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Evidence for the role of alveolar epithelial gp60 in active transalveolar albumin transport in the rat lung

机译:肺泡上皮gp60在大鼠肺中主动肺泡白蛋白转运中的作用的证据

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摘要

class="enumerated" style="list-style-type:decimal">Transcytosis of albumin, involving the 60 kDa albumin-binding glycoprotein, gp60, was studied in cultured type II alveolar epithelial cells obtained from rat lungs.Type II cells internalized the interfacial fluorescent dye RH 414, which marks for plasmalemma vesicles. Fluorescent forms of albumin and anti-gp60 antibody colocalized in the same plasmalemma vesicles.Antibody (100 μg ml−1) cross-linking of gp60 for brief periods (15 min) markedly stimulated vesicular uptake of fluorescently tagged albumin. The caveolar disrupting agent, filipin (10 nm), abolished the stimulated internalization of albumin.The vast majority of plasmalemmal vesicles carrying albumin also immunostained for caveolin-1; however, lysosomes did not stain for caveolin-1. Filipin depleted the epithelial cells of the caveolin-1-positive, albumin-transporting plasmalemma vesicles.Prolonged (> 1 h) stimulation of type II cells with cross-linking anti-gp60 antibody produced loss of cell-surface gp60 and abolished endocytic albumin uptake.Transalveolar transport of albumin was also studied in the isogravimetric rat lung preparation perfused at 37°C. 125I-labelled albumin was instilled into distal airspaces of lungs, and the resulting 125I-labelled albumin efflux into the vascular perfusate was determined.Unlabelled albumin (studied over a range of 0–10 g (100 instilled ml)−1) inhibited 40% of the transport of labelled albumin ((5.7 ± 0.4) × 105 counts (instilled ml)−1) with an IC50 value of 0.34 g (100 ml)−1.Filipin blocked the displacement-sensitive component of 125I-labelled albumin transport, but had no effect on the transport of the paracellular tracer 3[H]mannitol.Displacement-sensitive 125I-labelled albumin transport had a significantly greater Q10 (27–37 °C) than the non-displaceable component.Cross-linking of gp60 by antibody instillation stimulated only the displacement-sensitive 125I-labelled albumin transalveolar transport in intact rat lungs.To estimate the transport capacity of the displacement-sensitive system, the percentage of instilled 125I-labelled albumin counts remaining in lung tissue was compared in lungs treated with instillates containing either 0.05 g (100 ml)−1 unlabelled albumin or 5 g (100 ml)−1 unlabelled albumin. Approximately 25% of instilled 125I-labelled albumin was cleared from the lung preparations per hour by the displacement-sensitive transport pathway. This component was blocked by filipin.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在培养自大鼠肺的II型肺泡上皮细胞中研究了涉及60 kDa白蛋白结合糖蛋白gp60的白蛋白的胞吞作用。 II型细胞将界面荧光染料RH 414内在化。质膜囊泡。荧光形式的白蛋白和抗gp60抗体共定位在同一质膜囊泡中。 抗体(100μgml -1 )在短时间内(15分钟)交联gp60显着刺激了荧光标记的白蛋白的囊泡摄取。海绵体破坏剂菲律宾蛋白(10 nm)消除了刺激的白蛋白内在化。 绝大多数携带白蛋白的质膜囊泡也对Caveolin-1进行了免疫染色。但是,溶酶体对小窝蛋白1没有染色。磷脂耗尽了空洞蛋白1阳性,运输白蛋白的小窝膜小泡的上皮细胞。 用交联的抗gp60抗体长时间刺激(> 1小时)II型细胞会导致细胞凋亡。 在37°C灌注的等重量大鼠肺制剂中,还研究了白蛋白的肺泡转运。将 125 I标记的白蛋白滴注到肺的远端气隙中,并确定所得的 125 I标记的白蛋白排入血管灌注液中。 未标记的白蛋白(研究范围为0–10 g(滴入100 ml) -1 ),抑制了40%的标记白蛋白转运((5.7±0.4)×10 5 计数(滴入的毫升) -1 ),IC50值为0.34 g(100毫升) -1 菲律宾蛋白阻止了这种置换- 125 I标记的白蛋白转运的敏感成分,但对细胞旁示踪物 3 [H]甘露醇的转运没有影响。 位移-敏感的 125 I标记的白蛋白转运Q10(27-37°C)明显高于不可置换的组分。 仅通过抗体滴注刺激gp60的交联完整大鼠肺中对位移敏感的 125 I标记的白蛋白跨肺泡转运。 估计转运比较了位移敏感系统的容量,在用0.05 g(100 ml) -1 滴注液处理的肺中处理过的肺中残留的 125 I标记的白蛋白计数百分比/ sup>未标记白蛋白或5 g(100 ml) -1 未标记白蛋白。每小时约有25%的滴注的125 SupI标记的白蛋白通过置换敏感性转运途径从肺制剂中清除。该成分被菲林阻断。

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