Martin Connolly, S. Wort, B. Garfield, A. Crosby, N. Morrell, P. Kemp
{"title":"MiR-1-5p靶向TGF-ßR1,在肺动脉高压大鼠肥厚心脏中受到抑制","authors":"Martin Connolly, S. Wort, B. Garfield, A. Crosby, N. Morrell, P. Kemp","doi":"10.1183/13993003.congress-2019.pa5045","DOIUrl":null,"url":null,"abstract":"MicroRNAs (miRNAs) are small, non-coding RNAs, implicated in the control of myocardial homeostasis. miR-1 has been shown to be down-regulated in hypertrophying rodent hearts and its restoration an ameliorating factor. We used monocrotaline treatment to induce pulmonary hypertension in a cohort of rats and thereafter-showed miR-1 expression was reduced in the hypertrophying right ventricle (RV) (Fig. 1A). Bioinformatic analysis identified TGF-βR1 (ALK5) as a predicted target for miR-1, the expression of which was increased in the RV (Fig. 1B, C). Cell transfection with a miR-1-mimic reduced GFP expression from a reporter vector containing the ALK5 3’-UTR and also knocked down endogenous ALK5. Lastly, miR-1 reduced TGF-β activation of a SMAD2/3-dependent reporter. Taken together, these data confirm miR-1 targets TGF-βR1 thereby reducing TGF-β signalling, which may regulate cardiac hypertrophy.","PeriodicalId":20724,"journal":{"name":"Pulmonary hypertension","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"MiR-1-5p targets TGF-ßR1 and is suppressed in the hypertrophying hearts of rats with pulmonary arterial hypertension\",\"authors\":\"Martin Connolly, S. Wort, B. Garfield, A. Crosby, N. Morrell, P. Kemp\",\"doi\":\"10.1183/13993003.congress-2019.pa5045\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"MicroRNAs (miRNAs) are small, non-coding RNAs, implicated in the control of myocardial homeostasis. miR-1 has been shown to be down-regulated in hypertrophying rodent hearts and its restoration an ameliorating factor. We used monocrotaline treatment to induce pulmonary hypertension in a cohort of rats and thereafter-showed miR-1 expression was reduced in the hypertrophying right ventricle (RV) (Fig. 1A). Bioinformatic analysis identified TGF-βR1 (ALK5) as a predicted target for miR-1, the expression of which was increased in the RV (Fig. 1B, C). Cell transfection with a miR-1-mimic reduced GFP expression from a reporter vector containing the ALK5 3’-UTR and also knocked down endogenous ALK5. Lastly, miR-1 reduced TGF-β activation of a SMAD2/3-dependent reporter. Taken together, these data confirm miR-1 targets TGF-βR1 thereby reducing TGF-β signalling, which may regulate cardiac hypertrophy.\",\"PeriodicalId\":20724,\"journal\":{\"name\":\"Pulmonary hypertension\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pulmonary hypertension\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1183/13993003.congress-2019.pa5045\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pulmonary hypertension","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/13993003.congress-2019.pa5045","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
MiR-1-5p targets TGF-ßR1 and is suppressed in the hypertrophying hearts of rats with pulmonary arterial hypertension
MicroRNAs (miRNAs) are small, non-coding RNAs, implicated in the control of myocardial homeostasis. miR-1 has been shown to be down-regulated in hypertrophying rodent hearts and its restoration an ameliorating factor. We used monocrotaline treatment to induce pulmonary hypertension in a cohort of rats and thereafter-showed miR-1 expression was reduced in the hypertrophying right ventricle (RV) (Fig. 1A). Bioinformatic analysis identified TGF-βR1 (ALK5) as a predicted target for miR-1, the expression of which was increased in the RV (Fig. 1B, C). Cell transfection with a miR-1-mimic reduced GFP expression from a reporter vector containing the ALK5 3’-UTR and also knocked down endogenous ALK5. Lastly, miR-1 reduced TGF-β activation of a SMAD2/3-dependent reporter. Taken together, these data confirm miR-1 targets TGF-βR1 thereby reducing TGF-β signalling, which may regulate cardiac hypertrophy.