The effect of the IGF-I treated gingival and periodontal ligament fibroblast on osteoblasts.
- Author:
Mi Jeong KIM
1
;
Won Sik YANG
Author Information
1. Department of Orthodontics, College of Dentistry, Seoul National University, Korea. dentalkim@hotmail.net
- Publication Type:Original Article
- Keywords:
Insulin-like growth factor I;
Osteoblast;
Periodontal fibroblast
- MeSH:
Alkaline Phosphatase;
Animals;
Blotting, Western;
Cell Count;
Cell Proliferation;
Collagen;
Culture Media, Conditioned;
Fibroblasts*;
Humans;
Insulin-Like Growth Factor I*;
Male;
Osteoblasts*;
Periodontal Ligament*;
Periodontium;
Rabeprazole;
Rats;
Rats, Sprague-Dawley
- From:Korean Journal of Orthodontics
2001;31(6):589-600
- CountryRepublic of Korea
- Language:English
-
Abstract:
Insulin-like growth factor I (IGF-I) has the local tissue regulating actions. In bone, IGF-I increases the replication of osteoblastic lineage, probably preosteoblasts, and enhances osteoblastic collagen synthesis and matrix composition rates. The purpose of this study was to investigate the local regulatory effect of IGF-I on periodontium totally, both in an autocrine and paracrine manner. To examine the effect of IGF-I directly on osteoblast (OB) of test rats, and indirectly on OB via periodontal ligament fibroblast (PDLF), and the effect of gingival fibroblast (GF) on OB via cellular paracrine manner for the understanding of humoral action of adjacent tissue, GF and PDLF were obtained from male Sprague-Dawley rats of six to eight weeks of age. OB was obtained from frontal and parietal calvarial bone of Sprague-Dawley 21day-old-fetus. After each cell was incubated 24 hours, for collecting conditioned medium, different concentrations of IGF-I (1,10,100 ng/ml,1ml/well) was adding in the GF, PDLF cells, and the supernatant from these cultures was put into the primary OB culture with 1x104cell/ml/well. The experimental group was divided into six groups - control OB, IGF-I treated OB, OB culture with conditioned medium from PDLF, OB culture with conditioned medium from IGF-I treated PDLF, OB culture with conditioned medium from GF, OB culture with conditioned medium from IGF-I treated GF. After final IGF-I treatment, OB was incubated for 24 hours, and alkaline phosphatase activity assay, BMP expression, cell proliferation measurement using MTT assay, total protein measurement, collagen synthesis assay using western blot, and examination of bone nodule synthesis were done. Alkaline phosphatase expressions were increased in the group of PDLF-IGF-I supernatant treatment. Direct IGF-I treatment with concentrations of 100ng/ml showed increased viable cell number measured by MTT assay. And IGF-I treatment did not increase total protein amount. The entire experimental group showed BMP2, 4 expression in western blot, and there was no significant difference between control and experimental groups. These results suggested that supernatant from PDLF effects on increasing cellular activities of OB regardless of IGF-I, and at high concentration, IGF-I increases OB cell proliferation.
