Effects of porcine epidemic diarrhea virus infection on CD21+ B cells activation.

Porcine epidemic diarrhea virus (PEDV) is a devastating pathogen of acute- gastrointestinal infectious diseases, which can cause vomiting, diarrhea, dehydration and high morbidity and mortality among neonatal piglets. Humoral immunity plays a vital role in the host anti-PEDV infection process, but the mechanism of PEDV-induced B-cell immune response remains unknown. In this study, the effects of PEDV infection on CD21+ B cell activation were systematically analyzed through animal experiments. Enzyme-linked immunosorbent assays (ELISA) revealed that low levels of serum-specific IgA, IgM, or IgG were detected in piglets after PEDV infection, respectively. Serum interleukin (IL)-6 levels increased significantly at 4 d after infection, and the levels of IL-4, B-cell activating factor (BAFF), interferon (IFN)-γ, transforming growth factor (TGF)-ß and IL-10 decreased at 7 d after infection. Fluorescence-activated cell sorting (FACS) showed that expression levels of CD21, MHC Ⅱ, CD40, and CD38 on B cell surfaces were significantly higher. In contrast, the proportions of CD21+IgM+ B cells were decreased in peripheral blood mononuclear cells (PBMCs) from the infected piglets. No differences were found in the percentage of CD21+CD80+ and CD21+CD27+ B cells in PBMCs from the infected piglets. In addition, the number of CD21+B cells in PBMCs stimulated with PEDV in vitro was significantly lower. No significant change in the mRNA expression of BCR molecules was found while the expression levels of paired immunoglobulin-like receptor B (PIR-B), B cell adaptor molecule of 32 kDa (Bam32) and BAFF were decreased. In conclusion, our research demonstrates that virulent strains of PEDV profoundly impact B cell activation, leading to alterations in phenotypic expression and BCR signaling molecules. Furthermore, this dysregulation results in compromised specific antibody secretion and perturbed cytokine production, highlighting the intricate immunological dysfunctions induced by PEDV infection.

Monodispersed Molecular Phthalocyanine with Sulfur-Driven Electron Delocalization for Enhanced Electrochemical Biosensing.

Heterogenizing the molecular catalysts on conductive scaffolds to achieve the isolated molecular dispersion and expected coordination structures is significant yet still challenging. Herein, a sulfur-driving strategy to anchor monodispersed cobalt phthalocyanine on nitrogen and sulfur co-doped graphene (NSG-CoPc) is demonstrated. Experimental and theoretical analysis prove that the incorporation of S dramatically improves the adsorption capability of NSG and evokes the monodispersion of the CoPc molecule, promoting the axial Co─N coordination and the electron delocalization of the Co catalytic center. Benefiting from the reduced activation energy barrier and boosted electron transfer, as well as the maximized active site utilization, NSG-CoPc exhibits outstanding H2O2 oxidization and sensing performance (used as a representative reaction). Moreover, the usage of NSG as a substrate can be readily extended to other metal (Ni, Cu, and Fe) phthalocyanine molecules with molecular-level dispersion. This work clarifies the mechanism of heteroatoms decoration and provides a new paradigm in devising monodispersed molecular catalysts with modulated chemical surroundings for broad applications.

Superhydrophilicity Regulation of Carbon Nanotubes Boosting Electrochemical Biosensing for Real-time Monitoring of H2O2 Released from Living Cells.

Dynamic and accurate monitoring of cell-released electroactive signaling biomolecules through electrochemical techniques has drawn significant research interest for clinical applications. Herein, the functionalized carbon nanotubes (f-CNTs) featuring with gradient surface wettability from hydrophobicity to hydrophilicity, and even to superhydrophilicity, were regulated by thermolysis of an ionic liquid for exploration of the dependence of surface wettability on electrochemical biosensing performance to a cell secretion model of hydrogen peroxide (H2O2). The superhydrophilic f-CNTs demonstrated boosting electrocatalytic reduction activity for H2O2. Additionally, the molecular dynamic (MD) simulations confirmed the more cumulative number density distribution of H2O2 molecules closer to the superhydrophilic surface (0.20 vs 0.37 nm), which would provide a faster diffusional channel compared with the hydrophobic surface. Thereafter, a superhydrophilic biosensing platform with a lower detectable limit reduced by 200 times (0.5 vs 100 µM) and a higher sensitivity over 56 times (0.112 vs 0.002 µA µM cm-2) than that of the hydrophobic one was achieved. Given its excellent cytocompatibility, the superhydrophilic f-CNTs was successfully applied to determine H2O2 released from HeLa cells which were maintained alive after a 30 min real-time monitoring test. The surface hydrophilicity regulation of electrode materials presents a facile approach for real-time monitoring of H2O2 released from living cells and would provide new insights for other electroactive signaling targets at the cellular level.

Surface Hydrophobicity Engineering of Pt-Based Noble Metal Aerogels by Ionic Liquids toward Enhanced Electrocatalytic Oxygen Reduction.

Modulating the surface properties of electrocatalysts with ligands could effectively regulate their catalytic properties, while limited in-depth understanding of the surface ligands restricted their rational combination. Herein, ionic liquids (ILs) with different lengths of hydrophobic side chains were employed to regulate the surface hydrophobicity of noble metal aerogels, for comprehending the relationship between surface hydrophobicity and oxygen reduction reaction (ORR) activity and enhancing electrocatalytic ORR. The volcano-like trends between the hydrophobicity and the ORR activity for various Pt-based aerogels indicated that a suitable hydrophobic surface constructed by ILs was most favorable for contacting with oxygen molecules and the desorption of oxygen intermediates. Typically, the PtPd aerogel modified by ILs (PtPd aer-[MTBD][PFSI]) exhibited an inspiring ORR activity, with a 70 mV increase in half-wave potential and a 7.1-fold mass activity compared to the commercial Pt/C. Therefore, the regularity between the surface hydrophobicity and ORR activity of noble metal aerogels was uncovered and will facilitate the modulation of electrocatalysts for practical applications.

Ultrasmall Gold Nanoclusters-Enabled Fabrication of Ultrafine Gold Aerogels as Novel Self-Supported Nanozymes.

Metal aerogels represent an emerging type of functional porous materials with promising applications in diverse fields, but the fabrication of metal aerogels with specific structure and property still remains a challenge. Here, the authors report a new approach to fabricate metal aerogels by using ultrasmall metal nanoclusters (NCs) as functional building blocks. By taking D-penicillamine-stabilized gold NCs (AuNCs) with a diameter of 1.4 nm as an example, Au aerogels with ultrafine ligament size (3.5 nm) and good enzyme-mimic properties are synthesized. Detailed characterization shows that the obtained Au aerogels possess typical 3D self-supported porous network structure with high gold purity and surface area. Time-lapse spectroscopic and microscopic monitoring of the gelation process reveal that these ultrasmall AuNCs first grow into large nanoparticles before fusion into nanowire networks, during which both pH and the precursor concentration are identified to be the determining factor. Owing to their highly porous structure and abundant metal nodes, these self-supported Au aerogels display excellent peroxidase-like properties. This work provides a strategy for fabricating advanced metal aerogels by taking ultrasmall-sized metal NCs as building blocks, which also opens new avenues for engineering the structure and properties of metal aerogels for further advancing their applications.

Hierarchical self-assembly induced supramolecular polymer helical nanowires with white circularly polarized luminescence.

Novel CPL-active supramolecular helical nanowires (SHNWs) were successfully constructed, via the hierarchical self-assembly of supramolecular coordination polymers. The CPL colors of the resultant SHNWs are drastically regulated from blue to red, and pass through white.

1,8-Dioxapyrene-based electrofluorochromic supramolecular hyperbranched polymers.

A novel 1,8-dioxapyrene-based electrofluorochromic supramolecular polymer has been successfully constructed, through the coordination of terpyridine ligands with Eu3+ ions. The resulting polymer is capable of displaying multicolor tunable capacity and intriguing electrofluorochromic phenomena, and can be used in anti-counterfeiting inks.