Regeneration of sensory nerve branches in extraction socket and surrounding alveolar bone in rat: immunohistochemical observation of the axon and myelin sheath changes.

The purpose of this study was to investigate the process and derivation of the distribution of the sensory nerves that appear in the extraction socket and surrounding alveolar bone following tooth extraction. The right mandibular first molar of rats and periodontal ligament were extracted as a single mass, and the mandible was harvested after days 1, 3, 5, and 7 after extraction. Serial sections of 7 µm thickness were prepared for the proximal root (Section A), buccolingual root (Section B), and centrifugal root (Section C) of the first molar. H-E staining and immunohistochemical staining with anti-S100 antibody and anti-NF-L antibody were carried out. The presence of nerve fiber bundles in the blood clot was already evident on post-extraction day 3, and on post-extraction day 7. On day 3, the number of axons in Sections B and C had greatly decreased, indicating that, after extraction, the connection between peripheral nerve tissue and the trigeminal ganglion was temporarily markedly reduced in the region of the alveolar branch. Although the myelin sheaths were regenerating on day 5, the majority of the axons of the alveolar branches extending from the inferior alveolar nerve were seen to be extremely thin and scattered, despite their further regeneration. The above results suggest that the newly myelinated nerves are actually derived from the bone marrow to the extraction socket, so few nerves, rather than being derived from the alveolar branches that had innervated the extracted tooth.

Prominin-1 Modulates Rho/ROCK-Mediated Membrane Morphology and Calcium-Dependent Intracellular Chloride Flux.

Membrane morphology is an important structural determinant as it reflects cellular functions. The pentaspan membrane protein Prominin-1 (Prom1/CD133) is known to be localised to protrusions and plays a pivotal role in migration and the determination of cellular morphology; however, the underlying mechanism of its action have been elusive. Here, we performed molecular characterisation of Prom1, focussing primarily on its effects on cell morphology. Overexpression of Prom1 in RPE-1 cells triggers multiple, long, cholesterol-enriched fibres, independently of actin and microtubule polymerisation. A five amino acid stretch located at the carboxyl cytosolic region is essential for fibre formation. The small GTPase Rho and its downstream Rho-associated coiled-coil-containing protein kinase (ROCK) are also essential for this process, and active Rho colocalises with Prom1 at the site of initialisation of fibre formation. In mouse embryonic fibroblast (MEF) cells we show that Prom1 is required for chloride ion efflux induced by calcium ion uptake, and demonstrate that fibre formation is closely associated with chloride efflux activity. Collectively, these findings suggest that Prom1 affects cell morphology and contributes to chloride conductance.