A Novel Approach to Evaluating Crosstalk for Near-Infrared Spectrometers.

Multi-channel and multi-parameter near-infrared spectroscopy (NIRS) has gradually become a new research direction and hot spot due to its ability to provide real-time, continuous, comprehensive indicators of multiple parameters. However, multi-channel and multi-parameter detection may lead to crosstalk between signals. There is still a lack of benchmarks for the evaluation of the reliability, sensitivity, stability and response consistency of the NIRS instruments. In this study, a set of test methods (a human blood model test, ink drop test, multi-channel crosstalk test and multi-parameter crosstalk test) for analyzing crosstalk and verifying the reliability of NIRS was conducted to test experimental verification on a multi-channel (8-channel), multi-parameter (4-parameter) NIRS instrument independently developed by our team. Results show that these tests can be used to analyze the signal crosstalk and verify the reliability, sensitivity, stability and response consistency of the NIRS instrument. This study contributes to the establishment of benchmarks for the NIRS instrument crosstalk and reliability testing. These novel tests have the potential to become the benchmark for NIRS instrument reliability testing.

An Enhanced Hidden Markov Map Matching Model for Floating Car Data.

The map matching (MM) model plays an important role in revising the locations of floating car data (FCD) on a digital map. However, most existing MM models have multiple shortcomings, such as a low matching accuracy for complex roads, long running times, an inability to take full advantage of historical FCD information, and challenges in maintaining the topological adjacency and obeying traffic rules. To address these issues, an enhanced hidden Markov map matching (EHMM) model is proposed by adopting explicit topological expressions, using historical FCD information and introducing traffic rules. The EHMM model was validated against areal ground dataset at various sampling intervals and compared with the spatial and temporal matching model and the ordinary hidden Markov matching model. The empirical results reveal that the matching accuracy of the EHMM model is significantly higher than that of the reference models regarding real FCD trajectories at medium and high sampling rates. The running time of the EHMM model was notably shorter than those of the reference models. The matching results of the EHMM model retained topological adjacency and complied with traffic regulations better than the reference models.

IL-6 Released from Hepatic Stellate Cells Promotes Glycolysis and Migration of HCC Through the JAK1/vWF/TGFB1 Axis.

Purpose: The crosstalk between hepatocellular carcinoma (HCC) cells and hepatic stellate cells (HSCs) is one of the important mechanisms of liver cancer metastasis. The relationship between liver cancer metastasis and glycolysis has been extensively studied recently. However, the role of von Willebrand factor (vWF) mediated glycolysis mechanism in liver cancer metastasis is currently unknown. Methods: Western blot was used to verify the expression of vWF in HCC cells. PAS staining, glycogen and L-lactate content assays were used to reflect cellular glycolysis levels. The ability of cell migration was explored by Wound-healing and Transwell assays. Besides, the effect of vWF on the progression of HCC in vivo was also studied using subcutaneous xenograft model. Results: vWF derived from HCC cells promoted tumor migration by mediating glycolysis. Besides, vWF participated in the crosstalk between HCC cells and HSCs. HCC cells activated HSCs through vWF-mediated TGFB1 expression and secretion, and activated HSCs upregulated vWF expression in HCC cells through IL-6 secretion feedback. Further, in vitro and in vivo experiments also confirmed the importance of the JAK1/vWF/TGFB1 axis in regulating HSCs-derived IL-6 mediated HCC migration and growth. Conclusion: In summary, this article demonstrated that IL-6 released from hepatic stellate cells enhanced glycolysis and migration ability of liver cancer cells by activating JAK1/vWF/TGFB1 axis which may also be a potential target for inhibiting liver cancer metastasis.

[Study on the transmission of drug resistant human immunodeficiency virus-1 in Henan province].

OBJECTIVE: To survey the prevalence of HIV-1 drug resistance after five years antiretroviral treatment in Henan province. METHODS: Through the cross-sectional study, serum specimens of 69 HIV infected individuals that were 2 to 25 years old who were newly diagnosed according the WHO standard from November 2007 to August 2008 and did not receive antiretroviral treatment (ART) were collected. HIV-1 pol genetic mutations associated with drug resistance were identified with RT-PCR and interpreted. RESULTS: Out of 69 samples, 50 samples were successfully amplified and sequenced. Seven drug resistant mutation in reverse transcriptase region were detected and three mutations in protein region. In one specimen, a mutation (K103N) in reverse transcriptase was identified which caused high level resistance to NNRTIs, but no proteinase inhibitor mutation was found in protein region. According to the sampling and threshold surveillance criteria, the prevalence of drug resistant HIV-1 in Henan was less than 5%. CONCLUSION: The prevalence of drug resistant HIV-1 was still at low level in Henan. However, the proportion of resistant strains would be higher with the antiretroviral treatment. We should pay more attention to the transmission of resistant strains and continue the drug resistance surveillance.