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A nonenzymatic glucose fuel cell directly oxidizes glucose to gluconic acid as a Pt‐based abiotic catalyst in a proton exchange membrane environment and has various advantages (e. g., biocompatibility, chemical stability, high ionic conductivity). We report the permeability of a less hydrophobic diffusion layer for three flow‐field designs (serpentine, interdigitated, and parallel). In all cases, as the channel width of the flow path increases, the power density increases and the Ohmic resistance decreases. The serpentine shape (channel and rib widths: 1.5 and 0.5 mm, respectively) exhibits remarkable maximum power and current densities (cell voltage: 60 mV) of 103.4 μW cm−2 and 1,273 μA cm−2 compared to those of the parallel (46.5 μW cm−2 at 683 μA cm−2) and interdigitated (74.0 μW cm−2 at 878 μA cm−2) shapes, respectively. Furthermore, permeability and performance analyses according to the single‐cell temperature, glucose concentration, and flow rate changes provide various perspectives on glucose fuel cells. [ABSTRACT FROM AUTHOR]

Summary: An ultrathin layer composed of carbon nanotubes (CNTs) was deposited on the cathodic catalyst layer to boost performance of polymer electrolyte membrane fuel cell (PEMFC) under low to mid relative humidity (RH) conditions. The CNT‐deposited layer (CDL) was formed without modifying the PEMFC components. To investigate the behavior of water and reactants at the inner interface of the membrane electrode assembly (MEA), we characterized the morphology of the CDL (contact angle, pore size distribution, specific surface area, field emission scanning electron microscopy, and energy dispersive spectroscopy images). The CDL in PEMFCs was used as a contributor to enhance the membrane hydration. Thereby performances have been significantly enhanced. Additionally, the three‐dimensional nanostructure of the CDL expanded the active area by uniform dispersion of the reactants. The polarization curves of the conventional MEA and MEA with CDL were evaluated under diverse RH (100%, 70%, 50%, and 30% RH). In the low to mid RH conditions, the maximum power densities were increased by 29.7% (70% RH), 26.6% (50% RH), and 25.5% (30% RH) compared with the conventional MEA. Especially, the maximum power density of the MEA with CDL (0.547 W/cm2 at 70% RH) was higher than that of the conventional MEA (0.482 W/cm2 at 100% RH). Thus, MEA with CDL demonstrated excellent performance enhancement under low to mid RH conditions. [ABSTRACT FROM AUTHOR]

A novel method for replenishing platinum catalysts on an electrolyte membrane of polymer electrolyte membrane fuel cell (PEMFC) is studied. The method injects electrocatalyst‐supplementing ink into a pre‐assembled fuel cell in a simple and non‐destructive manner. For replenishing, straightforward catalyst‐replenishment equipment and corresponding protocol are proposed. The protocol consists of injection, penetration, and purge processes. As a feasibility study, the method is performed on fuel cells with pristine membranes. Target fuel cells for this study include a membrane‐assembled cell without catalyst layers (CLs) (Cell 1) and a cell assembled with a membrane‐coated cathodic CL (Cell 2). An open‐circuit voltage of 0.804 V in Cell 1 and a current of 77 mA in Cell 2 are measured, as supported through electrochemical impedance spectroscopy. Results of energy‐dispersive X‐ray spectroscopy and X‐ray photoelectron spectroscopy also support the presence of platinum catalysts. [ABSTRACT FROM AUTHOR]

The enhancement of recombinant therapeutic protein production in mammalian cell culture has been regarded as an important issue in the biopharmaceutical industry. Previous studies have reported that the addition of the recombinant 30Kc19 protein, a silkworm-derived plasma protein with simultaneous cell-penetrating and mitochondrial enzyme-stabilizing properties, can enhance the recombinant protein expression in Chinese hamster ovary (CHO) cell culture. Here, we produced an α-helix N-terminal domain of 30Kc19, called (30Kc19α), and investigated its effects on the production of human erythropoietin (EPO), a widely used therapeutic protein for the treatment of anemia, in recombinant CHO cell culture. Similar to the full-length 30Kc19, 30Kc19α was able to be mass-produced in a form of recombinant protein through an Escherichia coli expression system and delivered into EPO-producing CHO (EPO–CHO) cells. Supplementing the medium of EPO–CHO cell culture with 30Kc19α increased the intracellular NADPH/NADP+ ratio related to the flux of metabolic reducing power for protein biosynthesis, subsequently enhancing EPO production in serum-free culture. 30Kc19α is considered to have certain advantages in the downstream purification process of therapeutic protein production when it is used as a medium supplement due to its small size and low isoelectric point compared to the full-length 30Kc19. These results suggest that 30Kc19α has potential use for manufacturing biopharmaceutical proteins. [ABSTRACT FROM AUTHOR]

The generation of functional osteoblasts from human somatic cells could provide an alternative means of regenerative therapy for bone disorders such as osteoporosis. In this study, we demonstrated the direct phenotypic conversion of human dermal fibroblasts (HDFs) into osteoblasts by culturing them in osteogenic medium supplemented with valproic acid (VPA), a histone deacetylase (HDAC) inhibitor. HDFs cultured with the VPA in osteogenic medium exhibited expression of alkaline phosphatase and deposition of mineralized calcium matrices, which are phenotypical characteristics of functional osteoblasts. They also expressed osteoblast-specific genes such as alkaline phosphatase, osteopontin, and bone sialoprotein, which demonstrated their direct conversion into osteoblasts. In addition, co-treatment with VPA and a specific inhibitor for activin-like kinase 5 (ALK5i II) had a synergistic effect on direct conversion. It is considered that the inductive effect of VPA on the conversion into osteoblast-lineage is due to the opening of the nucleosome structure by HDAC inhibitor, which facilitates chromatin remodeling and cellular reprogramming. Our findings provide a novel insight into the direct conversion of human somatic cells into transgene-free osteoblasts with small chemical compounds, thus making bone regeneration using cellular reprogramming strategy more clinically feasible. [ABSTRACT FROM AUTHOR]

Although firms generally strive to enhance social evaluations, scholars have noted that such evaluations may not completely reflect actual performance of the firms. Extending this approach to the domain of environmental sustainability, we focus on the importance of social evaluation heuristics and explore how a firm's status, or generalized evaluation not directly linked to environmental performance, plays a key role in shaping audience perceptions on its environmental reputation. Using multiple sources of data on 178 global companies' green reputation, status, and environmental performance, our study shows that a firm's status significantly enhances its environmental reputation assessed by general consumers and that the status effect varies significantly according to media frames. These findings illuminate the richness and complexity in the relations between status, reputation, and media-provided information in the area of environmental sustainability. [ABSTRACT FROM AUTHOR]

Core binding factor β (Cbfβ) is a non‐DNA binding cofactor of Runx2 that potentiates DNA binding. Previously, it has been reported that Cbfβ plays an essential role in osteogenic differentiation and skeletal development by inhibition adipogenesis. Here, we delivered the recombinant Cbfβ protein into human mesenchymal stem cells (MSCs) and triggered osteogenic lineage commitment. The efficient delivery of Cbfβ was achieved by fusing 30Kc19 protein, which is a cell‐penetrating protein derived from the silkworm. After the production of the recombinant Cbfβ‐30Kc19 protein in the Escherichia coli expression system, and confirmation of its intracellular delivery, MSCs were treated with the Cbfβ‐30Kc19 once or twice up to 300 µg/ml. By investigating the upregulation of osteoblast‐specific genes and phenotypical changes, such as calcium mineralization, we demonstrated that Cbfβ‐30Kc19 efficiently induced osteogenic differentiation in MSCs. At the same time, Cbfβ‐30Kc19 suppressed adipocyte formation and downregulated the expression of adipocyte‐specific genes. Our results demonstrate that the intracellularly delivered Cbfβ‐30Kc19 enhances osteogenesis in MSCs, whereas it suppresses adipogenesis by altering the transcriptional regulatory network involved in osteoblast‐adipocyte lineage commitment. Cbfβ‐30Kc19 holds great potential for the treatment of bone‐related diseases, such as osteoporosis, by allowing transcriptional regulation in MSCs, and overcoming the limitations of current therapies. [ABSTRACT FROM AUTHOR]

CRISPR/Cas9 system has served a new insight in genome editing of eukaryotes, including human cells. In this system, delivery of Cas9 nuclease with guide RNA has been central challenge in developing safe and efficient techniques. The viral delivery of genes encoding these two components i.e. Cas9 and guide RNA may cause unexpected integration of the DNA sequence into the host cell genome, and lead to potential safety problems such as tumorigenesis. Herein, we report that the Cas9 protein can be directly delivered into the human cells through fusion with 30Kc19, a cell-penetrating and protein-stabilizing protein originating from silkworm. The 30Kc19-conjugated Cas9 (30Kc19-Cas9) showed higher stability than native Cas9 for thermal and chemical-induced inactivation in DNA-cleavable activity. In addition, it was demonstrated that 30Kc19-Cas9 was efficiently delivered into human cells and resulted in targeted gene disruption with single guide RNA by showing gene expression and site-specific mutations in the genome. With the advantages of efficient delivery in addition to the enhancement of Cas9 stability, this method is expected to provide a versatile strategy to advance non-viral and clinically-feasible genome editing for in vivo applications. [ABSTRACT FROM AUTHOR]

Ahkera Smart Tech is a technology start-up specialized in baggage loading, a niche market of airport baggage handling system. Its robotics technology has great potential to revolutionize baggage loading by improving operational efficiency, accuracy and safety in the airport. As Ahkera brings its innovation to a global stage, the management team is keen on Asian markets. Aviation industry in Asia has observed exploding demand for air traffic, providing great market opportunities for Ahkera. As a non-Asian startup, Ahkera faces significant challenges in market penetration and global strategic management in order to ride on Asian opportunities. [ABSTRACT FROM AUTHOR]

Abiotic catalyst, diffusion characteristic, flow channel architecture, nonenzymatic glucose fuel cell, proton exchange membrane Keywords: abiotic catalyst; diffusion characteristic; flow channel architecture; nonenzymatic glucose fuel cell; proton exchange membrane EN abiotic catalyst diffusion characteristic flow channel architecture nonenzymatic glucose fuel cell proton exchange membrane 1 1 1 10/28/22 20221026 NES 221026 B The Cover Feature b illustrates a glucose fuel cell that generates electricity through an electrochemical reaction with oxygen and glucose, which is an eco-friendly and abundant energy resource in nature. [Extracted from the article]

Polymer electrolyte membrane fuel cells were analyzed to investigate changes in the structure of the flow field and operating conditions. The cell performance, which was controlled by adjusting the width of the cathodic channel, improved as the backpressure increases. With the anodic and cathodic flow channels mismatched, the maximum power densities at 3.0 bar for a narrow cathodic channel were 1115 and 1024 mW/cm2, and those for a wide cathodic channel were 959 and 868 mW/cm2, respectively. The diffusion characteristics were investigated using the non-dimensional numbers Re (Reynolds), Sc (Schmidt), and Sh (Sherwood) to confirm the improvement of mass transport. The narrower the channel or the higher the operating pressure, the larger Re was and the smaller Sc and Sh became. In particular, the wider the anodic channel, the larger the value of Sh. [ABSTRACT FROM AUTHOR]

Extracellular vesicles (EVs), such as exosomes, are nano-sized vesicles derived from endocytic membranes and contain biomolecules such as proteins, lipids, RNAs, and DNAs for the transfer of signals to recipient cells, playing significant roles in cell-to-cell communication. Discovery of exosomes has attracted attention for possible use as next generation therapies in clinical applications; however, several studies suggest that cells secrete exosomes that perform as mediators in the tumor niche and play several roles in tumorigenesis, angiogenesis, and metastasis. Recently, stem cell-derived exosomes have been suggested as a desirable source for regenerative medicine due to their roles in the promotion of angiogenesis via migratory and proliferative mechanisms. This review is aimed at demonstrating the present knowledge of stem cell-derived exosomes and cell-engineered nanovesicles (CNVs) as proliferative, migratory, and anti-senescent therapeutic biomaterial for use in tissue regeneration; wound healing and anti-ageing are explained. We conclude this review by discussing the future perspectives of stem cell-derived exosomes and CNVs as a platform in therapeutic strategies for treatment of wound damage and skin aging. [ABSTRACT FROM AUTHOR]

Stem cells secrete numerous paracrine factors, such as cytokines, growth factors, and extracellular vesicles. As a kind of extracellular vesicle (EV), exosomes produced in the endosomal compartment of eukaryotic cells have recently emerged as a biomedical material for regenerative medicine, because they contain many valuable contents that are derived from the host cells, and can stably deliver those contents to other recipient cells. Although we have previously demonstrated the beneficial effects of human induced potent stem cell-derived exosomes (iPSC-Exo) on the aging of skin fibroblasts, low production yield has remained an obstacle for clinical applications. In this study, we generated cell-engineered nanovesicles (CENVs) by serial extrusion of human iPSCs through membrane filters with diminishing pore sizes, and explored whether the iPSC-CENV ameliorates physiological alterations of human dermal fibroblasts (HDFs) that occur by natural senescence. The iPSC-CENV exhibited similar characteristics to the iPSC-Exo, while the production yield was drastically increased compared to that of iPSC-derived EVs, including exosomes. The proliferation and migration of both young and senescent HDFs were stimulated by the treatment with iPSC-CENVs. In addition, it was revealed that the iPSC-CNEV restored senescence-related alterations of gene expression. Treatment with iPSC-CENVs significantly reduced the activity of senescence-associated-β-galactosidase (SA-β-Gal) in senescent HDFs, as well as suppressing the elevated expression of p53 and p21, key factors involved in cell cycle arrest, apoptosis, and cellular senescence signaling pathways. Taken together, these results suggest that iPSC-CENV could provide an excellent alternative to iPSC-exo, and be exploited as a resource for the treatment of signs of skin aging. [ABSTRACT FROM AUTHOR]