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Volumn 304, Issue 7, 2013, Pages

Loss of Cftr function exacerbates the phenotype of Na+ hyperabsorption in murine airways

Author keywords

F508 CFTR; Airway epithelia necrosis; Airway Inflammation; Cystic fibrosis; ENaC; Genetically modified mice

Indexed keywords

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EPITHELIAL SODIUM CHANNEL; VOLTAGE GATED SODIUM CHANNEL BETA SUBUNIT; CHLORIDE; SCNN1B PROTEIN, MOUSE; SODIUM;

EID: 84878234654     PISSN: 10400605     EISSN: 15221504     Source Type: Journal    
DOI: 10.1152/ajplung.00150.2012     Document Type: Article
Times cited : (39)

References (46)
  • 5
    • 34447116244 scopus 로고    scopus 로고
    • Identification of a key pathway required for the sterile inflammatory response triggered by dying cells
    • Chen CJ, Kono H, Golenbock D, Reed G, Akira S, Rock KL. Identification of a key pathway required for the sterile inflammatory response triggered by dying cells. Nat Med 13: 851-856, 2007.
    • (2007) Nat Med , vol.13 , pp. 851-856
    • Chen, C.J.1    Kono, H.2    Golenbock, D.3    Reed, G.4    Akira, S.5    Rock, K.L.6
  • 7
    • 0030466804 scopus 로고    scopus 로고
    • Increased survival of CFTR knockout mice with an oral osmotic laxative
    • Clarke LL, Gawenis LR, Franklin CL, Harline MC. Increased survival of CFTR knockout mice with an oral osmotic laxative. Lab Anim Sci 46: 612-618, 1996.
    • (1996) Lab Anim Sci , vol.46 , pp. 612-618
    • Clarke, L.L.1    Gawenis, L.R.2    Franklin, C.L.3    Harline, M.C.4
  • 8
    • 84856215739 scopus 로고    scopus 로고
    • CYP2F2-generated metabolites, not styrene oxide, are a key event mediating the mode of action of styrene-induced mouse lung tumors
    • Cruzan G, Bus J, Hotchkiss J, Harkema J, Banton M, Sarang S. CYP2F2-generated metabolites, not styrene oxide, are a key event mediating the mode of action of styrene-induced mouse lung tumors. Regul Toxicol Pharmacol 62: 214-220, 2012.
    • (2012) Regul Toxicol Pharmacol , vol.62 , pp. 214-220
    • Cruzan, G.1    Bus, J.2    Hotchkiss, J.3    Harkema, J.4    Banton, M.5    Sarang, S.6
  • 9
    • 36348979793 scopus 로고    scopus 로고
    • Sodium channels and cystic fibrosis
    • Donaldson SH, Boucher RC. Sodium channels and cystic fibrosis. Chest 132: 1631-1636, 2007.
    • (2007) Chest , vol.132 , pp. 1631-1636
    • Donaldson, S.H.1    Boucher, R.C.2
  • 10
    • 1642277855 scopus 로고    scopus 로고
    • Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model
    • Durie PR, Kent G, Phillips MJ, Ackerley CA. Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model. Am J Pathol 164: 1481-1493, 2004.
    • (2004) Am J Pathol , vol.164 , pp. 1481-1493
    • Durie, P.R.1    Kent, G.2    Phillips, M.J.3    Ackerley, C.A.4
  • 11
    • 0030882184 scopus 로고    scopus 로고
    • Intestinal physiology and pathology in genetargeted mouse models of cystic fibrosis
    • Grubb BR, Gabriel SE. Intestinal physiology and pathology in genetargeted mouse models of cystic fibrosis. Am J Physiol Gastrointest Liver Physiol 273: G258-G266, 1997.
    • (1997) Am J Physiol Gastrointest Liver Physiol , vol.273
    • Grubb, B.R.1    Gabriel, S.E.2
  • 18
    • 33748588664 scopus 로고    scopus 로고
    • Eosinophilic crystalline pneumonia as a major cause of death in 129S4/SvJae mice
    • Hoenerhoff MJ, Starost MF, Ward JM. Eosinophilic crystalline pneumonia as a major cause of death in 129S4/SvJae mice. Vet Pathol 43: 682-688, 2006.
    • (2006) Vet Pathol , vol.43 , pp. 682-688
    • Hoenerhoff, M.J.1    Starost, M.F.2    Ward, J.M.3
  • 20
    • 84866627429 scopus 로고    scopus 로고
    • CFTR regulates early pathogenesis of chronic obstructive lung disease in betaENaC-overexpressing mice
    • Johannesson B, Hirtz S, Schatterny J, Schultz C, Mall MA. CFTR regulates early pathogenesis of chronic obstructive lung disease in betaENaC-overexpressing mice. PLoS One 7: e44059, 2012.
    • (2012) PLoS One , vol.7
    • Johannesson, B.1    Hirtz, S.2    Schatterny, J.3    Schultz, C.4    Mall, M.A.5
  • 22
    • 80053376536 scopus 로고    scopus 로고
    • Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lung
    • Lazrak A, Jurkuvenaite A, Chen L, Keeling KM, Collawn JF, Bedwell DM, Matalon S. Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lung. Am J Physiol Lung Cell Mol Physiol 301: L557-L567, 2011.
    • (2011) Am J Physiol Lung Cell Mol Physiol , vol.301
    • Lazrak, A.1    Jurkuvenaite, A.2    Chen, L.3    Keeling, K.M.4    Collawn, J.F.5    Bedwell, D.M.6    Matalon, S.7
  • 25
    • 34249888226 scopus 로고    scopus 로고
    • Chloridedependent secretion of alveolar wall liquid determined by optical-sectioning microscopy
    • Lindert J, Perlman CE, Parthasarathi K, Bhattacharya J. Chloridedependent secretion of alveolar wall liquid determined by optical-sectioning microscopy. Am J Respir Cell Mol Biol 36: 688-696, 2007.
    • (2007) Am J Respir Cell Mol Biol , vol.36 , pp. 688-696
    • Lindert, J.1    Perlman, C.E.2    Parthasarathi, K.3    Bhattacharya, J.4
  • 27
    • 84864849180 scopus 로고    scopus 로고
    • Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammation
    • Livraghi-Butrico A, Kelly EJ, Klem ER, Dang H, Wolfgang MC, Boucher RC, Randell SH, O'Neal WK. Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammation. Mucosal Immunol 5: 397-408, 2012.
    • (2012) Mucosal Immunol , vol.5 , pp. 397-408
    • Livraghi-Butrico, A.1    Kelly, E.J.2    Klem, E.R.3    Dang, H.4    Wolfgang, M.C.5    Boucher, R.C.6    Randell, S.H.7    O'Neal, W.K.8
  • 29
  • 30
    • 33847289649 scopus 로고    scopus 로고
    • Cystic fibrosis and other respiratory diseases of impaired mucus clearance
    • Livraghi A, Randell SH. Cystic fibrosis and other respiratory diseases of impaired mucus clearance. Toxicol Pathol 35: 116-129, 2007.
    • (2007) Toxicol Pathol , vol.35 , pp. 116-129
    • Livraghi, A.1    Randell, S.H.2
  • 34
    • 0032433707 scopus 로고    scopus 로고
    • Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease
    • Matsui H, Grubb BR, Tarran R, Randell SH, Gatzy JT, Davis CW, Boucher RC. Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease. Cell 95: 1005-1015, 1998.
    • (1998) Cell , vol.95 , pp. 1005-1015
    • Matsui, H.1    Grubb, B.R.2    Tarran, R.3    Randell, S.H.4    Gatzy, J.T.5    Davis, C.W.6    Boucher, R.C.7
  • 36
    • 33747356489 scopus 로고    scopus 로고
    • Physiological regulation of ATP release at the apical surface of human airway epithelia
    • Okada SF, Nicholas RA, Kreda SM, Lazarowski ER, Boucher RC. Physiological regulation of ATP release at the apical surface of human airway epithelia. J Biol Chem 281: 22992-23002, 2006.
    • (2006) J Biol Chem , vol.281 , pp. 22992-23002
    • Okada, S.F.1    Nicholas, R.A.2    Kreda, S.M.3    Lazarowski, E.R.4    Boucher, R.C.5
  • 38
    • 34848847214 scopus 로고    scopus 로고
    • Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice
    • Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice. Gene Ther 14: 1492-1501, 2007.
    • (2007) Gene Ther , vol.14 , pp. 1492-1501
    • Ostrowski, L.E.1    Yin, W.2    Diggs, P.S.3    Rogers, T.D.4    O'Neal, W.K.5    Grubb, B.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.