We have studied the biosynthesis and transport of the endogenous caveo
lins in MDCK cells. We show that in addition to homooligomers of caveo
lin-1, heterooligomeric complexes of caveolin-1 and -2 are formed in t
he ER, The oligomers become larger, increasingly detergent insoluble,
and phosphorylated on caveolin-2 during transport to the cell surface.
In the TGN caveolin-1/-2 heterooligomers are sorted into basolateral
vesicles, whereas larger caveolin-1 homooligomers are targeted to the
apical side. Caveolin-1 is present on both the apical and basolateral
plasma membrane, whereas caveolin-2 is enriched on the basolateral sur
face where caveolae are present. This suggests that caveolin-1 and -2
heterooligomers are involved in caveolar biogenesis in the basolateral
plasma membrane. Anti-caveolin-1 antibodies inhibit the apical delive
ry of influenza virus hemagglutinin without affecting basolateral tran
sport of vesicular stomatitis virus G protein. Thus, we suggest that c
aveolin-1 homooligomers play a role in apical transport.