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首页> 外文期刊>The Journal of pediatrics >L-selectin expression on polymorphonuclear leukocytes and monocytes in premature infants: reduced expression after dexamethasone treatment for bronchopulmonary dysplasia.
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L-selectin expression on polymorphonuclear leukocytes and monocytes in premature infants: reduced expression after dexamethasone treatment for bronchopulmonary dysplasia.

机译:早产儿多形核白细胞和单核细胞上的L-选择素表达:地塞米松治疗支气管肺发育不良后表达降低。

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摘要

We examined the effect of dexamethasone on the expression of the adhesion molecule L-selectin on circulating polymorphonuclear leukocytes (PMLs) and monocytes from premature infants with bronchopulmonary dysplasia (BPD). Nineteen infants who received dexamethasone (Dex group) and 28 who did not receive dexamethasone (no Dex group) were studied. L-selectin expression, measured as mean fluorescence intensity, was lower on circulating PMLs (5.7 +/- 0.6 vs 10.6 +/- 0.7, p < 0.001) and monocytes (7.9 +/- 0.9 vs 12.5 +/- 0.9, p < 0.02) isolated from those who had received dexamethasone. Because L-selectin is important for the recruitment of PMLs to inflammatory foci in the lungs, we speculate that one of the mechanisms by which dexamethasone reduces inflammation in BPD is by impairing the ability of leukocytes to migrate into the BPD lesions.
机译:我们检查了地塞米松对支气管肺发育不良(BPD)早产儿的循环多形核白细胞(PMLs)和单核细胞上粘附分子L-选择蛋白表达的影响。研究了19例接受地塞米松的婴儿(Dex组)和28例未接受地塞米松的婴儿(无Dex组)。以平均荧光强度测量的L-选择素表达在循环PMLs(5.7 +/- 0.6 vs 10.6 +/- 0.7,p <0.001)和单核细胞(7.9 +/- 0.9 vs 12.5 +/- 0.9,p <0.001)较低0.02)与接受地塞米松的人隔离。因为L-选择素对于将PML募集到肺部炎症灶很重要,所以我们推测地塞米松减轻BPD炎症的机制之一是削弱白细胞迁移进入BPD病变的能力。

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