F. Braet et al., A NOVEL STRUCTURE INVOLVED IN THE FORMATION OF LIVER ENDOTHELIAL-CELLFENESTRAE REVEALED BY USING THE ACTIN INHIBITOR MISAKINOLIDE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(23), 1998, pp. 13635-13640
Hepatic endothelial fenestrae are dynamic structures that act as a sie
ving barrier to control the extensive exchange of material between the
blood and the liver parenchyma. Alterations in the number or diameter
of fenestrae by drugs, hormones, toxins, and diseases can produce ser
ious perturbations in liver function. Previous studies have shown that
disassembly of actin by cytochalasin B or latrunculin A caused a rema
rkable increase in the number of fenestrae and established the importa
nce of the actin cytoskeleton in the numerical dynamics of fenestrae.
So far, however, no mechanism or structure has been described to expla
in the increase in the number of fenestrae, Using the new actin inhibi
tor misakinolide, we observed a new structure that appears to serve as
a fenestrae-forming center in hepatic endothelial cells.