Abstract

Introduction. This study aimed to explore the effects of TGF-β1 on regulating activities of cementoblasts and osteoblasts with or without stress. Material and Methods. Human recombinant TGF-β1 was added with different doses. Immunohistochemical test of osteoprotegerin (OPG)/receptor activator of nuclear factor-kappaB ligand (RANKL) and Alizarin Red-S staining were conducted. Mechanical compressive stress was obtained by increasing the pressure of gaseous phase. OPG/RANKL expression was detected in both cells through quantitative real-time PCR. Results. Similar significant differences (P < 0.05) existed in OPG/RANKL change with increasing concentration of TGF-β1 without mechanical stress for cementoblasts and osteoblasts. However, under 3 h stress, OPG increased and RANKL decreased significantly (P < 0.01) but with similar OPG/RANKL change. Moreover, under 24 h stress, OPG change exhibited no difference (P > 0.05), but RANKL decreased significantly (P < 0.01) at 10 and 100 ng/mL TGF-β1 in cementoblasts. In osteoblasts, OPG increased significantly (P < 0.01) at 10 and 100 ng/mL, whereas RANKL decreased with statistical difference (P < 0.05) at 1 and 10 ng/mL. Conclusions. The effects of TGF-β1 on OPG/RANKL expression of cementoblasts and osteoblasts are similar even without mechanical stress. However, these effects are different under mechanical compressive stress.

Highlights

  • This study aimed to explore the effects of Transforming growth factor-β1 (TGF-β1) on regulating activities of cementoblasts and osteoblasts with or without stress

  • With the increasing TGF-β1 concentrations at 1, 10, and 100 ng/mL, OPG expression increased in OCCM-30 and MC3T3E1 cells (Figure 2), whereas receptor activator of nuclear factor-kappaB ligand (RANKL) expression decreased in both cells (Figure 3)

  • This finding indicated that TGF-β1 exhibits a negative effect on mineralization in cells, and the influence is more significant in OCCM-30 than in MC3T3-E1 (Figure 4)

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Summary

Introduction

This study aimed to explore the effects of TGF-β1 on regulating activities of cementoblasts and osteoblasts with or without stress. Similar significant differences (P < 0.05) existed in OPG/RANKL change with increasing concentration of TGF-β1 without mechanical stress for cementoblasts and osteoblasts. Under 24 h stress, OPG change exhibited no difference (P > 0.05), but RANKL decreased significantly (P < 0.01) at 10 and 100 ng/mL TGF-β1 in cementoblasts. The effects of TGF-β1 on OPG/RANKL expression of cementoblasts and osteoblasts are similar even without mechanical stress. These effects are different under mechanical compressive stress. As force-sensitive type of cells, both cementoblasts and osteoblasts change their functions and activities under mechanical stress to regulate the resorption and formation of bone and cementum [2]. The osteogenic cell lineage MC3T3-E1, which behaves to primary osteoblasts, and the cementogenic cell lineage OCCM-30, which expresses specific cementum-derived attachment protein and differentiates into terminally differentiated cementocytes, were considered good models for in vitro studies [4, 5]

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