Effects of ageing on proliferative ability, and the expressions of secreted protein, acidic and rich in cysteine (SPARC) and osteoprotegerin (osteoclastogenesis inhibitory factor) in cultures of human periodontal ligament cells
H. Shiba et al., Effects of ageing on proliferative ability, and the expressions of secreted protein, acidic and rich in cysteine (SPARC) and osteoprotegerin (osteoclastogenesis inhibitory factor) in cultures of human periodontal ligament cells, MECH AGE D, 117(1-3), 2000, pp. 69-77
Secreted protein, acidic and rich in cysteine (SPARC) has been suggested to
play an important role in wound repair and mineralization. Osteoprotegerin
/osteoclastogenesis inhibitory factor (OPG/OCIF) is a secreted protein that
inhibits the maturation, activity and survival of osteoclasts. An examinat
ion of the changes in expression of these proteins as well as their prolife
rative ability according to ageing in cultured cells may elucidate characte
ristic changes in periodontal tissues induced by ageing. In the present stu
dy, proliferative ability and the expression of SPARC and OPG/OCIF were com
pared between cultures of human periodontal ligament (HPL) cells obtained f
rom young and senior donors (in vivo cellular ageing) as well as in culture
s of HPL cells at early and late passages (in vitro cellular ageing). Cumul
ative population doubling levels and cell population doubling time of HPL c
ells from young donors were greater and shorter, respectively, than those o
f HPL cells from senior donors. Levels of SPARC mRNA in HPL cells increased
with cellular ageing in vivo. No change in the levels of OPG/OCIF mRNA in
HPL cells with cellular ageing in vivo was observed. The changes in prolife
rative ability and the mRNA levels of SPARC and OPG/OCIF with cellular agei
ng in vitro were similar to those with ageing in vivo. This study demonstra
ted for the first time a relationship between in vivo and in vitro cellular
ageing in the functional changes in HPL cells. These findings suggest that
the impairment of periodontal ligament repair with ageing is due to the de
crease in proliferative ability in HPL cells with ageing. Furthermore, the
increase in SPARC with ageing may be related to changes in metabolism of pe
riodontal ligament that occur with ageing. (C) 2000 Elsevier Science Irelan
d Ltd. All rights reserved.