Distribution of iodine 125-labeled alpha1-microglobulin in rats after intravenous injection.

Jörgen Larsson, K. Wingårdh, T. Berggård, Julia R. Davies, Lennart Lögdberg, Sven-Erik Strand, Bo Åkerström
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引用次数: 47

Abstract

The 28-kd plasma protein alpha(1)-microglobulin is found in the blood of mammals and fish in a free, monomeric form and as high-molecular-weight complexes with molecular masses above 200 kd. In this study, iodine 125-labeled free and high-molecular weight rat alpha(1)-microglobulin (a mixture of alpha(1)-microglobulin/alpha(1)-inhibitor-3 and alpha(1)-microglobulin/fibronectin complexes) were injected intravenously into rats. The distribution of the proteins was measured by using scintillation camera imaging. Both forms of (125)I-labeled alpha(1)-microglobulin were rapidly cleared from the blood, with a half-life of 2 and 16 minutes for the initial and late phase, respectively, for free alpha(1)-microglobulin; and a half-life of 3 and 130 minutes for the initial and late phase, respectively, for the complexes. After 45 minutes, 6%, 16%, 27%, 13%, and 34% of the free (125)I-labeled alpha(1)-microglobulin and 18%, 21%, 6%, 10%, and 42% of the (125)I-labeled alpha(1)-microglobulin complexes were found in the blood, gastrointestinal tract, kidneys, liver, and the remainder of the body, respectively. The local distribution of injected (125)I-labeled alpha(1)-microglobulin in intestines and kidneys was investigated by microscopy and autoradiography. In the intestine, both forms were distributed in the basal layers, villi, and luminal contents. The results also suggested intracellular labeling of epithelial cells. Well-defined local regions containing higher concentrations of injected protein could be seen in the intestine. In the kidneys, both forms were found mostly in the cortex. Free (125)I-labeled alpha(1)-microglobulin was found predominantly in epithelial cells of a subset of the tubules, whereas the (125)I-labeled complexes were more evenly distributed. Intracellular labeling was indicated for both alpha(1)-microglobulin forms. The results thus indicate a rapid transport of (125)I-labeled alpha(1)-microglobulin from the blood to most tissues.
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碘125标记α - 1微球蛋白在大鼠静脉注射后的分布。
28kd血浆蛋白α(1)-微球蛋白以游离单体形式存在于哺乳动物和鱼类的血液中,并以分子量大于200kd的高分子量复合物形式存在。本研究将碘125标记的游离高分子量大鼠α(1)-微球蛋白(α(1)-微球蛋白/ α(1)-抑制剂-3和α(1)-微球蛋白/纤连蛋白复合物的混合物)静脉注射到大鼠体内。利用闪烁照相机成像技术测量了蛋白质的分布。两种形式的(125)i标记α(1)-微球蛋白都能迅速从血液中清除,游离α(1)-微球蛋白的初始和晚期半衰期分别为2分钟和16分钟;复合物的初始和晚期的半衰期分别为3分钟和130分钟。45分钟后,在血液、胃肠道、肾脏、肝脏和身体其他部位分别发现6%、16%、27%、13%和34%的游离(125)i标记α(1)微球蛋白和18%、21%、6%、10%和42%的(125)i标记α(1)微球蛋白复合物。用显微镜和放射自显影技术观察注射(125)i标记α(1)-微球蛋白在肠道和肾脏的局部分布。在肠道中,两种形式均分布于基底层、绒毛和管腔内容物中。结果还提示上皮细胞的胞内标记。在肠道中可以看到含有高浓度注射蛋白的明确的局部区域。在肾脏中,这两种形式主要在皮质中发现。游离(125)i标记的α(1)微球蛋白主要存在于小管子集的上皮细胞中,而(125)i标记的复合物分布更均匀。细胞内标记用于α(1)-微球蛋白两种形式。因此,结果表明(125)i标记α(1)-微球蛋白从血液快速运输到大多数组织。
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