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Highlights: [•] SiGe porous nanorod arrays were synthesized via template-assisted method. [•] The SiGe porous nanorod arrays were used as anode materials of Li-ion batteries. [•] The SiGe porous nanorod arrays show better performance than planar electrode. [•] The porous structure and addition of Ge is responsible for the good performance. [ABSTRACT FROM AUTHOR]

RORγt and RORα are transcription factors of the RAR-related orphan nuclear receptor (ROR) family. They are expressed in Th17 cells and have been suggested to play a role in Th17 differentiation. Although RORγt signature genes have been characterized in mouse Th17 cells, detailed information on its transcriptional control in human Th17 cells is limited and even less is known about RORα signature genes which have not been reported in either human or mouse T cells. In this study, global gene expression of human CD4 T cells activated under Th17 skewing conditions was profiled by RNA sequencing. RORγt and RORα signature genes were identified in these Th17 cells treated with specific siRNAs to knock down RORγt or RORα expression. We have generated selective small molecule RORγt modulators and they were also utilized as pharmacological tools in RORγt signature gene identification. Our results showed that RORγt controlled the expression of a very selective number of genes in Th17 cells and most of them were regulated by RORα as well albeit a weaker influence. Key Th17 genes including IL-17A, IL-17F, IL-23R, CCL20 and CCR6 were shown to be regulated by both RORγt and RORα. Our results demonstrated an overlapping role of RORγt and RORα in human Th17 cell differentiation through regulation of a defined common set of Th17 genes. RORγt as a drug target for treatment of Th17 mediated autoimmune diseases such as psoriasis has been demonstrated recently in clinical trials. Our results suggest that RORα could be involved in same disease mechanisms and gene signatures identified in this report could be valuable biomarkers for tracking the pharmacodynamic effects of compounds that modulate RORγt or RORα activities in patients. [ABSTRACT FROM AUTHOR]

Abstract: We demonstrate the synthesis of order-aligned Mn3O4 nanostructures by electrochemically depositing Mn3O4 on a pre-fabricated Cu nanowire array current collector. When used as an electrode for lithium-ion batteries, it exhibits a capacity up to 637 and 494 mA h g−1 after 100 cycles at a current rate of 10 C and 20 C (10 C = 9.4 A g−1), respectively. The excellent cycling performance and superior rate capability can be attributed to the good electrical contact, fast electron transport and good strain accommodation of the order-aligned nanostructured electrodes. The relationship between the thickness of the Mn3O4 film and its electrochemical performance has also been investigated. [Copyright &y& Elsevier]

Abstract: We demonstrate the synthesis of new Cu–Si1−x Ge x core–shell nanowire array electrodes by directly depositing Si1−x Ge x layer on the surface of pre-synthesized Cu nanowire arrays via co-sputtering method. When used as anodes of lithium-ion batteries, the Cu–Si1−x Ge x (x =0.4) nanowire array electrodes show excellent electrochemical performance in terms of cycle stability and rate capability, which is much better than that of planar electrodes. The improved performance can be attributed to the good strain accommodation, fast electron transport and good electrical contact of the nanowire array electrodes. The effect of Ge content and the thickness of alloy film on the electrochemical performance of the three-dimensional electrodes have also been investigated. [Copyright &y& Elsevier]

Abstract: We have demonstrated large-scale synthesis of Si nanowire arrays (SiNA) on Ti substrate and their application as high-performance anode of Li-ion batteries. SiNA were controllably synthesized through hot-filament chemical vapour deposition (HFCVD) using Au films of different thickness as a catalyst. We found that the thickness of the Au film based catalysts played important role in controlling the morphology of Si nanostructures. The thick Au layer (e.g., 50nm) resulted in the formation of the SiNA, while the thin Au layer (e.g., 5nm) led to the disordered Si nanowires. The as-synthesized SiNA exhibited large reversible capacity (3600mAhg−1) and high initial Coulombic efficiency (86.4%), which is much better than the disordered Si nanowires. The good contact and adhesion of SiNA with current collectors, as well as excellent strain accommodation might be responsible for the enhanced performance as anode of Li-ion batteries. [Copyright &y& Elsevier]

The IL-23/IL-17 pathway is implicated in autoimmune diseases, particularly psoriasis, where biologics targeting IL-23 and IL-17 have shown significant clinical efficacy. Retinoid-related orphan nuclear receptor gamma t (RORγt) is required for Th17 differentiation and IL-17 production in adaptive and innate immune cells. We identified JNJ-54271074, a potent and highly-selective RORγt inverse agonist, which dose-dependently inhibited RORγt-driven transcription, decreased co-activator binding and promoted interaction with co-repressor protein. This compound selectively blocked Th17 differentiation, significantly reduced IL-17A production from memory T cells, and decreased IL-17A- and IL-22-producing human and murine γδ and NKT cells. In a murine collagen-induced arthritis model, JNJ-54271074 dose-dependently suppressed joint inflammation. Furthermore, JNJ-54271074 suppressed IL-17A production in human PBMC from rheumatoid arthritis patients. RORγt-deficient mice showed decreased IL-23-induced psoriasis-like skin inflammation and cytokine gene expression, consistent with dose-dependent inhibition in wild-type mice through oral dosing of JNJ-54271074. In a translational model of human psoriatic epidermal cells and skin-homing T cells, JNJ-54271074 selectively inhibited streptococcus extract-induced IL-17A and IL-17F. JNJ-54271074 is thus a potent, selective RORγt modulator with therapeutic potential in IL-23/IL-17 mediated autoimmune diseases. [ABSTRACT FROM AUTHOR]