Promoting Effect of Pinostrobin on the Proliferation, Differentiation, and Mineralization of Murine Pre-osteoblastic MC3T3-E1 Cells

• Published in: Molecules (Basel, Switzerland) Vol. 22; no. 10; p. 1735
• Main Authors: Gu, Chengbo, Fu, Linan, Yuan, Xiaohan, Liu, Zhiguo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 16.10.2017; MDPI
• Subjects: Alkaline phosphatase; Animals; Biocompatibility; Biomedical materials; Cell differentiation; Cell Differentiation - drug effects; Cell Line; Cell proliferation; Cell Proliferation - drug effects; Collagen (type I); Collagen - metabolism; Dexamethasone; Differentiation (biology); Flavanones - pharmacology; Gene expression; MC3T3-E1; Mice; Mineralization; mRNA; Osteoblastogenesis; Osteoblasts; Osteoblasts - cytology; Osteoblasts - drug effects; Osteocalcin; Osteogenesis - drug effects; osteogenic differentiation; Osteoporosis; Osteoporosis - metabolism; Pharmacology; pinostrobin; proliferation; proliferation; osteoporosis; osteogenic differentiation; MC3T3-E1; pinostrobin
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules22101735

Pinostrobin (PI), a natural flavonoid found in a variety of plants, is well known for its rich pharmacological activities. However, its osteogenic function remains unclear. The aim of this study is to evaluate the effect of PI on the proliferation, differentiation, and mineralization of murine pre-osteoblastic MC3T3-E1 cells in vitro using MTT, alkaline phosphatase (ALP) activity, the synthesis of collagen I (Col I) assay, and Von-Kossa staining, respectively. The expression of osteocalcin (OCN) mRNA in cells was detected by real-time PCR. The effect of PI on the differentiation of dexamethasone (DEX)-suppressed cells was also investigated. The results showed that PI greatly promoted the proliferation of MC3T3-E1 cells at 5-80 μg/mL ( < 0.05 or < 0.01), and caused a significant elevation of ALP activity, Col I content, and mineralization of osteoblasts at 10-40 μg/mL ( < 0.05 or < 0.01), and the expression levels of OCN gene were greatly upregulated after PI treatment ( < 0.01). Furthermore, PI could rescue the inhibition effect of cell differentiation induced by DEX. Taken together, these results indicated that PI could directly promote proliferation, differentiation, and mineralization of MC3T3-E1 cells and has potential for use as a natural treatment for osteoporosis.