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A novel-1364A/C aquaporin 5 gene promoter polymorphism influences the responses to salt loading of the renin-angiotensin-aldosterone system and of blood pressure in young healthy men

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Abstract

Background

The family of aquaporin water channels contributes to water and salt homeostasis. AQP5 is a ubiquitously expressed exocrine-type water channel. Functional single nucleotide polymorphisms in AQP5 which alter gene transcription have not yet been described. We, therefore, sequenced the human AQP5 promoter to detect novel sequence variants which could impact upon AQP5 expression and contribute to the phenotypic variability of the renin-angiotensin-aldosterone system (RAAS).

Method and results

Sequencing of the whole AQP5 promoter revealed a novel-1364A/C polymorphism. Substitution of C for A was associated with increased transcription factor binding as tested by electrophoretic mobility shift assay, but significantly reduced transcriptional activation of the AQP5 gene by cAMP and serum. The C allele was associated with significantly decreased mRNA in human heart and with decreased protein expression in erythrocyte membranes. Finally, we associated AQP5 genotypes with the variability of the RAAS in two independent study cohorts. First, we studied the phenotypic variability of the RAAS in 103 young (26 ± 3 years) healthy males under an increased dietary salt intake. Increasing salt intake decreased plasma angiotensin II by 25% in AC/CC genotypes but only by 2% in AA genotypes (P = 0.012), and it decreased serum aldosterone by 34% in subjects with AC/CC genotypes but only by 19% in the AA genotypes (P = 0.005). Both genotypes had increased blood pressure under salt diet (P < 0.01), which was significantly more pronounced in AA genotypes (P = 0.029). Second, we investigated associations with variables of the RAAS in 96 old patients (68 ± 10 years) with coronary artery disease scheduled for coronary artery bypass grafting. Aldosterone serum concentrations were 2-fold (P < 0.001) and angiotensin II plasma concentrations were 4-fold higher in AA genotypes than in AC/CC genotypes while ADH plasma concentrations did not differ.

Conclusion

A novel single nucleotide polymorphism in the AQP5 gene promoter alters AQP5 expression in different in vitro systems and cells, and is associated with alterations of variables of the RAAS both in young healthy males and in patients with coronary artery disease.

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References

  1. Agre P (2005) Membrane water transport and aquaporins: looking back. Biol Cell 97:355–356

    Article  PubMed  CAS  Google Scholar 

  2. Agre P, Bonhivers M, Borgnia MJ (1998) The aquaporins, blueprints for cellular plumbing systems. J Biol Chem 273:14659–14662

    Article  PubMed  CAS  Google Scholar 

  3. Bachmann HS, Siffert W, Frey UH (2003) Successful amplification of extremely GC-rich promoter regions using a novel ‘slowdown PCR’ technique. Pharmacogenetics 13:759–766

    Article  PubMed  CAS  Google Scholar 

  4. Delles C, Erdmann J, Jacobi J, Hilgers KF, Fleck E, Regitz-Zagrosek V, Schmieder RE (2001) Aldosterone synthase (CYP11B2) −344 C/T polymorphism is associated with left ventricular structure in human arterial hypertension. J Am Coll Cardiol 37:878–884

    Article  PubMed  CAS  Google Scholar 

  5. Holmer SR, Schunkert H (1996) Adaptive and genetic alterations of the renin angiotensin system in cardiac hypertrophy and failure. Basic Res Cardiol 91(Suppl 2):65–71

    Article  PubMed  CAS  Google Scholar 

  6. King LS, Nielsen S, Agre P (1997) Aquaporins in complex tissues. I. Developmental patterns in respiratory and glandular tissues of rat. Am J Physiol 273:C1541–C1548

    PubMed  CAS  Google Scholar 

  7. Klingbeil AU, Jacobi J, Langenfeld MR, John S, Hilgers KF, Schmieder RE (2000) Enhanced antinatriuresis in response to angiotensin II in essential hypertension. Am J Hypertens 13:986–993

    Article  PubMed  CAS  Google Scholar 

  8. Krane CM, Fortner CN, Hand AR, McGraw DW, Lorenz JN, Wert SE, Towne JE, Paul RJ, Whitsett JA, Menon AG (2001) Aquaporin 5-deficient mouse lungs are hyperresponsive to cholinergic stimulation. Proc Natl Acad Sci USA 98:14114–14119

    Article  PubMed  CAS  Google Scholar 

  9. Krane CM, Melvin JE, Nguyen HV, Richardson L, Towne JE, Doetschman T, Menon AG (2001) Salivary acinar cells from aquaporin 5-deficient mice have decreased membrane water permeability and altered cell volume regulation. J Biol Chem 276:23413–23420

    Article  PubMed  CAS  Google Scholar 

  10. Langenfeld MR, Schmieder RE (1995) Salt and left ventricular hypertrophy: what are the links? J Hum Hypertens 9:909–916

    PubMed  CAS  Google Scholar 

  11. Lee MD, Bhakta KY, Raina S, Yonescu R, Griffin CA, Copeland NG, Gilbert DJ, Jenkins NA, Preston GM, Agre P (1996) The human Aquaporin-5 gene. Molecular characterization and chromosomal localization. J Biol Chem 271:8599–8604

    Article  PubMed  CAS  Google Scholar 

  12. Ma T, Fukuda N, Song Y, Matthay MA, Verkman AS (2000) Lung fluid transport in aquaporin-5 knockout mice. J Clin Invest 105:93–100

    Article  PubMed  CAS  Google Scholar 

  13. Schlaich MP, Klingbeil AU, Jacobi J, Delles C, Schneider MP, Schmidt BM, Schmieder RE (2002) Altered aldosterone response to salt intake and angiotensin II infusion in young normotensive men with parental history of arterial hypertension. J Hypertens 20:117–124

    Article  PubMed  CAS  Google Scholar 

  14. Schmieder RE, Langenfeld MR, Friedrich A, Schobel HP, Gatzka CD, Weihprecht H (1996) Angiotensin II related to sodium excretion modulates left ventricular structure in human essential hypertension. Circulation 94:1304–1309

    PubMed  CAS  Google Scholar 

  15. Sidhaye V, Hoffert JD, King LS (2005) cAMP has distinct acute and chronic effects on aquaporin-5 in lung epithelial cells. J Biol Chem 280:3590–3596

    Article  PubMed  CAS  Google Scholar 

  16. Song Y, Fukuda N, Bai C, Ma T, Matthay MA, Verkman AS (2000) Role of aquaporins in alveolar fluid clearance in neonatal and adult lung, and in oedema formation following acute lung injury: studies in transgenic aquaporin null mice. J Physiol 525:771–779

    Article  PubMed  CAS  Google Scholar 

  17. Song Y, Verkman AS (2001) Aquaporin-5 dependent fluid secretion in airway submucosal glands. J Biol Chem 276:41288–41292

    Article  PubMed  CAS  Google Scholar 

  18. Steinfeld S, Cogan E, King LS, Agre P, Kiss R, Delporte C (2001) Abnormal distribution of aquaporin-5 water channel protein in salivary glands from Sjogren’s syndrome patients. Lab Invest 81:143–148

    PubMed  CAS  Google Scholar 

  19. Vandesompele J, De PK, Pattyn F, Poppe B, Van RN, De PA, Speleman F (2002) Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3:34–35

    Article  Google Scholar 

  20. Verbalis JG (2006) Whole-body volume regulation and escape from antidiuresis. Am J Med 119:S21–S29

    Article  PubMed  Google Scholar 

  21. Verbalis JG (2003) Disorders of body water homeostasis 3. Best Pract Res Clin Endocrinol Metab 17:471–503

    Article  PubMed  CAS  Google Scholar 

  22. Verkman AS, Yang B, Song Y, Manley GT, Ma T (2000) Role of water channels in fluid transport studied by phenotype analysis of aquaporin knockout mice. Exp Physiol 85:233S–241S

    Article  PubMed  CAS  Google Scholar 

  23. Yang F, Kawedia JD, Menon AG (2003) Cyclic AMP regulates aquaporin 5 expression at both transcriptional and post-transcriptional levels through a protein kinase A pathway. J Biol Chem 278:32173–32180

    Article  PubMed  CAS  Google Scholar 

  24. Yang JH, Shi YF, Cheng Q, Deng L (2006) Expression and localization of aquaporin-5 in the epithelial ovarian tumors. Gynecol Oncol 100:294–299

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Michael Adamzik MD.

Additional information

Returned for 1. Revision: 22 April 2008 1. Revision received: 25 July 2008

H. Schunkert, Lübeck, Germany served as guest editor for the manuscript and was responsible for all editorial decisions, including the selection of reviewers. The policy applies to all manuscripts with authors from the editor’s institution.

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Adamzik, M., Frey, U.H., Bitzer, K. et al. A novel-1364A/C aquaporin 5 gene promoter polymorphism influences the responses to salt loading of the renin-angiotensin-aldosterone system and of blood pressure in young healthy men. Basic Res Cardiol 103, 598–610 (2008). https://doi.org/10.1007/s00395-008-0750-z

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  • DOI: https://doi.org/10.1007/s00395-008-0750-z

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