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10.1161/CIRCRESAHA.109.206771 http://scihub22266oqcxt.onion/10.1161/CIRCRESAHA.109.206771 C2907241!2907241!20075334     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Circ+Res 2010 ; 106 (5): 992-1003 Nephropedia Template TP {{tp|p=20075334|t=2010. TRPM7-mediated Ca2+ signals confer fibrogenesis in human Atrial Fibrillation |pdf=|usr=}}{{20075334}} gab.com Text TRPM7-mediated Ca2+ signals confer fibrogenesis in human Atrial Fibrillation JO: Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=20075334 #FOAvip Rationale: Cardiac fibrosis contributes to pathogenesis of atrial fibrillation (AF), which is the most sustained arrhythmia and a major cause of morbidity and mortality. Although it has been suggested that Ca2+ signals are involved in fibrosis promotion, the molecular basis of Ca2+ signaling mechanisms and how Ca2+ signals contribute to fibrogenesis remain unknown. Objective: To determine the molecular mechanisms of Ca2+-permeable channel(s) in human atrial fibroblasts, and to investigate how Ca2+ signals contribute to fibrogenesis in human AF. Methods and Results: We demonstrate that the transient receptor potential melastatin related 7 (TRPM7) is the molecular basis of the major Ca2+-permeable channel in human atrial fibroblasts. Endogenous TRPM7 currents in atrial fibroblasts resemble the biophysical and pharmacological properties of heterologous expressed TRPM7. Knocking down TRPM7 by small hairpin RNA (shRNA) largely eliminates TRPM7 current and Ca2+ influx in atrial fibroblasts. More importantly, atrial fibroblasts from AF patients show a striking upregulation of both TRPM7 currents and Ca2+ influx and are more prone to myofibroblast differentiation, presumably due to the enhanced expression of TRPM7. TRPM7-shRNA markedly reduced basal AF fibroblast differentiation. Transforming growth factor ?1 (TGF-?1), the major stimulator of atrial fibrosis, requires TRPM7-mediated Ca2+ signal for its effect on fibroblast proliferation and differentiation. Furthermore, TGF-?1 induced differentiation of cultured human atrial fibroblasts is well correlated with an increase of TRPM7 expression induced by TGF-?1. Conclusions: Our results establish that TRPM7 is the major Ca2+-permeable channel in human atrial fibroblasts, and likely plays an essential role in TGF-?1-elicited fibrogenesis in human AF. Twit Text FOAVip TRPM7-mediated Ca2+ signals confer fibrogenesis in human Atrial Fibrillation ????Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=20075334 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=20075334 #FOAvip English Wikipedia <ref>{{Cite pmid|20075334}}</ref> TRPM7-mediated Ca2+ signals confer fibrogenesis in human Atrial Fibrillation #MMPMID20075334 Du J; Xie J; Zhang Z; Tsujikawa H; Fusco D; Silverman D; Liang B; Yue L Circ Res 2010[Mar]; 106 (5): 992-1003 PMID20075334show ga Rationale: Cardiac fibrosis contributes to pathogenesis of atrial fibrillation (AF), which is the most sustained arrhythmia and a major cause of morbidity and mortality. Although it has been suggested that Ca2+ signals are involved in fibrosis promotion, the molecular basis of Ca2+ signaling mechanisms and how Ca2+ signals contribute to fibrogenesis remain unknown. Objective: To determine the molecular mechanisms of Ca2+-permeable channel(s) in human atrial fibroblasts, and to investigate how Ca2+ signals contribute to fibrogenesis in human AF. Methods and Results: We demonstrate that the transient receptor potential melastatin related 7 (TRPM7) is the molecular basis of the major Ca2+-permeable channel in human atrial fibroblasts. Endogenous TRPM7 currents in atrial fibroblasts resemble the biophysical and pharmacological properties of heterologous expressed TRPM7. Knocking down TRPM7 by small hairpin RNA (shRNA) largely eliminates TRPM7 current and Ca2+ influx in atrial fibroblasts. More importantly, atrial fibroblasts from AF patients show a striking upregulation of both TRPM7 currents and Ca2+ influx and are more prone to myofibroblast differentiation, presumably due to the enhanced expression of TRPM7. TRPM7-shRNA markedly reduced basal AF fibroblast differentiation. Transforming growth factor ?1 (TGF-?1), the major stimulator of atrial fibrosis, requires TRPM7-mediated Ca2+ signal for its effect on fibroblast proliferation and differentiation. Furthermore, TGF-?1 induced differentiation of cultured human atrial fibroblasts is well correlated with an increase of TRPM7 expression induced by TGF-?1. Conclusions: Our results establish that TRPM7 is the major Ca2+-permeable channel in human atrial fibroblasts, and likely plays an essential role in TGF-?1-elicited fibrogenesis in human AF. äTRPM7-mediated Ca2+ signals confer fibrogenesis in human Atrial Fibril(epmc).pdf DeepDyve Pubget Overpricing