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活化嗜酸性粒细胞和中性粒细胞对豚鼠气道上皮细胞的体外作用。

The effects of activated eosinophils and neutrophils on guinea pig airway epithelium in vitro.

作者信息

Yukawa T, Read R C, Kroegel C, Rutman A, Chung K F, Wilson R, Cole P J, Barnes P J

机构信息

Department of Thoracic Medicine, National Heart and Lung Institute, Brompton Hospital, London, United Kingdom.

出版信息

Am J Respir Cell Mol Biol. 1990 Apr;2(4):341-53. doi: 10.1165/ajrcmb/2.4.341.

Abstract

Epithelial shedding is a characteristic feature of asthmatic airways and has been attributed to eosinophil products. We have examined the interaction of purified intraperitoneal guinea pig eosinophils with or without platelet-activating factor (PAF, 10(-7) M) or lyso-PAF (10(-7) M) with guinea pig tracheal epithelium in vitro. At 0, 4, 14, and 24 h, the percentage of ciliation of the tracheal circumference (CTC) was measured by light microscopy and the ciliary beat frequency (CBF) by photometry. PAF-activated eosinophils (50 x 10(6) cells/ml) disrupted the epithelium, mean CBF and CTC being reduced by 77.8 +/- 5.8% (mean +/- SEM; P less than 0.001 versus control) and 94.2 +/- 1.4% (P less than 0.001) over 24 h, respectively. PAF (10(-7) M) alone had no significant effect. Lyso-PAF with eosinophils (50 x 10(6) cells/ml) also reduced mean CBF and CTC but to a lesser extent. Eosinophils alone also led to a reduction of 36.2 +/- 11.4% in mean CBF and 53.0 +/- 15.5% in CTC, but these changes were not significant. The PAF antagonist, WEB 2086 (10(-6) M), significantly inhibited the mean CBF and CTC reduction due to PAF-activated eosinophils by 61.5 +/- 17.2% (P less than 0.01) and 20.8 +/- 6.5% (P less than 0.05), respectively. In addition, catalase (1,125 U/ml) partially inhibited the mean CBF and CTC reduction induced by PAF-activated eosinophils. Intraperitoneal neutrophils (PMN) (50 x 10(6) cells/ml) also disrupted epithelium but to a lesser extent (24-h reduction: 34.2 +/- 12.7% for mean CBF and 60.2 +/- 13.2% for CTC, respectively). Stimulation with PAF (10(-7) M) had no further effect. Marked exfoliation of the epithelial layer was observed after 14 h of incubation with activated eosinophils. We concluded the PAF-activated eosinophils are capable of grossly disrupting ciliated epithelium and may contribute to epithelial damage observed in asthma.

摘要

上皮细胞脱落是哮喘气道的一个特征性表现,且一直被认为与嗜酸性粒细胞产物有关。我们在体外研究了纯化的豚鼠腹腔嗜酸性粒细胞与豚鼠气管上皮细胞的相互作用,这些嗜酸性粒细胞分别添加或未添加血小板活化因子(PAF,10⁻⁷ M)或溶血PAF(10⁻⁷ M)。在0、4、14和24小时时,通过光学显微镜测量气管圆周纤毛化百分比(CTC),通过光度测定法测量纤毛摆动频率(CBF)。PAF激活的嗜酸性粒细胞(50×10⁶细胞/毫升)破坏了上皮细胞,在24小时内,平均CBF和CTC分别降低了77.8±5.8%(平均值±标准误;与对照组相比,P<0.001)和94.2±1.4%(P<0.001)。单独的PAF(10⁻⁷ M)没有显著影响。溶血PAF与嗜酸性粒细胞(50×10⁶细胞/毫升)一起也降低了平均CBF和CTC,但程度较小。单独的嗜酸性粒细胞也导致平均CBF降低36.2±11.4%,CTC降低53.0±15.5%,但这些变化不显著。PAF拮抗剂WEB 2086(10⁻⁶ M)分别显著抑制了由于PAF激活的嗜酸性粒细胞导致的平均CBF和CTC降低,抑制率分别为61.5±17.2%(P<0.01)和20.8±6.5%(P<0.05)。此外,过氧化氢酶(1125 U/毫升)部分抑制了PAF激活的嗜酸性粒细胞诱导的平均CBF和CTC降低。腹腔中性粒细胞(PMN)(50×10⁶细胞/毫升)也破坏了上皮细胞,但程度较小(24小时降低:平均CBF为34.2±12.7%,CTC为60.2±13.2%)。用PAF(10⁻⁷ M)刺激没有进一步影响。在用激活的嗜酸性粒细胞孵育14小时后,观察到上皮层明显剥脱。我们得出结论,PAF激活的嗜酸性粒细胞能够严重破坏纤毛上皮细胞,并可能导致哮喘中观察到的上皮损伤。

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