نتایج جستجو برای: cftr

تعداد نتایج: 5775  

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007
Markus W Wendeler Oliver Nufer Hans-Peter Hauri

The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-regulated chloride channel in the plasma membrane of several epithelial cells. Maturation of CFTR is inefficient in most cells, with only a fraction of nascent chains being properly folded and transported to the cell surface. The most common mutation in CFTR, CFTR-deltaF508, leads to the genetic disease cystic fibrosis. CF...

Journal: :Development 2013
Adam Navis Lindsay Marjoram Michel Bagnat

Regulated fluid secretion is crucial for the function of most organs. In vertebrates, the chloride channel cystic fibrosis transmembrane conductance regulator (CFTR) is a master regulator of fluid secretion. Although the biophysical properties of CFTR have been well characterized in vitro, little is known about its in vivo role during development. Here, we investigated the function of Cftr duri...

Journal: :The European respiratory journal 2010
J Bertrand B Boucherle A Billet P Melin-Heschel L Dannhoffer C Vandebrouck C Jayle C Routaboul M-C Molina J-L Décout F Becq C Norez

One of the major therapeutic strategy in cystic fibrosis aims at developing modulators of cystic fibrosis transmembrane conductance regulator (CFTR) channels. We recently discovered methylglyoxal alpha-aminoazaheterocycle adducts, as a new family of CFTR inhibitors. In a structure-activity relationship study, we have now identified GPact-11a, a compound able not to inhibit but to activate CFTR....

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
R E Ellsworth D C Jamison J W Touchman S L Chissoe V V Braden Maduro G G Bouffard N L Dietrich S M Beckstrom-Sternberg L M Iyer L A Weintraub M Cotton L Courtney J Edwards R Maupin P Ozersky T Rohlfing P Wohldmann T Miner K Kemp J Kramer I Korf K Pepin L Antonacci-Fulton R S Fulton P Minx L W Hillier R K Wilson R H Waterston W Miller E D Green

The identification of the cystic fibrosis transmembrane conductance regulator gene (CFTR) in 1989 represents a landmark accomplishment in human genetics. Since that time, there have been numerous advances in elucidating the function of the encoded protein and the physiological basis of cystic fibrosis. However, numerous areas of cystic fibrosis biology require additional investigation, some of ...

Journal: :International journal of oncology 2015
Jin Li Jie Ting Zhang Xiaohua Jiang Xiaoshun Shi Jianfei Shen Fenglan Feng Jingyi Chen Guihong Liu Ping He Juhong Jiang Lai Ling Tsang Yan Wang Rafael Rosell Long Jiang Jianxing He Hsiao Chang Chan

An increased risk of non-small cell lung cancer (NSCLC) in cystic fibrosis (CF) patients and carriers of CF transmembrane conductance regulator (CFTR) mutations has been proposed. However, the role of CFTR in lung cancer remains controversial. In the present study, CFTR expression was assessed in 165 NSCLC tumors and 22 normal lung samples with validation in an independent series of 131 samples...

Journal: :The Journal of biological chemistry 2000
B D Moyer M Duhaime C Shaw J Denton D Reynolds K H Karlson J Pfeiffer S Wang J E Mickle M Milewski G R Cutting W B Guggino M Li B A Stanton

Polarization of cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel to the apical plasma membrane in epithelial cells is critical for vectorial chloride transport. Previously, we reported that the C terminus of CFTR constitutes a PDZ-interacting domain that is required for CFTR polarization to the apical plasma membrane and interaction with the PDZ doma...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Sabrina Noel Christelle Faveau Caroline Norez Christian Rogier Yvette Mettey Frédéric Becq

The cystic fibrosis transmembrane conductance regulator (CFTR) represents the main Cl(-) channel in the apical membrane of epithelial cells for cAMP-dependent Cl(-) secretion. Here we report on the synthesis and screening of a small library of 6-phenylpyrrolo[2,3-b]pyrazines (named RP derivatives) evaluated as activators of wild-type CFTR, G551D-CFTR, and F508del-CFTR Cl(-) channels. Iodide eff...

Journal: :Genesis 2008
Craig A Hodges Calvin U Cotton Mark R Palmert Mitchell L Drumm

The cystic fibrosis transmembrane conductance regulator (CFTR) gene encodes a cAMP-regulated chloride channel that is important in controlling the exchange of fluid and electrolytes across epithelial cells. Mutation of CFTR can lead to cystic fibrosis (CF), the most common lethal genetic disease in Caucasians. CF is a systemic illness with multiple organ systems affected including pulmonary, ga...

2015
Firhan A. Malik Anja Meissner Illya Semenkov Steven Molinski Stan Pasyk Saumel Ahmadi Hai H. Bui Christine E. Bear Darcy Lidington Steffen-Sebastian Bolz Michael B. Butterworth

The cystic fibrosis transmembrane conductance regulator (CFTR) attenuates sphingosine-1-phosphate (S1P) signaling in resistance arteries and has emerged as a prominent regulator of myogenic vasoconstriction. This investigation demonstrates that S1P inhibits CFTR activity via adenosine monophosphate-activated kinase (AMPK), establishing a potential feedback link. In Baby Hamster Kidney (BHK) cel...

2016
Jinhong Park Poonam Khloya Yohan Seo Satish Kumar Ho K. Lee Dong-Kyu Jeon Sungwoo Jo Pawan K. Sharma Wan Namkung Jeffrey M. Beekman

The most common mutation of CFTR, affecting approximately 90% of CF patients, is a deletion of phenylalanine at position 508 (F508del, ΔF508). Misfolding of ΔF508-CFTR impairs both its trafficking to the plasma membrane and its chloride channel activity. To identify small molecules that can restore channel activity of ΔF508-CFTR, we synthesized and evaluated eighteen novel hydroxypyrazoline ana...

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