259 research outputs found
Optimization of Location-Routing for the Waste Household Appliances Recycling Logistics under the Uncertain Condition
Waste household appliances and electronic products usually contain harmful substances which need scientific and reasonable collection, classification, processing, recovery and disposal to achieve sustainable and effective recycling and utilization. In recent years, due to the poor management of waste household appliances recycling logistics system, safety accidents occur frequently, which seriously harm the health and life safety of the society. This paper studies the risk management of recycling waste household appliances under uncertain conditions and establishes a risk measurement model under fuzzy population density. Considering the multi-stage and classification diversity of waste household appliances recycling logistics, the multi-objective location routing model and location - routing model are established respectively. Based on the model complexity analysis, the solution method of multi-objective model is designed. Finally, the validity of the model and algorithm is verified by examples and tests
Identifying Subgroups of ICU Patients Using End-to-End Multivariate Time-Series Clustering Algorithm Based on Real-World Vital Signs Data
This study employed the MIMIC-IV database as data source to investigate the
use of dynamic, high-frequency, multivariate time-series vital signs data,
including temperature, heart rate, mean blood pressure, respiratory rate, and
SpO2, monitored first 8 hours data in the ICU stay. Various clustering
algorithms were compared, and an end-to-end multivariate time series clustering
system called Time2Feat, combined with K-Means, was chosen as the most
effective method to cluster patients in the ICU. In clustering analysis, data
of 8,080 patients admitted between 2008 and 2016 was used for model development
and 2,038 patients admitted between 2017 and 2019 for model validation. By
analyzing the differences in clinical mortality prognosis among different
categories, varying risks of ICU mortality and hospital mortality were found
between different subgroups. Furthermore, the study visualized the trajectory
of vital signs changes. The findings of this study provide valuable insights
into the potential use of multivariate time-series clustering systems in
patient management and monitoring in the ICU setting.Comment: Proceedings of Beijing Health Data Science Summit (HDSS) 202
Meta-optimized Joint Generative and Contrastive Learning for Sequential Recommendation
Sequential Recommendation (SR) has received increasing attention due to its
ability to capture user dynamic preferences. Recently, Contrastive Learning
(CL) provides an effective approach for sequential recommendation by learning
invariance from different views of an input. However, most existing data or
model augmentation methods may destroy semantic sequential interaction
characteristics and often rely on the hand-crafted property of their
contrastive view-generation strategies. In this paper, we propose a
Meta-optimized Seq2Seq Generator and Contrastive Learning (Meta-SGCL) for
sequential recommendation, which applies the meta-optimized two-step training
strategy to adaptive generate contrastive views. Specifically, Meta-SGCL first
introduces a simple yet effective augmentation method called
Sequence-to-Sequence (Seq2Seq) generator, which treats the Variational
AutoEncoders (VAE) as the view generator and can constitute contrastive views
while preserving the original sequence's semantics. Next, the model employs a
meta-optimized two-step training strategy, which aims to adaptively generate
contrastive views without relying on manually designed view-generation
techniques. Finally, we evaluate our proposed method Meta-SGCL using three
public real-world datasets. Compared with the state-of-the-art methods, our
experimental results demonstrate the effectiveness of our model and the code is
available
Topographical distribution of blubber in finless porpoises (Neophocaena asiaeorientalis sunameri): a result from adapting to living in coastal waters
Background: Blubber has many functions, among which energy storage, thermoregulation, buoyancy, and hydrodynamic streamlining are the most frequently cited. Within and between taxa, variations in its structure and distribution likely reflect different adaptations of a species to its life history requirements, environment, health, and function. Here, we use ultrasound to describe the distribution of blubber in the finless porpoise (Neophocaena asiaeorientalis sunameri) based on examinations of 34 fresh cadavers recovered as accidental fisheries bycatch
Time Course of Gene Expression Profiling in the Liver of Experimental Mice Infected with Echinococcus multilocularis
BACKGROUND: Alveolar echinococcosis (AE) is a severe chronic parasitic disease which behaves like a slow-growing liver cancer. Clinical observations suggest that the parasite, Echinococcus multilocularis (E. multilocularis) influences liver homeostasis and hepatic cell metabolism. However, this has never been analyzed during the time course of infection in the common model of secondary echinococcosis in experimental mice. METHODOLOGY/PRINCIPAL FINDINGS: Gene expression profiles were assessed using DNA microarray analysis, 1, 2, 3 and 6 months after injection of E. multilocularis metacestode in the liver of susceptible mice. Data were collected at different time points to monitor the dynamic behavior of gene expression. 557 differentially expressed genes were identified at one or more time points, including 351 up-regulated and 228 down-regulated genes. Time-course analysis indicated, at the initial stage of E. multilocularis infection (month 1-2), that most of up-regulated pathways were related to immune processes and cell trafficking such as chemokine-, mitogen-activated protein kinase (MAPK) signaling, and down-regulated pathways were related to xenobiotic metabolism; at the middle stage (month 3), MAPK signaling pathway was maintained and peroxisome proliferator-activated receptor (PPAR) signaling pathway emerged; at the late stage (month 6), most of up-regulated pathways were related to PPAR signaling pathway, complement and coagulation cascades, while down-regulated pathways were related to metabolism of xenobiotics by cytochrome P450. Quantitative RT-PCR analysis of a random selection of 19 genes confirmed the reliability of the microarray data. Immunohistochemistry analysis showed that proliferating cell nuclear antigen (PCNA) was increased in the liver of E. multilocularis infected mice from 2 months to 6 months. CONCLUSIONS: E. multilocularis metacestode definitely exerts a deep influence on liver homeostasis, by modifying a number of gene expression and metabolic pathways. It especially promotes hepatic cell proliferation, as evidenced by the increased PCNA constantly found in all the experimental time-points we studied and by an increased gene expression of key metabolic pathways
Angiotensin (1–7) reverses glucose-induced islet β cell dedifferentiation by Wnt/β-catenin/FoxO1 signalling pathway
Introduction: Recent studies have shown that a decline in islet β cells quality is due to β-cell dedifferentiation, not only β-cell apoptosis. Angiotensin (1–7) [Ang(1-7)] could attenuate high glucose-induced apoptosis and dedifferentiation of pancreatic β cells by combining with MAS receptors. However, the mechanism of such action has not been elucidated. Recent studies have revealed that Wnt/β-catenin and forkhead box transcription factor O1 (FoxO1) are associated with β-cell dedifferentiation. Our study aims to explore whether the effects of Ang(1-7)on islet b cell dedifferentiation are mediated through the Wnt/β-catenin/FoxO1 pathway.
Material and methods: Islet β cells were divided into 6 groups: a control group, a high-glucose group, high glucose with Ang(1-7) group, high-glucose with Ang(1-7) and A779 group, high-glucose with angiotensin(1-7) and CHIR99021 group, and high-glucose with CHIR99021 group. A779 is a kind of MAS receptor antagonist that blocks the action of Ang(1-7), and CHIR99021 is a Wnt pathway activator. The morphology of pancreatic β cells was observed in each group after 48 hours of intervention. β-cell insulin secretory function and expressions of relevant factors were measured.
Results: Compared with the control group, the cell morphology became degraded in the high-glucose group and the capability of insulin secretion was reduced. Meanwhile, the expressions of mature β cells markers [pancreatic and duodenal homeobox 1 (Pdx1) and MAF BZIP transcription factor A (MafA)] were reduced, while the expressions of endocrine progenitor cells makers [octamer-binding transcription factor 4 (Oct4) and Nanog] were increased. The addition of CHIR99021 resulted in profound deep destruction of β cells compared with the high-glucose group. However, such changes were dramatically reversed following the treatment of Ang(1-7). The addition of A779 significantly inhibited the improvement caused by Ang(1-7).
Conclusion: Ang(1-7) can effectively reverse β cell dedifferentiation through Wnt/β-catenin/FoxO1 pathway. It might be a new strategy for preventing and treating diabetes
Evolution of regulatory signatures in primate cortical neurons at cell-type resolution
The human cerebral cortex contains many cell types that likely underwent independent functional changes during evolution. However, cell-type-specific regulatory landscapes in the cortex remain largely unexplored. Here we report epigenomic and transcriptomic analyses of the two main cortical neuronal subtypes, glutamatergic projection neurons and GABAergic interneurons, in human, chimpanzee, and rhesus macaque. Using genome-wide profiling of the H3K27ac histone modification, we identify neuron-subtype-specific regulatory elements that previously went undetected in bulk brain tissue samples. Human-specific regulatory changes are uncovered in multiple genes, including those associated with language, autism spectrum disorder, and drug addiction. We observe preferential evolutionary divergence in neuron subtype-specific regulatory elements and show that a substantial fraction of pan-neuronal regulatory elements undergoes subtype-specific evolutionary changes. This study sheds light on the interplay between regulatory evolution and cell-type-dependent gene-expression programs, and provides a resource for further exploration of human brain evolution and function
A MicroRNA-7 Binding Site Polymorphism in HOXB5 Leads to Differential Gene Expression in Bladder Cancer
PURPOSE: To investigate the biological function of HOXB5 in human bladder cancer and explore whether the HOXB5 3'-UTR SNP (1010A/G), which is located within the microRNA-7 binding site, was correlated with clinical features of bladder cancer. METHODS: Expression of HOXB5 in 35 human bladder cancer tissues and 8 cell lines were examined using real-time PCR and immunohistochemistry. Next, we explored the biological function of HOXB5 in vitro using cell proliferation, migration and colony formation assays. Using bioinformatics, a SNP (1010A/G) was found located within the microRNA-7 binding site in the 3'-UTR of HOXB5. Real-time PCR was used to test HOXB5 expression affected by different alleles. Finally, multivariate logistic regression analysis was used to determine the relationship between SNP (1010A/G) frequency and clinical features in 391 cases. RESULTS: HOXB5 was frequently over-expressed both in bladder cancer tissues and cell lines. Inhibition of HOXB5 suppressed the oncogenic function of cancer cells. Next, we demonstrated that a SNP (1010A/G), located within the microRNA-7 binding site in the 3'-UTR of HOXB5, could affect HOXB5 expression in bladder cancer mainly by differential binding activity of microRNA-7 and SNP-related mRNA stability. Finally, we also showed the frequency of 1010G genotype was higher in cancer group compared to normal controls and correlated with the risk of high grade and high stage. CONCLUSION: HOXB5 is overexpressed in bladder cancer. A miRNA-binding SNP (1010A/G) located within 3'-UTR of HOXB5 is associated with gene expression and may be a promising prognostic factor for bladder cancer
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