T. Sato et al., MATURATION OF RAT DENDRITIC CELLS DURING INTRAHEPATIC TRANSLOCATION EVALUATED USING MONOCLONAL-ANTIBODIES AND ELECTRON-MICROSCOPY, Cell and tissue research, 294(3), 1998, pp. 503-514
Specific populations of hepatic sinusoidal cells were stained with mon
oclonal antibodies that recognize monocytes/macrophages (ED1), tissue
macrophages (Kupffer cells) (ED2), MHC class II (Ia) antigen (MRC OX6)
, and dendritic cells/gamma,delta T-cells (MRC OX62) and analyzed by l
ight and electron microscopy. The majority of ED1(+) and/or ED2(+) cel
ls were localized to the hepatic parenchyma, whereas OX6(+) and/or OX6
2(+) cells were more densely distributed within Glisson's sheath than
in the hepatic parenchyma. Double-immunoperoxidase staining of normal
liver for ED1, ED2, and OX6 identified dendritic cells (DC) of two dif
ferent phenotypes, ED1(+)ED2(-)OX6(+) and ED1(-)ED2(-)OX6(+). DC can b
e classified into three different types based on ultrastructural chara
cteristics. The first type (type I) is characterized by one or more lo
ng cytoplasmic processes and a well-developed lysosomal system. The se
cond type (type II) has an inconspicuous lysosomal system, abundant hy
aloplasm, and characteristic short cytoplasmic processes. The third ty
pe (type I-II) has cytologic features intermediate between those of ty
pe I and type II DC. At the electron-microscopic level, these three ce
ll types are found in the sinusoidal lumen, whereas the majority of ty
pe II DC are located in the space of Disse and Glisson's sheath. Furth
ermore, some OX6-labeled elongated DC appeared to traverse the lumen o
f sinusoids through endothelial pores to enter the space of Disse. One
hour after intravenous injection of latex particles (0.81 mu m in dia
meter), numerous latex-laden dendritic cells (ED1(+)OX6(+), type I and
type I-II) were detected in the lumen of hepatic sinusoids, but not i
n the space of Disse or Glisson's sheath. These findings suggest that
normal rat liver contains resident dendritic cells which downregulate
phagocytic activity and mature into potent accessory cells during migr
ation from the portal vein toward the central vein. These DC then trav
erse the sinusoidal lumen to the hepatic lymph system via the space of
Disse.