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Spin angular momentum associated with circular polarization is a fundamental and important aspect of photons both in classical and quantum optics. The interaction of this optical spin with matter and structures results in many intriguing optical effects and state-of-the-art applications covered under the emerging subject of spin optics. Distinct from longitudinal optical spin along the mean wavevector, transverse spin, the corresponding vector of which is perpendicular to the mean wavevector, prevails and plays a significant role in confined electromagnetic waves such as focused beams, guided waves, and evanescent waves. In the optical near-field, these transverse spins are generated owing to the spatial variation of the kinetic momentum of confined electromagnetic waves, where the spin and orbital angular momenta are strongly coupled, leading to many interesting topological spin structures and properties. Several reviews on optical transverse spins have been published in recent years in which their concepts and the various configurations producing them were introduced systematically. Here, we introduce in this review the underlying physics and dynamics of transverse spin and the resultant topological structures and properties such as the photonic skyrmions and merons. We term this sub-area ‘spin photonics’, its scope being to cover the design and research of spin structures in strongly confined electromagnetic fields with unique properties and applications. The concepts and framework reviewed have importance in optics, topological photonics, metrology, and quantum technologies and may be used to extend spin-dynamics concepts to fluidic, acoustic, and gravitational waves.

Polarimetry has been demonstrated essential in various disciplines, such as optical communications, imaging, and astronomy. On-chip nanostructures for polarization measurements are most expected to replace the conventional bulk elements, and hence minimize the polarimeter for integrated applications. Some on-chip nanophotonic polarimeter via polarization detection has been implemented, in which the separation of two spin polarized states is needed. However, due to the relatively low coupling efficiency or complicated photonic silicon circuits, on-chip polarimetry using a single device still remains challenging. Here, we introduce and investigate an on-chip polarimeter with nanostructures using the inverse design method. The developed device shows the ability to detect the four polarization components of light, two of which are the spin polarizations, and the other two are the linear polarizations. The retrieved Stokes parameters with experimentally tested data are in close agreement with the numerical results. We also show the proof of concept demonstration for high-speed Stokes vector optical signals detection. In the high-speed communication experiment with data rate up to 16 GBd, the detected optical signals via polarization measurements at multiple wavelengths in the C-band were recovered with the bit error rate below the 20% forward error correction threshold. The proposed on-chip polarimeter shows promising performance both in Stokes polarimetry and high-speed optical communication applications.

Polarization and related spin properties are important characteristics of electromagnetic waves and their manipulation is crucial in almost all photonic applications. Magnetic materials are often used for controlling light polarization through the magneto-optical Kerr or Faraday effects. Recently, complex topological structures of the optical spin have been demonstrated in the evanescent light field, which in the presence of the spin–orbit coupling may form photonic skyrmions. Here, we investigate the optical spin–orbit coupling in the presence of magnetization and the interaction between photonic skyrmions and magnetic domains. We demonstrate that the magnetization is responsible for the modulation of the optical spin distribution, resulting in twisted Neel-type skyrmions. This effect can be used for the visualization of magnetic domain structure with both in plane and polar orientation of magnetization, and in turn for creation of complex optical spin distributions using magnetization patterns. The demonstrated interplay between photonic skyrmions and magneto-optical effects may also provide novel opportunities for investigation and manipulation of magnetic skyrmions using optical spin–orbit coupling.

Topological spin textures, among which skyrmions and merons are typical examples, have with their swirling vectorial structures triggered enormous interest in physical systems including elementary particles and magnetic materials. Manipulating their symmetry and topology is important for understanding the mechanisms that underlie their topological phase transformation as well as offering tunable degrees of freedom to encode information, which has already been demonstrated in magnetic materials. Recently, the photonic counterparts of skyrmions and merons were constructed in a 2D wave system with deep-subwavelength features promising for optical sensing, imaging, and information decoding. However, their experimental realization relied on stringent excitation conditions that only support a single spin texture type on a specific structure. Here, we demonstrate for the first time the transformation between photonic skyrmion and meron spin lattices on the same metallic meta-surface having a well-designed structural period. We show experimentally the wavelength-tuned symmetry transformation of the photonic spin lattices, which are also found to be robust against disorder in the structure to a certain degree. This work provides new insights into controlling the electromagnetic field symmetry and topology, as well as in developing applications in spin optics and topological photonics. [ABSTRACT FROM AUTHOR]

Photonic skyrmions have applications in many areas, including the vectorial and chiral optics, optical manipulation, deep-subwavelength imaging and nanometrology. Much effort has been focused on the experimental characterization of photonic skyrmions. Here, we give an insight into the spin and orbital features of photonic skyrmions constructed by the p-polarized and s-polarized surface waves at an interface with various electric and magnetic properties by analyzing the continuity of chirality, energy flow and momentum densities through the electric and magnetic interface. The continuity of chirality density indicates that the photonic skyrmion has a property of the optical transverse spin. Most importantly, the continuity of energy flow and momentum densities results in four spin–orbit interaction quantities, which indicate the gradient of electric polarizability or permeability governs the spin–orbit interaction of photonic skyrmions and leads to the discontinuity and even the reversal of spin orientation through the optical interface. Our investigations on the spin–orbit properties of photonic skyrmions, which can give rise to the spin-dependent force and topological unidirectional transportation, is thorough and can be extended to other classical wave, such as acoustic and fluid waves. The findings help in understanding the spin–orbit feature of photonic topological texture and in constructing further optical manipulation, sensing, quantum and topological techniques.

The recently developed concept of optical skyrmions has introduced an exciting dimension to the emerging field of Poincaré engineering in optical lattices. There remains an unexplored territory in investigating system geometries to enhance the versatility of manipulating the topological landscape within optical lattices. Here, we present both experimental and theoretical evidence showcasing the periodic vectorial characteristics of field- and spin-based skyrmion lattices, generated by plasmonic vortices with varying topological charges. Our findings reveal that the geometric symmetry of the system plays a pivotal role in governing the periodic arrangement of these vortex patterns. Building upon this arrangement, the orbital–orbital coupling of plasmonic vortices gives rise to densely packed energy flow distributions, intricately bonded to topological charges. Consequently, this results in the formation of sublattices within the momentum space, each characterized by distinct k-vectors. Skyrmion and meron topologies, driven by the intrinsic spin–orbital coupling, are presented in these lattices. This proposed framework illuminates how symmetry serves as a fundamental tool in the manipulation of optical lattice topologies, opening up new avenues in fields ranging from optical trapping, laser writing, quantum gas microscopy, to electron quantum state control, each of which is poised to benefit from these nontrivial advances. [ABSTRACT FROM AUTHOR]

Monocytes (Mos) are believed to play important roles during the generation of immune response. In our previous study, CVC1302, a complex of PRRs agonists, was demonstrated to recruit Mo into lymph nodes (LNs) in order to present antigen and secret chemokines (CXCL9 and CXCL10), which attracted antigen-specific CD4+ T cells. As it is known that Mos in mice are divided into two main Mo subsets (Ly6C+ Mo and Ly6C− Mo), we aimed to clarify the CVC1302-recruiting Mo subset and functions in the establishment of immunity. In this study, we found that CVC1302 attracted both Ly6C+ Mo and Ly6C− Mo into draining LNs, which infiltrated from different origins, injection muscles and high endothelial venule (HEV), respectively. We also found that the numbers of OVA+ Ly6C+ Mo in the draining LNs were significantly higher compared with OVA+ Ly6C− Mo. However, the levels of CXCL9 and CXCL10 produced by Ly6C− Mo were significantly higher than Ly6C+ Mo, which plays important roles in attracting antigen-specific CD4+ T cells. Under the analysis of their functions in initiating immune responses, we found that the ability of the Ly6C+ monocyte was mainly capturing and presenting antigens, otherwise; the ability of the Ly6C− monocyte was mainly secreting CXCL9 and CXCL10, which attracted antigen-specific CD4+ T cells through CXCR3. These results will provide new insights into the development of new immunopotentiators and vaccines. [ABSTRACT FROM AUTHOR]

Strongly confined electromagnetic (EM) fields generated by tightly focused light beams are applied widely in nano‐optics due to their vectorial characteristics. The inclusion of the longitudinal polarized component plays a crucial role in both the physical characteristics and practical uses of tightly focused vector beams. The acquisition of the distributions of the three orthogonal polarized components of these fields is advantageous for the comprehensive examination of their captivating physical phenomena and possible applications. However, this continues to pose a noteworthy obstacle, especially in the case of the fields that are generated by high numerical aperture objectives. A novel approach is proposed to quantifying the three mutually perpendicular polarizations simultaneously in the focal plane. The method utilizes a dual‐mode waveguide probe that is composed of a dielectric nanoparticle and a metal‐dielectric waveguide. This design allows for the simultaneous support of both transverse electric (TE) and transverse magnetic (TM) modes. Consequently, it enables the polarization recognition of scattering light in k‐space. Importantly, this method effectively eliminates any interference originating from the background light. The work involves an analysis of the theoretical notion of the probe and followed by experimental investigations. This approach holds promise for augmenting optical nanoscopy methodologies and their associated applications. [ABSTRACT FROM AUTHOR]

The two-dimensional (2D) bulk photovoltaic effect (BPVE) is a cornerstone for future highly efficient 2D solar cells and optoelectronics. The ferromagnetic semiconductor 2H-FeCl2 is shown to realize a new type of BPVE in which spatial inversion (P), time reversal (T), and space–time reversal (PT) symmetries are broken (PT-broken). Using density functional theory and perturbation theory, we show that 2H-FeCl2 exhibits giant photocurrents, photo-spin-currents, and photo-orbital-currents under illumination by linearly polarized light. The injection-like and shift-like photocurrents coexist and propagate in different directions. The material also demonstrates substantial photoconductance, photo-spin-conductance, and photo-orbital-conductance, with magnitudes up to 4650 (nm·µA/V2), 4620 [nm·µA/V2ħ/(2e)], and 6450 (nm·µA/V2ħ/e), respectively. Furthermore, the injection-currents, shift-spin-currents, and shift-orbital-currents can be readily switched via rotating the magnetizations of 2H-FeCl2. These results demonstrate the superior performance and intriguing control of a new type of BPVE in 2H-FeCl2. [ABSTRACT FROM AUTHOR]

This study found a higher percentage of CD8+ T cells in piglets immunized with a CVC1302-adjuvanted inactivated foot-and-mouth disease virus (FMDV) vaccine. We wondered whether the CVC1302-adjuvanted inactivated FMDV vaccine promoted cellular immunity by promoting the antigen cross-presentation efficiency of ovalbumin (OVA) through dendritic cells (DCs), mainly via cytosolic pathways. This was demonstrated by the enhanced levels of lysosomal escape of OVA in the DCs loaded with OVA and CVC1302. The higher levels of ROS and significantly enhanced elevated lysosomal pH levels in the DCs facilitated the lysosomal escape of OVA. Significantly enhanced CTL activity levels was observed in the mice immunized with OVA-CVC1302. Overall, CVC1302 increased the cross-presentation of exogenous antigens and the cross-priming of CD8+ T cells by alkalizing the lysosomal pH and facilitating the lysosomal escape of antigens. These studies shed new light on the development of immunopotentiators to improve cellular immunity induced by vaccines. [ABSTRACT FROM AUTHOR]

Aims: Mesenchymal stem cells (MSCs) present in the heart cannot differentiate into cardiomyocytes, but may play a role in pathological conditions. Therefore, the aim of this study was to scrutinise the role and mechanism of MSC differentiation in vivo during heart failure. Methods and Results: We performed single-cell RNA sequencing of total non-cardiomyocytes from murine and adult human hearts. By analysing the transcriptomes of single cells, we illustrated the dynamics of the cell landscape during the progression of heart hypertrophy, including those of stem cell antigen-1 (Sca1)+ stem/progenitor cells and fibroblasts. By combining genetic lineage tracing and bone marrow transplantation models, we demonstrated that non-bone marrow-derived Sca1+ cells give rise to fibroblasts. Interestingly, partial depletion of Sca1+ cells alleviated the severity of myocardial fibrosis and led to a significant improvement in cardiac function in Sca1-CreERT2;Rosa26-eGFP-DTA mice. Similar non-cardiomyocyte cell composition and heterogeneity were observed in human patients with heart failure. Mechanistically, our study revealed that Sca1+ cells can transform into fibroblasts and affect the severity of fibrosis through the Wnt4-Pdgfra pathway. Conclusions: Our study describes the cellular landscape of hypertrophic hearts and reveals that fibroblasts derived from Sca1+ cells with a non-bone marrow source largely account for cardiac fibrosis. These findings provide novel insights into the pathogenesis of cardiac fibrosis and have potential therapeutic implications for heart failure. Non-bone marrow-derived Sca1+ cells differentiate into fibroblasts involved in cardiac fibrosis via Wnt4-PDGFRα pathway. [ABSTRACT FROM AUTHOR]

Photonic spin skyrmions with deep‐subwavelength features have aroused considerable interest in recent years. However, the manipulation of spin structure in the skyrmions in a desired manner is still a challenge, while this is crucial for developing the skyrmion‐based applications. Here, an approach of optical spin manipulation by utilizing the spin‐momentum equation is proposed to investigate the spin texture in a photonic skyrmion‐pair. With the benefit of the proposed approach, a unique spin texture with spin angular momentum varying linearly along the line connecting the two skyrmion centers is theoretically designed and experimentally verified. The optimized spin texture is then applied in a displacement‐sensing system, which is capable of attaining pico‐metric sensitivity. Compared with the conventional polarization and phase schemes, the spin‐based manipulation mechanism provides a new pathway for optical modulation, which is of great value in nanophotonics from both fundamental and application. [ABSTRACT FROM AUTHOR]

Background: CD34+ cells have been used to treat the patients with heart failure, but the outcome is variable. It is of great significance to scrutinize the fate and the mechanism of CD34+ cell differentiation in vivo during heart failure and explore its intervention strategy. Methods: We performed single-cell RNA sequencing (scRNA-seq) of the total non-cardiomyocytes and enriched Cd34-tdTomato+ lineage cells in the murine (male Cd34-CreERT2; Rosa26-tdTomato mice) pressure overload model (transverse aortic constriction, TAC), and total non-cardiomyocytes from human adult hearts. Then, in order to determine the origin of CD34+ cell that plays a role in myocardial fibrosis, bone marrow transplantation model was performed. Furthermore, to further clarify the role of CD34 + cells in myocardial remodeling in response to TAC injury, we generated Cd34-CreERT2; Rosa26-eGFP-DTA (Cre/DTA) mice. Results: By analyzing the transcriptomes of 59,505 single cells from the mouse heart and 22,537 single cells from the human heart, we illustrated the dynamics of cell landscape during the progression of heart hypertrophy, including CD34+ cells, fibroblasts, endothelial and immune cells. By combining genetic lineage tracing and bone marrow transplantation models, we demonstrated that non-bone-marrow-derived CD34+ cells give rise to fibroblasts and endothelial cells, while bone-marrow-derived CD34+ cell turned into immune cells only in response to pressure overload. Interestingly, partial depletion of CD34+ cells alleviated the severity of myocardial fibrosis with a significant improvement of cardiac function in Cd34-CreERT2; Rosa26-eGFP-DTA model. Similar changes of non-cardiomyocyte composition and cellular heterogeneity of heart failure were also observed in human patient with heart failure. Furthermore, immunostaining showed a double labeling of CD34 and fibroblast markers in human heart tissue. Mechanistically, our single-cell pseudotime analysis of scRNA-seq data and in vitro cell culture study revealed that Wnt-β-catenin and TGFβ1/Smad pathways are critical in regulating CD34+ cell differentiation toward fibroblasts. Conclusions: Our study provides a cellular landscape of CD34+ cell-derived cells in the hypertrophy heart of human and animal models, indicating that non-bone-marrow-derived CD34+ cells differentiating into fibroblasts largely account for cardiac fibrosis. These findings may provide novel insights for the pathogenesis of cardiac fibrosis and have further potential therapeutic implications for the heart failure. [ABSTRACT FROM AUTHOR]

Hyperbolic metamaterials can support extremely high‐k wavevectors, also known as volume plasmon polaritons, with highly directional propagation and light confinement to deep‐subwavelength scales. The number of high‐k modes has an inverse relationship with the overall thickness of hyperbolic metamaterials. Here, the optical spin textures from high‐k mode polaritons on the surface of silica–silver multilayer hyperbolic metamaterials are studied. The results demonstrate that with an increase in the overall thickness, the spin texture changes from a twisted structure to a Néel‐type photonic skyrmion, due to the decrease in the number of high‐k modes. Moreover, the size of a single photonic skyrmion is less than 1/2 of the light wavelength, and the full width at half maximum of the spin angular momentum is less than 1/9 of the light wavelength. This work is expected to facilitate new applications of hyperbolic metamaterials, such as spin‐dependent excitation and detection devices at the deep‐subwavelength level. [ABSTRACT FROM AUTHOR]

The ambiguous results of multiple CD34+ cell-based therapeutic trials for patients with heart disease have halted the large-scale application of stem/progenitor cell treatment. This study aimed to delineate the biological functions of heterogenous CD34+ cell populations and investigate the net effect of CD34+ cell intervention on cardiac remodeling. We confirmed, by combining single-cell RNA sequencing on human and mouse ischemic hearts and an inducible Cd34 lineage-tracing mouse model, that Cd34+ cells mainly contributed to the commitment of mesenchymal cells, endothelial cells (ECs), and monocytes/macrophages during heart remodeling with distinct pathological functions. The Cd34+-lineage-activated mesenchymal cells were responsible for cardiac fibrosis, while CD34+Sca-1high was an active precursor and intercellular player that facilitated Cd34+-lineage angiogenic EC-induced postinjury vessel development. We found through bone marrow transplantation that bone marrow-derived CD34+ cells only accounted for inflammatory response. We confirmed using a Cd34-CreERT2; R26-DTA mouse model that the depletion of Cd34+ cells could alleviate the severity of ventricular fibrosis after ischemia/reperfusion (I/R) injury with improved cardiac function. This study provided a transcriptional and cellular landscape of CD34+ cells in normal and ischemic hearts and illustrated that the heterogeneous population of Cd34+ cell-derived cells served as crucial contributors to cardiac remodeling and function after the I/R injury, with their capacity to generate diverse cellular lineages. [ABSTRACT FROM AUTHOR]

Rationale: CD34+ cells are believed being progenitors that may be used to treat cardiovascular disease. However, the exact identity and the role of CD34+ cells in physiological and pathological conditions remain unclear. Methods: We performed single-cell RNA sequencing analysis to provide a cell atlas of normal tissue/organ and pathological conditions. Furthermore, a genetic lineage tracing mouse model was used to investigate the role of CD34+ cells in angiogenesis and organ fibrosis. Results: Single-cell RNA sequencing analysis revealed a heterogeneous population of CD34+ cells in both physiological and pathological conditions. Using a genetic lineage tracing mouse model, we showed that CD34+ cells not only acquired endothelial cell fate involved in angiogenesis, but also, CD34+ cells expressing Pi16 may transform into myofibroblast and thus participate in organ fibrosis. Conclusion: A heterogeneous CD34+ cells serve as a contributor not only to endothelial regeneration but also a wound healing response that may provide therapeutic insights into fibrosis. [ABSTRACT FROM AUTHOR]

Mycoplasma hyopneumoniae is considered the major causative agent of porcine respiratory disease complex, occurs worldwide and causes major economic losses to the pig industry. To gain more insights into the pathogenesis of this organism, the high throughput cDNA microarray assays were employed to evaluate host responses of porcine alveolar macrophages to M. hyopneumoniae infection. A total of 1033 and 1235 differentially expressed genes were identified in porcine alveolar macrophages in responses to exposure to M. hyopneumoniae at 6 and 15 hours post infection, respectively. The differentially expressed genes were involved in many vital functional classes, including inflammatory response, immune response, apoptosis, cell adhesion, defense response, signal transduction, protein folding, protein ubiquitination and so on. The pathway analysis demonstrated that the most significant pathways were the chemokine signaling pathway, Toll-like receptor signaling pathway, RIG-I-like receptor signaling pathway, nucleotide-binding oligomerization domains (Nod)-like receptor signaling pathway and apoptosis signaling pathway. The reliability of the data obtained from the microarray was verified by performing quantitative real-time PCR. The expression kinetics of chemokines was further analyzed. The present study is the first to document the response of porcine alveolar macrophages to M. hyopneumoniae infection. The data further developed our understanding of the molecular pathogenesis of M. hyopneumoniae.