Munoz N M, Vita A J, Neeley S P, McAllister K, Spaethe S M, White S R, Leff A R
Department of Medicine, University of Chicago, Illinois.
J Pharmacol Exp Ther. 1994 Jan;268(1):139-43.
The inhibitory effect of beta-2 adrenergic receptor stimulation on leukotriene C4 (LTC4) secretion and eosinophil peroxidase (EPO) release caused by exogenous activation with 10(-8) to 10(-6) M formyl-met-leu-phe (fMLP) + 5 micrograms/ml of cytochalasin B (Cyto B) in purified human peripheral blood eosinophils was studied. Cells from normal subjects were isolated by negative immunoselection and remained > or = 98% viable as determined by trypan blue exclusion. Duplicate aliquots of eosinophils (10(5) cells/intervention) were activated with 1) fMLP + Cyto B alone, 2) fMLP + Cyto B after pretreatment with 10(-8) M albuterol, 3) 10(-8) M albuterol + fMLP + Cyto B after pretreatment with 10(-8) M propranolol or 4) vehicle control. After incubation, the supernatants were tested for concentration of LTC4 and EPO. Concentration-related release of EPO was demonstrated for 10(-8) M fMLP + 5 micrograms/ml of Cyto B to 10(-6) M fMLP + 5 micrograms/ml of Cyto B, and the greatest concentration of fMLP was used in all subsequent studies. FMLP + Cyto B caused substantial LTC4 secretion in eosinophils (300 +/- 83.0 pg/ml) as compared to sham-activated eosinophils (3.3 +/- 1.9 pg/ml; P < .02). Similarly, maximum EPO release increased from 277 +/- 17.8 to 3956 +/- 1230 ng/10(6) cells (P < .02) after activation with fMLP + Cyto B. Treatment with albuterol decreased markedly both LTC4 secretion to 144 +/- 54.0 pg/ml (P < .05 vs. fMLP + Cyto B-activated eosinophils) and EPO release to 1993 +/- 368 ng/10(6) cells (P < .05 vs. fMLP + Cyto B-activated eosinophils).(ABSTRACT TRUNCATED AT 250 WORDS)
研究了β-2肾上腺素能受体刺激对纯化的人外周血嗜酸性粒细胞中白三烯C4(LTC4)分泌和嗜酸性粒细胞过氧化物酶(EPO)释放的抑制作用,这些嗜酸性粒细胞通过10^(-8)至10^(-6) M的甲酰甲硫氨酸亮氨酸苯丙氨酸(fMLP)+ 5微克/毫升的细胞松弛素B(细胞松弛素B)进行外源性激活。通过阴性免疫选择从正常受试者中分离细胞,经台盼蓝排斥法测定,细胞存活率≥98%。将嗜酸性粒细胞的重复等分试样(10^5个细胞/干预)用以下方法激活:1)单独使用fMLP +细胞松弛素B;2)用10^(-8) M沙丁胺醇预处理后再用fMLP +细胞松弛素B;3)用10^(-8) M普萘洛尔预处理后再用10^(-8) M沙丁胺醇+ fMLP +细胞松弛素B;或4)溶剂对照。孵育后,检测上清液中LTC4和EPO的浓度。对于10^(-8) M fMLP + 5微克/毫升细胞松弛素B至10^(-6) M fMLP + 5微克/毫升细胞松弛素B,证明了EPO的浓度依赖性释放,并且在所有后续研究中使用了最高浓度的fMLP。与假激活的嗜酸性粒细胞(3.3±1.9皮克/毫升;P <.02)相比,fMLP +细胞松弛素B导致嗜酸性粒细胞中大量LTC4分泌(300±83.0皮克/毫升)。同样,用fMLP +细胞松弛素B激活后,最大EPO释放从277±17.8增加到3956±1230纳克/10^6个细胞(P <.02)。用沙丁胺醇治疗可使LTC4分泌显著降低至144±54.0皮克/毫升(与fMLP +细胞松弛素B激活的嗜酸性粒细胞相比,P <.05),EPO释放降低至1993±368纳克/10^6个细胞(与fMLP +细胞松弛素B激活的嗜酸性粒细胞相比,P <.05)。(摘要截断于250字)