LABELING OF HIGH-MOLECULAR-WEIGHT HYALURONAN WITH I-125 TYROSINE - STUDIES IN-VITRO AND IN-VIVO IN THE RAT

Citation
S. Gustafson et al., LABELING OF HIGH-MOLECULAR-WEIGHT HYALURONAN WITH I-125 TYROSINE - STUDIES IN-VITRO AND IN-VIVO IN THE RAT, Glycoconjugate journal, 11(6), 1994, pp. 608-613
Citations number
16
Categorie Soggetti
Biology
Journal title
ISSN journal
02820080
Volume
11
Issue
6
Year of publication
1994
Pages
608 - 613
Database
ISI
SICI code
0282-0080(1994)11:6<608:LOHHWI>2.0.ZU;2-Y
Abstract
Studies on the metabolism of the polysaccharide hyaluronan has previou sly been hampered by the lack of radioactive hyaluronan of high molecu lar weight (MW) and high specific activity. In the present study I-125 -tyrosine (T)-labelled hyaluronan was produced after CNBr-activation o f the polysaccharide. A specific activity of approximately 0.1 MBq mu g(-1) was achieved using 100 mu g of 0.5 x 10(6) Da hyaluronan labelle d for 2 h with 18 MBq I-125. The I-125-T-hyaluronan kept a high MW-pro file upon gel filtration chromatography and was found to be cleared fr om the circulation with the kinetics and organ distribution reported f or biosynthetically labelled hyaluronan of high MW. The I-125-labelled polysaccharide is also taken up by liver endothelial cells both in vi vo and in vitro, indicating that the labelling does not interfere with the binding to specific cell-surface receptors found on these cells. The intracellular degradation is slower than that earlier reported for biosynthetically labelled hyaluronan and seems to be halted at the le vel of low MW oligo- or mono-saccharides that eventually leave the org anism via the urine. Scintigraphic images of rats after intravenous in jection of I-125-T-hyaluronan showed rapid uptake in the liver and a r edistribution of radioactivity from liver to urine with time. Our resu lts indicate that the I-125-T-hyaluronan is suitable for studies of hy aluronan-metabolism in a number of ways. The gamma emitters I-125 and I-131 are easy to monitor and can be used also for in vivo 3D-imaging using single photon emission computer tomography.