Publications by authors named "Shunmei E"

Background: Bu-Shen-Huo-Xue (BSHX) decoction has been used in the postoperative rehabilitation of patients with spinal cord injury in China. In the present study, we aim to reveal the bioactive compounds in BSHX decoction and comprehensively explore the effects of BSHX decoction and the underlying mechanism in spinal cord injury recovery.

Methods: The main chemical constituents in BSHX decoction were determined by UPLC-MS/MS.

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Cartilage has a limited capacity to heal. Previously, we have shown that overexpression of Sox11 in rMSCs (Rat Mesenchymal Stem Cells) by lentivirus-mediated gene transfer leads to enhanced tri-lineage differentiation and accelerated bone formation in fracture model of rats. We observed that the fracture repair in the rats that received Sox11-modified rMSCs injection proceeded through an endochondral ossification process much faster than those in the control groups.

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Article Synopsis
  • Bacteria exposed to low doses of antibiotics, known as sub-minimal inhibitory concentrations (sub-MIC), can develop antibiotic resistance, but the exact mechanisms behind this are not fully understood.
  • In a study, researchers used a type of E. coli to see how sub-MIC levels of antibiotics Ciprofloxacin or Levofloxacin affected the transfer of plasmids (small DNA molecules) to Pseudomonas aeruginosa.
  • The results revealed that low doses of these antibiotics increased the transfer frequency of the plasmid, suggesting that sub-MIC conditions enhance gene expression related to plasmid transfer through mechanisms that do not rely on the bacterial SOS response.
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The effect of antibiotics on horizontal gene transfer (HGT) is controversial, and the underlying mechanism remains poorly understood. Here, using SM10λπ as the donor strain, which carries a chromosomally integrated RP4 plasmid, we investigated the effect of antibiotics on conjugational transfer of a mobilizable gentamicin (Gm) resistance plasmid. The results showed that an exposure to gentamicin that restricted the survival of recipient cells significantly enhanced SM10λπ- PAO1 conjugation, which was attenuated by a deficiency of , genes associated with the generation of the quorum sensing signals -acyl homoserine lactones (AHLs) in PAO1, or the deletion of the AHL receptor SdiA in SM10λπ.

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A taxonomic study was performed on strain SYSU D3-2T, isolated from coastal seawater near the estuary of Pearl River in southern China. The strain was observed to be Gram-reaction-negative, non-motile and non-spore-forming. Cells were found to be of coccobacilli shape.

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Conjugation is a key mechanism for horizontal gene transfer and plays an important role in bacterial evolution, especially with respect to antibiotic resistance. However, little is known about the role of donor and recipient cells in regulation of conjugation. Here, using an (λπ)- () conjugation model, we demonstrated that deficiency of /, genes associated with generation of the quorum sensing signals N-acyl homoserine lactones (AHLs) in , or deletion of the AHLs receptor SdiA in the donor λπ both facilitated conjugation.

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Grass carp (Ctenopharyngodon idella) is one of the most important species in China. Decabromodiphenyl ethane (DBDPE) is a brominated flame retardant that has been used widely in industry, and has been observed to accumulate in the tissues of fish from South China. Evidence has shown that DBDPE is toxic to aquatic animals, but the molecular response has been unclear.

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Pseudomonas aeruginosa is an opportunistic pathogen and a leading cause of nosocomial infections. Unfortunately, P. aeruginosa has low antibiotic susceptibility due to several chromosomally encoded antibiotic resistance genes.

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Article Synopsis
  • N-3-(Oxododecanoyl)-L-homoserine lactone (C12) is a bacterial signaling molecule from Pseudomonas aeruginosa that influences human immune responses without using TLR4 pathways.
  • C12-treated human dendritic cells (Mo-DCs) did not mature properly in response to lipopolysaccharide (LPS) and instead shifted to an immunosuppressive phenotype characterized by specific cytokine production changes.
  • The study reveals that C12 not only impairs the activation of Mo-DCs to stimulate T-cell proliferation but also promotes the formation of regulatory T-cells (iTregs), which can contribute to
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In mammalian cells, stress-induced expression of heat shock protein is controlled by heat shock factor 1 (HSF1). However, HSF1 functions as a regulator of additional genes. In this study, we observed that heat treatment effectively induced expression of Fas.

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Alpha-synuclein aggregation and cytotoxicity are widely considered to play a critical role in the process of Parkinson's disease. Heat shock proteins are a large family of cellular protective molecules in most kinds of cells. In this study, we examined the impact of dominant-positive heat shock transcription factor 1 (HSF1) on alpha-synuclein over-expression cellular model of Parkinson's disease.

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Macroautophagy is a regulated bulk degradation process of cellular components, mainly long-lived proteins or cytoplasmic organelles. Nutrient depletion is a classic inducer of macroautophagy. In this report, we have induced heat-mediated macroautophagy in several cell lines in the absence of nutrient depletion.

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Article Synopsis
  • - The study aimed to create immortalized embryonic fibroblast cell lines from both HSF1-deficient (HSF1-/-) and normal (HSF1+/+) mice to investigate the role of heat shock factor 1 (HSF1).
  • - Researchers used a specific vector to introduce SV40 large T antigen into the fibroblasts and confirmed successful integration and expression of this gene in both cell lines via various techniques.
  • - After six months of cultivation, the HSF1+/+ and HSF1-/- fibroblast lines displayed stable growth, but HSP70, a protein typically induced by heat shock, was not activated in the HSF1-/- cells.
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Objective: To observe the effect of heat shock factor 1 (HSF1) on heat stress-induced apoptosis in Raw264.7 macrophages.

Methods: Raw264.

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Objective: To determine the characteristics of a novel gene Mip5 (GenBank accession number AY553870) and its expression under physiological and pathological conditions.

Methods: The characteristics of Mip5 were analyzed by bioinformatic programs including BLAST, spidey, psort, ClustalW and so on. RT-PCR was performed to detect Mip5 expression.

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Objective: To observe the cleavage of nucleolin (C23) during apoptosis induced by oxidative stress and to clarify the effect of heat shock response (HSR) on the cleavage of nucleolin and its possible molecular mechanism.

Methods: We added 0.5 mmol/L peroxide hydrogen (H2O2 ) into cultured cells to mimic oxidative stress.

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Objective: To clarify the effect of nucleolin on the proliferation and apoptosis in C2C12 cells.

Methods: After inhibiting the expression of nucleolin using antisense oligonucleotides, the cellular proliferation was determined by MTT, and the apoptosis was detected by flow cytometry (FCM) assays and DNA ladder assays.

Results: After being transfected with antisense oligonucleotides for 24 hours, Western blotting showed that the expression of nucleolin was repressed significantly.

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