Polarization Modulation Research Articles

Tightly focusing metalens based on the high order Bessel function.

We propose a new, to the best of our knowledge, type of metalens of which the phase profile is extracted from the higher-order Bessel function. A light beam passing through this metalens would focus along the circular trajectory and produces a tightly focusing field. Utilizing phase binarization, we provide a method to design the geometric-phase dielectric metasurface both for phase and polarization modulations. We demonstrate two metalenses for circularly and radially polarized output beams at 633 nm, with the measured 0.737λ and 0.616λ focal spots, respectively. Theoretically, it can realize a super-diffraction-limit spot (0.38λ). This work can extend the way of realizing tightly focused optical devices.

P120 catenin enhances macrophage efferocytosis and facilitates resolution of lung inflammatory injury

Abstract Efficient clearance of apoptotic neutrophils (PMNs) (efferocytosis) after sepsis plays a crucial role in facilitating tissue repair, resolving inflammation, and maintaining immune system balance. Here, we identified p120 catenin (p120) as a pivotal regulator in efferocytosis and subsequent recovery from inflammatory lung injury. We found that specific macrophage p120 deletion had a profound delay in the resolution of PMN infiltration, extracellular protein accumulation, and lung edema and injury following LPS challenge. p120 deletion increased the levels of TNF-α and IL-6, and reduced the levels of TGF-β1 and IL-10. Depletion of p120 also led to a marked decrease in the phagocytosis of apoptotic PMNs by macrophages. The number of p120-depleted alveolar macrophages containing apoptotic PMNs in bronchoalveolar lavage fluid was significantly lower. p120 deficiency caused a reduction in the expression of key efferocytosis-related molecules, namely AXL and CD36. p120-depleted macrophages exhibited a shift in polarization towards the M1 phenotype. Apoptotic cells triggered the association and co-localization of p120 and PPAR, and p120 deletion decreased the activity of PPARgamma in response to apoptotic PMNs. Inhibition of PPAR abolished p120-mediated efferocytosis and the resolution of lung inflammation. These findings underscore the critical role of p120 in facilitating the resolution of lung inflammation through modulation of macrophage polarization and PPAR signaling pathway.

Spatial Polarization Modulation for Terahertz Single-Pixel Imaging

Spatial Polarization Modulation for Terahertz Single-Pixel Imaging

Adsorption and Structuration of PEG Thin Films: Influence of the Substrate Chemistry.

This study investigates polyethylene glycol (PEG) homopolymer thin film adsorption on gold surfaces of controlled surface chemistry. The conformational states of physisorbed PEG are analyzed through polarization modulation infrared reflection-absorption spectrometry (PM-IRRAS). The PM-IRRAS principle is based on specific optical selection rules allowing the detection of surface-specific FTIR response of thin polymer films on the basis of differential reflectivity at the polymer/substrate interface for p- and s-polarized light. The intensification of the electric field generated at the PEG/substrate interface for p-polarized IR light in comparison with s-polarized light permits the analysis of PEG chain anisotropy and conformational changes induced by the adsorption. Results showed that PEG adsorbs on model substrates having a rather hydrophilic character in a way that the PEG chains spread parallel to the surface. In the case of a very hydrophilic substrate, the adsorbed PEG chains are in a stable thermodynamic state which allows them to arrange and crystallize as stacked crystalline lamellae after adsorption. The surface topography and morphology of the PEG thin films were also investigated by atomic force microscopy (AFM). While in the bulk state, PEG crystallizes in the form of large spherulites; on substrates whose adsorption is favored by surface chemistry, PEG crystallizes in the form of stacked lamellae with a thickness equal to 20 nm. Conversely, on a hydrophobic substrate, the PEG chains do not crystallize and adsorption occurs in the statistical coil state.

Research progress on the role of macrophages in acne and regulation by natural plant products.

Acne vulgaris is one of the most common skin diseases. The current understanding of acne primarily revolves around inflammatory responses, sebum metabolism disorders, aberrant hormone and receptor expression, colonization by Cutibacterium acnes, and abnormal keratinization of follicular sebaceous glands. Although the precise mechanism of action remains incompletely understood, it is plausible that macrophages exert an influence on these pathological features. Macrophages, as a constituent of the human innate immune system, typically manifest distinct phenotypes across various diseases. It has been observed that the polarization of macrophages toward the M1 phenotype plays a pivotal role in the pathogenesis of acne. In recent years, extensive research on acne has revealed an increasing number of natural remedies exhibiting therapeutic efficacy through the modulation of macrophage polarization. This review investigates the role of cutaneous macrophages, elucidates their potential significance in the pathogenesis of acne, a prevalent chronic inflammatory skin disorder, and explores the therapeutic mechanisms of natural plant products targeting macrophages. Despite these insights, the precise role of macrophages in the pathogenesis of acne remains poorly elucidated. Subsequent investigations in this domain will further illuminate the pathogenesis of acne and potentially offer guidance for identifying novel therapeutic targets for this condition.

Noncollinear electro-optic detection of terahertz waves: Advantages and limitations

Electro-optic sampling of terahertz waves by noncollinearly propagating femtosecond laser pulses in electro-optic crystals can provide high efficiency and high spectral resolution of terahertz detection with various types of crystals and laser wavelengths, unlike the conventional collinear scheme. We develop an analytical theory of noncollinear electro-optic sampling detection technique that describes the modulation of the probe laser beam polarization as a result of nonlinear interaction between the optical and terahertz fields. The theory accounts for finite widths of the terahertz and probe beams. It is found that noncollinear scheme operates as a low-pass terahertz filter with the frequency cut-off determined by the width of the probe beam and the crossing angle of the terahertz and probe beams. We apply the theory to two practical situations: sampling of terahertz waves by fiber laser pulses (1.55 μm wavelength) in a GaAs crystal and sampling by Ti:sapphire laser pulses (800 nm wavelength) in a LiNbO3 crystal.

Role of transient receptor potential ankyrin 1 in idiopathic pulmonary fibrosis: modulation of M2 macrophage polarization

Idiopathic pulmonary fibrosis (IPF) poses significant challenges due to limited treatment options despite its complex pathogenesis involving cellular and molecular mechanisms. This study investigated the role of transient receptor potential ankyrin 1 (TRPA1) channels in regulating M2 macrophage polarization in IPF progression, potentially offering novel therapeutic targets. Using a bleomycin-induced pulmonary fibrosis model in C57BL/6J mice, we assessed the therapeutic potential of the TRPA1 inhibitor HC-030031. TRPA1 upregulation was observed in fibrotic lungs, correlating with worsened lung function and reduced survival. TRPA1 inhibition mitigated fibrosis severity, evidenced by decreased collagen deposition and restored lung tissue stiffness. Furthermore, TRPA1 blockade reversed aberrant M2 macrophage polarization induced by bleomycin, associated with reduced Smad2 phosphorylation in the TGF-β1-Smad2 pathway. In vitro studies with THP-1 cells treated with bleomycin and HC-030031 corroborated these findings, highlighting TRPA1's involvement in fibrotic modulation and macrophage polarization control. Overall, targeting TRPA1 channels presents promising therapeutic potential in managing pulmonary fibrosis by reducing pro-fibrotic marker expression, inhibiting M2 macrophage polarization, and diminishing collagen deposition. This study sheds light on a novel avenue for therapeutic intervention in IPF, addressing a critical need in the management of this challenging disease.Graphical abstract

Three-dimensional dipole orientation mapping with high temporal-spatial resolution using polarization modulation

Fluorescence polarization microscopy is widely used in biology for molecular orientation properties. However, due to the limited temporal resolution of single-molecule orientation localization microscopy and the limited orientation dimension of polarization modulation techniques, achieving simultaneous high temporal-spatial resolution mapping of the three-dimensional (3D) orientation of fluorescent dipoles remains an outstanding problem. Here, we present a super-resolution 3D orientation mapping (3DOM) microscope that resolves 3D orientation by extracting phase information of the six polarization modulation components in reciprocal space. 3DOM achieves an azimuthal precision of 2° and a polar precision of 3° with spatial resolution of up to 128 nm in the experiments. We validate that 3DOM not only reveals the heterogeneity of the milk fat globule membrane, but also elucidates the 3D structure of biological filaments, including the 3D spatial conformation of λ-DNA and the structural disorder of actin filaments. Furthermore, 3DOM images the dipole dynamics of microtubules labeled with green fluorescent protein in live U2OS cells, reporting dynamic 3D orientation variations. Given its easy integration into existing wide-field microscopes, we expect the 3DOM microscope to provide a multi-view versatile strategy for investigating molecular structure and dynamics in biological macromolecules across multiple spatial and temporal scales.

Multidimensional Multiplexing Liquid Crystal Holograms

AbstractAs a powerful platform for next‐generation display, planar liquid crystal (LC) optics exhibit attractive properties such as electro‐optical response, high efficiency, and broadband tunability. With planar LC optics applications taking off, multidimensional modulation and multiplexing capability of light wave is becoming crucial. Here, a Pancharatnam‐Berry phase LC hologram is demonstrated that enables the multidimensional modulation of amplitude, phase, and polarization of light, which increases the degree of freedom of multiplexing display to 4 at a single wavelength, realizing the simultaneous decoupling modulation in dual polarization channels in near and far fields. According to the quaternary degeneracy characteristics of the orientation angle of LC molecules implied in Malus' law, the LC holograms are designed using the optimized Gerchberg‐Saxton and annealing algorithms, and it is demonstrated that the spatial and polarization multiplexing of LC holograms have remarkable wavelength‐dependent electrical tunability. This LC hologram paves a promising pathway toward multifunctional LC optics for advanced display and imaging.

Hierarchical heterostructure Ni2P hollow carbon spheres derived from MOFs for efficient electromagnetic wave absorption

In this study, a hierarchical heterogeneous structure of Ni2P hollow carbon spheres (Ni2P-HCS) was synthesized through a two-step process involving carbonization and phosphorization of Ni-metal organic framework (Ni-MOF) precursors. During the construction of the Ni2P/C nanostructure, heterointerface recombination and secondary graphitization were observed, which contribute to the modulation of interface polarization. Structural analysis revealed that the Ni2P/C nanoparticles are uniformly dispersed, forming stable porous structured microspheres, thereby leveraging dielectric and magnetic losses. The combination of Ni2P with metal-organic frameworks (MOFs) can optimize impedance matching, enhance effective absorption bandwidth, and consequently improve electromagnetic wave absorption performance. The results show that Ni2P-HCS (Ni2P-HCS700) exhibited superior electromagnetic wave (EMW) absorption characteristics when the carbonization temperature is 700 ℃. It achieves a maximum reflection loss (RL) of −46.7 dB at a thickness of 2.9 mm and an effective absorption bandwidth (EAB) of 4.8 GHz at 1.71 mm thickness, almost covering the Ku-band (13.3 GHz−18 GHz). Radar cross-section (RCS) simulations utilizing CST indicated an optimal RCS reduction value of 41 dB m² at theta=0° for Ni2P-HCS700. This work introduces a universal approach to designing high-performance lightweight absorbers derived from MOFs, incorporating transition metal phosphides to form composites for impedance matching control.

Broadband achromatic and wide field of view metalens-doublet by inverse design

Metalenses, composed of patterned meta-atoms in various dimensions, offer tailored modulation of phase, amplitude, and polarization for diverse imaging applications across the visible and near-infrared spectra. However, simultaneously achieving achromatic and wide field of view (WFOV) imaging remains a significant challenge. In this paper, we propose a general inverse design framework for metalens-doublets that simultaneously enables broadband achromatic and WFOV imaging. The broadband achromatic and WFOV (BA&WFOV) metalens-doublet comprises a propagation phase metalens and a geometric phase metalens positioned on opposite sides of the substrate. This framework requires only once polarization conversion and mitigates aperture size constraints imposed by the limited group delay (GD) range of meta-atoms. We present a BA&WFOV metalens-doublet with an f-number of 3.9, a full field of view (FOV) of 68°, and a wavelength range from 640nm to 820nm. This metalens-doublet exhibits diffraction-limited focusing with an average absolute focusing efficiency of 16% and an average relative focusing efficiency of 60%. This innovative framework holds significant promise for applications in fields such as phone cameras, VR/AR, and endoscopes.

Effects of tamoxifen on the immune response phenotype in equine peripheral blood mononuclear cells.

Tamoxifen (TAM) is widely utilized in the prevention and treatment of human breast cancer and has demonstrated the potential to modulate the immune response. It has been proposed as a therapeutic tool for immune-mediated diseases. TAM has been investigated as a possible treatment for asthma-like conditions in horses, revealing specific impacts on the innate immune system. While the effects of TAM on equine neutrophils are well-documented, its influence on lymphocytes and the modulation of the immune response polarization remains unclear. This in vitro study employed peripheral blood mononuclear cells (PBMC) from healthy horses, exposing them to varying concentrations of the TAM and assessing the expression of genes involved in the polarization of the immune response (TBX21, IFNG, GATA3, IL4, IL10, FOXP3, and CTLA4) in PBMC stimulated or not with PMA/ionomycin. Additionally, the effect of TAM over the proportion of regulatory T cells (Treg) was also assessed. TAM did not significantly affect the expression of these genes and Treg at low concentrations. However, at the highest concentration, there was an impact on the expression of GATA3, IL4, IL10, and CTLA4 genes. These alterations in genes associated with a Th2 and regulatory response coincided with a noteworthy increase in drug-associated cytotoxicity but only at concentrations far beyond those achieved in pharmacological therapy. These findings suggest that the effects of TAM, as described in preclinical studies on asthmatic horses, may not be attributed to the modification of the adaptive response.

Design and fabrication of a liquid crystal retarder for the mid- and far-infrared wavelength ranges

We designed and fabricated a liquid crystal (LC) retarder that operates within mid-infrared (MIR) and far-infrared (FIR) wavelength regions. Fluorine-based mixed LCs and BaF2 substrates were employed to assemble the LC retarder on the basis of their absorption spectra. A thin NiCr film, which served as a semitransparent electrode in the infrared region, was also formed on the BaF2 substrate. The fabricated LC retarder showed transmittances of 40% and 42% at wavelengths of 3.88µm and 9.5µm, respectively. Here, we demonstrated phase shift that can be electrically controlled to exceed π/2. Our LC retarder can be applied to the polarization modulation in the MIR and FIR wavelength regions.

THz active modulation device by electric field turned modulation characteristics of titanium sulfide nanofilm device

AbstractAn effective approach to manipulate terahertz (THz) waves involves the utilization of a device structure. In this particular investigation, we have successfully fabricated a SnS2 nanofilm device using femtosecond laser direct ablation. The passive and active polarization‐sensitive characteristics of the SnS2 nanofilm device were examined within the THz frequency range, employing different line spaces of 500, 600, and 700 μm. The combination of the device effect and SnS2 absorption led to an enhanced passive polarization modulation. Moreover, when an external electric field was applied to the SnS2 nanofilm device along the device line, persistent switching and linear modulation of THz wave transmission were observed. These findings indicate that the integration of material properties and device structure in this SnS2 device renders it highly suitable for applications in ultrafast THz switches, filters, and modulation devices.

Tunable polarization holographic gratings obtained by varying the ratio of intensities of the recording beams

Polarization holography has been extensively applied in many fields, such as optical science, metrology, and biochemistry, due to its property of polarization modulation. However, the modulated polarization state of diffracted light corresponds strictly to that of incident light one by one. Here, a kind of tunable polarization holographic grating has been designed in terms of Jones matrices, and intensity-based polarization manipulation has been realized experimentally. The proposed tunable polarization holographic grating is recorded on an azobenzene liquid-crystalline film by a pair of coherent light beams with orthogonal polarization states and asymmetrically controlled intensities. It is found that the diffracted light can be actively manipulated from linearly to circularly polarized based on the light intensity of the recording holographic field when the polarization state of incident light keeps constant. Our work could enrich the field of light manipulation and holography.

Controlling the helicity of light by electrical magnetization switching.

Controlling the intensity of emitted light and charge current is the basis of transferring and processing information1. By contrast, robust information storage and magnetic random-access memories are implemented using the spin of the carrier and the associated magnetization in ferromagnets2. The missing link between the respective disciplines of photonics, electronics and spintronics is to modulate the circular polarization of the emitted light, rather than its intensity, by electrically controlled magnetization. Here we demonstrate that this missing link is established at room temperature and zero applied magnetic field in light-emitting diodes2-7, through the transfer of angular momentum between photons, electrons and ferromagnets. With spin-orbit torque8-11, a charge current generates also a spin current to electrically switch the magnetization. This switching determines the spin orientation of injected carriers into semiconductors, in which the transfer of angular momentum from the electron spin to photon controls the circular polarization of the emitted light2. The spin-photon conversion with the nonvolatile control of magnetization opens paths to seamlessly integrate information transfer, processing and storage. Our results provide substantial advances towards electrically controlled ultrafast modulation of circular polarization and spin injection with magnetization dynamics for the next-generation information and communication technology12, including space-light data transfer. The same operating principle in scaled-down structures or using two-dimensional materials will enable transformative opportunities for quantum information processing with spin-controlled single-photon sources, as well as for implementing spin-dependent time-resolved spectroscopies.

Liraglutide attenuates angiotensin II-induced aortic dissection and aortic aneurysm via inhibiting M1 macrophage polarization in APOE -/- mice

BackgroundAortic Aneurysm and Dissection (AAD) are severe cardiovascular conditions with potentially lethal consequences such as aortic rupture. Existing studies suggest that liraglutide, a long-acting glucagon-like peptide receptor (GLP-1R) agonist, offers protective benefits across various cardiovascular diseases. However, the efficacy of liraglutide in mitigating AAD development is yet to be definitively elucidated. MethodsAng II (Angiotension II) infusion of APOE-/- mouse model with intraperitoneal injection of liraglutide (200 μg/kg) to study the role of GLP-1R in AAD formation. Bone Marrow Derived Macrophages (BMDM) and Raw264.7 were incubated with LPS, liraglutide, exendin 9–39 or LY294002 alone or in combination. SMC phenotype switching was examined in a macrophage and vascular smooth muscle cell (VSMC) co-culture system. An array of analytical methods, including Western Blot, Immunofluorescence Staining, Enzyme-LinkedImmunosorbent Assay, Real-Time Quantitative Polymerase Chain Reaction, RNA-seq, and so on were employed. ResultsOur investigation revealed a significant increase in M1 macrophage polarization and GLP-1R expression in aortas of AD patients and Ang II-induced AAD APOE-/- mice. Administering liraglutide in APOE-/- mice notably reduced Ang II-induced AAD incidence and mortality. It was found that liraglutide inhibits M1 macrophage polarization primarily via GLP-1R activation, and subsequently modulates vascular smooth muscle cell phenotypic switching was the primary mechanism. RNA-Seq and subsequent KEGG enrichment analysis identified CXCL3, regulated by the PI3K/AKT signaling pathway, as a key element in liraglutide’s modulation of M1 macrophage polarization. ConclusionOur study found liraglutide exhibits protective effects against AAD by modulating M1 macrophage polarization, suppressing CXCL3 expression through the PI3K/AKT signaling pathway. This makes it a promising therapeutic target for AAD, offering a new avenue in AAD management.

Effect of Polarization‐Charge Modulation on the Carrier‐Injection Efficiency of AlGaN‐Based Ultraviolet‐B Laser Diodes Using Polarization Doping in the p‐Type AlGaN Cladding Layer

In this study, the effect of polarization modulation on the carrier‐injection efficiency of AlGaN‐based ultraviolet‐B laser diodes (LDs) using polarization doping in the p‐type AlGaN cladding layer is discussed. The structure of an intentional Al‐content drop at the interface between the p‐type AlGaN electron‐blocking layer and the p‐type AlGaN cladding layer is investigated. First, the usefulness of this structure using a device simulator is confirmed. The optimized structure is also verified by fabricating devices. The fabricated devices are evaluated at room temperature and under pulsed operation. The carrier injection efficiency of the ultraviolet‐B LD is confirmed to exceed 10%. By utilizing a structure with Al‐content drops in the AlGaN, it is found that the peak optical output power is improved by a factor of 6.2 and the carrier‐injection efficiency by a factor of 3.3, compared to a case without this structure.

Spin–orbit torque reconfigurable diffraction gratings

Spin–orbit torque (SOT) provides a convenient, fast, and efficient way to switch the magnetization and has been applied in memory, logic, and microwave devices. Here, we report the application of SOT in the spatial modulation of the optical field. We construct a diffraction grating composed of perpendicularly magnetized current channels that can be switched using the SOT current pulses, and the resulting periodic magnetization patterns are transferred into the polarization modulation of light through the magneto-optical effect. We demonstrate that the periodic structures and diffraction peaks of the grating can be reconfigured electrically. These results would open up an avenue to the application of the state-of-the-art spintronic technologies in fast tunable diffractive optics.

Insights into the mechanism of action of pterostilbene against influenza A virus-induced acute lung injury

BackgroundSevere respiratory system illness caused by influenza A virus infection is associated with excessive inflammation and abnormal apoptosis in alveolar epithelial cells (AEC). However, there are limited therapeutic options for influenza-associated lung inflammation and apoptosis. Pterostilbene (PTE, trans-3,5-dimethoxy-4-hydroxystilbene) is a dimethylated analog of resveratrol that has been reported to limit influenza A virus infection by promoting antiviral innate immunity, but has not been studied for its protective effects on virus-associated inflammation and injury in AEC. PurposeOur study aimed to investigate the protective effects and underlying mechanisms of PTE in modulating inflammation and apoptosis in AEC, as well as its effects on macrophage polarization during influenza virus infection. Study design and methodsA murine model of influenza A virus-mediated acute lung injury was established by intranasal inoculation with 5LD50 of mouse-adapted H1N1 viruses. Hematoxylin and eosin staining, immunofluorescence, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, western blotting, Luminex and flow cytometry were performed. ResultsPTE effectively mitigated lung histopathological changes and injury induced by H1N1 viruses in vivo. These beneficial effects of PTE were attributed to the suppression of inflammation and apoptosis in AEC, as well as the modulation of M1 macrophage polarization. Mechanistic investigations revealed that PTE activated the phosphorylated AMP-activated protein kinase alpha (P-AMPKα)/sirtui1 (Sirt1)/PPARγ coactivator 1-alpha (PGC1α) signal axis, leading to the inhibition of nuclear factor kappa-B (NF-κB) and p38 mitogen-activated protein kinase (MAPK) signaling induced by H1N1 viruses, thereby attenuating inflammation and apoptosis in AEC. PTE also forced activation of the P-AMPKα/Sirt1/PGC1α signal axis in RAW264.7 cells, counteracting the activation of phosphorylated signal transducer and activator of transcription 1 (P-STAT1) induced by H1N1 viruses and the augment of P-STAT1 activation in RAW264.7 cells with interferon-gamma (IFN-γ) pretreatment before viral infection, thereby reducing H1N1 virus-mediated M1 macrophage polarization as well as the enhancement of macrophages into M1 phenotypes elicited by IFN-γ pretreatment. Additionally, the promotion of the transition of macrophages towards the M2 phenotype by PTE was also related to activation of the P-AMPKα/Sirt1/PGC1α signal axis. Moreover, co-culturing non-infected AEC with H1N1 virus-infected RAW264.7 cells in the presence of PTE inhibited apoptosis and tight junction disruption, which was attributed to the suppression of pro-inflammatory mediators and pro-apoptotic factors in an AMPKα-dependent manner. ConclusionIn conclusion, our findings suggest that PTE may serve as a promising novel therapeutic option for treating influenza-associated lung injury. Its ability to suppress inflammation and apoptosis in AEC, modulate macrophage polarization, and preserve alveolar epithelial cell integrity highlights its potential as a therapeutic agent in influenza diseases.