Publications by authors named "YiJun Wu"

Article Synopsis
  • LPC acts as a physiological substrate for neuropathy target esterase in mice, but the reasons behind the differing symptoms in mice versus humans exposed to neuropathic organophosphates are still unclear.
  • The study compares the effects of LPC on intracellular calcium levels in mouse N2a cells and human SH-SY5Y neuroblastoma cells, finding that N2a cells exhibit a larger increase in calcium levels.
  • The mechanisms for calcium increases differ between the two cell types: N2a cells show membrane permeability, while SH-SY5Y cells rely more on L-type calcium channels and intracellular calcium release, suggesting that varying responses may not explain symptom differences seen between species.
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  • NTE-related esterase (NRE) is similar to the neuropathy target esterase (NTE) and its function has been largely unexplored until now.
  • Research successfully cloned and expressed the mouse NRE gene, demonstrating that it exhibits esterase activity in mammalian cells, particularly localized in the cytoplasm.
  • Gene expression analysis revealed that NRE is more prevalent in the brain and testis compared to other tissues, providing new insights into its distribution and confirming its functional activity.
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To explore the changes of the endogenous phosphorylation of brainstem mitochondrial and synaptosomal proteins in adult hens dosed with tri-o-cresyl phosphate (TOCP) following the development of organophosphate-induced delayed neurotoxicity (OPIDN). Verapamil (7mg/(kgday), i.m.

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Genetically engineered Escherichia coli, expressing the fusion protein of enhanced green fluorescent protein (EGFP) and carboxylesterase B1 (CarE B1), was successfully constructed by cloning the genes into the pET-28b vector and then transforming E. coli BL21 (DE3). Expression of the fusion protein was induced in E.

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Neuropathy target esterase (NTE) was originally identified as the primary target site of those organophosphorus compounds that induce delayed neuropathy in human and some animals. Here we examined the role of protein kinase C (PKC) in the regulation of the NTE activity in mammalian cells. Six-hour exposure of human neuroblastoma SK-N-SH cell to a PKC activator phorbol 12-myristate 13-acetate (PMA) decreased the activity of NTE, and this effect was blocked by the PKC inhibitor staurosporine.

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The residual level and dissipation rate of triazophos in wheat crops and the soil in which they were grown were determined by gas chromatography (GC). Maximum final residues of triazophos in wheat grain, stems and leaves, and soil were 1.865, 44.

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Lysophosphatidylcholine (LPC) is an important bioactive lipid. In the nervous system, elevated levels of LPC have been shown to produce demyelination. In the present study, we examined the effect of exogenous LPC on intracellular Ca2+ mobilization in human neuroblastoma SH-SY5Y cells.

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Article Synopsis
  • Neuropathy target esterase (NTE) is crucial for nerve development and is a key target of organophosphate compounds that lead to delayed neuropathy, characterized by nerve axon degeneration.
  • Researchers identified that Gbeta2 and Gbeta2-like I subunits can bind to the C-terminal of NTE, implying a potential regulatory role.
  • Experiments showed that reducing Gbeta2 levels through RNA interference decreased NTE activity without affecting its expression, indicating that Gbeta2 may be essential for maintaining NTE function.
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  • Cytoskeletal components are crucial for maintaining cell structure and function, influencing cell shape, division, and processes like neurite extension.
  • Exposure to tri-ocresyl phosphate (TOCP) for 12 hours resulted in a dose-dependent decrease in viability of neuroblastoma SK-N-SH cells, with high concentrations (5 mM) reducing viability to about 50%.
  • At these higher concentrations, TOCP inhibited key neurofilament and microtubule-associated proteins while altering neurite length and microfilament structure, indicating that cytoskeletal disruption is an early sign of TOCP toxicity in these cells.
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Article Synopsis
  • - The study aimed to create an RNA interference vector to express the human neuropathy target esterase (NTE) gene in mammalian cells.
  • - Researchers cloned an insert with a promoter and multiple cloning sites into a vector (pSUPER/neo), followed by ligating oligos that target NTE, leading to the creation of the pSUPER/neo-NTE vector, which was then introduced into specific cell types.
  • - The resulting vector successfully inhibited NTE activity in mammalian cells, demonstrating that a stable expression vector for double-stranded RNA of NTE was effectively constructed.
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Objective: To investigate the correlative factors of weight gain in very low birth weight infants (VLBW).

Methods: Fifty-one cases of VLBW from July 1998 to March 2004 were analyzed retrospectively.

Results: Twenty two cases were small for gestational age (SGA) and 29 cases were appropriate for gestational age (AGA).

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Carbamate esters are widely used as pesticides and can cause neurotoxicity in humans and animals; the exact mechanism is still unclear. In the present investigation, the effects of carbamates at sublethal concentration on neurite outgrowth and cytoskeleton as well as activities of acetylcholinesterase (AChE) and neuropathy target esterase (NTE) in differentiating human SK-N-SH neuroblastoma cells were studied. The results showed that 50 microM of either aldicarb or carbaryl significantly decreased neurite length in the retinoic acid-induced differentiation of the neuroblastoma cells, compared to cells treated with vehicle.

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Neuropathy target esterase (NTE) is inhibited and aged by organophosphorus compounds that induce delayed neuropathy in human and some sensitive animals. NTE has been proposed to play a role in neurite outgrowth and process elongation during neurodifferentiation. However, to date, there is no direct evidence of the relevance of NTE in neurodifferentiation under physiological conditions.

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Aim: To investigate the expression of cyclooxygenase-2 (COX-2) in gastric cancer and its relation with the liver metastasis and prognosis.

Methods: Expression of COX-2 mRNA and protein was examined in gastric cancer and its paired substantial normal tissue by semi-quantitative reverse transcription-polymerase chain reaction and immunohistochemistry. The relation between COX-2 expression and prognosis was investigated in 195 cases.

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Neuropathy target esterase (NTE) is phosphorylated and aged by oraganophosphorus compounds (OP) that induce delayed neuropathy in human and some animals. NTE has been proposed to play a role in neurite outgrowth and process elongation during neural differentiation. However, to date, there is no direct evidence of the relevance of NTE in neural differentiation under physiological conditions.

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Aim: Ischemia/reperfusion (I/R) injury is one of the major obstacles for intestinal transplantation (ITx). Urinary trypsin inhibitor (Ulinastatin, UTI) suppresses proteases and stabilizes lysosomal membranes. We supposed that Ulinastatin would diminish I/R injury of intestinal graft.

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To construct a hepatic stellate cells (HSCs) subtracted cDNA library to find differentially expressed genes in normal mice and mice infected with Schistosoma japonicum (S. japonicum). Suppression subtractive hybridization (SSH) was used.

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Article Synopsis
  • The study investigates how organophosphates (OPs) affect human neuroblastoma cells, focusing on their cytotoxic effects and delayed neurotoxicity.
  • At low concentrations, methamidophos increased cell proliferation but inhibited it at higher levels, while TOCP primarily inhibited cell growth and calcium uptake at high concentrations.
  • The findings suggest that OPs may disrupt nerve cell growth and calcium balance, contributing to their neurotoxic effects.
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Objective: To explore the effect of organophosphorus insecticides (OPs) on the nicotinic autoreceptor function (NAF) in rat cortical synaptosomes and to understand alternative target of the OPs for human and other animals.

Methods: In vitro experiment, synaptosomes from the rats were incubated with [(3)H] choline and then superfused with physiological buffer. The [(3)H] acetylcholine release from the synaptosomes after the addition of paraoxon or chlorpyrifos to the superfusion system was recorded and the changes of NAF were calculated.

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Article Synopsis
  • The study aimed to enhance the hamster-to-rat liver xenotransplant technique to reduce complications and to assess the effects of multiglycosides tripterygium wilfordii (T(II)) on immune rejection.
  • A total of 112 liver transplants were performed, with 30 cases randomly split into control and T(II) groups to measure survival and analyze liver tissue for rejection signs.
  • Results showed an 80% successful operation rate, with similar survival times for both groups, but the T(II) group experienced significantly less hyperemia and milder rejection than the control group, indicating that T(II) has some protective effects even though it did not extend survival.
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p73, a p53 family member, is highly similar to p53 in both structure and function. Like p53, the p73 protein contains an N-terminal activation domain, a DNA-binding domain, a tetramerization domain, and several PXXP motifs. Previously, we and others have shown that some functional domains in p53, such as the DNA-binding and tetramerization domains, are required for inducing both cell cycle arrest and apoptosis whereas others, such as the second activation domain, the proline-rich domain, and the C-terminal basic domain, are only required for inducing apoptosis.

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Acetylcholine (ACh) release is modulated pre-synaptically by both muscarinic and nicotinic receptor-mediated processes. While muscarinic autoreceptors inhibit ACh release, nicotinic autoreceptors enhance ACh release and thus disruption of these processes could potentially affect cholinergic toxicity following exposure to anticholinesterases. Marked age-related differences in sensitivity to some organophosphorus (OP) anticholinesterases have been reported.

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The Burkholderia cepacia complex consists of at least five well-documented bacterial genomovars, each of which has been isolated from the sputum of different patients with cystic fibrosis (CF). Although the world-wide prevalence of this opportunist pathogen in CF patients is low (1-3%), 'epidemic' clusters occur in geographically isolated regions. Prevalence in some of these clusters is as high as 30-40%.

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