Phytoremediation of Metals: A Numerical Analysis

A finite element code was used for investigating the effect of some relevant characteristics of a phytoremediation project (crop type and density, presence of an irrigation system, soil capping and root depth). The evolution of the plume of contamination of Cd²⁺, Pb²⁺, and Zn²⁺ was simulated taking into account reactive transport and root processes. The plant contaminant uptake model was previously calibrated using data from greenhouse experiments. The simulations adopted pedological and climatological data representative of a sub-tropical environment. Although the results obtained were specific for the proposed scenario, it was observed that, for more mobile contaminants, poor water conditions favor stabilization but inhibit plant extraction. Otherwise an irrigation system that decreases crop water stress had an opposite effect. For less mobile contaminants, the remediation process did not have appreciable advantages. Despite its simplifying assumptions, particularly about contaminant sorption in the soil and plant system, the numerical analysis provided useful insight for the phytoextraction process important in view of field experiments.     

Tenascin-C mRNA and Tenascin-C Protein Immunoreactivity Increase in Astrocytes after Activation by bFGF

Tenascin-C is an extracellular matrix glycoprotein with trophic and repulsive properties, involved in migratory processes in CNS. Previous reports demonstrated that this molecule is produced and secreted by astrocytes. Preliminary data on fibroblasts and astrocytes have suggested that bFGF may modulate tenascin-C expression. bFGF is a mitogenic growth factor, involved in cell differentiation and neovascularization. In the present study, we ex amined whether bFGF modulates the expression of tenascin-C in hippocampal astrocytes from newborn rats. Our results suggest that bFGF increases the production of tenascin-C by cultured hippocampal astrocytes. We found that both tenascin-C mRNA and protein immunoreactivity were increased after bFGF treatment. Our results also demonstrated that tenas cin-C polypeptides were secreted into the extracellular medium. In agreement with previous studies, we suggest that secreted tenascin-C is mainly the high molecular weight form. In addition, our results suggest that a cleavage of the high molecular weight form may occur in the extracellular medium causing production of proteolytic fragments, that may modify the biological properties of tenascin-C. The present results may be relevant to the understanding of lesion scarring and regeneration process.