Mechanism of Human Papillomavirus Binding to Human Spermatozoa and Fertilizing Ability of Infected Spermatozoa

Human papillomaviruses (HPVs) are agents of the most common sexually transmitted diseases in females and males. Precise data about the presence, mechanism of infection and clinical significance of HPV in the male reproductive tract and especially in sperm are not available. Here we show that HPV can infect human sperm, it localizes at the equatorial region of sperm head through interaction between the HPV capsid protein L1 and syndecan-1. Sperm transfected with HPV E6/E7 genes and sperm exposed to HPV L1 capsid protein are capable to penetrate the oocyte and transfer the virus into oocytes, in which viral genes are then activated and transcribed. These data show that sperm might function as vectors for HPV transfer into the oocytes, and open new perspectives on the role of HPV infection in males and are particularly intriguing in relation to assisted reproduction techniques

Microstructural Evolution of Boron Nitride Particles in Advanced 9Cr Power Plant Steels

The final publication is available at Springer via: http://dx.doi.org/10.1007/s11661-013-1642-x.B and N can be used to increase the creep strength of advanced 9Cr power plant steels by means of microstructural stabilization and precipitation strengthening; however, the formation of boron nitride (BN) particles removes B and N from solution and reduces the strengthening effect of B and N simultaneously. In the current study, the BN precipitation/dissolution conditions in 9Cr-3W-3Co-V-Nb steels have been investigated to understand how to prevent the formation of BN. A series of austenitizing heat treatments have been designed using thermodynamic predictions as a guide in an attempt to dissolve the BN present after the production of 9Cr-3W-3Co-V-Nb type steels and to prevent also the precipitation of BN during the subsequent heat treatments. Advanced electron microscopy has been carried out to investigate the evolution of the BN particles in relation to the austenitization temperature. Energy Dispersive X-ray spectroscopy (EDS) has been used to identify the B-containing phases, and a method has been developed using secondary electron images to quantify the amount of BN present within the microstructure. It has been found that BN solubility is sensitive to the B and N levels in the steel composition, as indicated by thermodynamic calculations. However, it is proposed that austenitizing heat treatments at temperatures ranging from 1448 K to 1473 K (from 1175 °C to 1200 °C) with durations from 1 to 7 hours can effectively prevent the precipitation of BN as well as dissolving most of the BN particles formed during initial steel manufacture

Intrinsic anion diffusivity in lead halide perovskites is facilitated by a soft lattice.

Facile ionic transport in lead halide perovskites plays a critical role in device performance. Understanding the microscopic origins of high ionic conductivities has been complicated by indirect measurements and sample microstructural heterogeneities. Here, we report the direct visualization of halide anion interdiffusion in CsPbCl3-CsPbBr3 single crystalline perovskite nanowire heterojunctions using wide-field and confocal photoluminescence measurements. The combination of nanoscale imaging techniques with these single crystalline materials allows us to measure intrinsic anionic lattice diffusivities, free from complications of microscale inhomogeneity. Halide diffusivities were found to be between 10-13 and ∼10-12 cm2/second at about 100 °C, which are several orders of magnitudes lower than those reported in polycrystalline thin films. Spatially resolved photoluminescence lifetimes and surface potential measurements provide evidence of the central role of halide vacancies in facilitating ionic diffusion. Vacancy formation free energies computed from molecular simulation are small due to the easily deformable perovskite lattice, accounting for the high equilibrium vacancy concentration. Furthermore, molecular simulations suggest that ionic motion is facilitated by low-frequency lattice modes, resulting in low activation barriers for vacancy-mediated transport. This work elucidates the intrinsic solid-state ion diffusion mechanisms in this class of semisoft materials and offers guidelines for engineering materials with long-term stability in functional devices

Thermochromic halide perovskite solar cells.

Smart photovoltaic windows represent a promising green technology featuring tunable transparency and electrical power generation under external stimuli to control the light transmission and manage the solar energy. Here, we demonstrate a thermochromic solar cell for smart photovoltaic window applications utilizing the structural phase transitions in inorganic halide perovskite caesium lead iodide/bromide. The solar cells undergo thermally-driven, moisture-mediated reversible transitions between a transparent non-perovskite phase (81.7% visible transparency) with low power output and a deeply coloured perovskite phase (35.4% visible transparency) with high power output. The inorganic perovskites exhibit tunable colours and transparencies, a peak device efficiency above 7%, and a phase transition temperature as low as 105 °C. We demonstrate excellent device stability over repeated phase transition cycles without colour fade or performance degradation. The photovoltaic windows showing both photoactivity and thermochromic features represent key stepping-stones for integration with buildings, automobiles, information displays, and potentially many other technologies