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في مارس 1999 م، سن المجلس الوطني لنواب الشعب قانون العقود الخاص بجمهورية الصين الشعبية، ما يدل على أن التشريعات المدنية الصينية قد دخلت مرحلة النضج النظامي. ورغم أن تاريخ هذا القانون لا يتجاوز 20 عاما، إلا أنه يؤدي وظيفة مهمة في تعزيز تنمية اقتصاد السوق المحلي في الصين. ومع ذلك، فقد نشأت قضايا جديدة ساعدت على تطوير قانون العقود ومنحه حيوية متجددة، وكذلك ظهرت صعوبات أثناء تفسيره وتطبيقه. وفي هذا الإطار، تساعد ترجمة قانون العقود هذه الباحثين في القانون المدني الصيني والناشطين في الممارسة القضائية على التكيّف مع المواقف الجديدة ومعالجة القضايا الناتجة عنها.

‘Autophagy’ refers to an evolutionarily conserved process through which cellular contents, such as damaged organelles and protein aggregates, are delivered to lysosomes for degradation. Different forms of autophagy have been described on the basis of the nature of the cargoes and the means used to deliver them to lysosomes. At present, the prevailing categories of autophagy in mammalian cells are macroautophagy, microautophagy and chaperone-mediated autophagy. The molecular mechanisms and biological functions of macroautophagy and chaperone-mediated autophagy have been extensively studied, but microautophagy has received much less attention. In recent years, there has been a growth in research on microautophagy, first in yeast and then in mammalian cells. Here we review this form of autophagy, focusing on selective forms of microautophagy. We also discuss the upstream regulatory mechanisms, the crosstalk between macroautophagy and microautophagy, and the functional implications of microautophagy in diseases such as cancer and neurodegenerative disorders in humans. Future research into microautophagy will provide opportunities to develop novel interventional strategies for autophagy- and lysosome-related diseases.Microautophagy involves direct engulfment of cytoplasmic components, including proteins and organelles, by lysosomes and late endosomes for degradation. Although it is one of three main types of autophagy — along with macroautophagy and chaperone-mediated autophagy — its mechanisms and physiological roles have only recently begun to emerge.

Flexible organic−inorganic hybrids are promising thermoelectric materials to recycle waste heat in versatile formats. However, current organic/inorganic hybrids suffer from inferior thermoelectric properties due to aggregate nanostructures. Here we demonstrate flexible organic−inorganic hybrids where size-tunable Bi 2 Te 3 nanoparticles are discontinuously monodispersed in the continuous conductive polymer phase, completely distinct from traditional bi-continuous hybrids. Periodic nanofillers significantly scatter phonons while continuous conducting polymer phase provides favored electronic transport, resulting in ultrahigh power factor of ~1350 μW m −1  K −2 and ultralow in-plane thermal conductivity of ~0.7 W m −1  K −1 . Consequently, figure-of-merit (ZT) of 0.58 is obtained at room temperature, outperforming all reported organic materials and organic−inorganic hybrids. Thermoelectric properties of as-fabricated hybrids show negligible change for bending 100 cycles, indicating superior mechanical flexibility. These findings provide significant scientific foundation for shaping flexible thermoelectric functionality via synergistic integration of organic and inorganic components. The potential of flexible organic/inorganic hybrids for thermoelectrics is limited by the inability to control their microstructure. Here, the authors demonstrate polymer-nanoparticle hybrids with a monodispersed, periodic nanophase that shows high thermoelectric performance at room temperature.

Unprotected gradient exchange in federated learning (FL) systems may lead to gradient leakage-related attacks. CKKS is a promising approximate homomorphic encryption scheme to protect gradients, owing to its unique capability of performing operations directly on ciphertexts. However, configuring CKKS security parameters involves a trade-off between correctness, efficiency, and security. An evaluation gap exists regarding how these parameters impact computational performance. Additionally, the maximum vector length that CKKS can once encrypt, recommended by Homomorphic Encryption Standardization, is 16384, hampers its widespread adoption in FL when encrypting layers with numerous neurons. To protect gradients’ privacy in FL systems while maintaining practical performance, we comprehensively analyze the influence of security parameters such as polynomial modulus degree and coefficient modulus on homomorphic operations. Derived from our evaluation findings, we provide a method for selecting the optimal multiplication depth while meeting operational requirements. Then, we introduce an adaptive segmented encryption method tailored for CKKS, circumventing its encryption length constraint and enhancing its processing ability to encrypt neural network models. Finally, we present FedSHE , a privacy-preserving and efficient Fed erated learning scheme with adaptive S egmented CKKS H omomorphic E ncryption. FedSHE is implemented on top of the federated averaging (FedAvg) algorithm and is available at https://github.com/yooopan/FedSHE . Our evaluation results affirm the correctness and effectiveness of our proposed method, demonstrating that FedSHE outperforms existing homomorphic encryption-based federated learning research efforts in terms of model accuracy, computational efficiency, communication cost, and security level.

In the realm of cancer research, the tumor microenvironment (TME) plays a crucial role in tumor initiation and progression, shaped by complex interactions between cancer cells and surrounding non-cancerous cells. Cytokines, as essential immunomodulatory agents, are secreted by various cellular constituents within the TME, including immune cells, cancer-associated fibroblasts, and cancer cells themselves. These cytokines facilitate intricate communication networks that significantly influence tumor initiation, progression, metastasis, and immune suppression. Pyroptosis contributes to TME remodeling by promoting the release of pro-inflammatory cytokines and sustaining chronic inflammation, impacting processes such as immune escape and angiogenesis. However, challenges remain due to the complex interplay among cytokines, pyroptosis, and the TME, along with the dual effects of pyroptosis on cancer progression and therapy-related complications like cytokine release syndrome. Unraveling these complexities could facilitate strategies that balance inflammatory responses while minimizing tissue damage during therapy. This review delves into the complex crosstalk between cytokines, pyroptosis, and the TME, elucidating their contribution to tumor progression and metastasis. By synthesizing emerging therapeutic targets and innovative technologies concerning TME, this review aims to provide novel insights that could enhance treatment outcomes for cancer patients.

Iron oxide nanoparticles (IONPs) have transitioned from conventional magnetic resonance imaging (MRI) contrast agents into structurally programmable combined imaging/treatment tools, leveraging their superparamagnetism, catalytic activity, and surface engineering versatility to achieve spatiotemporal control over drug delivery and immune modulation. Advances in nanofabrication now yield size-optimized aggregates with enhanced tumor accumulation through the enhanced permeability and retention (EPR) effect, while clinically approved formulations like ferumoxytol demonstrate intrinsic immunomodulatory functionality, positioning IONPs as pivotal tools for precision oncology. Conversely, cancer immunotherapy remains limited by the immunosuppressive tumor microenvironment (TME), where cellular suppression via M2-polarized macrophages and regulatory T cells (Tregs) synergizes with physical exclusion from dense extracellular matrices and metabolic sabotage through lactate-driven acidosis. These barriers establish “immune-cold” phenotypes characterized by deficient CD8⁺ T-cell infiltration and tertiary lymphoid structure formation, driving checkpoint inhibitor resistance with sub-30% response rates in solid tumors. To overcome these constraints, IONPs orchestrate multimodal immunotherapeutic strategies: they reprogram suppressive niches by polarizing macrophages toward M1 phenotypes, activate STING pathways, and induce immunogenic ferroptosis; enable precision delivery via magnetic lymph node targeting and cancer cell membrane-mediated homologous tumor homing; and facilitate real-time theranostics through MRI/magnetic particle imaging (MPI)-monitored immune cell trafficking. Preclinical validation confirms synergistic efficacy, with combinatorial regimens achieving over 50% complete tumor regression by converting immunologically cold microenvironments into inflamed states. This review systematically explores cutting-edge IONP-based innovations—spanning immune cell engineering, biohybrid systems, and energy-amplified therapies—that bridge localized tumor eradication with systemic antitumor immunity, while critically evaluating translational barriers for clinical implementation. Graphical abstract

How soft corona, the protein corona’s outer layer, contributes to biological identity of nanomaterials is largely because capturing protein composition of the soft corona in situ remains challenging. We herein develop an in situ Fishing method that can monitor the dynamic formation of protein corona on ultra-small chiral Cu 2 S nanoparticles (NPs) allowing us to directly separate and identify the corona protein composition. Our method detects spatiotemporal processes in the evolution of hard and soft coronas on chiral NPs, revealing subtle differences in NP − protein interactions even within several minutes. This study highlights the importance of in situ and dynamic analysis of soft/hard corona, provides insights into the role of soft corona in mediating biological responses of NPs, and offers a universal strategy to characterize soft corona to guide the rational design of biomedical nanomaterials. Characterizing the soft protein corona on nanoparticles i.e. the outer layer of the corona, remains a longstanding challenge. Here, the authors develop an in situ method to monitor the dynamic processes of multilayered corona formation and evolution that offers a universal strategy to characterize the soft corona proteome.

The traditional anti-inflammation disease-modifying anti-rheumatic drugs (DMARDs) have limited therapeutic effects in rheumatoid arthritis (RA) patients. We previously reported the safety and efficacy of umbilical cord mesenchymal stem cell (UC-MSC) treatment in RA patients that were observed for up to 8 months after UC-MSC infusion. The aim of this study is to assess the long-term efficacy and safety of UC-MSC along with DMARDs for the treatment of RA. 64 RA patients aged 18-64 years were recruited in the study. During the treatment, patients were treated with 40 mL UC-MSC suspension product (2 × 10 cells/20 mL) via intravenous injection immediately after the infusion of 100 mL saline. The serological markers tests were used to assess safety and the 28-joint disease activity score (DAS28) and the Health Assessment Questionnaire (HAQ) to assess efficacy. 1 year and 3 years after UC-MSC cells treatment, the blood routine, liver and kidney function and immunoglobulin examination showed no abnormalities, which were all in the normal range. The ESR, CRP, RF of 1 year and 3 years after treatment and anti-CCP of 3 years after treatment were detected to be lower than that of pretreatment, which showed significant change (P < 0.05). Health index (HAQ) and joint function index (DAS28) decreased 1 year and 3 years after treatment than before treatment (P < 0.05). UC-MSC cells plus DMARDs therapy can be a safe, effective and feasible therapeutic option for RA patients.

Wearable thermoelectric devices, capable of converting body heat into electrical energy, provide the potential driving power for the Internet of Things, artificial intelligence, and soft robotics. However, critical parameters have long been overlooked for these practical applications. Here, we report a three-dimensional flexible thermoelectric device with a structure featuring an inner rigid and outer flexible woven design. Such a structure includes numerous small static air pockets that create a stable out-of-plane temperature difference, enabling precise temperature signal detection (accuracy up to 0.02 K). Particularly, this structure exhibits excellent multi-signal decoupling capability, excellent elasticity (>10,000 compression cycles), ultra-fast compression response (20 ms), stable output signal under 50% compressive strain, high breathability (1300 mm s −1 ), and washability. All these metrics achieve the highest values currently reported, fully meeting the requirements for body heat and moisture exchange, as demonstrated in our designed integrated smart mask and smart glove systems based on vector machine learning technology. This work shows that our three-dimensional flexible thermoelectric device has broad applicability in wearable electronics. Wearable thermoelectric devices are promising, though fabricating a breathable, sensitive, and washable devices has been a challenge. This report shows a woven thermoelectric fabric, incorporating rigid and flexible layers, for smart wearable devices.

Ding Ma, Hui Wang, Xun Xu and colleagues report a genome-wide map of HPV integration sites in cervical cancer samples and cell lines. In addition to discovering new integration hot spots, the authors identify microhomology-mediated DNA repair as a likely mechanism by which HPV integrates into the human genome. Human papillomavirus (HPV) integration is a key genetic event in cervical carcinogenesis 1 . By conducting whole-genome sequencing and high-throughput viral integration detection, we identified 3,667 HPV integration breakpoints in 26 cervical intraepithelial neoplasias, 104 cervical carcinomas and five cell lines. Beyond recalculating frequencies for the previously reported frequent integration sites POU5F1B (9.7%), FHIT (8.7%), KLF12 (7.8%), KLF5 (6.8%), LRP1B (5.8%) and LEPREL1 (4.9%), we discovered new hot spots HMGA2 (7.8%), DLG2 (4.9%) and SEMA3D (4.9%). Protein expression from FHIT and LRP1B was downregulated when HPV integrated in their introns. Protein expression from MYC and HMGA2 was elevated when HPV integrated into flanking regions. Moreover, microhomologous sequence between the human and HPV genomes was significantly enriched near integration breakpoints, indicating that fusion between viral and human DNA may have occurred by microhomology-mediated DNA repair pathways 2 . Our data provide insights into HPV integration-driven cervical carcinogenesis.