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肺泡巨噬细胞在脂多糖诱导的中性粒细胞聚集中的作用。

Role of alveolar macrophages in lipopolysaccharide-induced neutrophil accumulation.

作者信息

Harmsen A G

机构信息

Trudeau Institute, Inc., Saranac Lake, New York 12983.

出版信息

Infect Immun. 1988 Aug;56(8):1858-63. doi: 10.1128/iai.56.8.1858-1863.1988.

Abstract

B6D2F1/TRU mice were exposed to a lipopolysaccharide (LPS) aerosol that resulted in a 1-h-postexposure lung burden of about 290 ng of LPS. This exposure caused an accumulation of neutrophils in the lung that peaked between 6 and 12 h after exposure. To determine the potential role of alveolar macrophages (AM) in the induction of neutrophil accumulation by LPS, 10(6) AM from normal or LPS-exposed mice were transferred to the lungs of groups of naive recipient mice. A third group of mice was instilled intratracheally with vehicle only. After 5 h, the lungs of the mice were lavaged and the numbers of neutrophils in the lavage fluids were determined. The instillation of AM from unexposed mice did not cause significantly more neutrophils to accumulate than did the instillation of vehicle only, whereas the instillation of AM from LPS-exposed mice caused nearly a threefold increase in the numbers of neutrophils in lavage fluids. Transfer of AM from LPS-exposed mice into cutaneous air pouches of naive mice also caused greater local neutrophil accumulation (10-fold) than did the transfer of AM from normal mice. Repeated freeze-thawing of the suspensions of AM before transfer to recipients significantly reduced the ability of the suspensions to induce neutrophil accumulation. This indicated that AM viability is necessary to cause a maximal neutrophil infiltration upon transfer of the AM. To determine the extent to which LPS-induced neutrophil accumulation depends on the presence of AM, the ability of LPS to elicit neutrophil accumulation when injected alone or together with AM into air pouches was determined. The injection of either AM or LPS alone caused few neutrophils to accumulate, whereas the injection of LPS and AM together caused a large number of neutrophils to accumulate. The results of this study indicate that LPS deposition in the lung can stimulate AM to induce neutrophil accumulation and that this may be the major mechanism by which LPS causes neutrophil accumulation.

摘要

将B6D2F1/TRU小鼠暴露于脂多糖(LPS)气溶胶中,暴露1小时后肺部LPS负荷约为290纳克。这种暴露导致肺部中性粒细胞积聚,在暴露后6至12小时达到峰值。为了确定肺泡巨噬细胞(AM)在LPS诱导中性粒细胞积聚中的潜在作用,将来自正常或LPS暴露小鼠的10⁶个AM转移到未接触过抗原的受体小鼠组的肺部。第三组小鼠仅气管内注入赋形剂。5小时后,对小鼠肺部进行灌洗,并测定灌洗液中中性粒细胞的数量。与仅注入赋形剂相比,注入未暴露小鼠的AM不会导致明显更多的中性粒细胞积聚,而注入LPS暴露小鼠的AM会使灌洗液中中性粒细胞数量增加近三倍。将LPS暴露小鼠的AM转移到未接触过抗原的小鼠的皮肤气袋中,也比转移正常小鼠的AM引起更大的局部中性粒细胞积聚(10倍)。在将AM悬液转移给受体之前对其进行反复冻融,显著降低了悬液诱导中性粒细胞积聚的能力。这表明AM的活力对于AM转移后引起最大程度的中性粒细胞浸润是必要的。为了确定LPS诱导的中性粒细胞积聚在多大程度上依赖于AM的存在,测定了单独注射LPS或与AM一起注入气袋时LPS引发中性粒细胞积聚的能力。单独注射AM或LPS都只会导致少量中性粒细胞积聚,而同时注射LPS和AM会导致大量中性粒细胞积聚。这项研究的结果表明,LPS在肺部的沉积可刺激AM诱导中性粒细胞积聚,这可能是LPS导致中性粒细胞积聚的主要机制。

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