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肺表面活性蛋白A(SP-A)可增强肺泡巨噬细胞对细菌的非血清依赖性吞噬作用。

Lung surfactant protein A (SP-A) enhances serum-independent phagocytosis of bacteria by alveolar macrophages.

作者信息

Manz-Keinke H, Plattner H, Schlepper-Schäfer J

机构信息

Faculty of Biology, University of Konstanz, Konstanz, Germany.

出版信息

Eur J Cell Biol. 1992 Feb;57(1):95-100.

PMID:1639094
Abstract

Surfactant protein A (SP-A) is the main protein component of lung surfactant. We studied the involvement of SP-A in body defense, i.e., effect of SP-A on the phagocytosis of bacteria by alveolar macrophages. We show here that SP-A enhances the phagocytosis of some non-opsonized bacteria: Escherichia coli growing logarithmically (E. coli/log), Pseudomonas aeruginosa/log as well as from stationary phase (P. aeruginosa/stat) and Staphylococcus aureus/log. Furthermore, not only serum-independent phagocytosis was effected by SP-A but also phagocytosis of serum-opsonized S. aureus/stat. No effect of SP-A on phagocytosis was observed with E. coli/stat neither on serum-independent nor on serum-dependent phagocytosis and on phagocytosis of non-opsonized S. aureus/stat. Thus, effect of SP-A on phagocytosis is dependent on bacterial species and on the growth phase of the microorganisms, and this effect is concentration dependent. We studied two different human recombinant SP-As and SP-A isolated from lung lavage material from proteinosis patients. These SP-A molecules contain different isomeric chains, and they differ in complexity of their structure. Qualitatively, we found the same effect with all three substances. Quantitatively, the proteinosis SP-A that forms the most complex structure was the most effective. Taken together, we demonstrated a stimulating effect of SP-A on serum-independent as well as on serum-dependent phagocytosis of bacteria by alveolar macrophages, both depending on species and growth phase of the bacteria.

摘要

表面活性蛋白A(SP-A)是肺表面活性剂的主要蛋白质成分。我们研究了SP-A在机体防御中的作用,即SP-A对肺泡巨噬细胞吞噬细菌的影响。我们在此表明,SP-A可增强对某些未调理细菌的吞噬作用:对数生长期的大肠杆菌(E. coli/log)、铜绿假单胞菌/log以及稳定期的铜绿假单胞菌(P. aeruginosa/stat)和对数生长期的金黄色葡萄球菌。此外,SP-A不仅影响非血清依赖性吞噬作用,还影响血清调理的金黄色葡萄球菌/stat的吞噬作用。未观察到SP-A对大肠杆菌/stat的吞噬作用有影响,无论是非血清依赖性还是血清依赖性吞噬作用,以及对未调理的金黄色葡萄球菌/stat的吞噬作用。因此,SP-A对吞噬作用的影响取决于细菌种类和微生物的生长阶段,且这种影响是浓度依赖性的。我们研究了两种不同的人重组SP-A以及从蛋白沉积症患者肺灌洗材料中分离出的SP-A。这些SP-A分子含有不同的异构链,其结构复杂性也不同。定性地说,我们发现这三种物质有相同的作用。定量地说,形成最复杂结构的蛋白沉积症SP-A最有效。综上所述,我们证明了SP-A对肺泡巨噬细胞非血清依赖性以及血清依赖性细菌吞噬作用具有刺激作用,这两种作用均取决于细菌的种类和生长阶段。

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Lung surfactant protein A (SP-A) enhances serum-independent phagocytosis of bacteria by alveolar macrophages.肺表面活性蛋白A(SP-A)可增强肺泡巨噬细胞对细菌的非血清依赖性吞噬作用。
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Pulmonary surfactant protein A enhances the host-defense mechanism of rat alveolar macrophages.肺表面活性物质蛋白A增强大鼠肺泡巨噬细胞的宿主防御机制。
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Surfactant protein A enhances alveolar macrophage phagocytosis of a live, mucoid strain of P. aeruginosa.表面活性蛋白A增强肺泡巨噬细胞对铜绿假单胞菌黏液样活菌株的吞噬作用。
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Surfactant protein D binds to Mycobacterium tuberculosis bacilli and lipoarabinomannan via carbohydrate-lectin interactions resulting in reduced phagocytosis of the bacteria by macrophages.表面活性蛋白D通过碳水化合物-凝集素相互作用与结核分枝杆菌及脂阿拉伯甘露聚糖结合,导致巨噬细胞对细菌的吞噬作用减弱。
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Opsonic activities of surfactant proteins A and D in phagocytosis of gram-negative bacteria by alveolar macrophages.表面活性蛋白A和D在肺泡巨噬细胞吞噬革兰氏阴性菌中的调理活性。
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Am J Respir Cell Mol Biol. 2014 Nov;51(5):604-14. doi: 10.1165/rcmb.2014-0095TR.
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Surfactant protein A binds flagellin enhancing phagocytosis and IL-1β production.表面活性蛋白A结合鞭毛蛋白可增强吞噬作用和白细胞介素-1β的产生。
PLoS One. 2013 Dec 2;8(12):e82680. doi: 10.1371/journal.pone.0082680. eCollection 2013.
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Staphylococcus aureus proteases degrade lung surfactant protein A potentially impairing innate immunity of the lung.
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J Innate Immun. 2013;5(3):251-60. doi: 10.1159/000345417. Epub 2012 Dec 11.
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An Insight into the Diverse Roles of Surfactant Proteins, SP-A and SP-D in Innate and Adaptive Immunity.深入了解表面活性剂蛋白 A 和 D 在先天和适应性免疫中的多种作用。
Front Immunol. 2012 Jun 7;3:131. doi: 10.3389/fimmu.2012.00131. eCollection 2012.
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Characterization of Virulence Factors of Staphylococcus aureus: Novel Function of Known Virulence Factors That Are Implicated in Activation of Airway Epithelial Proinflammatory Response.金黄色葡萄球菌毒力因子的特性:参与激活气道上皮促炎反应的已知毒力因子的新功能
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