Abstract

The sensory innervation of the dental mesenchyme is essential for tooth function and protection. Sensory innervation of the dental pulp is mediated by axons originating from the trigeminal ganglia and is strictly regulated in time. Teeth can develop from cultured re-associations between dissociated dental epithelial and mesenchymal cells from Embryonic Day 14 mouse molars, after implantation under the skin of adult ICR mice. In these conditions however, the innervation of the dental mesenchyme did not occur spontaneously. In order to go further with this question, complementary experimental approaches were designed. Cultured cell re-associations were implanted together with trigeminal ganglia for one or two weeks. Although axonal growth was regularly observed extending from the trigeminal ganglia to all around the forming teeth, the presence of axons in the dental mesenchyme was detected in less than 2.5% of samples after two weeks, demonstrating a specific impairment of their entering the dental mesenchyme. In clinical context, immunosuppressive therapy using cyclosporin A was found to accelerate the innervation of transplanted tissues. Indeed, when cultured cell re-associations and trigeminal ganglia were co-implanted in cyclosporin A-treated ICR mice, nerve fibers were detected in the dental pulp, even reaching odontoblasts after one week. However, cyclosporin A shows multiple effects, including direct ones on nerve growth. To test whether there may be a direct functional relationship between immunomodulation and innervation, cell re-associations and trigeminal ganglia were co-implanted in immunocompromised Nude mice. In these conditions as well, the innervation of the dental mesenchyme was observed already after one week of implantation, but axons reached the odontoblast layer after two weeks only. This study demonstrated that immunodepression per se does stimulate the innervation of the dental mesenchyme.

Highlights

  • Teeth can develop from cultured and implanted re-associations between dissociated dental epithelial and mesenchymal cells from Embryonic Day (ED) 14 mouse molars

  • Even when cell re-associations were implanted together with trigeminal ganglia, nerve fibers did not enter the dental pulp after one week (Figs. 2A–C; 0/29 samples)

  • For 3 of the 123 re-associations co-implanted with trigeminal ganglia for two weeks, immunostaining for peripherin was positive in the dental mesenchyme (2,44%)

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Summary

Introduction

Teeth can develop from cultured and implanted re-associations between dissociated dental epithelial and mesenchymal cells from Embryonic Day (ED) 14 mouse molars In these experimental conditions, it is possible to reproduce the epithelial-mesenchymal interactions, which control odontogenesis during embryonic development. It is possible to reproduce the epithelial-mesenchymal interactions, which control odontogenesis during embryonic development This approach allows the progressive steps involved in odontogenesis to proceed: crown morphogenesis, epithelial histogenesis, the initiation of root formation and the functional differentiation of odontoblasts, ameloblasts and cementoblasts [for review see [1]]. These steps were completed already after two weeks of implantation under the skin of adult ICR mice [2]. The other interacting tissue, the inductor, still needs to have a dental origin

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