Arteriosclerosis, Thrombosis, and Vascular Biology. 1999;19:552-561
(Arteriosclerosis, Thrombosis, and Vascular Biology. 1999;19:552-561.)
© 1999 American Heart Association, Inc.
Identification of Megalin/gp330 as a Receptor for Lipoprotein(a) In Vitro
Andreas Niemeier;
Thomas Willnow;
Hans Dieplinger;
Christian Jacobsen;
Nicolette Meyer;
Jan Hilpert;
Ulrike Beisiegel
AbstractLipoprotein(a)
[Lp(a)] is an atherogenic lipoprotein
of unknown
physiological function. The mechanism of Lp(a)
atherogenicity
as well as its catabolic pathways are only incompletely
understood
at present. In this report, we show that the low density
lipoprotein
receptor (LDLR) gene family member
megalin/glycoprotein (gp)
330 is capable of binding and
mediating the cellular uptake
and degradation of Lp(a) in vitro. A
mouse embryonic yolk sac
cell line with native expression of
megalin/gp330 but genetically
deficient in LDLR-related protein (LRP)
and a control cell line
carrying a double knockout for both LRP and
megalin/gp330 were
compared with regard to their ability to bind,
internalize,
and degrade
dioctadecyltetramethylindocarbocyanine perchlorate
(DiI)-fluorescencelabeled
Lp(a) as well as equimolar amounts
of
125I-labeled Lp(a) and
LDL. Uptake and degradation of
radiolabeled Lp(a) by the megalin/gp330-expressing
cells were, on
average, 2-fold higher than that of control cells.
This difference
could be completely abolished by addition of
the receptor-associated
protein, an inhibitor of ligand binding
to megalin/gp330.
Mutual suppression of the uptake of
125I-Lp(a)
and of
125I-LDL by both unlabeled Lp(a) and LDL suggested that
Lp(a)
uptake is mediated at least partially by apolipoprotein B100.
Binding
and uptake of DiI-Lp(a) resulted in strong signals on
megalin/gp330-expressing
cells versus background only on control cells.
In addition,
we show that purified megalin/gp330,
immobilized on a sensor
chip, directly binds Lp(a) in a
Ca
2+-dependent manner with an
affinity similar to that for
LDL. We conclude that megalin/gp330
binds Lp(a) in vitro and is capable
of mediating its cellular
uptake and degradation.
Key Words: megalin glycoprotein 330 lipoprotein(a) LDL LDLR gene family
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