Abstract

Mesenchymal stem cells (MSCs) have been identified in human dental tissues. Dental pulp stem cells (DPSCs) were classified within MSC family, are multipotent, can be isolated from adult teeth, and have been shown to differentiate, under particular conditions, into various cell types including osteoblasts. In this work, we investigated how the differentiation process of DPSCs toward osteoblasts is controlled. Recent literature data attributed to the nuclear receptor related 1 (NURR1), a still unclarified role in osteoblast differentiation, while NURR1 is primarily involved in dopaminergic neuron differentiation and activity. Thus, in order to verify if NURR1 had a role in DPSC osteoblastic differentiation, we silenced it during all the processes and compared the expression of the main osteoblastic markers with control cultures. Our results showed that the inhibition of NURR1 significantly increased the expression of osteoblast markers collagen I and alkaline phosphatase. Further, in long time cultures, the mineral matrix deposition was strongly enhanced in NURR1-silenced cultures. These results suggest that NURR1 plays a key role in switching DPSC differentiation toward osteoblasts rather than neuronal or even other cell lines. In conclusion, DPSCs represent a source of osteoblast-like cells and downregulation of NURR1 strongly prompted their differentiation toward the osteoblastogenesis process.

Highlights

  • The regenerative medicine is increasing its interest in using adult stem cells for the regeneration of mineralized tissues

  • We have reported in a previous work that Dental pulp stem cells (DPSCs) express the nuclear receptor nuclear receptor related 1 (NURR1) in basal and in osteogenic conditions [23], a surprising finding, considering that NURR1 is a member of the nuclear steroid/thyroid receptor superfamily, expressed primarily in the central nervous system, essential for the survival and development function of dopaminergic neurons of the ventral nuclei of the brain [30]

  • NURR1 is expressed in DPSCs, but its role in the osteogenic differentiation is still controversial and needs more investigations

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Summary

Introduction

The regenerative medicine is increasing its interest in using adult stem cells for the regeneration of mineralized tissues. DPSCs showed to differentiate into osteoblast-like cells, express the main bone matrix protein collagen I (Col1), the typical osteoblast enzyme alkaline phosphatase (ALP), and form nodules of mineralized matrix [2, 15, 22,23,24]. Col1 protein level increased in NURR1 silenced cells if compared with CTR cells at 2–6 days, confirming the mRNA data.

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