Electronic origin of spin-phonon coupling effect in transition-metal perovskites

By applying Wannier-based extended Kugel-Khomskii model, we carry out first-principles calculations and electronic structure analysis to understand the spin-phonon coupling effect in transition-metal perovskites. We demonstrate the successful application of our approach to SrMnO$_3$ and BiFeO$_3$. We show that both the electron orbitals under crystal field splitting and the electronic configuration should be taken into account in order to understand the large variances of spin-phonon coupling effects among various phonon modes as well as in different materials.Comment: 5 pages, 1 figur

A Generic Minimal Discrete Model for Toroidal Moments and Its Experimental Realization

It is well known that a closed loop of magnetic dipoles can give rise to the rather elusive toroidal moment. However, artificial structures required to generate the necessary magnetic moments are typically optically large, complex to make and easily compromised by the kinetic inductance at high frequencies. Instead of using magnetic dipoles, we propose a minimal model based on just three aligned discrete electric dipoles in which the occurrence of resonant toroidal modes is guaranteed by symmetry. The advantage of this model is its simplicity and the same model supports toroidal moments from the microwave regime up to optical frequencies as exemplified by a three-antenna array and a system consisting of three nano-sized plasmonic particles. Both the microwave and high-frequency configurations exhibit non-radiating "anapoles". Experiments in the microwave regime confirm the theoretical predictions.Comment: 21 pages, 6 figure

The transcriptional coactivator TAZ regulates reciprocal differentiation of T(h)17 cells and T(reg) cells

自身免疫性疾病是一类机体对自身抗原发生免疫反应而导致自身多器官、组织受累的慢性炎症性疾病。目前大量研究表明机体内促炎症的TH17细胞和抑制炎症Treg细胞在类群数量和活化状态的失衡是造成自身免疫疾病的主要致病因素。陈兰芬教授和周大旺教授团队的前期研究发现小鼠中Hippo信号通路中激酶Mst1/2缺失导致免疫缺陷，机体易受病原体感染并伴随着严重自身免疫疾病。该研究揭示了Hippo 信号通路转录共激活因子TAZ在决定CD4+初始T细胞分化为促进炎症的TH17效应细胞和抑制免疫反应的Treg调节性细胞过程中发挥着关键作用，拓展了当前对于Hippo信号通路的相关研究内容。 陈兰芬，博士，厦门大学生命科学学院教授。【Abstraact】An imbalance in the lineages of immunosuppressive regulatory T cells (Treg cells) and the inflammatory TH17 subset of helper T cells leads to the development of autoimmune and/or inflammatory disease. Here we found that TAZ, a coactivator of TEAD transcription factors of Hippo signaling, was expressed under T H17 cell–inducing conditions and was required for TH17 differentiation and TH17 cell–mediated inflammatory diseases. TAZ was a critical co-activator of the TH17-defining transcription factor RORγt. In addition, TAZ attenuated Treg cell development by decreasing acetylation of the Treg cell master regulator Foxp3 mediated by the histone acetyltransferase Tip60, which targeted Foxp3 for proteasomal degradation. In contrast, under T regcell–skewing conditions, TEAD1 expression and sequestration of TAZ from the transcription factors RORγt and Foxp3 promoted Treg cell differentiation. Furthermore, deficiency in TAZ or overexpression of TEAD1 induced Treg cell differentiation, whereas expression of a transgene encoding TAZ or activation of TAZ directed TH17 cell differentiation. Our results demonstrate a pivotal role for TAZ in regulating the differentiation of Treg cells and TH17 cells.J. Avruch for comments on the manuscript.Supported by the National Basic Research Program (973) of China (2015CB910502 to L.C.), the National Natural Science Foundation of China (81422018 to L.C.; 31625010 and U1505224 to D.Z.; U1405225 and 81372617 to L.C.; J1310027 to D.Z.; 81472229 to L.H.; and 31600698 to J. Geng), the 111 Projects (B12001 and B06016), China's 1000 Young Talents Program (D.Z., and L.C.), the Fundamental Research Funds for the Central Universities of China-Xiamen University (20720160071 to D.Z. and 20720160054 to L.H.) and Major disease research projects of Xiamen (3502Z20149029 to L.C.)

Enhancing motion forecasting of ship sailing in irregular waves based on optimized LSTM model and principal component of wave-height

Irregular waves exhibit complex and erratic behavior, posing significant challenges for accurate short-term ship motion forecasting. Reliable ship navigation depends on precise motion predictions, necessitating effective feature extraction from wave data to enhance predictive models. This study proposes a hybrid model integrating a wavelet principal component analysis (WPCA) for dimensionality reduction with an optimized double circulation-long short-term memory (DC-LSTM) network. The WPCA method retains key variance components, reducing redundant data while preserving critical wave characteristics. The DC-LSTM model is optimized using both internal and external circulation mechanisms to enhance learning efficiency and stability. Numerical simulation data are used to train and validate the model. Compared with conventional LSTM and PCA-LSTM models, the proposed WPCA-DC-LSTM model improves R2 by 14% and reduces RMSE by 12% in validation datasets. The model demonstrates robust generalization, effectively capturing nonlinear and high-dimensional wave features. The results indicate that the hybrid model effectively mitigates the influence of redundant data, reduces prediction randomness, and improves stability in handling wave-induced ship movements. The study highlights the broad applicability of the WPCA-DC-LSTM model for complex maritime data analysis and ship motion forecasting

Hippo Signaling Suppresses Cell Ploidy and Tumorigenesis through Skp2

大多数真核生物的体细胞是二倍体，即仅含有两组染色体，分别遗传自父本和母本。而一些特定组织如心脏、肝脏等就含有多倍体细胞，特别是肝脏组织含有较高比例的四、八倍体等多倍体细胞。肝脏是人体的重要解毒器官，同时酒精、肝炎病毒等毒性物质或毒性代谢物容易诱发肝细胞的基因突变，多倍体被认为有利于提供代偿性的正常基因来维持肝脏稳态。然而肝脏受损后，多倍体细胞将会受胁迫进行增殖，再生修复受损的肝组织。因此研究机体调控多倍体细胞产生及多倍体细胞进行细胞分裂的调控机理对于理解肝癌的发病机理和肝癌的治疗至关重要。Hippo信号通路在调节组织成体干细胞的分化和增殖，调控器官再生与尺寸大小中具有重要作用。深入研究发现, Hippo信号通路下游效应分子YAP通过AKT-SKP2信号促进二倍体细胞向多倍体转化及多倍体细胞的生长增殖。本项研究阐明了Hippo缺失及YAP激活促进多倍体细胞产生及增殖作为肝癌发生发展中的一个重要机制，为肝癌诊疗提供了新的策略。 周大旺，博士，厦门大学生命科学学院教授、副院长、国家杰出青年基金获得者。【Abstract】Polyploidy can lead to aneuploidy and tumorigenesis. Here, we report that the Hippo pathway effector Yap promotes the diploid-polyploid conversion and polyploid cell growth through the Akt-Skp2 axis. Yap strongly induces the acetyltransferase p300-mediated acetylation of the E3 ligase Skp2 via Akt signaling. Acetylated Skp2 is exclusively localized to the cytosol, which causes hyper-accumulation of the cyclin-dependent kinase inhibitor p27, leading to mitotic arrest and subsequently cell polyploidy. In addition, the pro-apoptotic factors FoxO1/3 are overly degraded by acetylated Skp2, resulting in polyploid cell division, genomic instability, and oncogenesis. importantly, the depletion or inactivation of Akt or Skp2 abrogated Hippo signal deficiency-induced liver tumorigenesis, indicating their epistatic interaction. Thus, we conclude that Hippo-Yap signaling suppresses cell polyploidy and oncogenesis through Skp2.该研究工作获得了国家自然科学基金委、国家重点基础研究发展计划(973)项目、青年千人计划和中央高校基本科研基金的资助。 The Yap (S127A) transgenic mice were kindly provided by Dr. Fernando Camargo from Harvard Medical School, Boston, MA. D.Z. and L.C. were supported by the National Natural Science Foundation of China (31625010,U1505224, and J1310027 to D.Z.; 81422018, U1405225, and 81372617 to L.C.; 81472229 to L.H.), the National Basic Research Program (973) of China (2015CB910502 to L.C.), the Fundamental Research Funds for the Central Universities of China-Xiamen University (20720140551 to L.C. and 2013121034 and 20720140537 to D.Z.)

Λ(t)\Lambda(t)CDM Model as a Unified Origin of Holographic and Agegraphic Dark Energy Models

Motivated by the fact that any nonzero $\Lambda$ can introduce a length scale or a time scale into Einstein's theory, $r_{\Lambda}=ct_{\Lambda}=\sqrt{3/|\Lambda|}$. Conversely, any cosmological length scale or time scale can introduce a $\Lambda (t)$, $\Lambda(t)=3/r^2_{\Lambda}(t)=3/(c^2t^2_{\Lambda}(t))$. In this letter, we investigate the time varying $\Lambda(t)$ corresponding to the length scales, including the Hubble horizon, the particle horizon and the future event horizon, and the time scales, including the age of the universe and the conformal time. It is found out that, in this scenario, the $\Lambda(t)$CDM model can be taken as the unified origin of the holographic and agegraphic dark energy models with interaction between the matter and the dark energy, where the interacting term is determined by $Q=-\dot{\rho}_{\Lambda}$. We place observational constraints on the $\Lambda(t)$CDM models originating from different cosmological length scales and time scales with the recently compiled "Union2 compilation" which consists of 557 Type Ia supernovae (SNIa) covering a redshift range $0.015\leq z \leq 1.4$. In conclusion, an accelerating expansion universe can be derived in the cases taking the Hubble horizon, the future event horizon, the age of the universe and the conformal time as the length scale or the time scale.Comment: 13 pages, 6 figures. Accepted for publication in PL