AN IMMUNOCYTOCHEMICAL STUDY FOR LYSOSOMAL CATHEPSIN-B AND CATHEPSIN-DRELATED TO THE INTRACELLULAR DEGRADATION OF TITANIUM AT THE BONE-TITANIUM INTERFACE
Y. Ayukawa et al., AN IMMUNOCYTOCHEMICAL STUDY FOR LYSOSOMAL CATHEPSIN-B AND CATHEPSIN-DRELATED TO THE INTRACELLULAR DEGRADATION OF TITANIUM AT THE BONE-TITANIUM INTERFACE, Journal of periodontology, 69(1), 1998, pp. 62-68
THE MORPHOLOGICAL RELATIONSHIP BETWEEN titanium and lysosomal proteina
ses, cathepsins B and D, at the bone-titanium interface using titanium
-coated plastic implants placed for 28 days in the tibiae of 6-week-ol
d rats was immunocytochemically investigated by the colloidal immunogo
ld-silver method. Under Light microscopy the titanium layer appeared t
o make direct contact with the bone and one or a few layers of slender
cells were interposed between the bone and titanium. Ultrastructurall
y, the titanium came in contact with the bone or the slender cell laye
r through a 20 to 40 nm thin amorphous zone. The slender cells at the
bone-titanium interface consisted of two types; one was an osteoblast
type with glycogen granules which was found along the newly-formed bon
e facing titanium layer. The other was a fibroblast type which came in
contact with the titanium layer and occasionally endocytosed the deta
ched titanium fragments. In addition, some of the slender cells also s
howed degenerative changes. Immunocytochemically, cathepsins B and/or
D were sometimes colocalized in some phagolysosomes with titanium frag
ments. These findings suggested that the fibroblast types at the bone-
titanium interface may act as scavengers to remove both cell debris an
d titanium by means of some endocytotic ability, and lysosomal catheps
ins also developed in response to the endocytosed titanium. The osteob
last type also appears to show a high degree of osteogenic activity ar
ound the titanium-coated plastic implants.