کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5826876 | 1558915 | 2015 | 35 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A functional tandem between transient receptor potential canonical channels 6 and calcium-dependent chloride channels in human epithelial cells
ترجمه فارسی عنوان
یک توالی کاربردی بین کانال های کانال 6 پتانسیل گیرنده گذرا و کانال های کلرید وابسته به کلسیم در سلول های اپیتلیال انسان
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
OAG1-Oleoyl-2-acetyl-sn-glycerolLarge-conductance Ca2+-activated K+ channelsTRPV channelsCFTRinh-172DIDSCFTRcACC - caccDMSO - DMSOSmall interfering RNA - RNA تداخل کوچکsiRNA - siRNAdiacylglycerol - دیسیل گلیسیرینDimethylsulfoxide - دیمتیل سولفواکسیدDAG - روزcystic fibrosis transmembrane conductance regulator - رگولاتور رسانایی فرابنفش فیبروز کیستیکHuman airway epithelial cells - سلول های اپیتلیال هواپیما انسانPharmacology - فارماکولوژی یا داروشناسیCystic fibrosis - فیبروز کیستیکBKCa channels - کانال های BKCaTRPC channels - کانال های TRPCCalcium-activated chloride channel - کانال کلرید فعال کلسیم
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب سلولی و مولکولی
چکیده انگلیسی
TRPC6 plays important human physiological functions, notably in artery and arterioles constriction, in regulation of vascular volume and in bronchial muscle constriction. It is implicated in pulmonary hypertension, cardiovascular disease, and focal segmental glomerulosclerosis and seems to play a role in cancer development. Previously, we identified Guanabenz, an α2-adrenergic agonist used for hypertension treatment (Wytensin®), as an activator of calcium-dependent chloride channels (CaCC) in human Cystic Fibrosis (CF) nasal epithelial cells by transiently increasing [Ca2+]i via an influx of extracellular Ca2+. In this study, using assays to measure chloride channel activity, we show that guanabenz is an activator of CaCC in freshly dissociated human bronchial epithelial cells from three CF patients with various genotypes (F508del/F508del, F508del/R1066C, F508del/H1085R). We further characterised the effect of guanabenz and show that it is independent of α-adrenergic receptors, is inhibited by the TRPC family inhibitor SKF-96365 but not by the TRPV family inhibitor ruthenium red. Using western-blotting, Ca2+ measurements and iodide efflux assay, we found that TRPC1 siRNA has no effect on guanabenz induced responses whereas TRPC6 siRNA prevented the guanabenz-dependent Ca2+ influx and the CaCC-dependent activity stimulated by guanabenz. In conclusion, we show that TRPC6 channel is pivotal for the activation of CaCC by guanabenz through a α2-adrenergic-independent pathway in human airway epithelial cells. We suggest propose a functional coupling between TRPC6 and CaCC and guanabenz as a potential TRPC6 activator for exploring TRPC6 and CaCC channel functions and corresponding channelopathies.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmacology - Volume 765, 15 October 2015, Pages 337-345
Journal: European Journal of Pharmacology - Volume 765, 15 October 2015, Pages 337-345
نویسندگان
Johanna Bertrand, Luc Dannhoffer, Fabrice Antigny, Laura Vachel, Christophe Jayle, Clarisse Vandebrouck, Frédéric Becq, Caroline Norez,