A design-based method for estimating glomerular number in the developing kidney

Author:

Cullen-McEwen Luise A.1,Armitage James A.1,Nyengaard Jens R.2,Moritz Karen M.3,Bertram John F.1

Affiliation:

1. Department of Anatomy and Developmental Biology, School of Biomedical Sciences, Monash University, Victoria;

2. Stereology and Electron Microscopy Laboratory and Centre for Stochastic Geometry and Advanced Bioimaging, University of Aarhus, Aarhus, Denmark; and

3. School of Biomedical Sciences, University of Queensland, Brisbane, Australia

Abstract

Low glomerular (nephron) endowment has been associated with an increased risk of cardiovascular and renal disease in adulthood. Nephron endowment in humans is determined by 36 wk of gestation, while in rats and mice nephrogenesis ends several days after birth. Specific genes and environmental perturbations have been shown to regulate nephron endowment. Until now, design-based method for estimating nephron number in developing kidneys was unavailable. This was due in part to the difficulty associated with unambiguously identifying developing glomeruli in histological sections. Here, we describe a method that uses lectin histochemistry to identify developing glomeruli and the physical disector/fractionator principle to provide unbiased estimates of total glomerular number ( Nglom). We have characterized Nglom throughout development in kidneys from 76 rats and model this development with a 5-parameter logistic equation to predict Nglom from embryonic day 17.25 to adulthood ( r2 = 0.98). This approach represents the first design-based method with which to estimate Nglom in the developing kidney.

Publisher

American Physiological Society

Subject

Physiology

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