1.Protease-activated receptors in periodontitis.
Xia QI ; Ling-xue KONG ; Meng DENG
Chinese Journal of Stomatology 2012;47(12):764-767
Animals
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Cardiovascular Diseases
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etiology
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metabolism
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Humans
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Inflammation
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metabolism
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Periodontitis
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complications
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metabolism
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microbiology
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Platelet Aggregation
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physiology
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Porphyromonas gingivalis
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pathogenicity
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RNA, Messenger
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metabolism
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Receptor, PAR-1
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metabolism
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Receptor, PAR-2
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genetics
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metabolism
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Receptors, Proteinase-Activated
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metabolism
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Receptors, Thrombin
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metabolism
2.The Role of Protease Activated Receptors and Proteases in Subtly Inflamed Diarrhea-Predominant Irritable Bowel Syndrome.
The Korean Journal of Gastroenterology 2014;63(1):59-61
No abstract available.
Animals
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Colon/*metabolism
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Constipation/*physiopathology
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Diarrhea/*physiopathology
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Female
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Ganglia, Spinal/*cytology
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Humans
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Irritable Bowel Syndrome/*physiopathology
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Male
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Nociceptors/*physiology
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Receptor, PAR-2/*physiology
3.Up regulation of interleukin-8 expressions induced by mast cell tryptase via protease activated receptor-2 in endothelial cell line.
Chao LU ; Feng-di ZHAO ; Xiao-Bo LI ; Lian-Hua YIN
Chinese Medical Journal 2005;118(22):1900-1906
BACKGROUNDProtease activated receptor-2 is cleaved and activated by trypsin or mast cell tryptase and may play an important role in inflammation. However, it is unknown whether PAR-2 can mediate tryptase-induced inflammatory reaction. This study was conduct to investigate whether PAR-2 could be the activated by mast cell tryptase and medicated the tryptase induced interleukin-8 expression in endothelial cells.
METHODSProtease activated receptor-2 expression was found in endothelial cell lines ECV304 cell by reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. Interleukin-8 stimulated by purified human mast cell tryptase was determined by RT-PCR and enzyme linked immunosorbent assay (ELISA). Data were analysed by the S-N-K one-way ANOVA test.
RESULTSThe present study shows that mRNA and protein of protease activated receptor-2 could be expressed in ECV304 cells, and tryptase upregulated the expression levels of both interleukin-8 mRNA and protein. The increased expression of interleukin-8 was inhibited by an antiprotease activated receptor-2 monoclonal antibody, SAM11. An additional band was observed by Western blotting after the incubation of ECV304 cells with tryptase for 2 hours, which suggested that protease activated receptor-2 was activated.
CONCLUSIONProtease activated receptor-2 can mediate the mast cell tryptase stimulated expression of interleukin-8 in ECV304 cell.
Antibodies, Monoclonal ; immunology ; Cell Line ; Endothelial Cells ; metabolism ; Gene Expression Regulation ; Humans ; Interleukin-8 ; genetics ; RNA, Messenger ; analysis ; Receptor, PAR-2 ; analysis ; genetics ; physiology ; Serine Endopeptidases ; physiology ; Tryptases ; Up-Regulation
4.Stress-induced Alterations in Mast Cell Numbers and Proteinase-activated Receptor-2 Expression of the Colon: Role of Corticotrophin-releasing Factor.
Dong Hoon KIM ; Young Ju CHO ; Jang Hee KIM ; Young Bae KIM ; Kwang Jae LEE
Journal of Korean Medical Science 2010;25(9):1330-1335
This study was performed in order to assess whether acute stress can increase mast cell and enterochromaffin (EC) cell numbers, and proteinase-activated receptor-2 (PAR2) expression in the rat colon. In addition, we aimed to investigate the involvement of corticotrophin-releasing factor in these stress-related alterations. Eighteen adult rats were divided into 3 experimental groups: 1) a saline-pretreated non-stressed group, 2) a saline-pretreated stressed group, and 3) an astressin-pretreated stressed group. The numbers of mast cells, EC cells, and PAR2-positive cells were counted in 6 high power fields. In proximal colonic segments, mast cell numbers of stressed rats tended to be higher than those of non-stressed rats, and their PAR2-positive cell numbers were significantly higher than those of non-stressed rats. In distal colonic segments, mast cell numbers and PAR2-positive cell numbers of stressed rats were significantly higher than those of non-stressed rats. Mast cell and PAR2-positive cell numbers of astressin-pretreated stressed rats were significantly lower than those of saline-pretreated stressed rats. EC cell numbers did not differ among the three experimental groups. Acute stress in rats increases mast cell numbers and mucosal PAR2 expression in the colon. These stress-related alterations seem to be mediated by release of corticotrophin-releasing factor.
Animals
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Colon/*metabolism
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Corticotropin-Releasing Hormone/antagonists & inhibitors/metabolism/pharmacology/*physiology
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Enterochromaffin Cells/cytology
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Male
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Mast Cells/*cytology/immunology/metabolism
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Peptide Fragments/pharmacology
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Rats
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Rats, Wistar
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Receptor, PAR-2/*metabolism
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Restraint, Physical
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*Stress, Physiological
5.Effect of thrombin on blood brain barrier permeability and its mechanism.
Jing-Xia GUAN ; Sheng-Gang SUN ; Xue-Bing CAO ; Zhi-Bin CHEN ; E-Tang TONG
Chinese Medical Journal 2004;117(11):1677-1681
BACKGROUNDPrevious studies have indicated that thrombin (TM) may play a major role in brain edema after intracerebral hemorrhages (ICHs). However, the mechanism of TM-induced brain edema is poorly understood. In this study, we explored the effect of TM on the permeability of the blood brain barrier (BBB) and investigated its possible mechanism, aiming at providing a potential target for brain edema therapy after ICHs.
METHODSTM or TM + cathepsin G (CATG) was stereotaxically injected into the right caudate nucleus of Sprague-Dawley rats in vivo. BBB permeability was measured by Evans-Blue extravasation. Brain water content was determined by the dry-wet weight method. Brain microvascular endothelial cells were then cultured in vitro. After TM or TM + CATG was added to the endothelial cell medium, changes in the morphology of cells were dynamically observed by phase-contrast light microscopy, and the expression of matrix metalloproteinase-2 (MMP-2) protein was measured by immunohistochemical method.
RESULTSBBB permeability increased at 6 hours after a TM injection into the ipsilateral caudate nucleus (P < 0.05), peaked between 24 hours (P < 0.01) and 48 hours (P < 0.05) after the injection, and then declined. Brain water content changed in parallel with the changes in BBB permeability. However, at all time points, BBB permeability and brain water content after a TM + CATG injection were not significantly different from the respective parameters in the control group (P > 0.05). TM induced endothelial cell contraction in vitro in a time-dependent manner and enhanced the expression of MMP-2 protein. After incubation with TM + CATG, cell morphology and MMP-2 expression did not change significantly as compared to the control group (P > 0.05).
CONCLUSIONSIncreased BBB permeability may be one of the mechanisms behind TM-induced cerebral edema. TM induces endothelial cell contraction and promotes MMP-2 expression by activating protease activated receptor-1 (PAR-1), possibly leading to the opening of the BBB.
Animals ; Blood-Brain Barrier ; drug effects ; Body Water ; metabolism ; Brain Edema ; etiology ; Cathepsin G ; Cathepsins ; pharmacology ; Cerebral Hemorrhage ; complications ; Matrix Metalloproteinase 2 ; analysis ; Permeability ; Rats ; Rats, Sprague-Dawley ; Receptor, PAR-1 ; physiology ; Serine Endopeptidases ; Thrombin ; toxicity
6.Protease activated receptor 2 and epidermal growth factor receptor are involved in the regulation of human sperm motility.
Karina ZITTA ; Martin ALBRECHT ; Stephan WEIDINGER ; Artur MAYERHOFER ; Frank KÖHN
Asian Journal of Andrology 2007;9(5):690-696
AIMTo investigate mechanisms of tryptase-induced reduction of sperm motility and explore whether epidermal growth factor receptor (EGF-R) and protease activated receptor 2 (PAR-2)- associated pathways are involved.
METHODSFresh semen was collected from healthy donors (n = 15). Semen parameters and quality were assessed in accordance with the World Health Organization (WHO) criteria. Swim-up sperm were fixed and subjected to immunocytochemistry and immunoelectronmicroscopy with specific antibodies directed against PAR-2 and EGF-R. Protein extractions from swim-up spermatozoa were analyzed by Western blotting with antibodies for both receptors. Motility of spermatozoa was evaluated by computer-assisted semen analysis.
RESULTSImmunocytochemistry found PAR-2 and EGF-R in approximately 30% of examined human ejaculated spermatozoa. Both receptors were localized in the plasma membrane. Like tryptase, the PAR-2 synthetic agonist SLIGKV reduced sperm motility, and this effect was inhibited by application of two specific EGF-R pathway blockers (AG1478 and PD168393).
CONCLUSIONThe observed reduction of sperm motility by tryptase through the PAR-2 receptor involves EGF-R pathways.
Ejaculation ; Enzyme Inhibitors ; pharmacology ; Humans ; Male ; Microscopy, Immunoelectron ; Oligopeptides ; pharmacology ; Quinazolines ; pharmacology ; Receptor, Epidermal Growth Factor ; antagonists & inhibitors ; drug effects ; physiology ; Receptor, PAR-2 ; physiology ; Reference Values ; Semen ; physiology ; Sperm Motility ; drug effects ; physiology ; Spermatozoa ; drug effects ; physiology ; ultrastructure ; Tyrphostins ; pharmacology
7.Effect of Pertussis Toxin and Herbimycin A on Proteinase-Activated Receptor 2-Mediated Cyclooxygenase 2 Expression in Helicobacter pylori-Infected Gastric Epithelial AGS Cells.
Ji Hye SEO ; Jeong Yeon SEO ; Hae Yun CHUNG ; Hyeyoung KIM
Yonsei Medical Journal 2011;52(3):522-526
Helicobacter pylori (H. pylori) is an important risk factor for chronic gastritis, peptic ulcer, and gastric cancer. Proteinase-activated receptor 2 (PAR2), subgroup of G-protein coupled receptor family, is highly expressed in gastric cancer, and chronic expression of cyclooxygenase-2 (COX-2) plays an important role in H. pylori-associated gastric carcinogenesis and inflammation. We previously demonstrated that H. pylori induced the expression of PAR2 and COX-2 in gastric epithelial cells. Present study aims to investigate whether COX-2 expression induced by H. pylori in Korean isolates is mediated by PAR2 via activation of Gi protein and Src kinase in gastric epithelial AGS cells. Results showed that H. pylori-induced COX-2 expression was inhibited in the cells transfected with antisense oligonucleotide for PAR2 or treated with Gi protein blocker pertussis toxin, Src kinase inhibitor herbimycin A and soybean trypsin inbitor, indicating that COX-2 expression is mediated by PAR2 through activation of Gi protein and Src kinase in gastric epithelial cells infected with H. pylori in Korean isolates. Thus, targeting the activation of PAR2 may be beneficial for prevention or treatment of gastric inflammation and carcinogenesis associated with H. pylori infection.
Benzoquinones/*pharmacology
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Cell Line, Tumor
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Cyclooxygenase 2/genetics/*metabolism
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Epithelial Cells/enzymology/metabolism/microbiology
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GTP-Binding Protein alpha Subunits, Gi-Go/metabolism
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Gastric Mucosa/enzymology/metabolism/*microbiology
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*Helicobacter pylori
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Humans
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Lactams, Macrocyclic/*pharmacology
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Oligonucleotides, Antisense
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Pertussis Toxin/*pharmacology
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RNA, Messenger/metabolism
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Receptor, PAR-2/*physiology
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src-Family Kinases/metabolism