This study aims to assess the extent of metal accumulation by plants found in a mining area in Hamedan Province in the central west part of Iran. It also investigates to find suitable plants for phytoextraction and phytostabilization as two phytoremediation strategies. Plants with a high bioconcentration factor (BCF) and low translocation factor (TF) have the potential for phytostabilization while plants with both BCFs and TFs greater than one have the potential to be used for phytoextraction. In this study, shoots and roots of the 12 plant species and the associated soil samples were collected. The collected samples were then analyzed by measurement of total concentrations of trace elements (Pb, Zn, Mn and Fe) using atomic absorption spectrophotometer. Simultaneously, BCF and TF parameters were calculated for each element. Results showed that although samples suitable for phytoextraction of Pb, Zn, Mn and Fe and phytostabilization of Fe were not detected, Scrophularia scoparia was the most suitable for phytostabilization of Pb, Centaurea virgata, Echinophora platyloba and Scariola orientalis had the potential for phytostabilization of Zn and Centaurea virgata and Cirsium congestum were the most efficient in phytostabilization of Mn. Present study showed that native plant species growing on contaminated sites may have the potential for phytoremediation.
Transforming growth factor (TGF)-β1 mediates glycosaminoglycan (GAG) chain hyperelongation on secreted proteoglycans and these modifications are associated with increased lipid binding in the vessel wall and the development of atherosclerosis. In vascular smooth muscle cells (VSMCs), TGF-β1 regulated GAG elongation via extracellular signal-regulated kinase (ERK) and p38 as well as Smad2 linker region phosphorylation. In this study, our aim was to identify the TGF-β1 mediated signalling pathway involving reactive oxygen species (ROS) and Smad2 linker region phosphorylation that regulate the mRNA expression of GAG synthesizing enzymes, chondroitin 4-O-sulfotransferase 1 (CHST11) and chondroitin sulfate synthase 1 (CHSY1) which are the rate limiting enzymes involved in GAG chain elongation. Signalling molecules were assessed by western blotting, quantitative real-time PCR was used for analysis of gene expression and intracellular ROS level was measured by a fluorescence based assay. TGF-β1 induced ROS production in VSMCs. Nicotinamide adenine dinucleotide phosphate oxidase (Nox) inhibitors, diphenyleneiodonium (DPI) and apocynin blocked TGF-β1 mediated Smad2 linker region phosphorylation. TGF-β1 treatment increased the mRNA levels of CHST11 and CHSY1. Pharmacological inhibition of Nox blocked TGF-β1 mediated mitogen activated protein kinases (MAPKs) phosphorylation and TGF-β1 stimulated CHST11 and CHSY1 mRNA expression. These findings demonstrated that TGF-β1 mediated expression of CHST11 and CHSY1 can occur via Nox-dependent pathways and Smad2 linker region phosphorylation. KeywordsAtherosclerosis . Nox . Reactive oxygen species . Mitogen activated protein kinases . Glycosaminoglycan Abbreviations CHST11 Chondroitin 4-Ο-sulfotransferase 1 CHSY1 Chondroitin synthase 1 DPI Diphenyleneiodonium ERK Extracellular signal-regulated kinase GAG Glycosaminoglycan JNK C-Jun N-terminal kinase MAPKs Mitogen activated protein kinases. Nox Nicotinamide adenine dinucleotide phosphate oxidase ROS Reactive oxygen species TGFBR1 Transforming growth factor-β receptor type 1 TGF-β1 Transforming growth factor β1 VSMCs Vascular smooth muscle cells * Hossein Babaahmadi-Rezaei
The current COVID-19 pandemic that is caused by SARS-CoV-2 has led all the people around the globe to implement preventive measures such as environmental cleaning using alcohol-based materials, and social distancing in order to prevent and minimize viral transmission via fomites. The role of environmental surface contamination in viral transmission in within hospital wards is still debatable, especially considering the spread of new variants of the virus in the world. The present comprehensive study aims to investigate environmental surface contamination in different wards of a hospital as well as the efficacy of two common disinfectants for virus inactivation, and tries to produce an estimate of plastic residue pollution as an environmental side effect of the pandemic. With regard to environmental surface contamination, 76 samples were taken from different wards of the hospital, from which 40 were positive. These samples were taken from contaminated environmental surfaces such as patient bed handles, the nursing station, toilet door handles, cell phones, patient toilet sinks, toilet bowls, and patient's pillows, which are regularly-touched surfaces and can pose a high risk for transmission of the virus. The number of positive samples also reveals that SARS-CoV-2 can survive on inanimate surfaces after disinfection by ethanol 70 % and sodium hypochlorite (0.001 %). The results correspond to the time that the VOC 202012/01 (lineage B.1.1.7) had emerged in the hospital and this should be considered that this variant could possibly have different traits, characteristics, and level of persistence in the environment. The plastic waste as an environmental side effect of the pandemic was also investigated and it was confirmed that the amount of plastic residue for a single (RT) PCR confirmatory test for COVID-19 diagnosis is 821.778 g of plastic residue/test. As a result, it is recommended that for improving plastic waste management programs, considering challenges such as minimizing plastic waste pollution, optimization of gas control technologies in incinerators, process redesign, reduction of single-use plastics and PPE, etc. Is of utmost importance.
Objectives TGF‐β through hyperelongation of glycosaminoglycan (GAG) chains leads to binding of low‐density lipoproteins to the proteoglycans. The vasoactive peptide, endothelin‐1 (ET‐1), plays a key role in the development of atherosclerosis. This study addressed the question whether ET‐1 by activating the Rho kinase and cytoskeletal rearrangement can transactivate the TGF‐β receptor leading to phosphorylation of the transcription factor Smad2 and increased expression of the GAG chain synthesizing enzyme such as chondroitin synthase‐1 (CHSY‐1) in bovine aortic endothelial cells (BAECs). Methods In this study, intermediates in ET‐1‐induced Smad2C phosphorylation and the protein level of CHSY‐1 were identified and quantified by Western blotting. Key findings Endothelin‐1 caused time‐dependent phosphorylation of Smad2C which was inhibited in the presence of the endothelin B receptor antagonist, BQ788. The response to ET‐1 was inhibited by the Rho/ROCK kinase antagonist, Y27632 and by cytochalasin D, an inhibitor of actin polymerization but the ET‐1‐mediated pSmad2C was not inhibited by the matrix metalloproteinase (MMP) inhibitor, GM6001. ET‐1 increased CHSY‐1 protein level, which was inhibited in the presence of BQ788, cytochalasin D and Y27632. Conclusions Endothelin‐1 signalling via the ETB receptor utilizes cytoskeletal rearrangement and Rho kinase but not MMPs leading to TβRI transactivation signalling and phosphorylation of Smad2C and through this pathway increased the level of CHSY‐1.
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