Liquid Metal-Promoted Graphene Oxide Supramolecular Film for Self-Healing Actuator with Multiple-Stimuli Responses.

The structural vulnerability and immobility of the multi-responsive actuators restrict its application in soft robots. Hence, self-healing film actuators based on interfacial supramolecular crosslinking and hierarchical structural design have been developed. The graphene oxide supramolecular film with asymmetric structure reveals excellent reversible deformation under different trigger signals like moisture, thermal, and infrared light. Meanwhile, it shows a good healing property based on supramolecular interaction, achieving the structure restoration and reconstitution of stimuli-responsive actuators (SRA). The re-edited SRA realizes reverse reversible deformation under the same external stimuli. To enhance the functionality of graphene oxide-based SRA, the reconfigurable liquid metal could be modified on the surface of the graphene oxide supramolecular film at low temperature (defined as LM-GO) due to its compatibility for hydroxyl. The fabricated LM-GO film displays satisfactory healing property and good conductivity. Besides, the self-healing film maintains strong mechanical strength, which can bear more than 20 grams of weight. This study provides a novel strategy to fabricate self-healing actuator with multiple responses, accomplishing the functional integration of the SRAs.

Microscopic imaging quality improvement through L0 gradient constraint model based on multi-fields of view analysis.

The degradation of optical microscopic imaging is space-variant, and how to fast restore optical degraded image remains a special problem. Based on point spread function (PSF) estimation under each field of view (FOV), a L0 gradient-constrained image restoration method is proposed to solve optical degradation in microscopic imaging. Firstly, the whole scene is segmented into several different regions according to different FOV. The PSFs for each region are estimated from modulation transfer function (MTF) measured in advance. Secondly, a penalty function is designed using L0 gradient constraint to deblur the degraded images of each sub-FOV. Finally, a weighted stitching approach is used to stitch the restored images of multiple FOV (m-FOV). Experimental results indicate that the m-FOV analysis could well solve the problem of space-variant degradation. Compared with the other methods, both subjective and objective evaluation results prove that the L0 norm idea could rapidly and effectively restore the degraded image. The approach could be well applied to a real product.

FTY720 Inhibits MPP+-Induced Microglial Activation by Affecting NLRP3 Inflammasome Activation.

Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons and excessive microglial activation in the substantia nigra pars compacta (SNpc). In the present study, we aimed to demonstrate the therapeutic effectiveness of the potent sphingosine-1-phosphate receptor antagonist fingolimod (FTY720) in an animal model of PD induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), and to identify the potential mechanisms underlying these therapeutic effects. C57BL/6J mice were orally administered FTY720 before subcutaneous injection of MPTP. Open-field and rotarod tests were performed to determine the therapeutic effect of FTY720. The damage to dopaminergic neurons and the production of monoamine neurotransmitters were assessed using immunohistochemistry, high-performance liquid chromatography, and flow cytometry. Immunofluorescence (CD68- positive) and enzyme-linked immunosorbent assay were used to analyze the activation of microglia, and the levels of activated signaling molecules were measured using Western blotting. Our findings indicated that FTY720 significantly attenuated MPTP-induced behavioral deficits, reduced the loss of dopaminergic neurons, and increased dopamine release. FTY720 directly inhibited MPTP-induced microglial activation in the SNpc, suppressed the production of interleukin (IL)-6, IL-1ß, and tumor necrosis factor-α in BV-2 microglial cells treated with 1-methyl-4-phenylpyridinium (MPP+), and subsequently decreased apoptosis in SH-SY5Y neuroblastoma cells. Moreover, in MPP+-treated BV-2 cells and primary microglia, FTY720 treatment significantly attenuated the increases in the phosphorylation of PI3K/AKT/GSK-3ß, reduced ROS generation and p65 activation, and also inhibited the activation of NLRP3 inflammasome and caspase-1. In conclusion, FTY720 may reduce PD progression by inhibiting NLRP3 inflammasome activation via its effects on ROS generation and p65 activation in microglia. These findings provide novel insights into the mechanisms underlying the therapeutic effects of FTY720, suggesting its potential as a novel therapeutic strategy against PD. Graphical Abstract FTY720 may reduce ROS production by inhibiting the PI3K/AKT/GSK-3ß signaling pathway, while at the same time reducing p65 phosphorylation, thus decreasing NLRP3 inflammasome activation through these two pathways, ultimately reducing microglia activation-induced neuronal damage.

Fingolimod targets cerebral endothelial activation to block leukocyte recruitment in the central nervous system.

Fingolimod (FTY720), an immunomodulator, is approved as an oral treatment for patients with relapsing forms of multiple sclerosis. Its effects are largely attributed to its mechanism of selectively retaining lymphocytes in the lymph nodes to reduce autoreactive T-cell recruitment in the CNS. In this study, we investigated the therapeutic effect of FTY720 on an animal model of CNS inflammation induced by intracerebral ventricle LPS injection. We found that FTY720 treatment significantly prevented LPS-induced neutrophil recruitment in the CNS by inhibiting leukocyte recruitment in cerebral microvessels. Furthermore, FTY720 also inhibited the expressions of adhesion molecules on the cerebral endothelium, but did not affect the expression levels of pro-inflammatory cytokines (TNF-α and IL-6) and chemokines (CXCL1 and CXCL2) in the CNS parenchyma. The inhibition of endothelial activation was accompanied by reduced phosphorylation of signaling molecules, including serine/threonine-specific protein kinase (Akt), STAT6, and nuclear factor-κB. This FTY720-attenuated inhibition of leukocyte recruitment and endothelial activation was reversed by blocking the functions of sphingosine kinase 2 or sphingosine-1-phosphate receptor 1. Our study demonstrated, for the first time, that FTY720 directly inhibits the phosphorylation of multiple signaling molecules in endothelial cells, thereby effectively blocking leukocyte recruitment in the CNS.

Airborne Laser Scanning Quantification of Disturbances from Hurricanes and Lightning Strikes to Mangrove Forests in Everglades National Park, USA.

Airborne light detection and ranging (LIDAR) measurements derived before and after Hurricanes Katrina and Wilma (2005) were used to quantify the impact of hurricanes and lightning strikes on the mangrove forest at two sites in Everglades National Park (ENP). Analysis of LIDAR measurements covering 61 and 68 ha areas of mangrove forest at the Shark River and Broad River sites showed that the proportion of high tree canopy detected by the LIDAR after the 2005 hurricane season decreased significantly due to defoliation and breakage of branches and trunks, while the proportion of low canopy and the ground increased drastically. Tall mangrove forests distant from tidal creeks suffered more damage than lower mangrove forests adjacent to the tidal creeks. The hurricanes created numerous canopy gaps, and the number of gaps per square kilometer increased from about 400~500 to 4000 after Katrina and Wilma. The total area of gaps in the forest increased from about 1~2% of the total forest area to 12%. The relative contribution of hurricanes to mangrove forest disturbance in ENP is at least 2 times more than that from lightning strikes. However, hurricanes and lightning strikes disturb the mangrove forest in a related way. Most seedlings in lightning gaps survived the hurricane impact due to the protection of trees surrounding the gaps, and therefore provide an important resource for forest recovery after the hurricane. This research demonstrated that LIDAR is an effective remote sensing tool to quantify the effects of disturbances such as hurricanes and lightning strikes in the mangrove forest.

Group delay and chromatic dispersion of thin-film-based, narrow bandpass filters used in dense wavelength-division-multiplexed systems.

Theoretical analysis is made for thin-film-based, 200- and 100-GHz narrow bandpass filters with respect to the intensity response as well as to the chromatic dispersion. The results indicate that the narrower the passband, the higher the chromatic dispersion. The maximum chromatic dispersion appears at the edges of the 0.5-dB passband, owing to the fast change of the group delay in the region. The deviation of chromatic dispersion induced by manufacturing error is simulated. Effective-medium approximation layers are added to simulate the contribution of surface roughness and the mixture interfaces to the passband ripple as well as the chromatic dispersion. The simulations are compared with the experimental results. The measured chromatic dispersion matches the general trend of the theoretical calculation. The imperfect surface and layer mismatch induce additional ripples across the 0.5-dB passband. The maximum chromatic dispersion within a 0.5-dB passband is 20.7 and 54.9 ps/nm for 200- and 100-GHZ narrow bandpass filters, respectively.