Assessment of running waters (Slovakia) using benthic macroinvertebrates — derivation of ecological quality classes with respect to altitudinal gradients

A method is presented for defining the five classes of ecological quality based on a multimetric index (MMI) of macroinvertebrates, as required for implementation of the Water Framework Directive for small (catchment area 10–100 km²), medium (101–1000 km²) and large (> 1000 km²) streams. Our method (expert judgment) allows us to overcome an absence of reference sites for some stream types. The key was selection of suitable metrics for all stream types. The whole procedure was divided into two parts. 1. Small streams with reference sites: suitable metrics were selected according to their ability to distinguish reference and monitoring sites — SI, Oligo [%], BMWP, RhiTI, Rheoindex, IBCR, % Aka+Lit+Psa [%] and EPT. Here the high-good boundary value was set as the 25^th (for metrics decreasing with increasing pollution) or 75^th percentile (for metrics increasing with increasing pollution). 2. Medium and large streams which lack reference sites: here the idea was applied that some metrics, the values of which change along an altitudinal gradient, also react to anthropogenic stress — SI, Oligo [%], BMWP, [%] metarhithral, RhiTI, Aka+Lit+Psa [%] and EPT for both medium and large streams with, in addition, IBCR and NFam for medium streams. This assumption was supported by regression analysis of altitude and metrics from small streams. Not all the metrics were related to altitude but metrics with a good ability to separate reference and monitoring sites did show a significant relationship to altitude. The boundary between high and good class for medium and large streams was set as the 95^th or 5^th percentiles.     

Cross-reactivity of an antiserum to the α-subunit of the Na+, K+-ATPase of toad (Bufo marinus) kidney with basal and apical membranes of transporting epithelia of the rat

Summary An antibody to the 96 kD -subunit of the Na⁺, K⁺ -ATPase from Bufo marinus has been used in immunostaining rat kidney and salivary glands. Intense staining was observed on basolateral membranes of distal tubules of the kidney and striated ducts of the three major salivary glands. Less intense staining was seen on the basolateral membranes of parotid acinar cells, but no staining was seen on the acinar cells of submandibular or sublingual glands. These sites of staining have been shown, by other methods, to posses substantial Na⁺, K⁺ -ATPase, indicating that the antibody recognizes antigenic determinants of the sodium pump highly conserved in the course of evolution. In addition, staining with this antibody was observed at the apical region of cells of the proximal straight tubule and of the papillary collecting duct in the kidney. Absorption studies suggest that the apical antigenic determinants are the same or closely related to each other but are distinct from basolateral antigenic determinants.     

ZNF746 plays cardinal roles on colorectal cancer (CRC) cell invasion and migration and regulates mitochondrial dynamics and morphological changes of CRC cells—Role of combined melatonin and 5-FU regimen

The underlying mechanism of colorectal cells developing into cancer cells has been extensively investigated, yet is still not fully delineated, resulting in the treatment of advanced colorectal cancer (CRC) remains regrettably an unmet need. Zinc Finger Protein 746/Parkin-interacting substrate (ZNF746/PARIS) has previously been identified to play a fundamental role on bladder cancer cell proliferation and metastasis that were effectively inhibited by melatonin (Mel). In this study, we utilized ex vivo/in vivo studies to verify whether the ZNF746 signaling was also crucial in CRC growth/invasion/migration. Tissue-bank specimens showed that the protein expression of ZNF746 was significantly increased in CRC than that of healthy colorectal tissues (p < 0.001). Additionally, in vitro study demonstrated that excessive expression of ZNF746 significantly inhibited mitochondrial activity via (1) interfering with the dynamic balance of mitochondrial fusion/fission and (2) inhibiting the protein expression of MFN1/MFN2/PGC1a (all p < 0.001). Furthermore, we identified that inhibition of ZNF746 protein expression significantly reduced the resistance of CRC cell lines to the anticancer drug of 5-FU (p < 0.001), whereas overexpression of ZNF746 significantly augmented resistance of CRC cells to 5-FU (all p < 0.001). Finally, using the cell culture method, we found that combined Mel and 5-FU was superior to merely one on promoting the CRC cell apoptosis (p < 0.001). Our results confirmed that ZNF746 signaling played a cardinal role of CRC cell proliferation/survival and combined Mel and 5-FU treatment attenuated the resistance of CRC cells to the drug mainly through suppressing this signaling.