4.4 Review

Investigating mechanisms of chronic kidney disease in mouse models

Journal

PEDIATRIC NEPHROLOGY
Volume 27, Issue 8, Pages 1233-1247

Publisher

SPRINGER
DOI: 10.1007/s00467-011-1938-2

Keywords

Fibrosis; Collagen; Animal models; Extracellular matrix; Chronic kidney disease; Unilateral ureteral obstruction

Funding

  1. National Institutes of Health [RO1DK54500, P50DK44757, K08DK073497, RO3DK083648, K08DK080926, R03DK58925]
  2. National Kidney Foundation
  3. American Society of Nephrology
  4. Seattle Children's Research Institute
  5. Robert O. Hickman Endowed Chair in Pediatric Nephrology

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Animal models of chronic kidney disease (CKD) are important experimental tools that are used to investigate novel mechanistic pathways and to validate potential new therapeutic interventions prior to pre-clinical testing in humans. Over the past several years, mouse CKD models have been extensively used for these purposes. Despite significant limitations, the model of unilateral ureteral obstruction (UUO) has essentially become the high-throughput in vivo model, as it recapitulates the fundamental pathogenetic mechanisms that typify all forms of CKD in a relatively short time span. In addition, several alternative mouse models are available that can be used to validate new mechanistic paradigms and/or novel therapies. Here, we review several models-both genetic and experimentally induced-that provide investigators with an opportunity to include renal functional study end-points together with quantitative measures of fibrosis severity, something that is not possible with the UUO model.

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