M. Kanai et al., PARTICIPATION OF ENDODERMAL EPITHELIAL-CELLS ON THE SYNTHESIS OF PLASMA LDL AND HDL IN THE CHICK YOLK-SAC, Microscopy research and technique, 35(4), 1996, pp. 340-348
We ultrastructually examined the chick yolk sac endodermal epithelium
and evaluated our findings in combination with the biochemical analysi
s of serum and yolk lipoproteins. Twenty-five to 30 nm-sized particles
were demonstrated to be a principal element of the extracellular yolk
mass and these were determined to be yolk very low density lipoprotei
n (VLDL). The particles were shown to be taken up by the epithelial ce
lls via coated pits and engulfed by plasma membrane invaginations toge
ther with yolk subdroplets, another element of the yolk mass. Through
apical vacuoles, the two yolk elements were incorporated into yolk dro
ps, which were identified to be one of the lysosomal structures by a c
ytochemical procedure using acid phosphatase (AcP)ase activity. During
the last week of incubation, which is the final third of the incubati
on period, the digestion seemed to progress rapidly in the yolk drops,
which came to resemble lipolysosomes; lipoprotein production became a
ctive as expressed by an enlarged Golgi apparatus. The newly produced
lipoprotein particles were electron-lucent and irregular in size (50-1
20 nm). They were sequestered in secretory vacuoles and secreted from
the vascular surface of the epithelial cells. Finally, the particles w
ere thought to be taken into the vitelline circulation as plasma lipop
roteins. The major component of lipoprotein in serum was determined to
be low density lipoprotein (LDL) and high density lipoprotein (HDL),
while cholesterol content was found to increase during incubation. We
concluded that endodermal epithelial cells participate the synthesis o
f plama LDL and HDL. For this synthesis the cells probably apply lipid
s and apo-protein generated from yolk VLDL degradation. (C) 1996 Wiley
-Liss, Inc.