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Evidence for changing nerve growth factor signalling mechanisms during development, maturation and ageing in the rat molar pulp
Author(s) -
Mahdee A.,
Eastham J.,
Whitworth J. M.,
Gillespie J. I.
Publication year - 2019
Publication title -
international endodontic journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.988
H-Index - 119
eISSN - 1365-2591
pISSN - 0143-2885
DOI - 10.1111/iej.12997
Subject(s) - calcitonin gene related peptide , nerve growth factor , pulp (tooth) , molar , ageing , odontoblast , calcitonin , endocrinology , medicine , sensory nerve , biology , receptor , neuropeptide , sensory system , dentistry , neuroscience
Aim To examine rat molar pulp innervation and identify complex cellular signalling systems involving nerve growth factor (NGF) and its p 75 receptors (NGFR) at different stages of development, maturation and ageing. Methodology Decalcified mandibular first molar mesial cusps from Wistar rats of ages 0 day; 1, 2, 3, 4, 6, 9, 12 and 24 weeks ( n = 5 per group) were sectioned (10 μm) and incubated with antibodies for NGF, NGFR, calcitonin gene‐related peptide (CGRP) and neurofilament. Nerve densities in worn and intact regions of 3‐ to 24‐week‐old rats were compared by anova , Bonferroni and t ‐tests. Results During odontogenesis, differences in NGF and NGFR expression were observed, with no evidence of nerve fibres, suggesting a signalling mechanism controlling cellular differentiation and dentine formation. Tooth wear in 4‐week rats was associated with reduced NGF expression and significantly decreased CGRP axons within affected odontoblast regions. The underlying subodontoblasts started expressing NGF which continued until 9 weeks. This may promote a significant increase in CGRP nerve density in affected regions. Nerve density in intact odontoblast regions increased gradually and reached significant levels in 12‐week rats. Reduction in nerve densities within worn and intact regions of cusps was observed at 24 weeks. Conclusions Age‐related changes and responses to tooth wear may be controlled by the NGF signalling mechanism, with roles in odontoblast/subodontoblast communication and control of sensory innervation at different stages of tooth development, maturation and ageing. Greater understanding of cellular and nerve regulation in the injured pulp may promote therapeutic strategies for pulp survival.