ABSTRACT:The effect of an external stress on the barrier properties of natural, bromobutyl, and nitrile rubber were studied using a modified ASTM permeation method. Stress-induced changes such as a decrease in the breakthrough time with mechanical elongation was observed. Upon application of a small mechanical deformation, little change was observed in terms of steady-state permeation flux. On the other hand, a stress-enhanced diffusion was observed for most of the solvent/rubber pairs studied.

A phenomenological model that incorporates swelling is adopted and used to solve the one-dimensional sorption problem. The model predictions are in good agreement with experimental data, involving the transport of dichloromethane, trichloroethylene, and benzene through high-density polyethylene and poly(vinyl chloride) geomembranes. The theoretical curves predict weight-gain and flux-time profiles, including the case where the flux goes through a maximum.

No abstract

No abstract

The (Pro)renin receptor ((P)RR), also known as ATP6AP2, is a single-transmembrane protein that is implicated in a multitude of biological processes. However, the exact role of ATP6AP2 during blood vessel development remains largely undefined. Here, we use an inducible endothelial cell (EC)-specific Atp6ap2 knockout mouse model to investigate the role of ATP6AP2 during both physiological and pathological angiogenesis in vivo. We observed that postnatal deletion of Atp6ap2 in ECs results in cell migration defects, loss of tip cell polarity and subsequent impairment of retinal angiogenesis. In vitro, Atp6ap2 deficient ECs similarly displayed reduced cell migration, impaired sprouting, and defective cell polarity. Transcriptional profiling of ECs isolated from Atp6ap2 mutant mice further indicated regulatory roles in angiogenesis, cell migration and extracellular matrix composition. Mechanistically, we showed that expression of various extracellular matrix components is controlled by ATP6AP2 via the extracellular-signal-regulated kinase (ERK) pathway. Furthermore, Atp6ap2 deficient retinas exhibited reduced revascularization in an oxygen induced retinopathy model. Collectively, our results demonstrated a critical role of ATP6AP2 as a regulator of developmental and pathological angiogenesis.