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Objective To explore the classification and changes of macrophage subsets in liver transplant rejection. Methods Rat liver transplantation model were established and divided into immune tolerance group (B-B), where the liver of BN rat donors was transplanted to BN rat recipients, and immune rejection group (L-B), in which the liver of Lewis rat donors was transplanted to BN rat recipients. Single-cell RNA sequencing and highthroughput RNA sequencing were used to distinguish the macrophage subsets of rat liver transplantation, and to find differential gene in rejection reactions. Immunohistochemistry was used to determine the changes and distribution of protein expression and cell subsets. Results CD68 positive macrophages were higher in the rejection group than that in the tolerance group (P < 0.05), and macrophages could be divided into 9 subsets. During the rejection reaction, the CXC chemokine ligand 9 (CXCL9) in the 8th subsets of macrophages was significantly increased, while the gene for white blood cell differentiation antigen 74 (CD74) in the 5th subsets was significantly increased (P < 0.05). CD74 ranked first in the differential gene synthesis of macrophages during rejection, followed by CXCL9. Compared with the tolerance group, a large number of CD74 positive macrophages were observed in the hepatic portal area of the rejection group, and the infiltration of CD74 positive macrophages in the hepatic sinuses was also significantly increased (P < 0.05), while a large number of CXCL9 positive macrophages were observed in the hepatic portal area and hepatic sinuses of the rejection group, especially in the portal area (P < 0.05), and CD14 positive cells were significantly increased (P < 0.05). Conclusions The CD74 positive macrophage subsets and CXCL9 positive macrophage subsets may be key subgroups in promoting liver transplant rejection, improving the mechanism of macrophage action in liver transplant rejection. [ABSTRACT FROM AUTHOR]

Building a comprehensive project-based curriculum based on the PBL teaching philosophy to meet the requirements of cultivating practical and comprehensive innovative talents in high-level, challenging, and innovative first-class courses in universities. Guided by STEAM and taking the course of "practice and innovation training based on ukulele" as an example, this paper designs the teaching objectives and content of PBL teaching, analyzes the corresponding teaching organization and teacher team construction according to the teaching characteristics, and conducts teaching research and practice. [ABSTRACT FROM AUTHOR]

Objective: To explore the genetic basis for 4 patients with globozoospermia., Methods: Semen and blood samples were collected from the patients for the determination of sperm concentration, viability, survival rate, morphology and acrosome antigen CD46. Meanwhile, DNA was extracted for whole exome sequencing (WES), and candidate variants were validated by Sanger sequencing., Results: All of the four patients were found to harbor variants of the DPY19L2 gene. Patients 1 ~ 3 had homozygous deletions of the DPY19L2 gene. Sanger sequencing confirmed that the DPY19L2 gene in patient 3 was disrupted at a recombination breakpoint area BP2, resulting in nonallelic homologous recombination and complete deletion of the DPY19L2 gene. Patients 2 and 3 respectively harbored novel homozygous deletions of exons 2 ~ 22 and exons 14 ~ 15. Patient 4 harbored heterozygous deletion of the DPY19L2 gene, in addition with a rare homozygous deletion of the 3' UTR region., Conclusion: DPY19L2 gene variants probably underlay the globozoospermia in the four patients, which has fit an autosomal recessive pattern of inheritance and the characteristics of genomic diseases.

Qi arrival is the meridian qi response to acupuncture stimulation. Through analyzing the relevant concepts of qi arrival and summarizing the general understanding of it in clinic and on the basis of the collection of the relevant literature at home and abroad on the determination of qi arrival and its strength, the characteristics are analyzed on the present method and the method for the determination of qi arrival and its strength is discussed in terms of the results in the needling sensation scale. It is believed that the needling sensation and its strength can be used to determine whether the qi is arrived or not and its strength. The components of different types of needling sensation are much better applicable for the analysis on the characteristics and rules on the influence on qi arrival. This method is in compliance not only with the theoretic connotation of qi arrival, but also with the clinical general understanding, which lays the foundation for the analysis on the scale results.

Objective: To screen for esophageal squamous cell carcinoma (ESCC)-associated long non-coding RNAs (lncRNA) and identify oncogenic lncRNA contributing to ESCC pathogenesis., Methods: A lncRNA array containing 7419 lncRNA was used to detect the transcriptional profiles of lncRNA of four pairs of ESCC and matched normal esophageal tissue. Bioinformatic analysis was employed to identify differentially expressed ESCC associated lncRNA (ESCCAL). Quantitative real-time PCR was used to verify selected dysregulated lncRNA on independent ESCC samples., Results: Genome-wide transcriptome profiling (coding and or noncoding RNA transcripts) was able to distinguish ESCC from normal tissue. Among these, bioinformatic analysis has identified 154 differentially expressed ESCC associated lncRNA (ESCCALs), which included 111 downregulated and 43 upregulated lncRNA in ESCC relative to the normal tissue (P< 0.01). The highest upregulated lncRNA (ESCCAL&#95;1) and known onco-lncRNA HOTAIR was further verified in 26 paired ESCC samples. ESCCAL&#95;1 and HOTAIR were found to be highly expressed in 17 ESCC and 18 ESCC compared with normal esophageal tissues., Conclusion: This investigation has revealed large scale aberrant expression of lncRNA in ESCC. About 70% of novel lncRNA-ESCCAL&#95;1, together with a known lncRNA-HOTAIR, are highly expressed in ESSC, suggesting that ESCCAL&#95;1 and HOTAIR may participate in the pathological process of ESCC. Furthermore, lncRNA could be potential diagnostic and prognostic biomarkers for ESCC.

Objective: To explore the effect of phosphorus, nitrogen on the production of microcystin under specific laboratory condition., Methods: The microcystis were ampliatively cultured for three times in N and P free culture. Then the microcysitis were inoculated in the culture at the concentrations of 0, 0.5, 1.0, 5.0 and 10.0 mg/L P for 20 days. The microcystis were inoculated in the BG-11 cultures at the concentrations of 0.05 mg/L and 5.0 mg/L P, NaNO3 were added in the culture according to the mol ratios of N/P were 5:1, 10:1, 20:1, 50:1, 100:1 and were cultured for 20 days. The changes of the count of the microcystis were observed. The microcystis cell were breaked at the 8th, 12th, 16th and 20th days after the beginning of culturing, the the microcystin were extracted and detected by HPLC., Results: When the concentrations of phosphorus were lower than 5.0 mg/L, The productions of microcystin increased with the phosphorus concentrations. But when the concentrations of phosphorus were 10.0 mg/L, the productions of microcystin significantly decreased. In the culture at the concentrations of 0.05 mg/L P, the microcystin concentration per cell (MCYST fg/cell) and the microcystin concentrations per milliliter (MCYST microg/ml culture) presented the greatest value when the N/P ratio was 50:1. But, In the culture at the concentrations of 5.0 mg/L P, the microcystin concentrations per cell (MCYST fg/cell) and the microcystin concentrations per milliliter (MCYST microg/ml culture) presented the greatest value when the N/P ratio was 20:1., Conclusion: P concentrations significantly incluence the production of microcystin. The P concentrations in water should be controlled through different way to control the production of microcystins.