, LPS is ingested by Kc and located in vacuoles and secondary lysosomes. Culture of Kc in the presence of 1-50 micrograms LPS/ml during 24 h did not affect the viability of the Kc as measured by trypan blue exclusion, neutral red uptake, lactate dehydrogenase leakage and cell survival and spreading. LPS treatment did not influence the ultrastructure of Kc. The exposure of Kc to LPS in vitro did not change the phagocytic activity. Several biochemical processes were stimulated: glucose consumption, MTT-tetrazolium salt reduction, total protein synthesis and secretion of proteins. LPS activated Kc to tumoricidal activity against L929 mouse fibrosarcoma cells. In the light of the above observations, it is concluded that purified LPS is not cytotoxic for pure Kc in culture. On the contrary, LPS stimulates several biochemical and functional processes.

摘要

研究了马流产沙门氏菌脂多糖(LPS)对大鼠枯否细胞(Kc)纯培养物的影响。在体外,Kc摄取LPS并将其定位在液泡和次级溶酶体中。在24小时内,在含有1 - 50微克/毫升LPS的条件下培养Kc,通过台盼蓝排斥法、中性红摄取法、乳酸脱氢酶泄漏法以及细胞存活和铺展情况测定,未影响Kc的活力。LPS处理不影响Kc的超微结构。体外将Kc暴露于LPS不会改变其吞噬活性。刺激了几个生化过程:葡萄糖消耗、MTT四氮唑盐还原、总蛋白质合成和蛋白质分泌。LPS激活Kc对L929小鼠纤维肉瘤细胞产生杀肿瘤活性。根据上述观察结果,得出结论:纯化的LPS对培养中的纯Kc无细胞毒性。相反,LPS刺激了几个生化和功能过程。

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1
Response of cultured rat Kupffer cells to lipopolysaccharide.培养的大鼠库普弗细胞对脂多糖的反应。
Arch Toxicol. 1988;62(4):316-24. doi: 10.1007/BF00332494.
2
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Br J Pharmacol. 2004 Feb;141(3):477-87. doi: 10.1038/sj.bjp.0705633. Epub 2004 Jan 12.

本文引用的文献

1
Increased production of superoxide anion by macrophages exposed in vitro to muramyl dipeptide or lipopolysaccharide.体外暴露于胞壁酰二肽或脂多糖的巨噬细胞中超氧阴离子生成增加。
J Exp Med. 1980 Jan 1;151(1):101-14. doi: 10.1084/jem.151.1.101.
2
Uptake by liver cells of endotoxin following its intravenous injection.静脉注射内毒素后肝细胞对其的摄取。
Lab Invest. 1981 Jul;45(1):38-45.
3
The response of isolated rabbit hepatic macrophages (H-M macrophage) to lipopolysaccharide (LPS).离体兔肝巨噬细胞(H-M巨噬细胞)对脂多糖(LPS)的反应。
Circ Shock. 1981;8(2):165-81.
4
Role of the RES in the pathogenesis of endotoxic hypoglycemia.网状内皮系统在内毒素性低血糖症发病机制中的作用。
Circ Shock. 1982;9(3):269-80.
5
Time course of cellular distribution of endotoxin in liver, lungs and kidneys of rats.内毒素在大鼠肝脏、肺和肾脏中的细胞分布时间进程。
Br J Exp Pathol. 1982 Feb;63(1):56-65.
6
The induction of a unique procoagulant activity in rabbit hepatic macrophages by bacterial lipopolysaccharides.细菌脂多糖诱导兔肝巨噬细胞产生独特的促凝血活性。
J Immunol. 1981 Oct;127(4):1596-600.
7
Human alveolar macrophages: effects of endotoxin in vitro.人肺泡巨噬细胞:内毒素的体外作用
Infect Immun. 1980 Dec;30(3):753-8. doi: 10.1128/iai.30.3.753-758.1980.
8
Macrophages as a source of tumoricidal activity (tumor-necrotizing factor).巨噬细胞作为肿瘤杀伤活性(肿瘤坏死因子)的来源。
Infect Immun. 1980 Nov;30(2):523-30. doi: 10.1128/iai.30.2.523-530.1980.
9
Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays.用于细胞生长和存活的快速比色测定法:应用于增殖和细胞毒性测定。
J Immunol Methods. 1983 Dec 16;65(1-2):55-63. doi: 10.1016/0022-1759(83)90303-4.
10
The fate of lipopolysaccharide in rats: evidence for chemical alteration in the molecule.大鼠体内脂多糖的命运:分子化学改变的证据。
Rev Infect Dis. 1984 Jul-Aug;6(4):483-7. doi: 10.1093/clinids/6.4.483.