{"title":"YM905是一种新型M3拮抗剂,可抑制人T细胞中通过毒蕈碱受体介导的Ca2+信号和c-fos基因表达","authors":"Takeshi Fujii, Koichiro Kawashima","doi":"10.1016/S0306-3623(01)00093-3","DOIUrl":null,"url":null,"abstract":"<div><p>Our earlier observations suggest that M<sub>3</sub> muscarinic acetylcholine (ACh) receptors (mAChRs) are involved in Ca<sup>2+</sup> signaling and regulation of c-<em>fos</em> gene expression in T lymphocytes. Here, we describe the effects of YM905, a novel M<sub>3</sub> antagonist, on evoked Ca<sup>2+</sup> signaling and c-<em>fos</em> gene expression in CEM human leukemic T cells. YM905 significantly inhibited increases in intracellular free Ca<sup>2+</sup> evoked by 10 μM oxotremorine-M, an M<sub>1</sub>/M<sub>3</sub> agonist (IC<sub>50</sub>=100 nM), and also inhibited 10 μM oxotremorine-M-induced upregulation of c-<em>fos</em> gene expression at 1 μM. These findings demonstrate that YM905 antagonizes the intracellular responses in T cells induced via mAChRs, possibly M<sub>3</sub> receptors.</p></div>","PeriodicalId":12607,"journal":{"name":"General Pharmacology-the Vascular System","volume":"35 2","pages":"Pages 71-75"},"PeriodicalIF":0.0000,"publicationDate":"2000-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-3623(01)00093-3","citationCount":"28","resultStr":"{\"title\":\"YM905, a novel M3 antagonist, inhibits Ca2+ signaling and c-fos gene expression mediated via muscarinic receptors in human T cells\",\"authors\":\"Takeshi Fujii, Koichiro Kawashima\",\"doi\":\"10.1016/S0306-3623(01)00093-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Our earlier observations suggest that M<sub>3</sub> muscarinic acetylcholine (ACh) receptors (mAChRs) are involved in Ca<sup>2+</sup> signaling and regulation of c-<em>fos</em> gene expression in T lymphocytes. Here, we describe the effects of YM905, a novel M<sub>3</sub> antagonist, on evoked Ca<sup>2+</sup> signaling and c-<em>fos</em> gene expression in CEM human leukemic T cells. YM905 significantly inhibited increases in intracellular free Ca<sup>2+</sup> evoked by 10 μM oxotremorine-M, an M<sub>1</sub>/M<sub>3</sub> agonist (IC<sub>50</sub>=100 nM), and also inhibited 10 μM oxotremorine-M-induced upregulation of c-<em>fos</em> gene expression at 1 μM. These findings demonstrate that YM905 antagonizes the intracellular responses in T cells induced via mAChRs, possibly M<sub>3</sub> receptors.</p></div>\",\"PeriodicalId\":12607,\"journal\":{\"name\":\"General Pharmacology-the Vascular System\",\"volume\":\"35 2\",\"pages\":\"Pages 71-75\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0306-3623(01)00093-3\",\"citationCount\":\"28\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"General Pharmacology-the Vascular System\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0306362301000933\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"General Pharmacology-the Vascular System","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0306362301000933","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
YM905, a novel M3 antagonist, inhibits Ca2+ signaling and c-fos gene expression mediated via muscarinic receptors in human T cells
Our earlier observations suggest that M3 muscarinic acetylcholine (ACh) receptors (mAChRs) are involved in Ca2+ signaling and regulation of c-fos gene expression in T lymphocytes. Here, we describe the effects of YM905, a novel M3 antagonist, on evoked Ca2+ signaling and c-fos gene expression in CEM human leukemic T cells. YM905 significantly inhibited increases in intracellular free Ca2+ evoked by 10 μM oxotremorine-M, an M1/M3 agonist (IC50=100 nM), and also inhibited 10 μM oxotremorine-M-induced upregulation of c-fos gene expression at 1 μM. These findings demonstrate that YM905 antagonizes the intracellular responses in T cells induced via mAChRs, possibly M3 receptors.