Asian
Science Seminar ASS-5
Mechanism of new bone formation by using immature stem cell KUSA/A1 for
bone tissue engineering in vivo study
Sathi Gulsan Ara1, 2, Andrea Paola Rodriguez2, 3, Hidetsugu Tsujigiwa2, Hitoshi Nagatsuka2
and
Noriyuki Nagai2
1Bangladesh
2Department of Oral Pathology and Medicine.
3Department of Oral Pathology.
The basic principle of bone tissue engineering is to seed stem cells in porous scaffold
. Stem cells can proliferate and differentiate into various
types of mature cells. On
the contrary, mature cells have low proliferation potential thereby not being
able to obtain sufficient amount of cells to promote tissue repair. In previous
study, we established an appropriate medium to maintain KUSA/A1 cells in
their immature stage. These immature cells placed in a diffusion chamber and
implanted intra-peritoneally, differentiated into osteoblast-like cells and produced bone-like tissue. In order to induce new
bone formation, immature KUSA/A1 cells were seeded into atelocollagen
honeycomb carrier. We evaluated the behavior of immature KUSA/A1 cells alone
or with honeycomb carrier implanted in subcutaneous tissues of SCID mice.
Transplants were subjected to radiographic, histological and immunohistochemical (CD34, Osteopontin,
PCNA and BMP-2) examinations after 1, 2 and 4 weeks of implantation. KUSA/A1
cells alone showed few, small islands of new bone formation surrounded by
scanty cells. On the other hand, KUSA/A1 with atelocollagen
revealed abundant new bone formation as well as cellular proliferation. To
clarify the cells implicated in new bone formation, same implantation was done
in GFP (green fluorescent protein) mice. The results showed evidence that GFP
positive host cells and GFP negative immature KUSA/A1 cells were both
responsible for this new bone formation. From this study we concluded that
there is a possibility of new bone formation induced by immature
KUSA/A1 and host stem cell within atelocollagen
honeycomb carrier in vivo.