Caveolae are 50-100 nm invaginations that represent an appendage or su
bcompartment of the plasma membrane. They are found in most cell types
but are abundant in fibroblasts, adipocytes, endothelial cells, type
I pneumocytes, epithelial cells, and smooth and striated muscle cells.
Functionally, caveolae have been implicated in three major processes:
endothelial transcytosis, potocytosis, and signal transduction. Caveo
lin, a 21-24 kD integral membrane protein is a principal component of
the caveolar membrane in vivo. Within caveolar microdomains, caveolin
functions as a multivalent docking site for recruiting and sequesterin
g signaling molecules. More specifically, caveolin interacts directly
in a regulated manner with multiple lipid-modified signaling molecules
(such as Src-tyrosine kinases, G alpha subunits, and H-Ras), preferri
ng the inactive conformation of these molecules. Here, the present a g
eneral overview of our current knowledge of caveolae and caveolin func
tioning and possible implications for treatment of human disease. (C)
1997, Elsevier Science Inc.