Background: Proper formation of cementum, a mineralized tissue lining the t
ooth root surface, is required for development of a functional periodontal
ligament. Further, the presence of healthy cementum is considered to be an
important criterion for predictable restoration of periodontal tissues lost
as a consequence of disease. Despite the significance of cementum to gener
al oral health, the mechanisms controlling development and regeneration of
this tissue are not well understood and research has been hampered by the l
ack of adequate in vitro experimental models.
Methods: In an effort to establish cementoblast cell populations, without t
he trappings of a heterogeneous population containing periodontal ligament
(PDL) cells, cells were obtained from the root surface of first mandibular
molars of OC-TAg transgenic mice. These mice contain the SV40 large T-antig
en (TAg) under control of the osteocalcin (OC) promoter. Therefore, only ce
lls that express OC also express TAg and are immortalized in vitro. Based o
n results of prior in situ studies, OC is expressed by cementoblasts during
root development, but not by cells within the PDL. Consequently, when popu
lations are isolated from developing molars using collagenase/trypsin diges
tion, only cementoblasts, not PDL cells, are immortalized and thus, will su
rvive in culture.
Results: The resulting immortalized cementoblast population (OC/CM) express
ed bone sialoprotein (BSP), osteopontin (OPN), and OC, markers selective to
cells lining the root surface. These cells also expressed type I and XII c
ollagen and type I PTH/PTHrP receptor (PTH1R). In addition to expression of
genes associated with cementoblasts, OC/CM cells promoted mineral nodule f
ormation and exhibited a PTHrP mediated cAMP response.
Conclusions: This approach for establishing cementoblasts in vitro provides
a model to study cementogenesis as required to enhance our knowledge of th
e mechanisms controlling development, maintenance, and regeneration of peri
odontal tissues.