The epithelial-mesenchymal transition (EMT) is an important factor in lung cancer metastasis, and targeting EMT is a potential therapeutic strategy. Fucosyltransferase IV (FUT4) and its synthetic cancer sugar antigen Lewis Y (LeY) was abnormally elevated in many cancers. In this study, a traditional Chinese medicine ginsenoside Rg3 was used to investigate whether its inhibition to EMT and invasion of lung cancer is by the glycobiology mechanism. We found that Rg3 treatment (25, 50, 100 μg/ml) inhibited cell migration and invasion by wound-healing and transwell assays. Rg3 could significantly alter EMT marker proteins with increased E-cadherin, but decreased Snail, N-cadherin and Vimentin expression. Rg3 also down-regulated FUT4 gene and protein expression in lung cancer cells by qPCR, Western blot and immunofluorescence. After FUT4 down-regulated with shFUT4, EMT was obviously inhibited. Furthermore, the activation of EGFR through decreased LeY biosynthesis was inhibited, which blocked the downstream MAPK and NF-κB signal pathways. In addition, Rg3 reduced tumor volume and weight in xenograft mouse model, and significantly decreased tumor metastasis nodules in lung tissues by tail vein injection. In conclusion, Rg3 inhibits EMT and invasion of lung cancer by down-regulating FUT4 mediated EGFR inactivation and blocking MAPK and NF-κB signal pathways. Rg3 may be a potentially effective agent for the treatment of lung cancer.

The low-angle bent-shaped molecules with 1,7-naphthalene central core and alkylthio tails can form a novel hexagonal columnar phase and a dark B4 phase. The columnar phase has a large two-dimensional hexagonal lattice with edges of 65–75 Å and exhibits polar switching with spontaneous polarization along the column axis. Calculated from the density (∼1 g·cm-3) and unit volume, the number of molecules that are necessary to fill a 4.6-Å stratum of each column were found to be ∼11. Such a large number of molecules can be accommodated only in the tube-like assembly, which may be the first example as formed by the usual bent-shaped molecule with a single alkylthio tail.

Laser surface texturing (LST) technique was utilised on a cylinder liner in a diesel engine. In order to analyse the effect of LST micro‐dimples on the lubrication and friction properties of cylinder liner–piston ring (CL–PR), we developed a new mixed lubrication model on the basis of the average Reynolds equation and asperity contacts equation. The model can consider the coupling effects between the surface roughness of non‐texturing regions and micro‐dimples and the synergistic effects of multi‐micro‐dimples. The results show that cylinder liner surface by LST can form effective hydrodynamic lubrication effect in most regions of the strokes, only near the dead points, the friction pair is in mixed lubrication state, asperity contact plays a major role in balancing the external load and the asperity friction force is obvious. The micro‐dimple parameters were optimised to obtain a better lubrication effect with the following optimised results: rp = 30–60 µm, Sp = 0.2–0.4 and e = 0.03–0.1. Copyright © 2012 John Wiley & Sons, Ltd.

Previous work in our laboratory demonstrated that exosomes derived from human amniotic epithelial cells (hAECs) accelerated wound healing by promoting the proliferation and migration of fibroblasts. It is reported that exosomes, which are carriers of the microRNAs (miRNAs) and proteins, play an important role in the regulation of cell-to-cell communication. However, it is still unclear precisely which molecule or which group of molecules carried within hAEC-derived exosomes (hAEC-Exos) mediated wound healing. Here, we explored purified hAEC-Exos together with either proteinase K (PROse) or RNase A on the effect of fibroblasts and cutaneous wound healing. Our experiments demonstrated that hAEC-Exos were positive for exosomal markers CD9, CD63, and CD81. Also, we found that hAEC-Exos could be internalized by fibroblasts and then stimulated cell migration and proliferation. However, the promotive effect of hAEC-Exos was abolished by pretreating hAEC-Exos with RNase A, not PROse. Importantly, in vivo wound healing assay showed that local injection of hAEC-Exos or PROse pretreated hAEC-Exos at skin wounds significantly accelerated wound healing. Our findings revealed an important role of exosomal miRNAs in wound healing.