An ultrastructural study of cellular response to variation in porosity in phase-pure hydroxyapatite

Hydroxyapatite has been shown to be biocompatible and bioactive. Incorporation of porosity has been shown to enhance osteointegration; however, difficulty in controlling the extent and type of porosity has limited investigation into determining the role of both macro‐ and microporosity. The current investigation reports on the synthesis of four types of phase‐pure hydroxyapatite with varying levels of porosity (HA1–HA4), and with defined levels of macro‐ and microporosities. Transmission electron microscopy was used to evaluate qualitatively the effect of these two parameters on cell–material interactions following a 30‐day incubation period. Biological mineralization was observed within vesicles and the needle‐like minerals were confirmed as hydroxyapatite using X‐ray microanalysis. This demonstrated the suitability of primary human osteoblast‐like cells as a tool to assess the extent of mineralization. Furthermore, internalization of hydroxyapatite particles was observed. Our findings show that the variation in macro‐ and microporosity does not affect the extent of cell–material interaction, with collagen synthesis evident in all samples.     

Evaluation of trace element contamination using Armadillo officinalis Duméril, 1816 (Crustacea,Isopoda) as a tool: An ultrastructural study

To estimate trace element bioaccumulation in Armadillo officinalis, specimens were collected from Ghar El Melh lagoon then exposed for 3 weeks in contaminated sediments with copper, zinc, and cadmium. From the first week until the end of the experiment, a decrease in A. officinalis growth related to the increase of Cd concentration in the sediment was recorded. However, a mass gain was highlighted under Cu and Zn exposures. At the end of experiment, body metal concentrations were measured using flame atomic emission spectrometry. Results of the bioaccumulation factor showed that the species could be considered as a macroconcentrator of copper (BAF > 2) and a deconcentrator of zinc (BAF < 2). Microscopy observations of hepatopancreas cells showed morphological and histological changes even at the lowest concentration. They consisted in the microvillus border destruction, lipid droplets modifications, trace element accumulation, and the condensation of the majority of cellular organelles. The degree of these alterations was found to be dose‐dependent. Through these results, the isopod A. officinalis could be used as relevant monitor organisms for soil metal contamination.     

MRT Letter: Spatial distribution of vancomycin‐induced damage in Staphylococcus epidermidis biofilm: An electron microscopic study

This study was planned to elucidate the efficacy of antibiotics on Staphylococcus epidermidis and Staphylococcus aureus biofilms by scanning electron microscopy (SEM). Biofilms of S. epidermidis ATCC 35984 and S. aureus ATCC 29213 were grown on black, polycarbonate membranes placed on tryptic soy agar plates for 48 h at 37°C, and then exposed to vancomycin or amikacin or ciprofloxacin at clinically achievable levels for 24 h at 37°C. The morphology of antibiotic‐treated and untreated biofilms was elucidated by SEM. SEM analysis indicated a differential affection of S. epidermidis ATCC 35984 in the center and periphery of biofilm upon treatment with vancomycin. The center of biofilm revealed damaged cells with sparse distribution, smaller size, and irregular shape, whereas cells in the periphery were unaffected. This differential distribution of susceptibility within S. epidermidis ATCC 35984 biofilms was specific for vancomycin only and was not observed on exposure to amikacin or ciprofloxacin. No such response was found in S.aureus ATCC 29213 biofilms. Thus, our study suggests a spatial distribution of vancomycin‐induced damage in S. epidermidis biofilms. To our knowledge, this is the first report that indicates a differential affection of S. epidermidis in the center and periphery of biofilm upon treatment with vancomycin. Studies on the factors controlling this differential distribution could provide valuable insights into the mechanisms of antimicrobial resistance in S. epidermidis biofilms. Microsc. Res. Tech., 2010. © 2010 Wiley‐Liss, Inc.