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Volumn 276, Issue 2 45-2, 1999, Pages

Adenosine and its nucleotides activate wild-type and R117H CFTR through an A(2B) receptor-coupled pathway

Author keywords

COS 7; Cystic fibrosis; G protein coupled receptor; Genetics; Secretion

Indexed keywords

ADENINE NUCLEOTIDE; ADENINE NUCLEOTIDE DERIVATIVE; ADENOSINE; ADENOSINE A2B RECEPTOR; ADENOSINE DIPHOSPHATE; ADENOSINE PHOSPHATE; ADENOSINE TRIPHOSPHATE; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; GUANINE NUCLEOTIDE BINDING PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0033019713     PISSN: 03636143     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpcell.1999.276.2.c361     Document Type: Article
Times cited : (83)

References (16)
  • 2
    • 0027480135 scopus 로고
    • Involvement of arachidonic acid in the chloride secretory response of intestinal epithelial cells
    • Cell Physiol. 33
    • Barrett, K. E., and T. D. Bigby. Involvement of arachidonic acid in the chloride secretory response of intestinal epithelial cells. Am. J. Physiol. 264 (Cell Physiol. 33): C446-C452, 1993.
    • (1993) Am. J. Physiol. , vol.264
    • Barrett, K.E.1    Bigby, T.D.2
  • 3
    • 0025333187 scopus 로고
    • Immune-related intestinal chloride secretion. II. Effect of adenosine on T84 cell line
    • Cell Physiol. 27
    • Barrett, K. E., J. A. Cohn, P. A. Huott, S. I. Wasserman, and K. Dharmsathaphorn. Immune-related intestinal chloride secretion. II. Effect of adenosine on T84 cell line. Am. J. Physiol. 258 (Cell Physiol. 27): C902-C912, 1990.
    • (1990) Am. J. Physiol. , vol.258
    • Barrett, K.E.1    Cohn, J.A.2    Huott, P.A.3    Wasserman, S.I.4    Dharmsathaphorn, K.5
  • 5
    • 0026532895 scopus 로고
    • Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)
    • Bear, C. E., C. H. Li, N. Kartner, R. J. Bridges, T. J. Jensen, M. Ramjeesingh, and J. R. Riordan. Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR). Cell 68: 809-818, 1992.
    • (1992) Cell , vol.68 , pp. 809-818
    • Bear, C.E.1    Li, C.H.2    Kartner, N.3    Bridges, R.J.4    Jensen, T.J.5    Ramjeesingh, M.6    Riordan, J.R.7
  • 7
    • 0028206480 scopus 로고
    • External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism
    • Cantiello, H. F., A. G. Prat, I. L. Reisin, L. B. Ercole, E. H. Abraham, J, F. Amara, R. J. Gregory, and D. A. Ausiello. External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism. J. Biol. Chem. 269: 11224-11232, 1994.
    • (1994) J. Biol. Chem. , vol.269 , pp. 11224-11232
    • Cantiello, H.F.1    Prat, A.G.2    Reisin, I.L.3    Ercole, L.B.4    Abraham, E.H.5    Amara, J.F.6    Gregory, R.J.7    Ausiello, D.A.8
  • 8
    • 0028906612 scopus 로고
    • The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regular (CFTR) have distinct functions in controlling channel activity
    • Carson, M. R., S. M. Travis, and M. J. Welsh. The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regular (CFTR) have distinct functions in controlling channel activity. J. Biol. Chem. 270: 1711-1717, 1995.
    • (1995) J. Biol. Chem. , vol.270 , pp. 1711-1717
    • Carson, M.R.1    Travis, S.M.2    Welsh, M.J.3
  • 9
    • 0025242929 scopus 로고
    • Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
    • Cheng, S. H., R. J. Gregory, J. Marshall, S. Paul, D. W. Souza, G. A. White, C. R. O'Riordan, and A. E. Smith. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 63: 827-834, 1990.
    • (1990) Cell , vol.63 , pp. 827-834
    • Cheng, S.H.1    Gregory, R.J.2    Marshall, J.3    Paul, S.4    Souza, D.W.5    White, G.A.6    O'Riordan, C.R.7    Smith, A.E.8
  • 10
    • 0025987020 scopus 로고
    • Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel
    • Cheng, S. H., D. P. Rich, J. Marshall, R. J. Gregory, M. J. Welsh, and A. E. Smith. Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel. Cell 66: 1027-1036, 1991.
    • (1991) Cell , vol.66 , pp. 1027-1036
    • Cheng, S.H.1    Rich, D.P.2    Marshall, J.3    Gregory, R.J.4    Welsh, M.J.5    Smith, A.E.6
  • 11
    • 20644445242 scopus 로고    scopus 로고
    • ATP metabolites activate CFTR through an A2 adenosine receptor in COS-7 cells
    • Clancy, J. P., F. Ruiz, and E. J. Sorscher, ATP metabolites activate CFTR through an A2 adenosine receptor in COS-7 cells (Abstract). Am. J. Respir. Crit. Care Med. 155: A47, 1997.
    • (1997) Am. J. Respir. Crit. Care Med. , vol.155
    • Clancy, J.P.1    Ruiz, F.2    Sorscher, E.J.3
  • 12
    • 0026670029 scopus 로고
    • Chloride secretory response to extracellular ATP in human normal and cystic fibrosis nasal epithelia
    • Cell Physiol. 32
    • Clarke, L. L., and R. C. Boucher. Chloride secretory response to extracellular ATP in human normal and cystic fibrosis nasal epithelia. Am. J. Physiol. 263 (Cell Physiol. 32): C348-C356, 1992.
    • (1992) Am. J. Physiol. , vol.263
    • Clarke, L.L.1    Boucher, R.C.2
  • 13
    • 0027319626 scopus 로고
    • Protein kinase C activates chloride conductance in C127 cells, stably expressing the cystic fibrosis gene
    • Dechecchi, M. C., A. Tamauini, G. Berton, and G. Cabrini. Protein kinase C activates chloride conductance in C127 cells, stably expressing the cystic fibrosis gene. J. Biol. Chem. 268: 11321-11325, 1993.
    • (1993) J. Biol. Chem. , vol.268 , pp. 11321-11325
    • Dechecchi, M.C.1    Tamauini, A.2    Berton, G.3    Cabrini, G.4
  • 15
    • 0025346025 scopus 로고
    • Long-term culture of normal and cystic fibrosis epithelial cells grown under serum-free condition
    • Gruenert, D. C., C. B. Basbaum, and J. H. Widdicombe. Long-term culture of normal and cystic fibrosis epithelial cells grown under serum-free condition. In Vitro Cell. Dev. Biol. 26: 411-418, 1990.
    • (1990) In Vitro Cell. Dev. Biol. , vol.26 , pp. 411-418
    • Gruenert, D.C.1    Basbaum, C.B.2    Widdicombe, J.H.3
  • 16
    • 0027517995 scopus 로고
    • Correlation between genotype and phenotype in patients with cystic fibrosis
    • Hamosh, A., and the Cystic Fibrosis Genotype-Phenotype Consortium. Correlation between genotype and phenotype in patients with cystic fibrosis. N. Engl. J. Med. 329: 1308-1313, 1993.
    • (1993) N. Engl. J. Med. , vol.329 , pp. 1308-1313
    • Hamosh, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.