Abstract

This study characterized alveolar periosteum-derived mesenchymal stem cells (P-MSCs) and examined the hypothesis that 1,25-(OH)2D3 (calcitriol) exerts osteoinductive effects on P-MSCs. The mRNA expressions of alkaline phosphatase (ALP), bone sialoprotein (BSP), core-binding factor alpha-1 (CBFA1), collagen-1 (Col-1), osteocalcin (OCN), and vitamin D3 receptor (VDR) were assessed after incubation with calcitriol for 2 weeks. Vitamin C as positive control (Vit. C-p) increased ALP and CBFA1 mRNA expression at both 1 and 2 weeks and increased BSP and Col-1 mRNA expression only at the first week. A concentration of 10−8 M calcitriol enhanced ALP, CBFA1, Col-1, and OCN mRNA expression at both weeks and BSP mRNA expression at the first week. Furthermore, 10−7 M calcitriol increased the mRNA expressions of all compounds at both weeks, except that of CBFA1 at the first week. 10−8 M calcitriol and Vit. C-p enhanced ALP activity at the second and third weeks. The results revealed that 10−9, 10−8, and 10−7 M calcitriol induced osteoinduction in alveolar P-MSCs by increasing ALP, CBFA1, Col-1, and OCN mRNA expression. A 10−7 M calcitriol yielded a higher mRNA expression than Vit. Cp on VDR and OCN mRNA expression at both weeks and on Col-1 mRNA at the second week.

Highlights

  • Mesenchymal stem cells (MSCs) can be isolated from various tissues, including long bone periosteum and dental tissues [1]

  • The present study examined the effects of calcitriolinduced osteogenic differentiation on human alveolar periosteum-derived MSCs (P-MSCs) and assessed the optimal calcitriol concentration and incubation period required for osteogenic induction

  • The results revealed that periosteum-derived cells (PDCs) could be decent subpassaged and potentially differentiated into periosteum-derived mesenchymal stem cells (P-MSCs)

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Summary

Introduction

Mesenchymal stem cells (MSCs) can be isolated from various tissues, including long bone periosteum and dental tissues [1]. Low Vit. D3 levels are associated with skeletal fragility and fractures; Vit. D3metabolites are major contributors of bone and mineral homeostasis, including the effect of 24R,25(OH)2D3on the osteoblastic differentiation of human MSCs [14]. Calcitriol, the most biologically active form of Vit. D3, serves various physiological functions in the body, the most crucial being the maintenance of the calcium and phosphorus balance, which affects bone health. Calcitriol stimulates the in vitro differentiation of human MSCs into osteoblasts, which can be monitored on the basis of the increase in the alkaline phosphatase (ALP) enzyme activity or osteocalcin (OCN) gene expression [14]. Few studies have investigated the dose–response and dose–time effects of calcitriol on human P-MSCs for bone tissue engineering

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