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Translational Approaches to Assess Kidney Disease

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Tanecia Mitchell

Tanecia Mitchell

University of Alabama at Birmingham, Department of Urology

Dr. Tanecia Mitchell is an Assistant Professor in the Department of Urology at the University of Alabama at Birmingham, School of Medicine. Dr. Mitchell has contributed significantly to the study of mitochondria and oxidative stress in kidney related disorders. She obtained her PhD from the University of Arkansas for Medical Sciences under the mentorship of Dr. Lee Ann MacMillan-Crow. She determined that mitochondrial reactive oxygen species play a significant role in cold storage (ischemia) injury and this could be reduced by the mitochondrial targeted antioxidant, mitoquinone. As a postdoctoral fellow in the laboratory of Dr. Victor Darley-Usmar at UAB, Dr. Mitchell discovered that increased oxidative stress and disruption in mitochondrial quality control contributed to beta cell injury in a Type 1 diabetes model. She also contributed to the development of a method evaluating cellular bioenergetics in immune cells, in an effort to potentially monitor health status and disease progression in humans. Dr. Mitchell was subsequently appointed to a faculty position in the UAB Department of Urology, where she investigated the role of monocyte cellular bioenergetics in patients with kidney stone disease. Her current research focuses on studying the impact of diet on crystalluria and macrophage immunometabolism during kidney stone disease using experimental models and clinical trials. Dr. Mitchell aims to discover relevant scientific information to further understand kidney stone formation and to identify potential therapeutic and diagnostic approaches to reduce stone risk.

Collection Overview

Kidney disease is a major healthcare problem that causes significant morbidity and mortality. More than 850 million individuals have been diagnosed with kidney disease worldwide. In addition, kidney disease results in increased healthcare costs, diminishes the quality of life of patients, and is becoming more prevalent. The most common types of kidney disease include Chronic Kidney Disease, Acute Kidney Injury, Diabetic Nephropathy, and Kidney Stones. These conditions are associated with each other and other metabolic diseases such as hypertension, diabetes, and obesity. Several basic science and clinical advances have greatly improved the well-being of individuals impacted by kidney disease. However, the precise mechanisms leading to these diseases are not fully elucidated. Thus, innovative methods are needed to understand the mechanisms leading to kidney disease and to develop therapies to prevent and/or treat kidney injury and failure. This collection aims to highlight current methods used to study kidney disease, and other methods that could potentially be translated into the clinical setting to improve the diagnosis and prognosis of kidney disease. This series should provide an overview of both basic and translational approaches to understand kidney pathophysiology.

Editorial

Novel Translational Approaches To Study Kidney Disease

Novel Translational Approaches To Study Kidney Disease

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2022

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Articles

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
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Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis

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Cited by 4

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2021

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Abstracts

Simultaneous quantification of equilibrium angiotensin 1, angiotensin 2, and aldosterone using LC-MS/MS

Vineetha Garimella1,

Christine Klemens*1

1University of South Florida