Influence of dissolved organic carbon on multimedia distribution and toxicity of fipronil and its transformation products in lotic waterways.

Environmental fate and ecological impacts of fipronil and its transformation products (FIPs) in aquatic environment have caused worldwide attention, however, the influence of dissolved organic carbon (DOC) on multimedia distribution, bioavailability, and toxicity of FIPs in field waterways was largely unknown. Here, we collected 11 companion water and sediment samples along a lotic stream in Guangzhou, South China. FIPs were ubiquitous with total water concentrations ranging from 1.22 to 43.2 ng/L (14.8 ± 12.9 ng/L) and fipronil sulfone was predominant in both water and sediment. More than 70% of FIPs in aqueous phase were bound to DOC and the KDOC values of FIPs were approximately 1-2 orders of magnitude higher than Kd-s/KOC, emphasizing the significance of DOC in phase partitioning and transport of FIPs in aquatic environment. Water and sediment samples were more toxic to Chironomus dilutus than Hyallela azteca, and FIPs (especially fipronil sulfone) pronouncedly contributed toxicity to C. dilutus. Toxic units (TU) based on freely dissolved concentrations in water determined by solid phase microextraction significantly improved toxicity estimation of FIPs to the invertebrates compared to TUs based on aqueous concentrations. The present study highlights the significance of DOC association on fate and ecological risk of hydrophobic insecticides in lotic ecosystem.

Bioassay-based identification and removal of target and suspect toxicants in municipal wastewater: Impacts of chemical properties and transformation.

Municipal wastewater contains numerous chemicals and transformation products with highly diverse physiochemical properties and intrinsic toxicity; thus, it is imperative but challenging to identify major toxicants. Herein, toxicity identification evaluation (TIE) was applied to identify major toxicants in a typical municipal wastewater treatment plant (WWTP). Impacts of chemical properties on the removal of contaminants and toxicity at individual treatment stages were also examined. The WWTP influent caused 100% death of Daphnia magna and zebrafish embryos, and toxicity characterization suggested that organics, metals, and volatiles all contributed to the toxicity. Toxicity identification based on 189 target and approximately one-thousand suspect chemicals showed that toxicity contributions of organic contaminants, metals, and ammonia to D. magna were 77%, 4%, and 19%, respectively. Galaxolide, pyrene, phenanthrene, benzo[a]anthracene, fluoranthene, octinoxate, silver, and ammonia were identified as potential toxicants. Comparatively, the detected transformation products elicited lower toxicity than their respective parent contaminants. In contrast, the analyzed contaminants showed negligible contributions to the toxicity of zebrafish embryos. Removal efficiencies of these toxicants in WWTP were highly related to their hydrophobicity. Diverse transformation and removal efficiencies of contaminants in WWTPs may influence the chemical compositions in effluent and ultimately the risk to aquatic organisms in the receiving waterways.

Legacy and Emerging Per- and Polyfluoroalkyl Substances Behave Distinctly in Spatial Distribution and Multimedia Partitioning: A Case Study in the Pearl River, China.

Per- and polyfluoroalkyl substances (PFASs) have attracted worldwide attention due to their ubiquitous occurrence, bioaccumulation, and toxicological effects, yet the fate of PFASs in a lotic ecosystem is largely unknown. To elucidate spatial distribution and multimedia partitioning of legacy and emerging PFASs in a lotic river flowing into an estuary, PFASs were synchronously analyzed in water, suspended particulate matter (SPM), sediment, and biota samples collected along Guangzhou reach of the Pearl River, South China. Geographically, the concentrations of PFASs in the water phase showed a decreasing trend from the upper and middle sections (urban area) to the down section (suburban area close to estuary) of the river. While perfluorooctanoic acid predominated in water and SPM, more diverse compositions were observed in sediment and biota with the increase in contributions of long-chain PFASs. Field-derived sediment-water partitioning coefficients (Kd) and bioaccumulation factors (BAFs) of PFASs increased with the increase in perfluorinated carbons. Besides hydrophobicity, water pH and salinity significantly affected the multimedia partitioning of PFASs in a lotic ecosystem. In addition, 87 homologues (63 classes) were identified as emerging PFASs in four media using suspect analysis. Interestingly, Kd and BAF of the emerging PFASs were often higher than legacy PFASs containing the same perfluorinated carbons, raising a special concern on the environmental risk of emerging PFASs.

Protein kinase Cα inhibits myocardin-induced cardiomyocyte hypertrophy through the promotion of myocardin phosphorylation.

Myocardin plays a key role in the development of cardiac hypertrophy. However, the upstream signals that control the stability and transactivity of myocardin remain to be fully understood. The expression of protein kinase Cα (PKCα) also induces cardiac hypertrophy. An essential downstream molecule of PKCα, extracellular signal-regulated kinase 1/2, was reported to negatively regulate the activities of myocardin. But, the effect of cooperation between PKCα and myocardin and the potential molecular mechanism by which PKCα regulates myocardin-mediated cardiac hypertrophy are unclear. In this study, a luciferase assay was performed using H9C2 cells transfected with expression plasmids for PKCα and myocardin. Surprisingly, the results showed that PKCα inhibited the transcriptional activity of myocardin. PKCα inhibited myocardin-induced cardiomyocyte hypertrophy, demonstrated by the decrease in cell surface area and fetal gene expression, in cardiomyocyte cells overexpressing PKCα and myocardin. The potential mechanism underlying the inhibition effect of PKCα on the function of myocardin is further explored. PKCα directly promoted the basal phosphorylation of endogenous myocardin at serine and threonine residues. In myocardin-overexpressing cardiomyocyte cells, PKCα induced the excessive phosphorylation of myocardin, resulting in the degradation of myocardin and a transcriptional suppression of hypertrophic genes. These results demonstrated that PKCα inhibits myocardin-induced cardiomyocyte hypertrophy through the promotion of myocardin phosphorylation.

Ca²âº signal-induced cardiomyocyte hypertrophy through activation of myocardin.

Hypertrophic growth of cardiomyocytes in response to pressure overload is an important stage during the development of many cardiac diseases. Ca(2+) overload as well as subsequent activation of Ca(2+) signaling pathways has been reported to induce cardiac hypertrophy. Myocardin, a transcription cofactor of serum response factor (SRF), is a key transducer of hypertrophic signals. However, the direct role of myocardin in Ca(2+) signal-induced cardiomyocyte hypertrophy has not been explained clearly. In the present study, we discovered that embryonic rat heart-derived H9c2 cells responded to the stimulation of calcium ionophore A23187 with a cell surface area enlargement and an increased expression of cardiac hypertrophy marker genes. Increased Ca(2+) also induces an organization of sarcomeres in neonatal rat cardiomyocytes, as revealed by α-actinin staining. Increased Ca(2+) could upregulate the expression of myocardin. Knockdown of myocardin by shRNA attenuates hypertrophic responses triggered by increased intracellular Ca(2+), suggesting that Ca(2+) signals induce cardiomyocyte hypertrophy partly through activation of myocardin. Furthermore, A23187 treatment directly activates myocardin promoter, chelation of Ca(2+) by EGTA inhibits this activation and knockdown of myocardin expression using shRNA also abrogates A23187-induced ANF and SK-α-actin promoter activity. CSA (calcineurin inhibitor) and KN93 (CaMKII inhibitor) inhibit A23187-induced the increase in myocardin expression. These results suggest that myocardin plays a critical role in Ca(2+) signal-induced cardiomyocyte hypertrophy, which may serve as a novel mechanism that is important for cardiac hypertrophy.