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Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

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The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
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Drug Metabolism: Phase I Reactions01:17

Drug Metabolism: Phase I Reactions

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A phase I reaction is a biochemical process that introduces a functionally reactive polar group to a substance. This transformation predominantly occurs in the liver, facilitated by the cytochrome P450 system of hemoproteins situated in the lipophilic endoplasmic reticulum of cells. The metabolite generated through this process can have varying polarities. If it is sufficiently polar, it can be easily excreted in the urine due to its water compatibility. However, if the metabolite is nonpolar,...
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Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

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During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
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Peroxisomes and Mitochondria01:30

Peroxisomes and Mitochondria

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Peroxisomes and mitochondria are two important oxygen-utilizing organelles in eukaryotic cells. Mitochondria carry out cellular respiration—the process that converts energy from food into ATP. Peroxisomes carry out a variety of functions, primarily breaking down different substances, such as fatty acids.
The peroxisome is a single membrane-bound cellular organelle that can perform several different functions, including lipid metabolism and chemical detoxification. The enzymes within...
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Peroxisomes01:24

Peroxisomes

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Peroxisomes are specialized organelles present in fungi, plant, and animal cells. It can vary in number, size, morphology, and activity depending on the type of tissue and the nutritional state of the cell. For example, cells with active lipid metabolism, such as adipocytes, neurons, and hepatocytes, have more peroxisomes than other cells in the body. Besides their primary role in breaking down complex organic molecules, peroxisomes can also synthesize specific macromolecules and participate in...
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The Electron Transport Chain01:30

The Electron Transport Chain

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The electron transport chain or oxidative phosphorylation is an exothermic process in which free energy released during electron transfer reactions is coupled to ATP synthesis. This process is a significant source of energy in aerobic cells, and therefore inhibitors of the electron transport chain can be detrimental to the cell's metabolic processes.
Inhibitors of the electron transport chain
Rotenone, a widely used pesticide, prevents electron transfer from Fe-S cluster to ubiquinone or Q...
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Related Experiment Video

Updated: Jun 5, 2025

Isolation, Characterization, And High Throughput Extracellular Flux Analysis of Mouse Primary Renal Tubular Epithelial Cells
09:40

Isolation, Characterization, And High Throughput Extracellular Flux Analysis of Mouse Primary Renal Tubular Epithelial Cells

Published on: June 20, 2018

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Measuring renal cortical cell-specific mitochondrial metabolism.

Kyle Feola1,2, Andrea H Venable1,2, Tatyana Broomfield3

  • 1Department of Internal Medicine (Nephrology), University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Biorxiv : the Preprint Server for Biology
|December 9, 2024
PubMed
Summary

Kidney cells show diverse mitochondrial functions. This study reveals cell-specific metabolic differences in proximal and distal tubules, crucial for understanding kidney disease and developing targeted therapies.

Keywords:
cellular metabolic heterogeneitykidneymetabolismmitochondriatubular epithelium

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Author Spotlight: Oxygen-Independent Assays to Measure Mitochondrial Function in Mammals
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Related Experiment Videos

Last Updated: Jun 5, 2025

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Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
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Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice

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Author Spotlight: Oxygen-Independent Assays to Measure Mitochondrial Function in Mammals
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Author Spotlight: Oxygen-Independent Assays to Measure Mitochondrial Function in Mammals

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Area of Science:

  • Nephrology
  • Mitochondrial Biology
  • Cellular Metabolism

Background:

  • Kidney metabolic health is key to preventing kidney disease progression.
  • Kidney structural and functional heterogeneity limits understanding of cell-specific metabolism.
  • Intra-renal mitochondrial heterogeneity is hypothesized to drive cell-specific kidney metabolism.

Purpose of the Study:

  • To investigate mitochondrial functional capacities and metabolomes in distinct kidney cell types.
  • To explore cell-specific mitochondrial metabolism in early proximal tubule (PT), late PT, and distal convoluted tubule (DCT).
  • To assess how fasting impacts mitochondrial metabolism in these kidney segments.

Main Methods:

  • Utilized a novel mitochondrial tagging technique (MITO-Tag) in mouse models.
  • Generated cell-type specific mouse models targeting early PT, late PT, and DCT using Cre-driver lines.
  • Performed functional assays (respiratory, fatty acid oxidation) and metabolomics on isolated mitochondria.

Main Results:

  • Revealed differential mitochondrial respiratory and fatty acid oxidation (FAO) capacities across early PT, late PT, and DCT.
  • Demonstrated dynamic changes in these capacities during fasting.
  • Observed increased FAO in the late PT during fasting, indicated by metabolomic changes.

Conclusions:

  • The kidney cortex exhibits significant mitochondrial metabolic and functional diversity across different cell populations.
  • Understanding cell-specific mitochondrial metabolism is critical for developing targeted therapies for kidney diseases.
  • The MITO-Tag model effectively captures differential mitochondrial metabolism in distinct kidney cell types under fed and fasted conditions.