Rabe K F, Muñoz N M, Vita A J, Morton B E, Magnussen H, Leff A R
Krankenhaus Grosshansdorf, Zentrum für Pneumologie und Thoraxchirurgie, LVA Hamburg, Germany.
Am J Physiol. 1994 Sep;267(3 Pt 1):L326-34. doi: 10.1152/ajplung.1994.267.3.L326.
We assessed the effect of activated eosinophils isolated from human peripheral blood in causing contraction of explanted human bronchi in vitro. Sixty-three epithelium-intact fifth generation airway sections were obtained from 16 subjects undergoing lung resection for carcinoma. Eosinophils were isolated by negative immunoselection, and activation with 10(-7) M platelet-activating factor (PAF) was confirmed by measurements of eosinophil peroxidase (EPO) secretion and superoxide (O2-.) generation. EPO secretion increased from 68.6 +/- 13.4 ng/10(6) cells to 420 +/- 125 ng/10(6) cells after activation with PAF (P < 0.05). Similarly, PAF-induced O2-. generation increased from 15.3 +/- 4.64 nmol cytochrome c reduced/10(5) cells to 44.2 +/- 8.50 nmol cytochrome c reduced/10(5) cells (P < 0.05). Cells were instilled into an isolated airway pouch preparation, and, 60 min later, airway contractile responses were determined by optical micrometry as percent decrease in lumenal diameter (%decrease) and percent increase in wall thickness (%increase) using a calibrated magnifying lens. Treatment with either vehicle, PAF alone, or untreated eosinophils had no effect on airway caliber or thickness. PAF-activated cells caused a 30.5 +/- 1.52% decrease in airway caliber (P < 0.001 vs. untreated cells) and a 36.6 +/- 2.54% increase in wall thickness (P < 0.001 vs. untreated cells). Preincubation with A63162, a 5-lipoxygenase inhibitor, caused concentration-dependent inhibition of airway narrowing. After 10(-5) M A63162, decrease in airway diameter caused by PAF was 8.00 +/- 0.10% vs. 30.5 +/- 1.52% for PAF alone (P < 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)
我们评估了从人外周血中分离出的活化嗜酸性粒细胞在体外引起人离体支气管收缩的作用。从16例因肺癌接受肺切除术的受试者中获取了63个上皮完整的第五代气道节段。通过阴性免疫筛选分离嗜酸性粒细胞,并用嗜酸性粒细胞过氧化物酶(EPO)分泌和超氧化物(O₂⁻)生成的测量来确认其用10⁻⁷M血小板活化因子(PAF)的活化情况。用PAF活化后,EPO分泌从68.6±13.4 ng/10⁶个细胞增加到420±125 ng/10⁶个细胞(P<0.05)。同样,PAF诱导的O₂⁻生成从15.3±4.64 nmol细胞色素c还原/10⁵个细胞增加到44.2±8.50 nmol细胞色素c还原/10⁵个细胞(P<0.05)。将细胞滴入离体气道囊制备物中,60分钟后,使用校准的放大镜通过光学显微镜测量气道收缩反应,以管腔直径减小百分比(%减小)和壁厚增加百分比(%增加)来确定。用赋形剂、单独的PAF或未处理的嗜酸性粒细胞处理对气道口径或厚度均无影响。PAF活化的细胞导致气道口径降低30.5±1.52%(与未处理细胞相比,P<0.001),壁厚增加36.6±2.54%(与未处理细胞相比,P<0.001)。用5-脂氧合酶抑制剂A63162预孵育导致气道狭窄的浓度依赖性抑制。在10⁻⁵M A63162处理后,PAF引起的气道直径减小为8.00±0.10%,而单独PAF处理为30.5±1.52%(P<0.01)。(摘要截断于250字)