메뉴 건너뛰기




Volumn 7, Issue 8, 2001, Pages 523-534

Control of the Proinflammatory State in Cystic Fibrosis Lung Epithelial Cells by Genes from the TNF-αR/NFκB Pathway

Author keywords

[No Author keywords available]

Indexed keywords

1,3-DIPROPYL-8-CYCLOPENTYLXANTHINE; 8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE; CFTR PROTEIN, HUMAN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 8; TRANSMEMBRANE CONDUCTANCE REGULATOR; TUMOR NECROSIS FACTOR RECEPTOR; XANTHINE DERIVATIVE;

EID: 0035431701     PISSN: 10761551     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf03401858     Document Type: Article
Times cited : (78)

References (37)
  • 2
    • 0024453308 scopus 로고
    • Identification of the cystic fibrosis gene: Chromosome walking and jumping
    • Rommens JM, Lannuzzi MC, Karem B-S, et al. (1989) Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 245: 1059-1065.
    • (1989) Science , vol.245 , pp. 1059-1065
    • Rommens, J.M.1    Lannuzzi, M.C.2    Karem, B.-S.3
  • 3
    • 0024424270 scopus 로고
    • Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
    • Riordan JR, Rommens JM, Karem B-S, et al. (1989) Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA. Science 245: 1066-1073.
    • (1989) Science , vol.245 , pp. 1066-1073
    • Riordan, J.R.1    Rommens, J.M.2    Karem, B.-S.3
  • 4
    • 0024423668 scopus 로고
    • Identification of the cystic fibrosis gene: Genetic analysis
    • Kerem B-S Rommens JM, Buchanan JA, et al. (1989) Identification of the cystic fibrosis gene: genetic analysis. Science 245: 1073-1080.
    • (1989) Science , vol.245 , pp. 1073-1080
    • Kerem, B.-S.1    Rommens, J.M.2    Buchanan, J.A.3
  • 5
    • 0025242929 scopus 로고
    • Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
    • Cheng SH, Gregory RJ, Marshall J, et al. (1990) Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 63: 827-834.
    • (1990) Cell , vol.63 , pp. 827-834
    • Cheng, S.H.1    Gregory, R.J.2    Marshall, J.3
  • 6
    • 0028559511 scopus 로고
    • Conformational maturation of CFTR but not its mutant counterpart (ΔF508) occurs in the endoplasmic reticulum and requires ATP
    • Lukacs GL, Mohamed A, Kartner N, Chang X-B, Riordan JR, Grinstein S. (1994) Conformational maturation of CFTR but not its mutant counterpart (ΔF508) occurs in the endoplasmic reticulum and requires ATP. EMBO J. 13: 6076-6086.
    • (1994) EMBO J. , vol.13 , pp. 6076-6086
    • Lukacs, G.L.1    Mohamed, A.2    Kartner, N.3    Chang, X.-B.4    Riordan, J.R.5    Grinstein, S.6
  • 7
    • 0028006681 scopus 로고
    • Intracellular turnover of Cystic Fibrosis Transmembrane Conductance Regulator. Inefficient processing and rapid degradation of wild type and mutant protein
    • Ward CL, Kopito RR. (1994) Intracellular turnover of Cystic Fibrosis Transmembrane Conductance Regulator. Inefficient processing and rapid degradation of wild type and mutant protein. J. Biol. Chem. 269: 25710-25718.
    • (1994) J. Biol. Chem. , vol.269 , pp. 25710-25718
    • Ward, C.L.1    Kopito, R.R.2
  • 8
    • 0027488993 scopus 로고
    • The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment
    • Yang Y, Janich S, Cohn JA, Wilson JM. (1993) The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment. Proc. Natl. Acad. Sci. U.S.A. 90: 9480-9484.
    • (1993) Proc. Natl. Acad. Sci. U.S.A. , vol.90 , pp. 9480-9484
    • Yang, Y.1    Janich, S.2    Cohn, J.A.3    Wilson, J.M.4
  • 9
    • 0026611093 scopus 로고
    • Al adenosine-receptor antagonists activate chloride efflux from cystic fibrosis cells
    • Eidelman O, Guay-Broder C, van Galen PJM, et al. (1992) Al adenosine-receptor antagonists activate chloride efflux from cystic fibrosis cells. Proc. Natl. Acad. Sci. U.S.A. 89: 5562-5566.
    • (1992) Proc. Natl. Acad. Sci. U.S.A. , vol.89 , pp. 5562-5566
    • Eidelman, O.1    Guay-Broder, C.2    Van Galen, P.J.M.3
  • 10
    • 0034099743 scopus 로고    scopus 로고
    • Sodium 4-phenylbutyrate downregulates Hsc70: Implications for intracellular trafficking of ΔF508-CFTR
    • Rubenstein RC, Zeitlin PL. (2000) Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of ΔF508-CFTR. Am. J. Physiol. Cell Physiol 278: C259-C267.
    • (2000) Am. J. Physiol. Cell Physiol , vol.278
    • Rubenstein, R.C.1    Zeitlin, P.L.2
  • 11
    • 0027274608 scopus 로고
    • Interleukin-8 concentrations are elevated in bronchoalveolar lavage, sputum and sera of children with cystic fibrosis
    • Dean TP, Dai Y, Shute JK, Church MK, Warner JO. (1993) Interleukin-8 concentrations are elevated in bronchoalveolar lavage, sputum and sera of children with cystic fibrosis. Pediatr. Res. 34: 159-161.
    • (1993) Pediatr. Res. , vol.34 , pp. 159-161
    • Dean, T.P.1    Dai, Y.2    Shute, J.K.3    Church, M.K.4    Warner, J.O.5
  • 12
    • 0032081281 scopus 로고    scopus 로고
    • Activation of NFκB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells
    • DiMango E, Ratner AJ, Bryan R, Tabibi S, Prince A. (1998) Activation of NFκB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells. J. Clin. Invest. 101: 2598-2605.
    • (1998) J. Clin. Invest. , vol.101 , pp. 2598-2605
    • DiMango, E.1    Ratner, A.J.2    Bryan, R.3    Tabibi, S.4    Prince, A.5
  • 13
    • 0029124837 scopus 로고
    • Nitric oxide and interleukin-8 as inflammatory components of cystic fibrosis
    • Francoeur C, Denis M. (1995) Nitric oxide and interleukin-8 as inflammatory components of cystic fibrosis. Inflammation 19: 587-598.
    • (1995) Inflammation , vol.19 , pp. 587-598
    • Francoeur, C.1    Denis, M.2
  • 14
    • 0027251739 scopus 로고
    • Interleukin-8: An important chemoattractant in sputum of patients with chronic inflammatory airway diseases
    • Richman-Eisenstat JB, Jorens PG, Hebert CA, Ueki I, Nadel JA. (1993) Interleukin-8: an important chemoattractant In sputum of patients with chronic inflammatory airway diseases. Am. J. Physiol. 264: L413-L418.
    • (1993) Am. J. Physiol. , vol.264
    • Richman-Eisenstat, J.B.1    Jorens, P.G.2    Hebert, C.A.3    Ueki, I.4    Nadel, J.A.5
  • 15
    • 0029054666 scopus 로고
    • Faecal interleukin-8 and tumour necrosis factor- Alpha concentrations in cystic fibrosis
    • Briars GL, Dean TP, Murphy JL, Rolles CJ, Warner JO. (1995) Faecal interleukin-8 and tumour necrosis factor- alpha concentrations in cystic fibrosis. Arch. Dis. Child. 73: 74-76.
    • (1995) Arch. Dis. Child. , vol.73 , pp. 74-76
    • Briars, G.L.1    Dean, T.P.2    Murphy, J.L.3    Rolles, C.J.4    Warner, J.O.5
  • 17
    • 0033276659 scopus 로고    scopus 로고
    • Pharmacogenomics of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and the Cystic Fibrosis Drug CPX using genome microarray analysis
    • Srivastava M, Eidelman O, Pollard HE. (1999) Pharmacogenomics of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and the Cystic Fibrosis Drug CPX using genome microarray analysis. Mol. Med. 5: 753-767.
    • (1999) Mol. Med. , vol.5 , pp. 753-767
    • Srivastava, M.1    Eidelman, O.2    Pollard, H.E.3
  • 18
    • 0031017468 scopus 로고    scopus 로고
    • Salmonella typhi stimulation of human intestinal epithelial cells induces secretion of epithelial cell-derived interleukin-6
    • Weinstein DL, O'Neill B, Metcalf ES. (1997) Salmonella typhi stimulation of human intestinal epithelial cells induces secretion of epithelial cell-derived interleukin-6. Infect. Immun. 65: 395-404.
    • (1997) Infect. Immun. , vol.65 , pp. 395-404
    • Weinstein, D.L.1    O'Neill, B.2    Metcalf, E.S.3
  • 20
    • 0026687233 scopus 로고
    • Defective regulation of outwardly rectifying Cl-channels by protein kinase A corrected by insertion of CFTR
    • Egan M, Flotte T, Afione S, et al. (1992) Defective regulation of outwardly rectifying Cl-channels by protein kinase A corrected by insertion of CFTR. Nature 358: 581-584.
    • (1992) Nature , vol.358 , pp. 581-584
    • Egan, M.1    Flotte, T.2    Afione, S.3
  • 21
    • 0033831270 scopus 로고    scopus 로고
    • Exaggerated activation of nuclear factor κB and altered IκB-β processing in cystic fibrosis bronchial epithelial cells
    • Venkatakrishnan A, Stecenko AA, King G, et al. (2000) Exaggerated activation of nuclear factor κB and altered IκB-β processing in cystic fibrosis bronchial epithelial cells. Am. J. Respir. Cell. Mol. Biol. 23: 396-403.
    • (2000) Am. J. Respir. Cell. Mol. Biol. , vol.23 , pp. 396-403
    • Venkatakrishnan, A.1    Stecenko, A.A.2    King, G.3
  • 23
    • 0032489513 scopus 로고    scopus 로고
    • Direct activation of Cystic Fibrosis Transmembrane Conductance Regulator by 8-cyclopentyl-1,3-dipropylxanthine and 1,3- Diallyl-8-cyclohexylxanthine
    • Arispe N, Ma J, Jacobson KA, Pollard HB. (1998) Direct activation of Cystic Fibrosis Transmembrane Conductance Regulator by 8-cyclopentyl-1,3-dipropylxanthine and 1,3- Diallyl-8-cyclohexylxanthine. J. Biol Chem. 273: 5724-5734.
    • (1998) J. Biol Chem. , vol.273 , pp. 5724-5734
    • Arispe, N.1    Ma, J.2    Jacobson, K.A.3    Pollard, H.B.4
  • 24
    • 0030926711 scopus 로고    scopus 로고
    • DNA fragmentation is a feature of cystic fibrosis epithelial cells: A disease with inappropriate apoptosis?
    • Maiuri L, Raia V, De Marco G, et al. (1997) DNA fragmentation is a feature of cystic fibrosis epithelial cells: a disease with inappropriate apoptosis? FEBS Lett. 408: 225- 231.
    • (1997) FEBS Lett. , vol.408 , pp. 225-231
    • Maiuri, L.1    Raia, V.2    De Marco, G.3
  • 25
    • 0032745888 scopus 로고    scopus 로고
    • Fas and Fas ligand expression in cystic fibrosis airway epithelium
    • Durieu I, Amsellem C, Paulin C, et al. (1999) Fas and Fas ligand expression in cystic fibrosis airway epithelium. Thorax 54: 1093-1098.
    • (1999) Thorax , vol.54 , pp. 1093-1098
    • Durieu, I.1    Amsellem, C.2    Paulin, C.3
  • 26
    • 0029983188 scopus 로고    scopus 로고
    • Mutant cystic fibrosis transmembrane conductance regulator inhibits acidification and apoptosis in C127 cells possible relevance to cystic fibrosis
    • Gottlieb RA, Dasanjh A. (1996) Mutant cystic fibrosis transmembrane conductance regulator inhibits acidification and apoptosis in C127 cells possible relevance to cystic fibrosis. Proc. Natl. Acad. Sci. U.S.A. 93: 3587-3591.
    • (1996) Proc. Natl. Acad. Sci. U.S.A. , vol.93 , pp. 3587-3591
    • Gottlieb, R.A.1    Dasanjh, A.2
  • 28
    • 0033929391 scopus 로고    scopus 로고
    • Pseudomonas aeruginosa exoenzyme S induces transcriptional expression of pro-inflammatory cytokines and chemokines
    • Epelman S, Bruno TF, Neely GG, Woods DE, Mody CH. (2000) Pseudomonas aeruginosa exoenzyme S induces transcriptional expression of pro-inflammatory cytokines and chemokines. Infect. Immun. 68: 4811-4814.
    • (2000) Infect. Immun. , vol.68 , pp. 4811-4814
    • Epelman, S.1    Bruno, T.F.2    Neely, G.G.3    Woods, D.E.4    Mody, C.H.5
  • 29
    • 0032955681 scopus 로고    scopus 로고
    • Chemokine expression in CF epithelia: Implications for the role of CFTR in RANTES expression
    • Schweibert LM, Estell K, Propst SM. (1999) Chemokine expression in CF epithelia: implications for the role of CFTR in RANTES expression. Am. J. Physiol. 276: C700-C710.
    • (1999) Am. J. Physiol. , vol.276
    • Schweibert, L.M.1    Estell, K.2    Propst, S.M.3
  • 30
    • 0028222602 scopus 로고
    • Immunohistochemical localization of transforming growth factor-beta 1 in the lungs of patients with systemic sclerosis, cryptogenic fibrosing alveolitis and other lung disorders
    • Corrin B, Butcher D, McAnulty BJ, et al. (1994) Immunohistochemical localization of transforming growth factor-beta 1 in the lungs of patients with systemic sclerosis, cryptogenic fibrosing alveolitis and other lung disorders. Histopathology 24: 145-150.
    • (1994) Histopathology , vol.24 , pp. 145-150
    • Corrin, B.1    Butcher, D.2    McAnulty, B.J.3
  • 31
    • 0034102868 scopus 로고    scopus 로고
    • TGF-beta(1) genotype and accelerated decline in lung function in patients with cystic fibrosis
    • Arkwright PD, Laurie S, Super M, et al. (2000) TGF-beta(1) genotype and accelerated decline in lung function in patients with cystic fibrosis. Thorax 55: 459-462.
    • (2000) Thorax , vol.55 , pp. 459-462
    • Arkwright, P.D.1    Laurie, S.2    Super, M.3
  • 32
    • 0032694890 scopus 로고    scopus 로고
    • Cytokine expression in bronchial biopsies of cystic fibrosis patients with and without acute exacerbation
    • Wojnarowski C, Frischer T, Hofbauer E, et al. (1999) Cytokine expression in bronchial biopsies of cystic fibrosis patients with and without acute exacerbation. Eur. Respir. J. 14: 1136-1144.
    • (1999) Eur. Respir. J. , vol.14 , pp. 1136-1144
    • Wojnarowski, C.1    Frischer, T.2    Hofbauer, E.3
  • 33
    • 0032584744 scopus 로고    scopus 로고
    • An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton
    • Short DB, Trotter KW, Reczek D, et al. (1998) An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton. J. Biol. Chem. 273: 19797-19801.
    • (1998) J. Biol. Chem. , vol.273 , pp. 19797-19801
    • Short, D.B.1    Trotter, K.W.2    Reczek, D.3
  • 34
    • 0344390884 scopus 로고    scopus 로고
    • A PDZ- Interacting domain in CFTR is an apical membrane polarization signal
    • Moyer BD, Denton J, Karlson KH, et al. (1999) A PDZ- interacting domain in CFTR is an apical membrane polarization signal. J. Clin. Inv. 104: 1353-1361.
    • (1999) J. Clin. Inv. , vol.104 , pp. 1353-1361
    • Moyer, B.D.1    Denton, J.2    Karlson, K.H.3
  • 35
    • 0034703069 scopus 로고    scopus 로고
    • E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells
    • Sun F, Hug MJ, Bradbury NA, Frizzell RA. (2000) E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells. J. Biol. Chem. 275: 29539- 29546.
    • (2000) J. Biol. Chem. , vol.275 , pp. 29539-29546
    • Sun, F.1    Hug, M.J.2    Bradbury, N.A.3    Frizzell, R.A.4
  • 36
    • 0034640510 scopus 로고    scopus 로고
    • Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin
    • Sun F, Hug MJ, Lewarchik CM, Yun C, Bradbury NA, Frizzell RA. (2000) Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin. J. Biol. Chem. 275: 14360-14366.
    • (2000) J. Biol. Chem. , vol.275 , pp. 14360-14366
    • Sun, F.1    Hug, M.J.2    Lewarchik, C.M.3    Yun, C.4    Bradbury, N.A.5    Frizzell, R.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.