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1.
Korean J Parasitol ; 59(4): 427-432, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34470096

ABSTRACT

The infection status of zoonotic trematode metacercariae (ZTM) was investigated in total 568 freshwater fishes (19 species) from the irrigation canal of Togyo-jeosuji (Reservoir) in Cheorwon-gun, Gangwon-do, the Republic of Korea for 3 years (2018-2020). All fishes were examined using the artificial digestion method. The metacercariae of Clonorchis sinensis (CsMc) were detected in 180 (43.8%) out of 411 fish of positive species, and their infection intensity was 38 per fish infected (PFI). Especially, in 2 fish species, i.e., Pseudorasbora parva and Puntungia herzi, the prevalence was 82.1% and 31.3%, and the infection intensity with CsMc was 88 and 290 PFI, respectively. Metagonimus spp. metacercariae (MsMc) were found in 403 (74.1%) out of 544 fish of positive species, and their infection intensity was 62 PFI. In the pale chub, Zacco platypus, the prevalence of MsMc was 98.6%, and their infection intensity was 144 PFI. Centrocestus armatus metacercariae were detected in 171 (38.9%) out of 440 fish of positive species, and their infection intensity was 1,844 PFI. Echinostoma spp. metacercariae were found in 94 (19.6%) out of 479 fish of positive species, and their infection intensity was 3 PFI. Metorchis orientalis metacercariae were detected in 43 (29.3%) out of 147 fish of positive species, and their infection intensity was 4 PFI. By the present study, it has been confirmed that some species of ZTM, including CsMc and MsMc, are prevalent in fishes from the irrigation canal of Togyo-jeosuji in Cheorwon-gun, Gangwon-do, Korea.


Subject(s)
Fish Diseases , Trematoda , Trematode Infections , Animals , Fish Diseases/epidemiology , Fishes , Metacercariae , Republic of Korea/epidemiology , Trematode Infections/epidemiology , Trematode Infections/veterinary
2.
Psychopathology ; 48(3): 137-44, 2015.
Article in English | MEDLINE | ID: mdl-25831960

ABSTRACT

BACKGROUND: Patients with panic disorder have higher rates of suicide than the general population. Among panic disorder subjects, early onset, female gender, alcohol abuse, and mood disorder increase the risk of suicidality. However, less is known about the unique relationships between discrete DSM-IV panic symptoms and higher suicidality. Therefore, in the current study we examined the panic symptom profile that is associated with higher suicidality in a sample of outpatients with panic disorder. METHODS: This cross-sectional study included 427 patients diagnosed with current panic disorder on the basis of the DSM-IV-TR. In order to assess the contribution of the clinical variables, a univariate logistic regression was carried out examining the relationships between the demographic variables, suicidality from the suicide module of the Korean version of the MINI International Neuropsychiatric Interview Plus, and DSM-IV panic symptoms. Additionally, a multivariate logistic regression was performed to identify specific panic symptoms that were significant risk factors for suicidality among patients with current panic disorder. RESULTS: We found that 74 (17.33%) panic disorder patients experienced high suicidality. Univariate analyses showed that high suicidality was significantly associated with a younger age (OR = 13.66; 95% CI 2.68-69.70), comorbid depressive disorders (OR = 4.57; 95% CI 2.57-8.11), and the following panic symptoms: palpitations (OR = 2.20; 95% CI 0.90-5.35), trembling (OR = 0.61; 95% CI 0.362-1.18), nausea or abdominal distress (OR = 1.77; 95% CI 0.96-3.27), fear of losing control or going crazy (OR = 2.18; 95% CI 1.12-4.23), and paresthesia (OR = 1.57; 95% CI 0.83-2.98). Multivariate logistic regression analyses demonstrated that specific panic symptoms, such as palpitations (adjusted OR = 2.69; 95% CI 1.08-6.73) and fear of losing control or going crazy (adjusted OR = 2.28; 95% CI 1.21-4.31), were related to suicidality after controlling for confounding factors. CONCLUSION: Some panic symptoms (e.g. palpitations and fear of losing control or going crazy) are associated with a risk of suicidality among patients with panic disorder. A priori identification of high-risk suicidal subjects could lead to effective treatment strategies for panic disorder.


Subject(s)
Panic Disorder/psychology , Suicide/psychology , Suicide/statistics & numerical data , Adolescent , Adult , Age Factors , Alcoholism/epidemiology , Alcoholism/psychology , Child , Comorbidity , Cross-Sectional Studies , Depressive Disorder/epidemiology , Depressive Disorder/psychology , Diagnostic and Statistical Manual of Mental Disorders , Fear , Female , Humans , Interview, Psychological , Logistic Models , Male , Middle Aged , Odds Ratio , Outpatients/psychology , Outpatients/statistics & numerical data , Panic Disorder/physiopathology , Republic of Korea/epidemiology , Risk Assessment , Risk Factors , Suicidal Ideation , Surveys and Questionnaires
3.
Arch Virol ; 156(5): 887-92, 2011 May.
Article in English | MEDLINE | ID: mdl-21234769

ABSTRACT

Among 312 rotavirus-positive samples collected from eight hospitals across South Korea during 2008 and 2009, the most prevalent circulating G genotype was G1 (35.9%), followed by G3 (24.7%), G2 (17.0%), G4 (7.7%), and G9 (2.6%). Notably, one unusual G11 lineage III strain-the first hypoendemic infection case in the world-was found. Of the P genotypes, P[8] (43.9%) was the most common, followed by P[6] (29.5%), P[4] (9.3%) and P[9] (0.6%). Determining G- and P-type combinations showed that G1P[8] was the most prevalent (20.5%), followed by G2P[6] (12.8%) and G3P[8] (12.8%). These findings provide new information concerning the current prevalence and spread of the rare G11 rotavirus.


Subject(s)
Diarrhea/epidemiology , Diarrhea/virology , Rotavirus Infections/epidemiology , Rotavirus Infections/virology , Rotavirus/classification , Rotavirus/genetics , Child, Preschool , Cluster Analysis , Genotype , Humans , Infant , Infant, Newborn , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , RNA, Viral/genetics , Republic of Korea/epidemiology , Rotavirus/isolation & purification , Sequence Analysis, DNA
4.
Plant Mol Biol ; 68(3): 263-75, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18587653

ABSTRACT

Recombinant proteins have been previously synthesized in a transgenic rice cell suspension culture system with the rice amylase 3D promoter, which can be induced via sugar starvation. However, the secreted recombinant proteins have been shown to be rapidly decreased as the result of proteolytic degradation occurring during prolonged incubation. The secreted proteases were identified via two-dimensional electrophoresis (2-DE) and ESI/Q-TOF mass spectrometry analyses. The internal amino acid sequences of 8 of 37 spots corresponded to cysteine proteinase (CysP), which is encoded for by Rep1 and EP3A. This result shows that CysP is a major secreted protease in rice cell suspension cultures following induction via sugar starvation. Intron-containing self-complementary hairpin RNA (ihpRNA)-mediated post-transcriptional gene silencing (PTGS) was applied to suppress the expression of CysP in rice cell suspension cultures. The reduction of rice CysP mRNA and the detection of siRNA specific to CysP, an initiator of RNAi, were verified via Northern blot analysis and RNase protection assays, respectively, thereby indicating that PTGS operated successfully in this system. The analysis of total secreted protease and CysP activities evidenced lower activity than was observed with the wild-type. Furthermore, suspension cultures of rice cells transformed with both hGM-CSF and the gene expressing the ihpRNA of CysP evidenced a reduction in total protease and CysP activities, and an up to 1.9-fold improvement in hGM-CSF production as compared to that observed in a rice cell line expressing hGM-CSF only. These results demonstrate the feasibility of the suppression of CysP via RNA interference to reduce protease activity and to increase target protein accumulation in rice cell suspension cultures.


Subject(s)
Cysteine Endopeptidases/genetics , Cysteine Endopeptidases/metabolism , Granulocyte-Macrophage Colony-Stimulating Factor/biosynthesis , Oryza/genetics , RNA Interference , Electrophoresis, Gel, Two-Dimensional , Gene Expression Regulation, Plant , Genetic Vectors/genetics , Granulocyte-Macrophage Colony-Stimulating Factor/genetics , Humans , Oryza/metabolism , Plants, Genetically Modified , RNA, Messenger/genetics , Recombinant Proteins
5.
Mol Cells ; 22(1): 70-7, 2006 Aug 31.
Article in English | MEDLINE | ID: mdl-16951553

ABSTRACT

Platelets are anucleate cytoplasmic fragments derived from bone marrow megakaryocytes, and endothelial cells constitute the barrier between bloodstream and adjacent tissues. Although platelets are thought to regulate the biological functions of endothelial cells, the molecular mechanisms involved are poorly understood. With human umbilical vein endothelial cells and freshly isolated platelets, we established an in vitro model of platelet-induced endothelial cell proliferation. Platelets stimulated endothelial cell proliferation in a dose-dependent manner and transwell experiments with semi-permeable membranes suggested that direct cell-to-cell contacts were required. We developed mAbs against platelets and selected a mAb that blocks their proliferative effect. We purified the antigen by immunoprecipitation and identified it by Q-TOF MS analysis as the tetraspanin CD9. Since both platelets and endothelial cells expressed CD9 strongly on their surfaces we carried out a pre-treatment experiment that showed that CD9 molecules on the endothelial cells participate in the mitogenic effect of the platelets. The inhibitory effect of our mAb was comparable to that of a well-known functional anti-CD9 mAb. These results suggest that the tetraspanin CD9 plays an important role in endothelial regeneration.


Subject(s)
Antibodies, Monoclonal/immunology , Antigens, CD/physiology , Blood Platelets/physiology , Cell Proliferation/drug effects , Endothelium, Vascular/cytology , Membrane Glycoproteins/physiology , Antigens, CD/immunology , Coculture Techniques , Endothelium, Vascular/drug effects , Humans , Membrane Glycoproteins/immunology , Tetraspanin 29
6.
J Immunol ; 175(3): 1658-64, 2005 Aug 01.
Article in English | MEDLINE | ID: mdl-16034106

ABSTRACT

Stromal cells in the lymphoid organs provide a microenvironment where lymphocytes undergo various biological processes such as development, homing, clonal expansion, and differentiation. Follicular dendritic cells (FDCs) in the primary and secondary follicles of the peripheral lymphoid tissues interact with lymphocytes by contacting directly or producing diffusible molecules. To understand the biological role of human FDC at the molecular level, we developed a mAb, 3C8, that recognizes FDC but not bone marrow-derived cells. Through expression cloning and proteome analysis, we identified the protein that is recognized by 3C8 mAb, which revealed that FDC expresses prostacyclin synthase. The 3C8 protein purified from FDC-like cells indeed displayed the enzymatic activity of prostacyclin synthase and converted PGH2 into prostacyclin. In addition, prostacyclin significantly inhibited proliferation of T cells but delayed their spontaneous apoptosis. These findings may help explain why T cells constitute only a minor population compared with B cells in the germinal center.


Subject(s)
Cell Proliferation , Cytochrome P-450 Enzyme System/biosynthesis , Dendritic Cells, Follicular/enzymology , Dendritic Cells, Follicular/immunology , Intramolecular Oxidoreductases/biosynthesis , Lymphocyte Count , T-Lymphocyte Subsets/cytology , Amino Acid Sequence , Apoptosis/drug effects , Apoptosis/immunology , Cell Line , Cell Proliferation/drug effects , Cell Survival/drug effects , Cell Survival/immunology , Cells, Cultured , Cloning, Molecular , Cytochrome P-450 Enzyme System/isolation & purification , Epoprostenol/analogs & derivatives , Epoprostenol/pharmacology , Germinal Center/cytology , Germinal Center/enzymology , Germinal Center/immunology , Growth Inhibitors/pharmacology , Humans , Intramolecular Oxidoreductases/isolation & purification , Molecular Sequence Data , T-Lymphocyte Subsets/enzymology , T-Lymphocyte Subsets/immunology
7.
Exp Mol Med ; 35(4): 310-6, 2003 Aug 31.
Article in English | MEDLINE | ID: mdl-14508072

ABSTRACT

We have used a surface plasmon resonance biosensor (SPR, BIACORE 2000) to detect antibodies against glucose 6-phosphate isomerase (GPI) in synovial fluids of rheumatoid arthritis (RA) and osteoarthritis (OA). Recombinant human GPI proteins fused with or without NusA were expressed in E. coli, purified to homogeneity and immobilized in flow cells of CM5 sensor chips. The flow cells immobilized with NusA protein or bovine serum albumin were used to monitor non-specific binding. Synovial fluid samples from RA patients showed a significantly higher level of binding to recombinant GPI proteins than samples from OA patients. Proteins which bound to the recombinant GPI proteins were confirmed to be immunoglobulin through the administration of anti-human immunoglobulin. NusA fusion protein was excellent for this assay because of a low background binding activity in the SPR analysis and its advantage of increased solubility in recombinant protein production. These results suggested a useful utilization of recombinant NusA-GPI fusion protein for the detection of autoantibodies against GPI in RA patients.


Subject(s)
Antibodies/immunology , Arthritis, Rheumatoid/immunology , Glucose-6-Phosphate Isomerase/immunology , Synovial Fluid/immunology , Aged , Escherichia coli Proteins , Female , Glucose-6-Phosphate Isomerase/genetics , Glucose-6-Phosphate Isomerase/metabolism , Humans , Male , Middle Aged , Osteoarthritis/immunology , Peptide Elongation Factors/genetics , Peptide Elongation Factors/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Surface Plasmon Resonance , Transcription Factors/genetics , Transcription Factors/metabolism , Transcriptional Elongation Factors
8.
Mol Cells ; 14(1): 115-21, 2002 Aug 31.
Article in English | MEDLINE | ID: mdl-12243340

ABSTRACT

The role of interleukin-4 (IL-4) in the inflammatory process has emerged recently. In this study, we investigated the effect of IL-4 on the angiogenic process in an in vitro experimental system. IL-4 significantly inhibited the proliferation of human umbilical vein endothelial cells (HUVEC) that was induced by the vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). VEGF- or bFGF-induced HUVEC chemotaxis was abrogated by the IL-4 treatment. In addition, the formation of tube-like structures by HUVEC in the presence of VEGF or bFGF was also severely down-regulated by IL-4. The inhibitory effects on the critical steps of angiogenesis were not observed with IL-6 that is abundantly found in the inflamed tissue. Our results suggest that IL-4 may play a regulatory role in normal physiology and provide the potential possibility for IL-4 as a therapeutic agent in the intervention of angiogenesis-related diseases.


Subject(s)
Endothelial Growth Factors/pharmacology , Fibroblast Growth Factor 2/pharmacology , Intercellular Signaling Peptides and Proteins/pharmacology , Interleukin-4/pharmacology , Lymphokines/pharmacology , Neovascularization, Physiologic/drug effects , Chemotaxis/drug effects , Down-Regulation , Drug Antagonism , Humans , In Vitro Techniques , Neovascularization, Physiologic/physiology , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
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