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DOI 10.1016/j.jsb.2012.12.005

Медицинская библиотека · Journal of structural biology · 2012

Structural analysis of reactionary dentin formed in response to polymicrobial invasion.

Charadram Nattida, Austin Christine, Trimby Patrick, Simonian Mary, Swain Michael V, Hunter Neil

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

In response to microbial invasion of dentin odontoblasts secrete an altered calcified matrix termed reactionary dentin (Rd). 3D reconstruction of focused-ion-beam scanning electron microscopy (FIB-SEM) image slices revealed helical tubular structures in Rd that contrasted with regular cylindrical tubules characteristic of dentin from healthy teeth and affected so-called physiological dentin (Pd) lying exterior to Rd. This helical structure in Rd provided effective constriction of tubule lumen diameter that formed a barrier to bacterial advance towards the dental pulp. SEM of resin cast preparations revealed altered extension of odontoblast processes through Rd. The distribution of key mineral elements was studied by combination of 3D reconstruction of focused-ion-beam based X-ray microanalysis (FIB-EDS), laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). There was a marked redistribution of calcium and phosphorous in Rd together with an increase of diffusely deposited magnesium compatible with the mineral deposition phase of synthesis of this altered matrix. Changes in tubule structure and mineral content characteristic of Rd are consistent with reduced hardness and lower elastic modulus reported for this matrix. Findings provide insight into the unique structure of Rd synthesised as a primary response to infection.

Для цитирования: Charadram Nattida, Austin Christine, Trimby Patrick, Simonian Mary, Swain Michael V, Hunter Neil. Structural analysis of reactionary dentin formed in response to polymicrobial invasion.. Journal of structural biology. 2012. DOI: 10.1016/j.jsb.2012.12.005.

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