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Journal of Lipid Research, Vol 32, 1-8, Copyright © 1991 by Lipid Research, Inc.
AM Lees and RS Lees
99MTechnetium-labeled low density lipoprotein (99MTc-labeled LDL) was
developed to detect atherosclerosis by external imaging with the gamma
scintillation camera (Lees, et al. J. Nucl. Med. 1985. 26: 1056-1062; Lees,
et al. Arteriosclerosis. 1988. 8: 461-470). The present study examined high
affinity LDL receptor recognition and intracellular sequestration of
99MTc-labeled LDL by fibroblasts. There were no significant differences
between 99MTc-labeled LDL and 125I-labeled LDL in binding parameters or
percent inhibition of accumulation, which indicated that 99MTc labeling did
not alter receptor recognition of LDL. At 4 degrees C the Kd (+SE) for
99MTc-labeled LDL and 125I-labeled LDL, respectively, was 1.52 +/- 0.24 and
1.45 +/- 0.14 micrograms/ml; Bmax (+/- SE) was 5.45 +/- 0.48 and 4.89 +/-
0.25 ng/well, respectively. Binding was saturated at about 2 micrograms/ml.
The complete linearity of 99MTc-labeled LDL accumulation from 0-6 h and the
positive slope from 6-24 h indicated that radiolabel that entered cells as
99MTc-labeled LDL was sequestered; pulse-chase experiments, which measured
residual cell-associated radioactivity out to 24 h, also showed that
radiolabel was trapped. Because radiolabel sequestration was essentially
complete, and because 99MTc-labeled LDL was recognized by the LDL receptor
equally as well as 125I-labeled LDL, it should be useful not only for
imaging atherosclerosis, but also for quantitatively determining sites of
utilization and degradation of LDL.
ARTICLES
99mTechnetium-labeled low density lipoprotein: receptor recognition and intracellular sequestration of radiolabel
Arteriosclerosis Center, New England Deaconess Hospital, Boston, MA.
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