Transmission electron microscopy image of a renal collecting duct cell from a Sprague-Dawley rat with a 3D reconstruction of mitochondria shown in blue surrounding the cell nucleus shown in yellow. The image illustrates the spatial organization and distribution of mitochondria within the cell. 3D reconstruction of mitochondria in renal collecting duct cells

Pictured are transmission electron microscopy images of renal collecting duct cells from a Sprague-Dawley rat. Approximately 50 serial sections 0.09 microns thick were stacked, aligned and reconstructed using Reconstruct version 1.1 (SynapseWeb) to generate a 3D representation of mitochondria (blue) surrounding the cell nucleus (yellow).

Mitochondrial structure, function and metabolic dysregulation

The lab studies the role of mitochondrial dysfunction and altered cellular metabolism in the progression of autosomal dominant polycystic kidney disease. Mitochondria play a central role in cellular energetics, redox balance and metabolic regulation. Abnormalities in these pathways may occur early in disease progression.

Research combines metabolomics, mitochondrial imaging and functional studies in preclinical models and patients with autosomal dominant polycystic kidney disease to identify pathways associated with disease severity and progression.

Areas of investigation include:

  • Mitochondrial morphology and dynamics.
  • Metabolic reprogramming in autosomal dominant polycystic kidney disease.
  • Tissue and biofluid metabolomics.
  • Early biomarkers of mitochondrial dysfunction.
  • Effects of hypoxia and metabolic stress on kidney injury.

The lab also has developed and optimized protocols for metabolomic analyses and tissue preservation to improve reproducibility and reliability in kidney metabolomics studies.

Scatter plots show longitudinal changes in kidney citrate and lactate levels in wild-type and Pkd1RC/RC mice at multiple time points during disease progression. Data are separated by sex and genotype, demonstrating dynamic metabolic changes over time in Pkd1RC/RC kidneys compared with wild-type controls. Dynamic changes in kidney metabolite levels during preclinical autosomal dominant polycystic kidney disease progression

Longitudinal changes in kidney citrate and lactate levels in wild-type and Pkd1RC/RC mice over time. Dynamic alterations in kidney metabolite levels accompany total kidney volume and cystic growth patterns in Pkd1RC/RC mice during disease progression.

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