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补体可溶性复合物可增加大鼠肺单根微血管的水导率。

Soluble complex of complement increases hydraulic conductivity in single microvessels of rat lung.

作者信息

Ishikawa S, Tsukada H, Bhattacharya J

机构信息

Department of Medicine, College of Physicians and Surgeons, Columbia University, St. Luke's-Roosevelt Hospital Center, New York 10019.

出版信息

J Clin Invest. 1993 Jan;91(1):103-9. doi: 10.1172/JCI116157.

Abstract

We determined the effect of sera enriched with the soluble complex of complement (SC5b-9), on hydraulic conductivity (Lp) of single pulmonary venules (diameter 20-30 microns). Sera free of anticoagulants and blood cells were prepared from rat and human blood. Lp were determined by our split drop technique in isolated, blood-perfused lungs prepared from anesthetized rats (2% halothane; Sprague Dawley, 500 g; n = 73). Zymosan-activated (ZAS) and control sera were used for Lp determinations. In ZAS prepared from human serum, SC5b-9 concentration was > 300 micrograms/ml (control: < 1 microgram/ml) as determined by ELISA. At baseline, Lp averaged 3.4 +/- .4 x 10(-7) ml/(cm2.s.cm H2O), but it increased by 217 +/- 32% with undiluted ZAS (P < 0.05). The Lp increase correlated significantly with different ZAS dilutions for rat serum and with SC5b-9 concentration for human serum. Lp did not increase significantly with ZAS prepared from heat-treated sera, C6- and C8-deficient sera; or with ZAS in which SC5b-9 had been depleted by immunoprecipitation. The ZAS-induced increase of Lp was blocked completely by venular preinfusion with the arginine-glycine-aspartic acid (RGD) tripeptide (1 mg/ml, 10 min). We report for the first time that: (a) SC5b-9 increases lung endothelial Lp; and (b) the increase of Lp is attributable to an integrin-dependent mechanism.

摘要

我们测定了富含补体可溶性复合物(SC5b-9)的血清对单个肺小静脉(直径20 - 30微米)水导率(Lp)的影响。从大鼠和人血液中制备不含抗凝剂和血细胞的血清。Lp通过我们的分滴技术在由麻醉大鼠(2%氟烷;Sprague Dawley,500克;n = 73)制备的离体、血液灌注肺中进行测定。酵母聚糖激活(ZAS)血清和对照血清用于Lp测定。通过ELISA测定,在人血清制备的ZAS中,SC5b-9浓度> 300微克/毫升(对照:< 1微克/毫升)。在基线时,Lp平均为3.4 ± 0.4 × 10⁻⁷毫升/(平方厘米·秒·厘米水柱),但未稀释的ZAS使其增加了217 ± 32%(P < 0.05)。Lp的增加与大鼠血清不同ZAS稀释度以及人血清SC5b-9浓度显著相关。用热处理血清、C6和C8缺陷血清制备的ZAS,或SC5b-9已通过免疫沉淀去除的ZAS,Lp均未显著增加。ZAS诱导的Lp增加被小静脉预先注入精氨酸 - 甘氨酸 - 天冬氨酸(RGD)三肽(1毫克/毫升,10分钟)完全阻断。我们首次报道:(a)SC5b-9增加肺内皮细胞Lp;(b)Lp的增加归因于整合素依赖性机制。

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