Novel composite meshes to evaluate their structural property and in vivo biocompatibility for tissue repair

404-410Composite meshes of different types have been prepared and used for tissue repair in pelvic floor disorder. An interlocking texture mesh (inter-mesh) and a membrane coated mesh (electro-mesh) have been used based on their structural property and biocompatibility. The proportion of degradation material in inter-mesh (69.6%) is found extremely higher than that of electro-mesh (3.22%), thus leading to higher product weight (65.50±2.31 g/m2) and thickness (0.500±0.025 mm). After 4 weeks of implantation in animal experiment, inter-mesh with surrounding tissues is observed to have higher breaking strength in tensile behavoir and better flexibility. Tissues on inter-mesh are found to grow faster with larger thickness (0.76±0.033 mm). The surface area loss of inter-mesh (2.49±0.25%) is much less than that of electro-mesh (7.49±0.63 %) within the first 2 weeks of implantation. However, the material’s degradation is accelerated after 2 weeks, leading to a higher shrinkage of 13.12±1.48 %

Novel composite meshes to evaluate their structural property and in vivo biocompatibility for tissue repair

Composite meshes of different types have been prepared and used for tissue repair in pelvic floor disorder. An interlocking texture mesh (inter-mesh) and a membrane coated mesh (electro-mesh) have been used based on their structural property and biocompatibility. The proportion of degradation material in inter-mesh (69.6%) is found extremely higher than that of electro-mesh (3.22%), thus leading to higher product weight (65.50±2.31 g/m2) and thickness (0.500±0.025 mm). After 4 weeks of implantation in animal experiment, inter-mesh with surrounding tissues is observed to have higher breaking strength in tensile behavoir and better flexibility. Tissues on inter-mesh are found to grow faster with larger thickness (0.76±0.033 mm). The surface area loss of inter-mesh (2.49±0.25%) is much less than that of electro-mesh (7.49±0.63 %) within the first 2 weeks of implantation. However, the material’s degradation is accelerated after 2 weeks, leading to a higher shrinkage of 13.12±1.48 %

The OX40/OX40L Axis Regulates T Follicular Helper Cell Differentiation: Implications for Autoimmune Diseases

T Follicular helper (Tfh) cells, a unique subset of CD4+ T cells, play an essential role in B cell development and the formation of germinal centers (GCs). Tfh differentiation depends on various factors including cytokines, transcription factors and multiple costimulatory molecules. Given that OX40 signaling is critical for costimulating T cell activation and function, its roles in regulating Tfh cells have attracted widespread attention. Recent data have shown that OX40/OX40L signaling can not only promote Tfh cell differentiation and maintain cell survival, but also enhance the helper function of Tfh for B cells. Moreover, upregulated OX40 signaling is related to abnormal Tfh activity that causes autoimmune diseases. This review describes the roles of OX40/OX40L in Tfh biology, including the mechanisms by which OX40 signaling regulates Tfh cell differentiation and functions, and their close relationship with autoimmune diseases

LAMOST meets Gaia: The Galactic Open Clusters

Open Clusters are born and evolve along the Milky Way plane, on them is imprinted the history of the Galactic disc, including the chemical and dynamical evolution. Chemical and dynamical properties of open clusters can be derived from photometric, spectroscopic, and astrometric data of their member stars. Based on the photometric and astrometric data from the Gaia mission, the membership of stars in more than 2000 Galactic clusters has been identified in the literature. The chemical and kinematical properties, however, are still poorly known for many of these clusters. In synergy with the large spectroscopic survey LAMOST (data release 8) and Gaia (data release 2), we report a new comprehensive catalogue of 386 open clusters. This catalogue has homogeneous parameter determinations of radial velocity, metallicity, and dynamical properties, such as orbit, eccentricity, angular momenta, total energy, and 3D Galactic velocity. These parameters allow the first radial velocity determination and the first spectroscopic [Fe/H] determination for 44 and 137 clusters, respectively. The metallicity distribution of majority clusters shows falling trends in the parameter space of the Galactocentric radius, the total energy, and the Z component of angular momentum -- except for two old groups that show flat tails in their own parameter planes. Cluster populations of ages younger and older than 500 Myrs distribute diversely on the disc. The latter has a spatial consistency with the Galactic disc flare. The 3-D spatial comparison between very young clusters (< 100 Myr) and nearby molecular clouds revealed a wide range of metallicity distribution along the Radcliffe gas cloud wave, indicating a possible inhomogeneous mixing or fast star formation along the wave. This catalogue would serve the community as a useful tool to trace the chemical and dynamical evolution of the Milky Way.Comment: accepted for publication on A&

Robust estimation of bacterial cell count from optical density

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals &lt;1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

Application of hot melt extrusion to enhance the dissolution and oral bioavailability of oleanolic acid

The aim of this study was to improve the in vitro dissolution rate and oral bioavailability of oleanolic acid (OA), a water insoluble drug belonging to BCS class IV. Hot melt extrusion (HME) was applied to develop OA amorphous solid dispersions. The characterizations of the optimal formulation were performed by differential scanning calorimetry, X-ray powder diffraction, Fourier transform infrared spectroscopy and in vitro dissolution test. The in vivo pharmacokinetic study was conducted in rats. As a result, OA solid dispersion based on PVP VA 64 (OA-PVP) was successfully prepared. In the dissolution medium containing 0.3% SDS, OA-PVP dramatically increased the releasing rate of OA compared with the physical mixture (PM-PVP) and commercial tablet. Furthermore, OA-PVP exhibited higher AUC (P < 0.05) and Cmax (P < 0.05) than PM-PVP and commercial tablet. The superior dissolution property and bioavailability of OA-PVP mainly attributed to the amorphous state of OA in PVP VA64 and the well dispersion caused by thermal melting and shearing. Overall, hot melt extrusion was an efficient strategy to enhance the dissolution rate and oral bioavailability of OA