Renal Epithelial Casts

Renal epithelial casts are cylindrical structures formed within kidney tubules when shed renal epithelial cells become embedded in a protein matrix and molded by the tubular lumen. They typically arise when tubular injury or stress causes epithelial cells to detach, while uromodulin, also called Tamm-Horsfall protein, provides the matrix that binds cellular debris into a cast. In developmental biology, recognizing these casts helps distinguish abnormal tubular damage from normal patterns of nephron formation in tissue sections and experimental models. Their morphology can therefore support microscopic assessment of epithelial integrity, kidney injury, and how developing renal tissues respond to genetic or environmental perturbations.

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JoVE EoE - Urinary Tract Cancer

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In this video, we demonstrate the steps to isolate and purify renal tubular epithelial cells for a wide range of molecular biology and cell culture studies.

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JoVE Journal - Biology
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Cited by 43 •

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Acute kidney injury (AKI) in humans is a common clinical problem caused by damage to the epithelial cells that comprise kidney nephrons, and AKI is associated with high mortality rates of 50-70%1. Following epithelial cell destruction, nephrons have a limited ability to regenerate, though the mechanisms and limitations that guide this phenomenon remain poorly understood. In this video article, we describe our technique for targeted laser ablation of kidney nephron cells in the zebrafish...

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Here, we describe the protocols for obtaining primary cultures of human renal tubular epithelial cells (HRTEC) from the kidney cortex to develop monolayers and three-dimensional cultures on an extracellular matrix (3D-HRTEC).

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Cited by 17 •

2015

This protocol describes decellularization of Sprague Dawley rat kidneys by antegrade perfusion of detergents through the vasculature, producing acellular renal extracellular matrices that serve as templates for repopulation with human renal epithelial cells. Recellularization and use of the resazurin perfusion assay to monitor growth is performed within specially-designed perfusion bioreactors.

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Cited by 3 •

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We present an optimized protocol for processing whole human kidneys to isolate and culture primary renal proximal tubule epithelial cells and the application of these cells in a three-dimensional, microfluidic, microphysiological platform to recapitulate the renal proximal tubule.

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