Publications by authors named "Henry Magloire"

Nerve growth factor (NGF) is a key regulator of the development and differentiation of neuronal and non-neuronal cells. In the present study we examined the distribution of NGF and its low and high-affinity receptors, p75 and TrkA respectively, in permanent human teeth under normal and pathological conditions. In intact functional teeth, NGF, p75 and TrkA are weakly expressed in dental pulp fibroblasts and odontoblasts that are responsible for dentine formation, while the NGF and p75 molecules are strongly expressed in nerve fibres innervating the dental pulp.

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Dental pain arises from exposed dentin following bacterial, chemical, or mechanical erosion of enamel and/or recession of gingiva. Thus, dentin tissue and more specifically patent dentinal tubules represent the first structure involved in dentin sensitivity. Interestingly, the architecture of dentin could allow for the transfer of information to the underlying dental pulp via odontoblasts (dentin-forming cells), via their apical extension bathed in the dentinal fluid running in the tubules, or via a dense network of trigeminal sensory axons intimately related to odontoblasts.

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  • - MAP-1B is a microtubule-associated protein crucial for stabilizing microtubules during the development of nerve cells, particularly in odontoblasts involved in tooth formation, and its expression is regulated by FMRP.
  • - The study employed various methods like real-time PCR and immunochemistry to analyze MAP-1B expression, discovering it in adult and embryonic human dentin-forming cells, especially in response to differentiation states.
  • - Findings suggest that MAP-1B plays a significant role in the terminal differentiation of odontoblasts, alongside other proteins like MAP2 and tau, indicating its importance in both healthy development and dental conditions.
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  • - KLF4 and KLF5 are transcription factors that influence tooth development, and their expression patterns during this process in mice were studied from embryonic day E12.5 to postnatal day PN3.
  • - KLF4 was found to be specifically expressed in polarizing odontoblasts and ameloblasts during later stages of tooth development, while KLF5 was primarily expressed in secretory ameloblasts and odontoblasts, as well as in proliferating epithelial cells at earlier stages.
  • - The findings suggest KLF4 is linked to the differentiation of odontoblasts and ameloblasts, while KLF5 may play roles in both early cell proliferation and later mineralization of tooth structures.
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Odontoblasts are organized as a single layer of specialized cells responsible for dentine formation and presumably for playing a role in tooth pain transmission. Each cell has an extension running into a dentinal tubule and bathing in the dentinal fluid. A dense network of sensory unmyelinated nerve fibers surrounds the cell bodies and processes.

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  • Odontoblasts are essential for creating dentin through the production of organic matrix and mineralization, and new techniques have been developed to study both mature and newly formed odontoblasts.
  • A comparison of gene expression profiles between native and cultured odontoblasts revealed notable similarities, particularly in the expression levels of genes related to neuronal proteins.
  • Findings indicated that cultured odontoblasts closely mimic the gene expression patterns of native ones, highlighting their potential for in vitro research and supporting the idea that odontoblasts may function as sensory cells.
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The Nav1.9 sodium channel is expressed in nociceptive DRG neurons where it contributes to spontaneous pain behavior after peripheral inflammation. Here, we used a newly developed antibody to investigate the distribution of Nav1.

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  • * A study using cDNA gene arrays on human dental pulp cells revealed that EVI1, a transcription factor that inhibits TGF-beta/BMP signaling, is under-expressed in odontoblast-like cells compared to pulp fibroblast-like cells.
  • * EVI1 levels were confirmed through PCR and immunohistochemistry, showing that its expression varies in the dental pulp, potentially impacting odontoblast differentiation and the overall healing process in dental therapeutics.
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  • Odontoblasts are cells that create dentin in teeth and may also play a role in tooth pain, but this function has not been definitively proven before.
  • New research shows that human odontoblasts can generate electrical signals and action potentials, indicating they have excitability similar to nerve cells.
  • The study finds that odontoblasts have specific sodium channel subunits which cluster with nerve fibers, suggesting they could act as sensor cells involved in transmitting tooth pain signals.
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  • Gram-positive bacteria entering the dental tissue can affect the immune response in the dental pulp, with odontoblasts being the first cells to encounter these bacteria.
  • The study found that odontoblasts expressed certain pattern recognition receptors and showed a strong response to lipoteichoic acid (LTA), a component of Gram-positive bacterial walls, enhancing the release of specific chemokines like CCL2 and CXCL10.
  • Interestingly, while LTA triggered an immune response and chemokine production to recruit immune cells, it also decreased the expression of genes related to dentin matrix synthesis, highlighting a trade-off between immune activation and odontoblast function.
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Previous reports have shown the expression of several mechanosensitive ionic channels on the plasma membrane in odontoblasts, which are the cells responsible for dentin formation. The membrane characteristics of odontoblasts imply that they could play critical roles in the mechano-transduction of fluid displacement within dentinal tubules into the electrical cell signals, to carry dentin sensation to the central nervous system. However, the direct ionic mechanism underlying such a dentin nociceptive function remains unclear.

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Semaphorin 7A (SEMA 7A) is a membrane-anchored member of the semaphorin family of guidance proteins, previously identified in the immune system. Expressed in central and peripheral nervous system during embryonic and post-natal stages, it can mediate neuronal functions by promoting axonal growth. We show here that SEMA 7A is expressed in human odontoblasts in vivo and in vitro and that its expression is correlated with the establishment of dentin-pulp complex terminal innervation .

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Reelin is a large extracellular matrix (ECM) glycoprotein strongly expressed during embryonic development in the central nervous system and involved in architectonic brain development. It could participate in axon plasticity processes or adhesion-recognition between nerve fibers in adulthood. Previously identified from a subtractive cDNA library of fully differentiated human odontoblasts, reelin might be involved in the relationship between dental nerves and odontoblasts in as so far the latter are in close association with pulpal nerve fibers.

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Purpose: The aim of this study was to investigate dental pulp reactions after a neodynium:yttrium aluminum perovskite laser pulse on the dentinal floor of occlusal cavities in an in vitro model.

Methods: A Lokki dt laser was used at 30 Hz, 5 W, and 160 mJ for 0.5 s.

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Odontoblasts, the cells responsible for the dentine formation, are organized as a single layer of highly polarized and differentiated post-mitotic cells along the interface between the dental pulp and the mineralized tubules. They lay down the physiological secondary dentine throughout the life of the teeth. Odontoblasts play a central role in the transportation of calcium to the dentine and they possibly mediate early stages of sensory processing in teeth.

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An antiserum was generated from synthetic peptides highly conserved between different mammalian species to immunolocalise the small leucine-rich proteoglycan osteoadherin (OSAD) in murine teeth. In 19-day-old embryos of rats and mice, a positive staining was found in incisor predentin and alveolar bone surrounding developing incisors and molars. In newborns, OSAD was detected at the tip of the first molar cusp where it accumulated in predentin concomitantly with odontoblast differentiation.

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Transforming growth factor beta 1 (TGF beta 1) is generally considered to be a potent inducer of dentin formation. In order to further assess this role, we studied the influence of this factor in human dental pulp cells on the expression of osteoadherin (OSAD), a newly described proteoglycan found in bone and dentin and suspected to play a role in mineralization events. We performed TGF beta 1 stimulation both in cultures of human tooth thick slices including mature odontoblasts and in pulp explant cultures giving rise to early secretory odontoblasts or pulpal fibroblasts.

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