TLR2 controls random motility, while TLR7 regulates chemotaxis of microglial cells via distinct pathways

Microglial cells are the pathologic sensor of the brain, and any pathologic event triggers microglial activation, which involves migration of these cells to a lesion site. Employing different migration assays, we show that ligands for toll-like receptor (TLR) 2 stimulate random motility, while TLR7 ligands are chemoattractants. The subtype specificity of the TLR ligands was verified by using different TLR-deficient (TLRKO) mouse lines. PI3K and Rac inhibition impairs both TLR2- and TLR7-stimulated microglial migration. In contrast, Akt phosphorylation is only required for the TLR2-, but not for the TLR7-stimulated pathway. Interestingly, P2Y12 receptor signaling is involved in the TLR2 activation-induced microglial migration but not TLR7. Furthermore, TLR7 mRNA expression is down-regulated by TLR2 and TLR7 activation. We conclude that TLRs control the migratory behavior of microglia in a distinct manner

Fabrication of Chitin Nanofiber-Reinforced PLA Nanocomposites by an Environmentally Friendly Process

Polylactic acid (PLA) reinforced with chitin nanofibers was produced from a mixture of a colloidal suspension of PLA particles with chitin nanofiber suspension. The dispersion medium was solely water, which was removed by filtration and drying. Nanocomposites were obtained by compression molding of the filtrates. Static tensile test and dynamic mechanical analysis were performed to evaluate the reinforcement as a function of nanofiber content. Chitin nanofibers delivered reinforcement similar to cellulose nanofibers, being especially effective at up to 70 wt% fiber load. The ultimate tensile modulus and strength reached 7.7 GPa and 110 MPa, respectively, at a nanofiber content of 70 wt%

The N-terminal sequence of the extrinsic PsbP protein modulates the redox potential of Cyt b(559) in photosystem II

This work was supported in part by JST PRESTO (K.I.), by JSPS KAKENHI (grant no. 26660087 to K.I.; 26840091 to R.N.; 24000018 and 25291033 to T.No.), and MEXT KAKENHI (grant no. 24107003 to T.No.). The JST CREST also contributed to this work (part to J.N.). T.Ni. is supported as a JSPS research fellow (grant no. 15J08254)

Identification of the basic amino acid residues on the PsbP protein involved in the electrostatic interaction with photosystem II

AbstractThe PsbP protein is an extrinsic subunit of photosystem II (PSII) that is essential for photoautotrophic growth in higher plants. Several crystal structures of PsbP have been reported, but the binding topology of PsbP in PSII has not yet been clarified. In this study, we report that the basic pocket of PsbP, which consists of conserved Arg48, Lys143, and Lys160, is important for the electrostatic interaction with the PSII complex. Our release-reconstitution experiment showed that the binding affinities of PsbP-R48A, -K143A, and -K160A mutated proteins to PSII were lower than that of PsbP-WT, and triple mutations of these residues greatly diminished the binding affinity to PSII. Even when maximum possible binding had occurred, the R48A, K143A, and K160A proteins showed a reduced ability to restore the rate of oxygen evolution at low chloride concentrations. Fourier transform infrared resonance (FTIR) difference spectroscopy results were consistent with the above finding, and suggested that these mutated proteins were not able to induce the normal conformational change around the Mn cluster during S1 to S2 transition. Finally, chemical cross-linking experiments suggested that the interaction between the N-terminus of PsbP with PsbE was inhibited by these mutations. These data suggest that the basic pocket of PsbP is important for proper association and interaction with PSII. This article is part of a Special Issue entitled: Photosynthesis Research for Sustainability: Keys to Produce Clean Energy

Preparation of chitin nanofibers by surface esterification of chitin with maleic anhydride and mechanical treatment

Esterification with maleic anhydride significantly improved the mechanical disintegration of chitin into uniform 10-nm nanofibers. Nanofibers with 0.25° of esterification were homogeneously dispersed in basic water due to the carboxylate salt on the surface. Esterification proceeded on the surface and did not affect the relative crystallinity. A cast film of the esterified chitin nanofibers was highly transparent, since the film was free from light scattering

Activation of Ca 2+ -dependent K + Channels Is Essential for Bradykinin-induced Microglial Migration

Summary Bradykinin (BK) is produced and acts at the site of injury and inflammation not only in periphery but also in the brain. In the central nervous system, migration of microglia towards damaged tissue plays a role in regeneration under pathological condition. In the present study, we found that bradykinin (BK) induced migration of cultured microglia, which was blocked by charybdotoxin, a blocker of large conductance Ca 2+ -dependent K + channels, but not by pertussis toxin (PTX). These results indicate that activation of large conductance Ca 2+ -activated K + channel is required for BK-induced microglial migration, while activation of PTX-sensitive G protein is not. Our findings may help to understand the function of kinins in the brain and the role of microglia in response to brain injury

Protein/CaCO3/Chitin Nanofiber Complex Prepared from Crab Shells by Simple Mechanical Treatment and Its Effect on Plant Growth

A protein/CaCO3/chitin nanofiber complex was prepared from crab shells by a simple mechanical treatment with a high-pressure water-jet (HPWJ) system. The preparation process did not involve chemical treatments, such as removal of protein and calcium carbonate with sodium hydroxide and hydrochloric acid, respectively. Thus, it was economically and environmentally friendly. The nanofibers obtained had uniform width and dispersed homogeneously in water. Nanofibers were characterized in morphology, transparency, and viscosity. Results indicated that the shell was mostly disintegrated into nanofibers at above five cycles of the HPWJ system. The chemical structure of the nanofiber was maintained even after extensive mechanical treatments. Subsequently, the nanofiber complex was found to improve the growth of tomatoes in a hydroponics system, suggesting the mechanical treatments efficiently released minerals into the system. The homogeneous dispersion of the nanofiber complex enabled easier application as a fertilizer compared to the crab shell flakes