Proliferation of lipolysosomes is one of the characteristic aspects of
embryonic chick hepatocytes. Formation of lipolysosomes is observed i
n the well-developed trans-Golgi network, with the highest frequency o
ccurring from 11 to 14 days of incubation. The lipolysosomes usually c
ontain a small and electron-dense lipid inclusion; however, during dev
elopment, they gradually enlarge with an accompanying reduction in the
electron density of the inclusion. Lipolysosomes isolated from neonat
al chick liver homogenates were mainly composed of esterified choleste
rol and showed considerably high activity of lysosomal enzymes. Moreov
er, the lipolysosome fraction is clearly shown to be a function of int
ralysosomal lipolysis via acid lipase, This accumulation of esterified
cholesterol within lipolysosomes might be attributed to an excessive
uptake and conversion of plasma lipoproteins to lipolysosomes. This co
ncept is supported by the appearance of an abundance of coated pits an
d both ''early'' and ''late'' endosomes. The major components of plasm
a lipoprotein are low density lipoprotein (LDL) and high density lipop
rotein (HDL), the cholesterol-rich lipoproteins, whose cholesterol con
tent increases during the last week of incubation when the lipolysosom
es quickly enlarge. Plasma lipoprotein particles are produced in tile
yolk sac epithelium from yolk very low density lipoprotein (VLDL) and
transferred via the vitelline circulation to the chick liver. After ha
tching, when the supply of nutrients from the yolk sac is terminated,
lipolysosomes immediately decrease in size and number. The cholesterol
and fatty acids released are useful as an energy source and lipid met
abolism in general, especially after hatching. Food intake induces the
use of and accelerates the disappearance of lipolysosomes. instead of
lipolysosomes, lipid droplets appear and increase in number and size
with concomitant increases of triglyceride concentrations in the liver
homogenates, suggesting that lipogenesis has begun in the chick hepat
ocyte. (C) 1997 Wiley-Liss, Inc.