Literature DB >> 31339774

In vivo measurements of kidney glomerular number and size in healthy and Os/+ mice using MRI.

Edwin J Baldelomar1,2, Jennifer R Charlton3, Kimberly A deRonde3, Kevin M Bennett1,4.   

Abstract

The development of chronic kidney disease (CKD) is associated with the loss of functional nephrons. However, there are no methods to directly measure nephron number in living subjects. Thus, there are no methods to track the early stages of progressive CKD before changes in total renal function. In this work, we used cationic ferritin-enhanced magnetic resonance imaging (CFE-MRI) to enable measurements of glomerular number (Nglom) and apparent glomerular volume (aVglom) in vivo in healthy wild-type (WT) mice (n = 4) and mice with oligosyndactylism (Os/+; n = 4), a model of congenital renal hypoplasia leading to nephron reduction. We validated in vivo measurements of Nglom and aVglom by high-resolution ex vivo MRI. CFE-MRI measured a mean Nglom of 12,220 ± 2,028 and 6,848 ± 1,676 (means ± SD) for WT and Os/+ mouse kidneys in vivo, respectively. Nglom measured in all mice in vivo using CFE-MRI varied by an average 15% from Nglom measured ex vivo in the same kidney (α = 0.05, P = 0.67). To confirm that CFE-MRI can also be used to track nephron endowment longitudinally, a WT mouse was imaged three times by CFE-MRI over 2 wk. Values of Nglom measured in vivo in the same kidney varied within ~3%. Values of aVglom calculated from CFE-MRI in vivo were significantly different (~15% on average, P < 0.01) from those measured ex vivo, warranting further investigation. This is the first report of direct measurements of Nglom and aVglom in healthy and diseased mice in vivo.

Entities:  

Keywords:  cationic ferritin; glomerulus; magnetic resonance imaging; mouse; nephron number; oligosyndactylism

Mesh:

Year:  2019        PMID: 31339774      PMCID: PMC6843043          DOI: 10.1152/ajprenal.00078.2019

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


  35 in total

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Authors:  K M Bennett; John F Bertram; Scott C Beeman; Norbert Gretz
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  9 in total

1.  Mapping vascular and glomerular pathology in a rabbit model of neonatal acute kidney injury using MRI.

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Review 4.  New imaging tools to measure nephron number in vivo: opportunities for developmental nephrology.

Authors:  K M Bennett; E J Baldelomar; D Morozov; R L Chevalier; J R Charlton
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5.  Mapping nephron mass in vivo using positron emission tomography.

Authors:  Edwin J Baldelomar; David E Reichert; Kooresh I Shoghi; Scott C Beeman; Jennifer R Charlton; Lori Strong; Nikki Fettig; Amanda Klaas; Kevin M Bennett
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6.  Image analysis techniques to map pyramids, pyramid structure, glomerular distribution, and pathology in the intact human kidney from 3-D MRI.

Authors:  Jennifer R Charlton; Yanzhe Xu; Neda Parvin; Teresa Wu; Fei Gao; Edwin J Baldelomar; Darya Morozov; Scott C Beeman; Jamal Derakhshan; Kevin M Bennett
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7.  Small Blob Detector Using Bi-Threshold Constrained Adaptive Scales.

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8.  Magnetic resonance imaging accurately tracks kidney pathology and heterogeneity in the transition from acute kidney injury to chronic kidney disease.

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9.  Nephron number and its determinants: a 2020 update.

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  9 in total

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