Papers by Author: Jing Qiu Cheng

Abstract: With the outstanding biocompatibility of hydroxyapatite (HA) and biodegradation of poly(D,L)lactide(PDLLA), and the expected good bio-mechanical compatibility, nano-HA / PDLLA (n-HA/PDLLA)composite has been paid great interests in hard tissue repair. One of the key factors affecting the potential of the composite is the degradation of the composite. That is what the mechanism of degradation in the composite is and if the degradation of the materials would induce the crack of the composite or a porous structure facile for tissue ingrowth would be formed. In this study, an n-HA/ PDLLA composite containing about 40% n-HA (wt%) was prepared and the degradation of the composite in bony tissue of rabbits and tissue response were studied by implanting composite rods and control HA rods into the femora of 16 New Zealand rabbits. After definite intervals, the histological analysis was completed by light microscopy and the degradation behavior was observed by scanning electron microscopy. The results suggested that a nano-HA/PDLLA composite was obtained and the materials showed good biocompatibility and osteoconductivity. The substantial degradation of the composite occurred at 8 weeks in vivo. After a longer period of implantation, the further degradation of the composite led to the formation of interconnected microporous and macroporous structure in the materials that might facilitate the tissue ingrowth in the composite.

Abstract: The aim of this experiment is to investigate whether MSCs from Banna Minipig Inbred Line (BMI) could be immortalized by introducing SV40 large T antigen gene. MSCs were isolated from BMI and transfected with pSV3neo plasmid. Normal BMI-MSCs would apoptosis and senescence during proliferation while its population doubling (PD) number exceeded 20. However, SV40-transfected cells were immortal. As same as that of normal BMI-MSCs, transfected MSCs were positive for stem cell markers and negative for differentiated osteoblast specific marker. After cultured in osteogenesis supplement media, cbfa1 and calcium deposit on stimulated cells were enhanced obviously. There were no data to prove the tumorigenicity potential of the immortalized cells. Furthermore, histological analysis demonstrated that bone formation was initiated in the pores of HA/TCP implants loaded immortalized BMI-MSCs 7 weeks postimplantation. BMI-MSCs were immortalized by introducing SV40 large T antigen into the cells and still kept the stem cell characters and might be used as seeding cells for tissue engineering as well as stable test cells for biocompatibility of bone biomaterials.