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暴露于人类血液单核细胞产物的牙龈细胞中前列腺素E生成的刺激作用。

Stimulation of production of prostaglandin E in gingival cells exposed to products of human blood mononuclear cells.

作者信息

D'Souza S M, Englis D J, Clark A, Russell R G

出版信息

Biochem J. 1981 Aug 15;198(2):391-6. doi: 10.1042/bj1980391.

Abstract
  1. Supernatant media from cultures of unstimulated human peripheral blood mononuclear cells contained one or more factors that increased by several hundred-fold the production of prostaglandin E by fibroblast-like cells derived from both inflamed and normal human gingival tissue. 2. This stimulation occurred in a dose-dependent manner and was completely inhibited by 14 microM-indomethacin. 3. Responsiveness to the factor declined as the age of the cell culture increased. 4. An increase in prostaglandin E production was first observed after a 2h exposure to the mononuclear cell factor(s) and could be prevented by cycloheximide. 5. Brief exposure (0.5 and 1.0 h) to mononuclear cell factor did not increase prostaglandin E production by the cells in a subsequent 72 h incubation in the absence of mononuclear cell factor. 6. Addition of arachidonate (10 microM and 15 microM) further enhanced stimulation of prostaglandin E production in response to mononuclear cell factor. 7. The stimulatory activity was resistant to digestion by trypsin, but was heat-labile, so that only 17% remained after treatment at 56 degrees C for 30 min.
摘要
  1. 未刺激的人外周血单核细胞培养物的上清培养基中含有一种或多种因子,这些因子可使源自发炎和正常人牙龈组织的成纤维细胞样细胞产生前列腺素E的量增加数百倍。2. 这种刺激呈剂量依赖性,并且被14微摩尔的吲哚美辛完全抑制。3. 随着细胞培养年龄的增加,对该因子的反应性下降。4. 在暴露于单核细胞因子2小时后首次观察到前列腺素E产量增加,并且可以被放线菌酮阻止。5. 在随后72小时无单核细胞因子的孵育中,短暂暴露(0.5小时和1.0小时)于单核细胞因子并不会增加细胞产生前列腺素E的量。6. 添加花生四烯酸(10微摩尔和15微摩尔)进一步增强了对单核细胞因子刺激前列腺素E产生的反应。7. 刺激活性对胰蛋白酶消化有抗性,但对热不稳定,因此在56℃处理30分钟后仅保留17%。

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Prostaglandin E2 levels and human periodontal disease.前列腺素E2水平与人类牙周病
Prostaglandins. 1974 Apr 10;6(1):81-5. doi: 10.1016/s0090-6980(74)80043-2.

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