T. Honma et T. Hamasaki, ULTRASTRUCTURE OF BLOOD-VESSEL REGRESSION IN INVOLUTION OF FOREIGN-BODY GRANULOMA, Journal of submicroscopic cytology and pathology, 30(1), 1998, pp. 31-44
The diversity of endothelial cell deletion in regressing blood vessels
during involution of granulation tissue was investigated in foreign-b
ody granulomas induced by a collagen sponge implanted into the dorsum
of the rat. Small blood vessel density counts were performed to determ
ine the degree of blood Vessel regression in the involution of granula
tion tissue in foreign-body granuloma. The density of these small bloo
d vessels significantly decreased between 100 and 130 days after spong
e implantation. The detachment of endothelial cells from their underly
ing basement membrane and the consequent protrusion into and/or out of
the lumen in the vascular network of granulation tissue was observed
by electron microscopy. Based on the pattern of manifestation in the e
ndothelium and the characteristic deformation of nuclei, the detached
endothelial cells were classified into two groups: 1) the endothelial
cell apoptosis group and 2) the endothelial cell degeneration group. T
he essential difference between the two groups was easily distinguisha
ble as the nucleus of the former group displayed chromatin condensatio
n and margination as the hallmark of early apoptotic changes, while th
e nucleus of the latter group displayed a pinch structure and intranuc
lear pocket formation. However, the process by which the detached endo
thelial cells were shed into the vascular lumen and eventually elimina
ted from circulation was the same in both groups. The occurrence of bo
th groups increased on the 90th day after sponge implantation and reac
hed a maximum on the 110th day, indicating that the appearance of the
groups was synchronized. These results suggest that the two major proc
esses of apoptosis and degeneration of endothelial cells occur during
endothelial cell deletion as a mechanism contributing to blood vessel
regression.