FcγRIIb Exacerbates LPS-Induced Neuroinflammation by Binding with the Bridging Protein DAP12 and Promoting the Activation of PI3K/AKT Signaling Pathway in Microglia.

Introduction: This paper focuses on the expression and role of FcγRIIb in neuroinflammation, exploring the molecular mechanisms by which FcγRIIb interacts with the bridging protein DAP12 to regulate the PI3K-AKT signaling pathway that promote neuroinflammation and aggravate neuronal injury. Methods: LPS-induced neuroinflammation models in vivo and in vitro were constructed to explore the role and mechanism of FcγRIIb in CNS inflammation. Subsequently, FcγRIIb was knocked down or overexpressed to observe the activation of BV2 cell and the effect on PI3K-AKT pathway. Then the PI3K-AKT pathway was blocked to observe its effect on cell activation and FcγRIIb expression. We analyzed the interaction between FcγRIIb and DAP12 by Immunoprecipitation technique. Then FcγRIIb was overexpressed while knocking down DAP12 to observe its effect on PI3K-AKT pathway. Finally, BV2 cell culture supernatant was co-cultured with neuronal cell HT22 to observe its effect on neuronal apoptosis and cell activity. Results: In vivo and in vitro, we found that FcγRIIb expression was significantly increased and activated the PI3K-AKT pathway. Contrary to the results of overexpression of FcγRIIb, knockdown of FcγRIIb resulted in a significant low level of relevant inflammatory factors and suppressed the PI3K-AKT pathway. Furthermore, LPS stimulation induced an interaction between FcγRIIb and DAP12. Knockdown of DAP12 suppressed inflammation and activation of the PI3K-AKT pathway in BV2 cells, and meantime overexpression of FcγRIIb suppressed the level of FcγRIIb-induced AKT phosphorylation. Additionally, knockdown of FcγRIIb inhibited microglia activation, which induced neuronal apoptosis. Discussion: Altogether, our experiments indicate that FcγRIIb interacts with DAP12 to promote microglia activation by activating the PI3K-AKT pathway while leading to neuronal apoptosis and exacerbating brain tissue injury, which may provide a new target for the treatment of inflammatory diseases in the central nervous system.

Efficient CO2 Separation of Multi-Permselective Mixed Matrix Membranes with a Unique Interfacial Structure Regulated by Mesoporous Nanosheets.

A facile strategy to elevate gas separation performances of polymers is to introduce a versatile particle. In this study, the novel F-Ce nanosheets are synthesized, and then F-Ce is functionalized with 1-ethyl-3-methylimidazole thiocyanate (ionic liquids, ILs), obtaining multifunctional f-F-Ce nanosheets by the facile and environment-friendly methods. The multifunctional f-F-Ce nanosheets are incorporated into the Pebax (Pebax 1657) matrix to fabricate mixed matrix membranes (MMMs) for efficient CO2 separation. The f-F-Ce nanosheets play versatile parts in elevating membrane gas separation performance. On the one hand, f-F-Ce tends to arrange horizontally and constructs a unique interfacial structure for cross-layer CO2 transport in MMMs. On the other hand, the abundant mesopores from f-F-Ce construct high-speed CO2 transport channels in MMMs and notably elevate the gas permeability. Moreover, the as-prepared MMMs separate CO2 efficiently due to the comprehensive improvements of diffusivity selectivity, solubility selectivity, and reactivity selectivity. First, the high aspect ratio of f-F-Ce provides the tortuous pathways for gas transport and generates the rigid interface between the Pebax matrix and f-F-Ce nanosheets, increasing the diffusivity selectivity. Second, SCN- groups from ILs show excellent affinity to CO2, enhancing the solubility selectivity. Third, amine groups from ILs with abundant methylimidazole generate reversible reaction with CO2 to elevate reactivity selectivity. Consequently, the f-F-Ce-doped MMMs display excellent CO2 permeability and CO2/CH4 selectivity. In particular, the MMM incorporated with 8 wt % f-F-Ce displays a CO2 permeability of 1823 Barrer and a CO2/CH4 selectivity of 35, overcoming the Robeson upper bound line (2008).

Treatment of Ni-EDTA containing wastewater by electrocoagulation using iron scraps packed-bed anode.

The unique electrocoagulator proposed in this study is highly efficient at removing Ni-EDTA, providing a potential remediation option for wastewater containing lower concentrations of Ni-EDTA (Ni ≤ 10 mg L-1). In the electrocoagulation (EC) system, cylindrical graphite was used as a cathode, and a packed-bed formed from iron scraps was used as an anode. The results showed that the removal of Ni-EDTA increased with the application of current and favoured acidic conditions. We also found that the iron scrap packed-bed anode was superior in its treatment ability and specific energy consumption (SECS) compared with the iron rod anode. In addition, the packed density and temperature had a large influence on the energy consumption (ECS). Over 94.3% of Ni and 95.8% of TOC were removed when conducting the EC treatment at an applied current of 0.5 A, initial pH of 3, air-purged rate 0.2 L min-1, anode packed density of 400 kg m-3 temperature of 313 K and time of 30 min. SEM analysis of the iron scraps indicated that the specific area of the anode increased after the EC. The XRD analysis of flocs produced during EC revealed that hematite (α-Fe2O3) and magnetite (Fe3O4) were the main by-products under aerobic and anoxic conditions, respectively. A kinetic study demonstrated that the removal of Ni-EDTA followed a first-order model with the current parameters. Moreover, the removal efficiency of real wastewater was essentially consistent with that of synthetic wastewater.

Pd/RGO modified carbon felt cathode for electro-Fenton removing of EDTA-Ni.

Ethylenediaminetetraacetic acid (EDTA) forms stable complexes with toxic metals such as nickel due to its strong chelation. The electro-Fenton (EF) process using a cathode made from palladium (Pd), reduced graphene oxide (RGO) and carbon felt, fed with air, exhibited high activities and stability for the removal of 10 mg L(-1) EDTA-Ni solution. Pd/RGO catalyst was prepared by one-pot synthesis; the scanning electron microscopy and X-ray diffraction analysis indicated nanoparticles and RGO were well distributed on carbon felt, forming three dimensional architecture with both large macropores and a mesoporous structure. The cyclic voltammetric results showed that the presence of RGO in Pd/RGO/carbon felt significantly increased the current response of two-electron reduction of O2 (0.45 V). The key factors influencing the removal efficiency of EDTA-Ni, such as pH, current and Fe(2+) concentration, were investigated. Under the optimum conditions, the removal efficiency of EDTA-Ni reached 83.8% after 100 min EF treatment. Mechanism analysis indicated that the introduction of RGO in Pd/RGO/carbon felt significantly enhanced the electrocatalytic activities by inducing •OH in the EF process; direct H2O2 oxidation still accounted for a large amount of EDTA-Ni removal efficiency.