A small but significant portion of the thyroid hormones that circulate
in human plasma is associated with lipoproteins. Although the major l
ipoprotein carrier is HDL, the role of these interactions on T4 entry
into cells was tested first with LDL and human fibroblasts because of
the well-characterized LDL receptors and the availability of cells wit
h genetically absent receptors. It was shown that LDL enhanced the upt
ake of T4 by cultured fibroblasts in which the LDL receptors were expr
essed. The T4-binding sites on apolipoproteins B-100 and E, as well as
apoA-I, have been partially characterized, and they exhibit considera
ble homology. A number of possible physiologic consequences of thyroid
hormone-lipoprotein interactions have been put forward as topics for
further investigation.