Literature DB >> 19493966

Dissecting the genetic basis of kidney tubule response to hyperoxaluria using chromosome substitution strains.

John H Wiessner1, Michael R Garrett, Richard J Roman, Neil S Mandel.   

Abstract

Whether genetics may play a role in the pathophysiologic response of kidney tubules to oxalate exposure remains unexplored despite that as many as 15% of the U.S. population annually will experience a kidney stone composed of calcium oxalate. To explore this issue, we utilized a panel of chromosome substitution strains in which one chromosome at a time was transferred from the Brown Norway (BN) rat onto the Dahl salt-sensitive (SS) genetic background. Hyperoxaluria was induced by adding hydroxyproline (HP) to the drinking water. A dose-response (0-2% HP) study found that both SS and BN exhibited the same level of oxalate excretion as HP concentration increased, but only the BN exhibited changes in urothelial pathology and demonstrated crystal deposition at sites of urothelial injury as a function of dose (at 1.5-2.0%). The consomic panel was treated with 2.0% HP and evaluated for hyperoxaluria, renal injury, and crystal deposition. Tubular injury (% Area) and crystal deposition (% Area) were similar between the resistant SS and SS-4, -6, -7, -8, -9, -11, -16, and -20(BN) consomic rats. However, tubular injury was significantly increased in SS-2(BN) compared with the SS parental (9.8 +/- 1.56 and 4.2 +/- 1.09%, respectively). Crystal deposition was observed in SS-2(BN) and SS-18(BN) (4.7 +/- 0.70 and 3.5 +/- 1.3%, respectively) to the same extent as seen in the susceptible BN (3.2 +/- 0.44%). The fact that crystal deposition was observed in SS-18(BN) without extensive overall tubule injury, compared with the more severe widespread tubular injury seen in SS-2(BN), suggests that the underlying mechanism of each locus is different. In conclusion, these studies establish that BN rats demonstrate oxalate-associated pathology and they retain calcium oxalate crystals coincident with urothelial injury but SS rats do not. These observations establish that BN rat chromosome 2 and 18 harbor genes that contribute to these processes.

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Year:  2009        PMID: 19493966      PMCID: PMC2724241          DOI: 10.1152/ajprenal.00009.2009

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  31 in total

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Authors:  Mark I McCarthy; Gonçalo R Abecasis; Lon R Cardon; David B Goldstein; Julian Little; John P A Ioannidis; Joel N Hirschhorn
Journal:  Nat Rev Genet       Date:  2008-05       Impact factor: 53.242

2.  Modeling of hyperoxaluric calcium oxalate nephrolithiasis: experimental induction of hyperoxaluria by hydroxy-L-proline.

Authors:  S R Khan; P A Glenton; K J Byer
Journal:  Kidney Int       Date:  2006-07-19       Impact factor: 10.612

Review 3.  Genetic hypercalciuria.

Authors:  Orson W Moe; Olivier Bonny
Journal:  J Am Soc Nephrol       Date:  2005-02-02       Impact factor: 10.121

4.  Quantitative genetic basis of arterial phenotypes in the Brown Norway rat.

Authors:  Lalitha Kota; Mary Osborne-Pellegrin; Herbert Schulz; Jacques Behmoaras; Michèle Coutard; Maolian Gong; Norbert Hübner
Journal:  Physiol Genomics       Date:  2007-03-13       Impact factor: 3.107

Review 5.  Kidney stones: pathophysiology and medical management.

Authors:  Orson W Moe
Journal:  Lancet       Date:  2006-01-28       Impact factor: 79.321

6.  The natural history of calcium urolithiasis.

Authors:  F L Coe; J Keck; E R Norton
Journal:  JAMA       Date:  1977-10-03       Impact factor: 56.272

Review 7.  Update on primary hypercalciuria from a genetic perspective.

Authors:  Giuseppe Vezzoli; Laura Soldati; Giovanni Gambaro
Journal:  J Urol       Date:  2008-03-17       Impact factor: 7.450

8.  Localization of genetic loci controlling hydronephrosis in the Brown Norway rat and its association with hematuria.

Authors:  Lalitha Kota; Herbert Schulz; Samreen Falak; Norbert Hübner; Mary Osborne-Pellegrin
Journal:  Physiol Genomics       Date:  2008-06-03       Impact factor: 3.107

Review 9.  Genetics of hypercalciuric stone forming diseases.

Authors:  O Devuyst; Y Pirson
Journal:  Kidney Int       Date:  2007-08-08       Impact factor: 10.612

10.  Chromosome substitution reveals the genetic basis of Dahl salt-sensitive hypertension and renal disease.

Authors:  David L Mattson; Melinda R Dwinell; Andrew S Greene; Anne E Kwitek; Richard J Roman; Howard J Jacob; Allen W Cowley
Journal:  Am J Physiol Renal Physiol       Date:  2008-07-23
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  2 in total

1.  Improved methodology to induce hyperoxaluria without treatment using hydroxyproline.

Authors:  John H Wiessner; Michael R Garrett; Linda Y Hung; David F Wille; Neil S Mandel
Journal:  Urol Res       Date:  2011-03-04

2.  Chromosome 2 Fragment Substitutions in Dahl Salt-Sensitive Rats and RNA Sequencing Identified Enpep and Hs2st1 as Vascular Inflammatory Modulators.

Authors:  Olga Berillo; Sofiane Ouerd; Noureddine Idris-Khodja; Asia Rehman; Chantal Richer; Daniel Sinnett; Anne E Kwitek; Pierre Paradis; Ernesto L Schiffrin
Journal:  Hypertension       Date:  2020-11-09       Impact factor: 10.190

  2 in total

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