Forward Signal Research Articles

EphA4 mediates ephrinB1-dependent adhesion in retinal ganglion cells

Eph/ephrin signaling is crucial for organizing retinotopic maps in vertebrates. Unlike other EphAs, which are expressed in the embryonic ventral retina, EphA4 is found in the retinal ganglion cell (RGC) layer at perinatal stages, and its role in mammalian visual system development remains unclear. Using classicin vitrostripe assays, we demonstrate that, while RGC axons are repelled by ephrinB2, they grow on ephrinB1 stripes through EphA4-mediated adhesion. In vivo, retinal axons from EphA4-deficient mice from either sex show impaired arborization in the medial, but not lateral, regions of the superior colliculus that express ephrinB1. Gain-of-function experiments further reveal that ephrinB1-mediated adhesion depends on EphA4 tyrosine kinase activity but it is independent of its Sterile Alpha Motif. Together, our findings suggest that EphA4/ephrinB1 forward signaling likely facilitates adhesion between retinal axon terminals and cells in the medial colliculus, contributing to the establishment of proper connectivity within the visual system.Significance statementThe significance of our findings goes beyond unveiling the mechanisms underlying topographic visual map formation. By discovering a dual role for EphA4 in mediating both repulsion and adhesion, which challenges the conventional understanding of EphA4/ephrin interactions, this work opens up new avenues for exploring EphA4 broader implications in other cellular contexts, including cell differentiation, migration and synaptic plasticity.

Multifunctional and tunable bandpass filters with RF codesigned isolator and impedance matching capabilities

Abstract This paper presents the radio frequency (RF) design and experimental validation of a multifunctional bandpass filtering (BPF) concept with center frequency tunability and RF codesigned isolator and impedance matching functionality. The multifunctional bandpass filter/isolator (BPFI) concept combines frequency-tunable reciprocal resonators and nonreciprocal frequency-selective stages (NFSs) to realize center frequency tunability and fully directional transfer characteristics. The NFS, as the core component of the BPFI concept, exhibits frequency-selective transmission response in the forward direction and signal cancellation in the reverse direction. Its tunability is achieved by combining a transistor-based network with a tunable capacitively loaded coupled-line section. Furthermore, the NFS facilitates matching of different source loads allowing for the BPFIs to be used as reconfigurable matching networks. For experimental validation, an NFS and two BPFIs were designed, manufactured, and measured at L band. Their features include (i) NFS: center frequency tuning from 1.55 to 1.9 GHz with maximum directivity from 20 to 52 dB and gain from 0.3 to 1.3 dB. (ii) BPFI (topology A): center frequency tuning from 1.52 to 1.9 GHz with maximum directivity from 20 to 44 dB and gain from −1.5 to −0.5 dB. (iii) BPFI (topology C): ability to match complex loads with 26 + j18 Ω and 26 − j14 Ω.

Cell-cell contact-dependent secretion of large-extracellular vesicles from EFNBhigh cancer cells accelerates peritoneal dissemination.

Large non-apoptotic vesicles released from the plasma membrane protrusions are classified as large-EVs (LEVs). However, the triggers of LEV secretion and their functions in tumors remain unknown. Coculture system of cancer cells, peritoneal mesothelial cells (PMCs), and macrophages (MΦs) was conducted to observe cell-cell contact-mediated LEV secretion. Lineage tracing of PMCs was performed using Wt1CreERT2-tdTnu mice to explore the effects of LEVs on PMCs in vivo, and lymphangiogenesis was assessed by qRT-PCR and flow-cytometry. In peritoneal dissemination, cancer cells expressing Ephrin-B (EFNB) secreted LEVs upon the contact with PMCs expressing ephrin type-B (EphB) receptors, which degraded mesothelial barrier by augmenting mesothelial-mesenchymal transition. LEVs were incorporated in subpleural MΦs, and these MΦs transdifferentiated into lymphatic endothelial cells (LEC) and integrated into the lymphatic vessels. LEC differentiation was also induced in PMCs by interacting with LEV-treated MΦs, which promoted lymphangiogenesis. Mechanistically, activation of RhoA-ROCK pathway through EFNB reverse signaling induced LEV secretion. EFNBs on LEVs activated EphB forward signaling in PMC and MΦs, activating Akt, ERK and TGF-β1 pathway, which were indispensable for causing MMT and LEC differentiation. LEVs accelerated peritoneal dissemination and lymphatic invasions by cancer cells. Blocking of EFNBs on LEVs using EphB-Fc-fusion protein attenuated these events. EFNBhigh cancer cells scattered LEVs when they attached to PMCs, which augmented the local reactions of PMC and MΦ (MMT and lymphangiogenesis) and exaggerated peritoneal dissemination.

Heterogeneous Kinetics of Nanobubble Ultrasound Contrast Agent and Angiogenic Signaling in Head and Neck Cancer.

Recently developed nanobubble ultrasound contrast agents are a promising tool for imaging and drug delivery in tumors. To better understand their unusual kinetics, we implemented a novel pixel clustering analysis, which provides unique information by accounting for spatial heterogeneity. By combining ultrasound results with proteomics of the imaged tumors, we show that this analysis is highly predictive of protein expression and that specific types of nanobubble time-intensity curve are associated with upregulation of different metabolic pathways. We applied this method to study the effects of two proteins, EphB4 and ephrinB2, which control tumor angiogenesis through bidirectional juxtacrine signaling, in mouse models of head and neck cancer. We show that ephrinB2 expression by endothelial cells and EphB4 expression by cancer cells have similar effects on tumor vasculature, despite sometimes opposite effects on tumor growth. This implicates a cancer-cell-intrinsic effect of EphB4 forward signaling and not angiogenesis in EphB4's action as a tumor suppressor.

Neuregulin1 Nuclear Signaling Influences Adult Neurogenesis and Regulates a Schizophrenia Susceptibility Gene Network within the Mouse Dentate Gyrus.

Neuregulin1 (Nrg1) signaling is critical for neuronal development and function from fate specification to synaptic plasticity. Type III Nrg1 is a synaptic protein which engages in bidirectional signaling with its receptor ErbB4. Forward signaling engages ErbB4 phosphorylation, whereas back signaling engages two known mechanisms: (1) local axonal PI3K-AKT signaling and (2) cleavage by γ-secretase resulting in cytosolic release of the intracellular domain (ICD), which can traffic to the nucleus (Bao et al., 2003; Hancock et al., 2008). To dissect the contribution of these alternate signaling strategies to neuronal development, we generated a transgenic mouse with a missense mutation (V321L) in the Nrg1 transmembrane domain that disrupts nuclear back signaling with minimal effects on forward signaling or local back signaling and was previously found to be associated with psychosis (Walss-Bass et al., 2006). We combined RNA sequencing, retroviral fate mapping of neural stem cells, behavioral analyses, and various network analyses of transcriptomic data to investigate the effect of disrupting Nrg1 nuclear back signaling in the dentate gyrus (DG) of male and female mice. The V321L mutation impairs nuclear translocation of the Nrg1 ICD and alters gene expression in the DG. V321L mice show reduced stem cell proliferation, altered cell cycle dynamics, fate specification defects, and dendritic dysmorphogenesis. Orthologs of known schizophrenia (SCZ)-susceptibility genes were dysregulated in the V321L DG. These genes coordinated a larger network with other dysregulated genes. Weighted gene correlation network analysis and protein interaction network analyses revealed striking similarity between DG transcriptomes of V321L mouse and humans with SCZ.

Damage-related imbalance identification for UAV composite propeller blades based on bidirectional temporal convolutional network and a flexible sensing system

Abstract Damage to the composite propeller blades could lead to rotational imbalance, which seriously affects the operational safety of unmanned aerial vehicles (UAVs), therefore, a novel method combining the Teager energy operator (TEO) and bidirectional temporal convolutional network (BiTCN) is proposed for detecting, localizing, and quantifying the damage-related imbalance in the blades. A flexible sensing system that contains Micro electro mechanical sensor accelerometers, signal conditioning, and wireless transmission is integrated with the composite propeller for in-situ signal acquisition of the propeller blades. TEO is applied to demodulate and enhance the pulse compositions in vibration signals and singular value decomposition (SVD) is employed to suppress random noise, resulting in denoised Teager energy spectrums for model input. Temporal convolutional network (TCN) has been widely used in sequence signal modeling because the causal dilated convolution could learn the context information of sequence signals while maintaining the advantages of parallel computing. To fully extract the signal features, BiTCN models are established to learn both the forward and backward signal features. Experimental verification results show that the proposed method detects the existence of imbalance with 100% accuracy, and the accuracies of localization and quantization are 99.65% and 98.61%, respectively, which are much higher than those of the models with the original signal as input. In addition, compared with the other four different algorithms, BiTCN is superior in terms of convergence speed and prediction accuracy.

The intracellular domain of Sema6A is essential for development of the zebrafish retina.

Semaphorin6A (Sema6A) is a repulsive guidance molecule that plays many roles in central nervous system, heart and bone development, as well as immune system responses and cell signaling in cancer. Loss of Sema6A or its receptor PlexinA2 in zebrafish leads to smaller eyes and improper retinal patterning. Here, we investigate a potential role for the Sema6A intracellular domain in zebrafish eye development and dissect which phenotypes rely on forward signaling and which rely on reverse signaling. We performed rescue experiments on zebrafish Sema6A morphants with either full-length Sema6A (Sema6A-FL) or Sema6A lacking its intracellular domain (Sema6A-ΔC). We identified that the intracellular domain is not required for eye size and retinal patterning, however it is required for retinal integrity, the number and end feet strength of Müller glia and protecting against retinal cell death. This novel function for the intracellular domain suggests a role for Sema6A reverse signaling in zebrafish eye development.

EphB2 activation in neural stem cells in the basolateral amygdala facilitates neurogenesis and enhances long-term memory

Many brain diseases lead to a reduction in the number of functional neurons and it would be of value to be able to increase the number of neurons in the affected brain areas. In this study, we examined whether we can promote neural stem cells to produce mature neurons and whether an increase in the mature neurons can affect cognitive performance. We detected that the EphB2 receptor is localized in immature basolateral amygdala (BLA) neurons. We therefore aimed to increase the level of EphB2 activity in neural stem cells (NSCs) in the BLA and examine the effects on the production of mature neurons and cognition. Toward that end, we utilized a photoactivatable EphB2 construct (optoEphB2) to increase EphB2 forward signaling in NSCs in the BLA. We revealed that the activation of optoEphB2 in NSCs in the BLA increased the level of immature and mature neurons in the BLA. We further found that activation of optoEphB2 in BLA NSCs enhanced auditory, but not contextual, long-term fear memory formation. Impairing EphB2 forward signaling did not affect the level of immature and mature neurons in the BLA. This study provides evidence that NSCs can be promoted to produce mature neurons by activating EphB2 to enhance specific brain functions.

Ephrin Forward Signaling Controls Interspecies Cell Competition in Pluripotent Stem Cells.

In the animal kingdom, evolutionarily conserved mechanisms known as cell competition eliminate unfit cells during development. Interestingly, cell competition also leads to apoptosis of donor cells upon direct contact with host cells from a different species during interspecies chimera formation. The mechanisms underlying how host animal cells recognize and transmit cell death signals to adjacent xenogeneic human cells remain incompletely understood. In this study, we developed an interspecies cell contact reporter system to dissect the mechanisms underlying competitive interactions between mouse and human pluripotent stem cells (PSCs). Through single-cell RNA-seq analyses, we discovered that Ephrin A ligands in mouse cells play a crucial role in signaling cell death to adjacent human cells that express EPHA receptors during interspecies PSC co-culture. We also demonstrated that blocking the Ephrin A-EPHA receptor interaction pharmacologically, and inhibiting Ephrin forward signaling genetically in the mouse cells, enhances the survival of human PSCs and promotes chimera formation both in vitro and in vivo . Our findings elucidate key mechanisms of interspecies PSC competition during early embryogenesis and open new avenues for generating humanized tissues or organs in animals, potentially revolutionizing regenerative medicine.

Large-scale self-normalizing neural networks

Self-normalizing neural networks (SNN) regulate the activation and gradient flows through activation functions with the self-normalization property. As SNNs do not rely on norms computed from minibatches, they are more friendly to data parallelism, kernel fusion, and emerging architectures such as ReRAM-based accelerators. However, existing SNNs have mainly demonstrated their effectiveness on toy datasets and fall short in accuracy when dealing with large-scale tasks like ImageNet. They lack the strong normalization, regularization, and expression power required for wider, deeper models and larger-scale tasks. To enhance the normalization strength, this paper introduces a comprehensive and practical definition of the self-normalization property in terms of the stability and attractiveness of the statistical fixed points. It is comprehensive as it jointly considers all the fixed points used by existing studies: the first and second moment of forward activation and the expected Frobenius norm of backward gradient. The practicality comes from the analytical equations provided by our paper to assess the stability and attractiveness of each fixed point, which are derived from theoretical analysis of the forward and backward signals. The proposed definition is applied to a meta activation function inspired by prior research, leading to a stronger self-normalizing activation function named “bi-scaled exponential linear unit with backward standardized” (bSELU-BSTD). We provide both theoretical and empirical evidence to show that it is superior to existing studies. To enhance the regularization and expression power, we further propose scaled-Mixup and channel-wise scale & shift. With these three techniques, our approach achieves 75.23% top-1 accuracy on the ImageNet with Conv MobileNet V1, surpassing the performance of existing self-normalizing activation functions. To the best of our knowledge, this is the first SNN that achieves comparable accuracy to batch normalization on ImageNet.

EphB2 Receptor Promotes Dermal Fibrosis in Systemic Sclerosis.

Erythropoietin-producing hepatocellular (Eph)/Ephrin cell-cell signaling is emerging as a key player in tissue fibrogenesis. The aim of this study was to test the hypothesis that the receptor tyrosine kinase EphB2 mediates dermal fibrosis in systemic sclerosis (SSc). We assessed normal and SSc human skin biopsies for EphB2 expression. The in vivo role of EphB2 in skin fibrosis was investigated by subjecting EphB2-knockout mice to both bleomycin-induced and tight skin (Tsk1/+) genetic mouse models of skin fibrosis. EphB2 kinase-dead and overactive point mutant mice were used to evaluate the role of EphB2 forward signaling in bleomycin-induced dermal fibrosis. In vitro studies were performed on dermal fibroblasts from patients with SSc and healthy controls, which was followed by in vivo analysis of fibroblast-specific Ephb2-deficient mice. Expression of EphB2 is up-regulated in SSc skin tissue and explanted SSc dermal fibroblasts compared with healthy controls. EphB2 expression is elevated in two animal models of dermal fibrosis. In mice, EphB2 drives dermal fibrosis in both the bleomycin and the Tsk1/+ models of skin fibrosis. EphB2 forward signaling is a critical mediator of dermal fibrosis. Transforming growth factor-β (TGF-β) cytokines up-regulate EphB2 in dermal fibroblasts via noncanonical TGF-β/mother against decapentaplegic signaling, and silencing EPHB2 in human dermal fibroblasts is sufficient to dampen TGF-β-induced fibroblast-to-myofibroblast differentiation. Moreover, mice with fibroblast-specific deletion of EphB2 showed impaired fibroblast-to-myofibroblast differentiation and reduced skin fibrosis upon bleomycin challenge. Our data implicate TGF-β regulation of EphB2 overexpression and kinase-mediated forward signaling in the development of dermal fibrosis in SSc. EphB2 thus represents a potential new therapeutic target for SSc.

The role of glial and neuronal Eph/ephrin signaling in Drosophila mushroom body development and sleep and circadian behavior

The Eph receptor, a prototypically large receptor protein tyrosine kinase, interacts with ephrin ligands, forming a bidirectional signaling system that impacts diverse brain functions. Eph receptors and ephrins mediate forward and reverse signaling, affecting neurogenesis, axon guidance, and synaptic signaling. While mammalian studies have emphasized their roles in neurogenesis and synaptic plasticity, the Drosophila counterparts are less studied, especially in glial cells, despite structural similarities. Using RNAi to modulate Eph/ephrin expression in Drosophila neurons and glia, we studied their roles in brain development and sleep and circadian behavior. Knockdown of neuronal ephrin disrupted mushroom body development, while glial knockdown had minimal impact. Surprisingly, disrupting ephrin in neurons or glial cells altered sleep and circadian rhythms, indicating a direct involvement in these behaviors independent from developmental effects. Further analysis revealed distinct sleep phenotypes between neuronal and glial knockdowns, underscoring the intricate interplay within the neural circuits that govern behavior. Glia-specific knockdowns showed altered sleep patterns and reduced circadian rhythmicity, suggesting an intricate role of glia in sleep regulation. Our findings challenge simplistic models of Eph/ephrin signaling limited to neuron-glia communication and emphasize the complexity of the regulatory networks modulating behavior. Future investigations targeting specific glial subtypes will enhance our understanding of Eph/ephrin signaling's role in sleep regulation across species.

A Signal Matching Method of In-Orbit Calibration of Altimeter in Tracking Mode Based on Transponder

In this paper, a matching method for altimeter and transponder signals in Sub-optimal Maximum Likelihood Estimate (SMLE) tracking mode is proposed. In the in-orbit calibration of the altimeter in SMLE tracking mode using the reconstructive transponder, it is necessary to separate the forwarding signal from the ground echo signal. At the same time, the fluctuations in the received signal of the altimeter, which are caused by the forwarding signal of the transponder, can be eliminated. The transponder generates a bias when measuring the arrival time of the transmitting signal from the altimeter and embeds this bias in both the transponder-recorded data and the altimeter-recorded data. Therefore, the two sets of data have one-to-one correspondence, and they are superimposed using the sliding sum method. Moreover, the distance between the altimeter and the transponder is a parabolic geometric relationship, and the outliers are eliminated by the fitting error minimization decision, and the transponder signal is separated from the ground echo. The final altimeter transmitting–receiving signal path is obtained. Furthermore, the principles underlying this method can be used for any transponder that can adjust the response signal delay during calibration.

Abstract 6866: Investigating the role of Epha2 in breast cancer-mediated myeloid cell expansion and function

Abstract Bone metastases are present in over 70% of metastatic breast cancer patients, and current therapy reduces osteolysis in tumor-induced bone disease (TIBD) but does not improve overall survival. Frequently, TIBD is characterized by an increase in osteoclast proliferation and bone-resorbing activity, and patients often experience pain and pathologic fractures. Increased bone resorption releases growth factors that aid in the progression of tumor growth causing the ‘vicious cycle’. Additionally, bone metastatic patients are often resistant to first- and second-line therapies highlighting an importance for research in this area. The receptor tyrosine kinase, Ephrin-type-A 2 receptor (EphA2), participates in both forward and reverse signaling during receptor/ligand engagement and participates in many physiological and pathological processes, including bone homeostasis, immunity, and cancer. Interestingly, EphA2 is highly expressed in bone metastases, and previous evidence suggests that EphA2 can promote TIBD and reduce anti-tumor immunity. We therefore hypothesize that increased expression of EphA2 in breast cancer cells at the site of bone metastasis promotes expansion of myeloid cells, leading to TIBD. Previous data shows a reduction in osteoclast number and bone lesions following EphA2 knockout. However, the mechanism by which EphA2 mediates the expansion of osteoclasts is not well understood. In agreement with previous work, our data shows that EphA2 deletion in murine breast cancer (BC) cell line, 4T1, reduces bone lesion area and number and the presence of bone metastasis-associated macrophages. Additionally, we observed a significant reduction in Ly6Chi cells. To assess the effects of EphA2 deletion on the behavior of 4T1 cells, we conducted a wound healing assay and observed a decrease in wound healing capacity in 4T1 cells following EphA2 deletion. This suggests that EphA2 expression in 4T1 cells may increase their metastatic potential. We will repeat these studies and incorporate factors from the bone marrow. Our future studies will investigate the role of EphA2 signaling and reverse signaling in BC cell lines, myeloid progenitor cells, osteoclasts, and bone metastasis-associated macrophages. We will utilize murine and human BC cell lines to elucidate the effects of EphA2 deletion in BC on immune cell populations, bone metastasis, and tumor progression. Additionally, we will investigate how EphA2 reverse signaling impacts osteoclasts’ ability to modulate immune cells. We aim to reduce TIBD and tumor burden by reducing the expansion of osteoclasts and shifting the immune cells to an anti-tumorigenic phenotype. Our studies will provide additional insight into the underlying mechanisms of the vicious cycle which will offer new treatment strategies for patients with osteolytic breast cancer. Citation Format: Dominique Parker, Verra Ngwa, Jin Chen, Julie Rhoades. Investigating the role of Epha2 in breast cancer-mediated myeloid cell expansion and function [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 6866.

Time Delay Study of Ultrasonic Gas Flowmeters Based on VMD-Hilbert Spectrum and Cross-Correlation.

The accuracy of ultrasonic flowmeter time delay measurement is directly affected by the processing method of the ultrasonic echo signal. This paper proposes a method for estimating the time delay of the ultrasonic gas flowmeter based on the Variational Mode Decomposition (VMD)-Hilbert Spectrum and Cross-Correlation (CC). The method improves the accuracy of the ultrasonic gas flowmeter by enhancing the quality of the echo signal. To denoise forward and reverse ultrasonic echo signals collected at various wind speeds, a Butterworth filter is initially used. The ultrasonic echo signals are then analyzed by Empirical Mode De-composition (EMD) and VMD analysis to obtain the Intrinsic Mode Function (IMF) containing distinct center frequencies, respectively. The Hilbert spectrum time-frequency diagram is used to evaluate the results of the VMD and EMD decompositions. It is found that the IMF decomposed by VMD has a better filtering performance and better anti-interference performance. Therefore, the IMF with a better effect is selected for signal reconstruction. The ultrasonic time delay is then calculated using the Cross-Correlation algorithm. The self-developed ultrasonic gas flowmeter was tested on the experimental platform of the gas flow standard devices using this signal processing method. The results show a maximum indication error of 0.84% within the flow range of 60-606 m3/h, with a repeatability of no more than 0.29%. These results meet the 1-level accuracy requirements as outlined in the national ultrasonic flowmeters calibration regulation JJG1030-2007.

Sema6D forward signaling impairs T cell activation and proliferation in head and neck cancer.

Immune checkpoint inhibitors (ICIs) are indicated for a diverse range of cancer types, and characterizing the tumor immune microenvironment is critical for optimizing therapeutic strategies, including ICIs. T cell infiltration and activation status in the tumor microenvironment greatly affects the efficacy of ICIs. Here, we show that semaphorin 6D (Sema6D) forward signaling, which is reportedly involved in coordinating the orientation of cell development and migration as a guidance factor, impaired the infiltration and activation of tumor-specific CD8+ T cells in murine oral tumors. Sema6D expressed by nonhematopoietic cells was responsible for this phenotype. Plexin-A4, a receptor for Sema6D, inhibited T cell infiltration and partially suppressed CD8+ T cell activation and proliferation induced by Sema6D stimulation. Moreover, mouse oral tumors, which are resistant to PD-1-blocking treatment in wild-type mice, showed a response to the treatment in Sema6d-KO mice. Finally, analyses of public data sets of human head and neck squamous cell carcinoma, pan-cancer cohorts, and a retrospective cohort study showed that SEMA6D was mainly expressed by nonhematopoietic cells such as cancer cells, and SEMA6D expression was significantly negatively correlated with CD8A, PDCD1, IFNG, and GZMB expression. Thus, targeting Sema6D forward signaling is a promising option for increasing ICI efficacy.

Alzheimer's disease-associated P460L variant of EphA1 dysregulates receptor activity and blood-brain barrier function.

Genome-wide association studies link susceptibility to late-onset Alzheimer's disease (LOAD) with EphA1. Sequencing identified a non-synonymous substitution P460L as a LOAD risk variant. Other Ephs regulate vascular permeability and immune cell recruitment. We hypothesized that P460L dysregulates EphA1 receptor activity and impacts neuroinflammation. EphA1/P460L receptor activity was assayed in isogenic Human Embryonic Kidney (HEK) cells. Soluble EphA1/P460L (sEphA1/sP460L) reverse signaling in brain endothelial cells was assessed by T-cell recruitment and barrier function assays. EphA1 and P460L were expressed in HEK cells, but membrane and soluble P460L were significantly reduced. Ligand engagement induced Y781 phosphorylation of EphA1 but not P460L. sEphA1 primed brain endothelial cells for increased T-cell recruitment; however, sP460L was less effective. sEphA1 decreased the integrity of the brain endothelial barrier, while sP460L had no effect. These findings suggest that P460L alters EphA1-dependent forward and reverse signaling, which may impact blood-brain barrier function in LOAD. EphA1-dependent reverse signaling controls recruitment of T cells by brain endothelial cells. EphA1-dependent reverse signaling remodels brain endothelial cell contacts. LOAD-associated P460L variant of EphA1 shows reduced membrane expression and reduced ligand responses. LOAD-associated P460L variant of EphA1 fails to reverse signal to brain endothelial cells.

Cooperative Relaying in a Three User Downlink NOMA System Using Dynamic Power Allocation

Non-orthogonal multiple access (NOMA) represents the latest addition to the array of multiple access techniques, enabling simultaneous servicing of multiple users within a singular resource block in terms of time, frequency, and code. A typical NOMA configuration comprises a base station along with proximate and distant users. The proximity users experience more favorable channel conditions in contrast to distant users, resulting in a compromised performance for the latter due to the less favorable channel conditions. When cooperative communication is integrated with NOMA, the overall system performance, including spectral efficiency and capacity, is further elevated. This study introduces a cooperative NOMA setup in the downlink, involving three users, and employs dynamic power allocation (DPA). Within this framework, User 2 acts as a relay, functioning under the decode-and-forward protocol, forwarding signals to both User 1 and User 3. This arrangement aims to bolster the performance of the user positioned farthest from the base station, who is adversely affected by weaker channel conditions. Theoretical and simulation outcomes reveal enhancements within the system’s performance.

CD40L modulates CD4+ T-cell activation through receptor for activated C kinase 1.

Inhibition of the co-stimulatory ligand CD40L has shown beneficial effects in many experimental models of autoimmune disease and inflammation. Here, we show that CD40L deficiency in T cells in mice causes a reduction of CD4+ T-cell activation and specifically a strong reduction in IFN-γ-producing Th1 cells. In vitro, we could not reproduce this antigen presenting cell-dependent effects, but found that T-cell CD40L affects cell death and proliferation. We identified receptor of activated C kinase, the canonical PKC binding partner and known to drive proliferation and apoptosis, as a mediator of CD40L reverse signaling. Furthermore, we found that CD40L clustering stabilizes IFN-γ mediated Th1 polarization through STAT1, a known binding partner of receptor of activated C kinase. Together this highlights the importance of both CD40L forward and reverse signaling.

Robust free-space optical frequency transfer in time-varying link distances conditions

Future inter-satellite clock comparison on high orbit will require optical time and frequency transmission technology between moving objects. Here, we demonstrate robust optical frequency transmission under the condition of variable link distance. This variable link is accomplished by the relative motion of a single telescope fixed on the experimental platform to a corner-cube reflector (CCR) installed on a sliding guide. Two acousto–optic modulators with different frequencies are used to separate forward signal from backward signal. With active phase noise suppression, when the CCR moves back and forth at a constant velocity of 20 cm/s and an acceleration of 20 cm/s2, we achieve the best frequency stability of 1.9 × 10−16 at 1 s and 7.9 × 10−19 at 1000 s indoors. This work paves the way for future studying optical frequency transfer between ultra-high-orbit satellites.