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肺癌患者肺泡巨噬细胞一氧化氮活性研究 被引量:3

A study on the activity of nitric oxide in alveolarmacrophages from patients with lung cancer
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摘要 用镀铜镉还原-Griess法检测肺癌患者BALF及肺泡巨噬细胞(AM)培养上清液中NO水平;RT-PCR检测AMiNOSmRNA表达。结果显示,肺癌组BALF及AM培养上清液中NO水平均明显低于对照组。两组AMiNOSmRNA表达阳性率分别为69%和91%(P>0.05),但表达强度肺癌组明显弱于对照组(P<0.01)。经GM-CSF刺激后,AMiNOS表达强度及培养上清液中NO水平均显著提高。提示肺癌局部AM抗肿瘤功能可能存在某些缺陷; Nitrite and nitrate (NO_2^-/NO_2^-) in the bronchus alveolar lavage fluid (BALF) and the supernatants of incubated alveolar macrophages(AMs) from patients with primary lung cancer were measured by coppercoated cadmium reduction and Griess metehod. mRNA expression of AM induced nitric oxide synthase(iNOS) were analyzed by RTPCR. There was NO-2/NO-2 in BALF either from lung cancer patients or from control subjects. When compared with control group and the nontumorbearing lung, the level of NO-2/NO-2 was lower in BALF from the tumorbearing lung [5.18±1.1 vs 2.47±0.67nmol·mg protein-1 (P<0.01); 4.65±2.46 vs 2.47±0.67nmol·mg protein-1 (P<0.01)]. We also found a lower level of NO-2/NO-2 in the supernatants of incubated AMs from the lung of cancer patients than from control and nontumorbearing lung [95.03±21.76 vs 63.37±17.58nmol (P<0.01); 85.61±16.70 vs 63.37±17.58nmol (P<0.05)]. No significant difference existed between the mRNA expression of AM iNOS in lung cancer patients (69%) and that of control subjects (91%). After the AMs were stimulated with granulocytemacrophage colony stimulating factor (GMCSF), the level of NO-2/NO-2 in the supernatants was significantly increased (P<0.01); while the mRNA expression of AM iNOS from patients with lung cancer resulted in an increase of 16.85±7.58% vs 33.38±8.21% of control group (P<0.05). These observation suggest that some defects of antitumor function occur in the AMs at the tumor region. GMCSF can stimulate AMs and thus potentiate their NO activity.
出处 《湖南医科大学学报》 CSCD 1998年第2期157-160,共4页 Bulletin of Hunan Medical University
关键词 肺肿瘤 肺泡 巨噬细胞 一氧化氮 pulmonary neoplasm alveolus macrophage nitric oxide synthase gene expression
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