(C) 2010 Elsevier B.V. All rights reserved.”
“The seed bank of a seasonally flowing

river was sampled to assess ecosystem resilience this website and evidence of connectivity. Seed banks were sampled from ‘Floodplain’, ‘Top of Bank’ and ‘In Channel’ hydrogeomorphic areas in seven reaches of the Wannon River, and the distribution of species and water plant functional groups (WPFGs) among these sites was assessed. The seed bank material was exposed to two treatments (damp and flooded) to stimulate germination of terrestrial (Tdr Tda), flooding-tolerant (ATe, ATI, ARp, ATw) and flooding-dependent (ARf, Se, Sr, Sk) species. There was a high degree of similarity among seed banks from all parts of the river, and all hydrogeomorphic areas. Few species were restricted to any one area (i.e., ‘In Channel’, ‘Top of Bank’, ‘Floodplain’) BAY 80-6946 or any one reach of the river. This indicates that the wetland areas of the Wannon River have a high degree of longitudinal and lateral connectivity, and the riparian zone retains the capacity to provide resources to wetland fauna, even with large variation in the natural flow regime and long-term

agricultural land-use. Provided the seed bank remains intact, the perennial vegetation is allowed to regenerate, and a natural flow regime is maintained, seasonal rivers like the Wannon are likely to be resilient to the consequences of climate change, despite the surrounding agricultural land-use and the influx of saline ground-water. Crown Copyright (c) 2015 Published by Elsevier B.V. All rights reserved.”
“Autophagy is an apoptosis-independent mechanism of cell death that protects the cell from environmental imbalances and infection by pathogens. We identified a novel small molecule, 2-(3-Benzyl-4-oxo-3,4,5,6,7,8-hexahydro-benzo[4,5]thieno[2,3-d]pyrimidin-2-ylsulfanylmethyl)-oxazole-4-carboxylic acid (2-pyrrolidin-1-yl-ethyl)-amide (referred as

autophagonizer), using high-content cell-based screening and the autophagosome marker EGFP-LC3. Autophagonizer inhibited growth and induced cell death in the human tumor cell lines ASP2215 clinical trial MCF7, HeLa, HCT116, A549, AGS, and HT1080 via a caspase-independent pathway. Conversion of cytosolic LC3-I to autophagosome-associated LC3-II was greatly enhanced by autophagonizer treatment. Transmission electron microscopy and acridine orange staining revealed increased autophagy in the cytoplasm of autophagonizer-treated cells. In conclusion, autophagonizer is a novel autophagy inducer with unique structure, which induces autophagic cell death in the human tumor cell lines. (C) 2010 Elsevier Inc. All rights reserved.”
“BACKGROUND & AIMS: Toll-like receptors (TLR) are innate immune receptors involved in recognition of the intestinal microflora; they are expressed by numerous cell types in the intestine, including epithelial cells, myeloid cells, and lymphocytes.