Fine Structure of the Inner Enamel in Human Permanent Teeth

Using SEM after EDTA etching, the mid-coronal inner enamel of human permanent teeth was classified into three regions of the 1st, 2nd, and 3rd zones. The 1st zone showing a highly negative birefringence was the innermost 10 - 15 μm enamel. This zone consisted of arcade and circular initial prisms, and the succeeding arcade prisms only. These initial prisms arising perpendicularly to the dentine surface resembled pseudoprisms because these prisms showed a somewhat centripetal arrangement of crystal lites and indistinct prism boundaries. The succeeding prisms were frequently bent following a faint slit within the prism. The 2nd zone adjacent to the 1st zone measured 20 - 40 μm in thickness. This zone was mainly composed of horseshoe-shaped prisms with EDTA-insoluble prism sheaths in the deep-etched prism boundaries, but the inner-half layer had dotted irregular prisms including circular, double marginal, and spiral shapes with the prism sheaths. Prismless structures were rarely seen in the 2nd zone. The 3rd zone was mainly occupied by horseshoe-shaped prisms without EDTA-insoluble prism sheaths in the deep-etched prism boundaries, although tuft prisms in the 3rd zone contained a large amount of EDTA-insoluble substances in the prisms, interprismatic regions, and the boundaries

Use of Chitosan-Siloxane Porous Hybrid Scaffold as Novel Burr Hole Covers

Chitosan-siloxane porous hybrids have high potential as tissue scaffolds. This manuscript focuses on the regeneration of skull bone after a burr hole. This was done using hybrids incorporated with calcium or coated with hydroxyapatite after soaking in a phosohate solution. The specimens fitted the burr hole and the cells migrated into the pores form surrounding bone tissue. After implanation no inflammation was observed and the specimens degraded 12 months later. A coating of hydroxyapatite accelerated bone formation compared

Mechanisms of organelle division and inheritance and their implications regarding the origin of eukaryotic cells

Mitochondria and plastids have their own DNAs and are regarded as descendants of endosymbiotic prokaryotes. Organellar DNAs are not naked in vivo but are associated with basic proteins to form DNA-protein complexes (called organelle nuclei). The concept of organelle nuclei provides a new approach to explain the origin, division, and inheritance of organelles. Organelles divide using organelle division rings (machineries) after organelle-nuclear division. Organelle division machineries are a chimera of the FtsZ (filamentous temperature sensitive Z) ring of bacterial origin and the eukaryotic mechanochemical dynamin ring. Thus, organelle division machineries contain a key to solve the origin of organelles (eukaryotes). The maternal inheritance of organelles developed during sexual reproduction and it is also probably intimately related to the origin of organelles. The aims of this review are to describe the strategies used to reveal the dynamics of organelle division machineries, and the significance of the division machineries and maternal inheritance in the origin and evolution of eukaryotes

Role of systemic T-cells and histopathological aspects after subcutaneous implantation of various carbon nanotubes in mice

ArticleCarbon. 44(6):1079-1092 (2006)journal articl

In vivo immunological toxicity in mice of carbon nanotubes with impurities

ArticleCarbon. 47(5):1365-1372 (2009)journal articl

Manipulating transgenes using a chromosome vector

Recent technological advances have enabled us to visualize the organization and dynamics of local chromatin structures; however, the comprehensive mechanisms by which chromatin organization modulates gene regulation are poorly understood. We designed a human artificial chromosome vector that allowed manipulation of transgenes using a method for delivering chromatin architectures into different cell lines from human to fish. This methodology enabled analysis of de novo construction, epigenetic maintenance and changes in the chromatin architecture of specific genes. Expressive and repressive architectures of human STAT3 were established from naked DNA in mouse embryonic stem cells and CHO cells, respectively. Delivery of STAT3 within repressive architecture to embryonic stem cells resulted in STAT3 activation, accompanied by changes in DNA methylation. This technology for manipulating a single gene with a specific chromatin architecture could be utilized in applied biology, including stem cell science and regeneration medicine

Neurogenic muscular atrophy and low density of large myelinated fibres of sural nerve in chorea-acanthocytosis

In three cases of chorea-acanthocytosis (acanthocytosis and neurological disease, or familial degeneration of the basal ganglia with acanthocytosis), biopsies of short peroneal muscles and sural nerves were studied histologically. The muscles showed groups of atrophic fibres with clumping of sarcolemmal nuclei in all cases. It was concluded that neurogenic muscular atrophy should be included as one of the main pathological findings in chorea-acanthocytosis. The sural nerves showed a small number of large myelinated fibres in two cases. This finding remains to be confirmed in other cases