The Effect Of Hyaluronic Acid On Mouse Calvaria Pre-Osteoblasts Osteogenesis In Vitro.
- Author:
Yong Min CHO
1
;
Seung Ki MIN
;
Soo Nam KIM
;
Yong Ouk YOU
Author Information
1. Department of Oral and Maxillofacial Surgery, School of Dentistry, Won-kwang University, Korea. omsmin@wonkwang.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Hyaluronic acid (HA);
Mesenchymal cell;
Pre-osteoblast;
Bone osteogenesis
- MeSH:
Alkaline Phosphatase;
Animals;
Cell Proliferation;
Collagen;
Embryonic Development;
Extracellular Matrix;
Female;
Fractures, Bone;
Hyaluronic Acid*;
Mice*;
Molecular Weight;
Osteogenesis*;
Pregnancy;
Skull*;
Wounds and Injuries
- From:Journal of the Korean Association of Oral and Maxillofacial Surgeons
2002;28(3):216-225
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Hyaluronic acid (HA) is an almost essential component of extracellular matrices. Early in embryogenesis mesenchymal cells migrate, proliferate and differentiate, in part, because of the influence of HA. Since the features of embryogenesis are revisited during wound repair, including bone fracture repair, this study was initiated to evaluate whether HA has an effect on calcification and bone formation in an in vitro system of osteogenesis. Mouse calvaria Pre-osteoblast (MC3T3-E1) cells were cultured in alpha-MEM medium with microorganism-derivative hyaluronic acid that was produced by Strep. zooepidemicus which of molecular weight was 3 million units. The dosages were categorized in each 0.5, 1.0 and 2.0 mg/ml concentration experimental groups. After 2 and 4 days cultures in expeirmental and control groups, the tendency of cell proliferation, MTT assay, protein synthesis ability, collagen synthesis and alkaline phosphatase activity were analysed and bone nodule formation capacity were measured with Alizarin Red S stain after 29 days cultures. The cell proliferation was increased in time, especially the group of 0.5 and 1.0 mg/ml concentration of HA were showed prominent cell proliferation. After 2 and 4 days culture, experimental groups in general were greater cell activity in MTT assay. The protein synthesis was increased in all experimental groups compared to control group, especially most prominent in 1.0 mg/ml concentration group. The collagen synthesis capacity were increased in HA experimental groups, especially prominent in 1.0 mg/ml group and the activity of alkaline phosphatase were increased, especially also prominent in 1.0 mg/ml group, compared to control group. Above these, the activity of mouse carvarial pre-osteoblast cells was showed greater bone osteogenesis activity in all applied HA experimental group, especially group of 1.0 mg/ml concentration of HA.
