J. Larsson et al., Distribution of iodine 125-labeled alpha(1)-microglobulin in rats after intravenous injection, J LA CL MED, 137(3), 2001, pp. 165-175
Citations number
68
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
The 28-kd plasma protein al-microglobulin is found in the blood of mammals
and fish in a free, monomeric form and as high-molecular-weight complexes w
ith molecular masses above 200 kd. In this study, iodine 125-labeled free a
nd high-molecular weight rat alpha (1)-microglobulin (a mixture of alpha (1
)-microglobulin/alpha (1) -inhibitor-3 and alpha (1)-microglobulin/fibronec
tin complexes) were injected intravenously into rats. The distribution of t
he proteins was measured by using scintillation camera imaging. Both forms
of (125)l-labeled alpha (1)-microglobulin were rapidly cleared from the blo
od, with a half-life of 2 and 16 minutes for the initial and late phase, re
spectively, for free alpha (1)-microglobulin; and a half-life of 3 and 130
minutes for the initial and late phase, respectively, for the complexes. Af
ter 45 minutes, 6%, 16%, 27%, 13%, and 34% of the free (125)l-labeled alpha
(1)-microglobulin and 18%, 21%, 6%, 10%, and 42% of the (125)l-labeled alp
ha (1)-microglobulin complexes were found in the blood, gastrointestinal tr
act, kidneys, liver, and the remainder of the body, respectively. The local
distribution of injected (125)l-labeled alpha (1)-microglobulin in intesti
nes and kidneys was investigated by microscopy and autoradiography. In the
intestine, both forms were distributed in the basal layers, villi, and lumi
nal contents. The results also suggested intracellular labeling of epitheli
al cells. Well-defined local regions containing higher concentrations of in
jected protein could be seen in the intestine. In the kidneys, both forms w
ere found mostly in the cortex. Free (125)l-labeled al-microglobulin was fo
und predominantly in epithelial cells of a subset of the tubules, whereas t
he (125)l-labeled complexes were more evenly distributed. Intracellular lab
eling was indicated for both al-microglobulin forms. The results thus indic
ate a rapid transport of (125)l-labeled alpha (1)-microgiobulin from the bl
ood to most tissues.