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Extracellular matrix (ECM)-mimicking biomaterials are considered effective tissue-engineered scaffolds for regenerative medicine because of their biocompatibility, biodegradability, and bioactivity. ECM-mimicking biomaterials preserve natural microstructures and matrix-related bioactive components and undergo continuous matrix remodeling upon transplantation. The interaction between host immune cells and transplanted ECM-mimicking biomaterials has attracted considerable attention in recent years. Transplantation of biomaterials may initiate injuries and early pro-inflammation reactions characterized by infiltration of neutrophils and M1 macrophages. Pro-inflammation reactions may lead to degradation of the transplanted biomaterial and drive the matrix into a fetal-like state. ECM degradation leads to the release of matrix-related bioactive components that act as signals for cell migration, proliferation, and differentiation. In late stages, pro-inflammatory cells fade away, and anti-inflammatory cells emerge, which involves macrophage polarization to the M2 phenotype and leukocyte activation to T helper 2 (Th2) cells. These anti-inflammatory cells interact with each other to facilitate matrix deposition and tissue reconstruction. Deposited ECM molecules serve as vital components of the mature tissue and influence tissue homeostasis. However, dysregulation of matrix remodeling results in several pathological conditions, such as aggressive inflammation, difficult healing, and non-functional fibrosis. In this review, we summarize the characteristics of inflammatory responses in matrix remodeling after transplantation of ECM-mimicking biomaterials. Additionally, we discuss the intrinsic linkages between matrix remodeling and tissue regeneration. Extracellular matrix (ECM)-mimicking biomaterials are effectively used as scaffolds in tissue engineering and regenerative medicine. However, dysregulation of matrix remodeling can cause various pathological conditions. Here, the review describes the characteristics of inflammatory responses in matrix remodeling after transplantation of ECM-mimicking biomaterials. Additionally, we discuss the intrinsic linkages between matrix remodeling and tissue regeneration. We believe that understanding host immune responses to matrix remodeling of transplanted biomaterials is important for directing effective tissue regeneration of ECM-mimicking biomaterials. Considering the close relationship between immune response and matrix remodeling results, we highlight the need for studies of the effects of clinical characteristics on matrix remodeling of transplanted biomaterials. Schematic of ideal pro-regenerative matrix remodeling induced by host immune cells in the context of ECM-mimicking biomaterials. After the transplantation of ECM-mimicking biomaterials, ECM is remodeled into a fetal-like state for pro-regenerative reactions and then switch to a mature state for tissue homeostasis and function recovery. Neutrophils, Macrophage and Th cells are main cell types responsible for matrix remodeling during tissue regeneration. [Display omitted] [ABSTRACT FROM AUTHOR]

By using artificial lightning of standardized Waveform A, this study explored the lightning strike protection (LSP) effect of zirconium carbide (ZrC) and copper (Cu) modified short-carbon-fiber-reinforced boron phenolic resin composites under a current peak of 200 kA. Based on the results of visual observation, micro-morphologies characterization, three-dimensional shapes and X-ray detection, we observed a remarkable LSP effect in this composite, which can be attributed to the high bending strength of the laminated structure, and the well thermal resistance of ZrC. Meanwhile, the addition of Cu powders with concentrations of 10% was demonstrated to enable efficiently withstand the lightning strike and prevent crack propagation since the electrically conductive path. Our findings proposed a promising LSP skin material for the aircraft, which will maintain structural stability under the impact of a lightning strike. [ABSTRACT FROM AUTHOR]

The NiFe spinel material itself has good thermal stability and emissivity and can be prepared as an infrared high radiation coating for energy saving applications in industrial high temperature furnace applications. In this study, Cr3+ and Cu2+ doped spinel NiFe 2 O 4 was prepared by solid phase reaction at 1250 °C for 3 h and the microstructure and physicochemical properties of the powder and coating were characterised by XRD, SEM, EDS and IR radiometry. The effect of Cr3+ and Cu2+ doping on the infrared emissivity of spinel NiFe 2 O 4 was investigated and energy saving assessment was carried out in a resistance furnace. The results show that the doping of Cr3+ and Cu2+ can significantly affect the emissivity of spinel powders in the 2.5–10 μm band, and the coatings prepared from the four powders have an emissivity of up to 0.95 in the 2.5–10 μm band. using this high temperature infrared radiation energy saving coating in a resistance furnace resulted in significant energy savings compared to no coating. The furnace was tested for energy saving by holding the furnace for 2 h and 5 h, and the energy saving efficiency reached 20.7% and 17.0% respectively. The coating was subjected to 10 thermal shock tests from room temperature to 700 °C. The coating bonded well and had good thermal shock resistance. Therefore, the coating has wide application prospects for energy saving applications in the field of industrial high temperature furnaces. [ABSTRACT FROM AUTHOR]

Protein Kinase A catalytic subunit α (PKACα), plays an important role in the PKA and NF-κB signaling pathway in mammals. However, the function of PKACα in teleost fish remains largely unknown. In this study, PKACα from black carp (bcPKACα) has been cloned and its role in the innate immune antiviral signaling pathway was investigated. The open reading frame of bcPKACα gene contains 1056 nucleotides and the immunofluorescence assay verified that PKACα was mainly distributed in the cytoplasm. The reporter assay showed that bcPKACα expression and co-expression of bcPKACα and black carp TAK1 (bcTAK1) could activate the transcription of NF-κB. However, bcTAK1/bcIRF7-mediated IFN transcription was inhibited by bcPKACα. Knockdown of bcPKACα showed slightly enhanced antiviral activity against spring viremia of carp virus (SVCV) compared with control group. Accordingly, the antiviral activity against SVCV and grass carp reovirus (GCRV) of EPC cells co-expressing bcPKACα, bcTAK1 and bcIRF7 was obviously lower than that of EPC cells co-expressing bcTAK1 and bcIRF7. The similar subcellular distribution and interaction between bcPKACα and bcTAK1 were detected by immunofluorescent staining and co-immunoprecipitation assay separately. The data generated in this study demonstrates that bcPKACα associates with bcTAK1 and positively regulates NF-κB signaling, however, negatively regulates TAK1/IRF7 signaling pathway. • bcPKACα interacted with bcTAK1. • bcPKACα positively regulates NF-κB signaling pathway. • bcPKACα negatively regulates TAK1/IRF7 signaling pathway. [ABSTRACT FROM AUTHOR]

Dihydroxyacetone kinase (DAK) functions as a negative regulator of melanoma differentiation-associated gene 5 (MDA5)-mediated interferon (IFN) production in human. To explore its role in teleost fish, DAK homologue of black carp (Mylopharyngodon piceus) has been cloned and characterized in this paper. The transcription of black carp DAK (bcDAK) variated in host cells in response to LPS, poly (I:C) and virus stimulation, and bcDAK was majorly distributed in the cytoplasm. Overexpressed bcDAK in EPC cells showed little IFN promoter-inducing ability in the reporter assay and no antiviral activity in plaque assay. When co-expressed with black carp MDA5 (bcMDA5) in EPC cells, bcDAK obviously inhibited bcMDA5-mediated IFN promoter transcription in reporter assay and the antiviral activity in plaque assay. The knockdown of bcDAK enhanced the antiviral activity of the host cells. The association between bcDAK and bcMDA5 has been identified through immunofluorescent staining and co-immunoprecipitation (co-IP) assay. Thus, the data generated in this study support the conclusion that black carp DAK interacts with MDA5 and negatively regulates MDA5-mediated antiviral signaling. 1. bcDAK interacted with bcMDA5. 2. Overexpressed bcDAK inhibited bcMDA5-mediated IFN signaling. 3. Knocking down bcDAK enhanced host antiviral activity. [ABSTRACT FROM AUTHOR]