首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Erythrocyte Catabolism by Macrophages In Vitro THE EFFECT OF HYDROCORTISONE ON ERYTHROPHAGOCYTOSIS AND ON THE INDUCTION OF HEME OXYGENASE
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Erythrocyte Catabolism by Macrophages In Vitro THE EFFECT OF HYDROCORTISONE ON ERYTHROPHAGOCYTOSIS AND ON THE INDUCTION OF HEME OXYGENASE

机译:巨噬细胞对红细胞的体外代谢作用氢化可的松对红细胞吞噬作用和血红素加氧酶诱导的影响

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摘要

Phagocytosis of erythrocytes was studied in vitro in an incubation system consisting of rat peritoneal macrophages and antibody-coated 59Fe-labeled erythrocytes. The system was characterized in terms of the rate and magnitude of erythrophagocytosis, determined by the interiorization of the 59Fe label. On incubation of 150 × 106 macrophages with 75 × 106 antibodycoated erythrocytes, erythrophagocytosis began within a few minutes and was essentially completed after 2 h when 50% of the offered red cells had been ingested by the macrophages. Heme oxygenase (HO) activity, which is very low in native macrophages, increased 4- to 10- fold in response to the ingested erythrocytes; this enzyme stimulation occurred with a delay of 3 h in relation to erythrophagocytosis. Actinomycin D or puromycin prevented the increase of HO activity without affecting erythrophagocytosis, which suggests that the enzyme stimulation was due to substrate-mediated enzyme induction.Hydrocortisone (HC) (0.1 mg/ml medium) dissociated erythrophagocytosis from HO induction, leaving the former unimpaired but completely suppressing the latter. The suppressive effect of HC on the enzyme induction was completely prevented by 5 mg glucose and 0.02 U insulin/ml of the medium. In macrophages engaged in erythrophagocytosis. HC also lowered glucose removal from the medium and reduced formation of 14CO2 from [1-14C]glucose.These results suggest that induction of HO in macrophages by the hemoglobin of ingested erythrocytes requires intact transport or metabolism of glucose. Glucose utilization appears to be impaired by HC, but is restored by additional glucose and insulin. The findings suggest that plasma steroid concentrations in the pharmacological range could reduce bilirubin formation in phagocytic cells in vivo without affecting the sequestration and degradation of erythrocytes. This provides a possible explanation for the observation that in patients with hepatogenous jaundice, steroids often lower the serum bilirubin level.
机译:在由大鼠腹膜巨噬细胞和抗体包被的 59 Fe标记的红细胞组成的培养系统中,对红细胞的吞噬作用进行了体外研究。该系统的特征是通过 59 Fe标签的内在化确定了红细胞吞噬作用的速率和程度。将150×10 6 巨噬细胞与75×10 6 抗体包被的红细胞孵育后,红细胞吞噬作用在几分钟内开始,并在2小时后基本完成,此时提供的50%红细胞细胞已被巨噬细胞摄取。血红素加氧酶(HO)的活性在天然巨噬细胞中非常低,响应摄取的红细胞增加了4到10倍。与红细胞吞噬作用有关的这种酶刺激延迟了3小时。放线菌素D或嘌呤霉素在不影响红细胞吞噬作用的情况下阻止了HO活性的增加,这表明酶刺激是由于底物介导的酶诱导而引起的。氢化可的松(HC)(0.1 mg / ml培养基)使红细胞吞噬作用与HO诱导解离,使前者不受损害。但完全压制了后者。 5 mg葡萄糖和0.02 U胰岛素/ ml的培养基完全阻止了HC对酶诱导的抑制作用。在巨噬细胞中参与红细胞吞噬作用。 HC还降低了培养基中葡萄糖的去除,并减少了[1- 14 C]葡萄糖中 14 CO2的形成。这些结果表明,巨噬细胞中的血红蛋白可诱导HO的形成。摄入的红细胞需要完整的葡萄糖转运或代谢。 HC似乎会损害葡萄糖的利用,但额外的葡萄糖和胰岛素会恢复葡萄糖的利用。这些发现表明,药理学范围内的血浆类固醇浓度可以减少体内吞噬细胞中的胆红素形成,而不会影响红细胞的螯合和降解。这为肝源性黄疸患者中的类固醇经常降低血清胆红素水平提供了可能的解释。

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