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With the progression of big data and cloud computing technologies, there has been an escalating trend in cross-institutional data sharing and interaction within the financial sector. However, the frequent occurrence of privacy breaches poses significant challenges to ensuring data security protection. This necessitates the elevation of requirements for identity authentication across data centers and other technologies related to data security management. The traditional centralized identity authentication schemes are inherently flawed in security and scalability, which hampers their ability to meet the demands of high-frequency cross-center data sharing applications. The blockchain technology has emerged as a potential solution, offering exceptional characteristics such as a distributed nature, tamper-proof properties, traceability, and the ability to achieve multi-party consensus. In practical application scenarios, it is essential to not only protect the privacy of user identities but also to effectively regulate anonymous identities. An anonymous and supervisable cross-data center identity authentication scheme based on blockchain was proposed. This scheme did not necessitate alterations to the original architecture of each data center. Instead, a distributed multi-center consortium blockchain was formed by leveraging more than one server from each data center to establish a data center union. Blockchain technology was utilized to ensure the transparency and reliability of the identity authentication process. Additionally, attribute signatures were employed to safeguard user identity privacy while simultaneously creating an identity mapping table that facilitated the tracking of real user identities. Consequently, the scheme was designed to protect user privacy during cross-data center identity authentication and to enable effective supervision over anonymous identities. A thorough security analysis and the results of experiments demonstrate that the proposed scheme possesses the following attributes: it does not require users to re-register, it exhibits characteristics of unforgeability and traceability, and it is capable of withstanding various network attacks, including replay attacks, denial of service attacks, tampering attacks, and man-in-the-middle attacks.

Musk secreted by male forest musk deer (Moschus berezovskii) musk glands is an invaluable component of medicine and perfume. Musk secretion depends on musk gland maturation; however, the mechanism of its development remains elusive. Herein, using single cell multiome ATAC + gene expression coupled with several bioinformatic analyses, a dynamic transcriptional cell atlas of musk gland development was revealed, and key genes and transcription factors affecting its development were determined. Twelve cell types, including two different types of acinar cells (Clusters 0 and 10) were identified. Single‐nucleus RNA and single‐nucleus ATAC sequencing analyses revealed that seven core target genes associated with musk secretion (Hsd17b2, Acacb, Lss, Vapa, Aldh16a1, Aldh7a1, and Sqle) were regulated by 12 core transcription factors (FOXO1, CUX2, RORA, RUNX1, KLF6, MGA, NFIC, FOXO3, ETV5, NR3C1, HSF4, and MITF) during the development of Cluster 0 acinar cells. Kyoto Encyclopedia of Genes and Genomes enrichment showed significant changes in the pathways associated with musk secretion during acinar cell development. Gene set variation analysis also revealed that certain pathways associated with musk secretion were enriched in 6‐year‐old acinar cells. A gene co‐expression network was constructed during acinar cell development to provide a precise understanding of the connections between transcription factors, genes, and pathways. Finally, intercellular communication analysis showed that intercellular communication is involved in musk gland development. This study provides crucial insights into the changes and key factors underlying musk gland development, which serve as valuable resources for studying musk secretion mechanisms and promoting the protection of this endangered species. [ABSTRACT FROM AUTHOR]

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The gut microbiota is closely associated with human health, and alterations in gut microbiota can influence various physiological and pathological activities in the human body. Therefore, microbiota regulation has become an important strategy in current disease treatment, albeit facing numerous challenges. Nanomaterials, owing to their excellent protective properties, drug release capabilities, targeting abilities, and good biocompatibility, have been widely developed and utilized in pharmaceuticals and dietary fields. In recent years, significant progress has been made in research on utilizing nanomaterials to assist in regulating gut microbiota for disease intervention. This review explores the latest advancements in the application of nanomaterials for microbiota regulation and offers insights into the future development of nanomaterials in modulating gut microbiota. [ABSTRACT FROM AUTHOR]

Musk is a scarce and precious medical resource secreted by male forest musk deer (FMD). Current research to promote musk secretion in FMD has used almost exclusively hormone injections, but this approach can be detrimental to the health of FMD. In order to conserve this endangered species as much as possible while increasing the production of musk, this study first used bioinformatics methods to predict the function of quercetin, a flavonoid that promotes testosterone (T) production and prevents late‐onset male hypogonadism. On the basis of good prediction effect, different concentrations of quercetin were added to the diet of FMD. The results showed that quercetin could change the levels of T, luteinizing hormone releasing hormone, luteinizing hormone, and estradiol, and regulate the structure of intestinal microorganisms and musk microorganisms of FMD. Moreover, there is a correlation among musk components, hormones, intestinal microorganisms, and musk microorganisms, which indicates that the production of musk may be regulated by these three at the same time, and the addition of quercetin with 800 mg per kg diet could significantly increase the yield of muscone (P < 0.05), the most effective ingredient in musk. In addition, quercetin decreased the high level of cortisol during musk secretion, which may relieve the stress on FMD in this process. This may help to protect the health of FMD. Combined with the results of software prediction, we finally proposed a possible mechanism for the complex process of musk secretion in FMD with a view to providing ideas for further studies. [ABSTRACT FROM AUTHOR]

Human immunodeficiency virus (HIV) infection is still a global public health issue, and the development of an effective prophylactic vaccine inducing potent neutralizing antibodies remains a significant challenge. This study aims to explore the inflammation‐related proteins associated with the neutralizing antibodies induced by the DNA/rTV vaccine. In this study, we employed the Olink chip to analyze the inflammation‐related proteins in plasma in healthy individuals receiving HIV candidate vaccine (DNA priming and recombinant vaccinia virus rTV boosting) and compared the differences between neutralizing antibody‐positive (nab +) and –negative(nab‐) groups. We identified 25 differentially expressed factors and conducted enrichment and correlation analysis on them. Our results revealed that significant expression differences in artemin (ARTN) and C‐C motif chemokine ligand 23 (CCL23) between nab+ and –nab‐ groups. Notably, the expression of CCL23 was negatively corelated to the ID50 of neutralizing antibodies and the intensity of the CD4+ T cell responses. This study enriches our understanding of the immune picture induced by the DNA/rTV vaccine, and provides insights for future HIV vaccine development. [ABSTRACT FROM AUTHOR]

To reduce energy consumption and save economic costs, waste-derived secondary resources can be considered as cement substitutes for emulsified asphalt. Considering emulsion type and red mud–based alkali-activated materials dosage and curing time, this study determined the feasibility of using red mud–based geopolymer to replace the commonly used cement in emulsified asphalt. Experimental tests, including pH tests, optical microscopy tests, dynamic shear rheological (DSR) tests, and Fourier-transform infrared (FTIR) spectroscopy tests were performed to characterize the rheological properties, interaction, and microstructure characteristic of red mud–based geopolymer emulsified asphalt composite binder (REACB). Cement emulsified asphalt composite binder (CEACB) was selected for comparison. The pH test and optical microscope tests demonstrated that the influence of red mud–based geopolymer on demulsification speed of stearyl trimethyl ammonium chloride (STAC) emulsion was greater than that of sodium dodecylbenzene sulfonate (SDBS) emulsion. The dynamic shear rheological test results showed that with the increase of curing time and red mud–based alkali-activated materials dosage, both the deformation resistance and the elastic recovery ability of REACB were improved, and the interaction ability between red mud–based geopolymer and SDBS emulsified asphalt gradually became stronger than that of STAC emulsified asphalt. Moreover, geopolymerization reactions in two kinds of REACB were proved using stretching vibration peaks of the asymmetric functional group T-O-Si. This study will promote the utilization of red mud–based aluminosilicate waste in emulsified asphalt. [ABSTRACT FROM AUTHOR]

Objective: The aim of this study was to investigate the molecular mechanism by which the transcription factor ETS1 regulates N‐myc downstream regulatory gene 1 (NDRG1) to provide a new theoretical basis for the study of oral squamous cell carcinoma (OSCC). Methods: In this study, eight human OSCC and paraneoplastic samples were collected. The expressions of NDRG1, ETS1, and Ki67 were detected by immunohistochemistry; apoptosis was detected by tdt‐mediated dUTP notched end labeling; cell migration and invasion were detected by Transwell; quantitative real‐time PCR was performed to detect the expression of NDRG1; RNA‐binding protein immunoprecipitation (RIP) assays detected NDRG1 expression; immunofluorescence assays detected ETS1 expression. Results: NDRG1 and ETS1 expression was significantly upregulated in cancer tissues and CAL‐27 and SCC‐6 cells. Knockdown of NDRG1 and ETS1 inhibited cell proliferation, migration, invasion, cloning, and EMT while promoting apoptosis and inhibited tumor development; ETS1 positively regulated NDRG1 expression; Finally, overexpression of NDRG1 in vivo and in vitro reversed the effect of ETS1 knockdown on CAL‐27 and SCC‐6 cells. Conclusions: ETS1 positively regulates the expression of NDRG1 and promotes OSCC. Therefore, ETS1 may serve as a new target for the clinical diagnosis and treatment of OSCC. [ABSTRACT FROM AUTHOR]