“…There is a limitation in the investigation of lipid droplets by conventional thin-section electron microscopy as a result of the extraction of lipids by organic solvents during dehydration and embedding (Korn and Weisman, 1966;Collet, 1979). The freeze-replica method avoids this specific problem, because it does not use organic solvents in the preparation of specimens (Daikoku et al, 1973;Williams, 1978). Nevertheless, it is not easy to identify lipid droplets of the It0 cells in freeze-replica images, since Ito cells are relatively small in size, constitute only 1.4% of parenchymal volume of the liver (Blouin et al, 19771, and have relatively few lipid droplets in their cytoplasm in the normal state (Wake, 1971;Kobayashi et al, 1973).…”