Literature DB >> 24969531

Why to compare absolute numbers of mitochondria.

Sabine Schmitt1, Sabine Schulz1, Eva-Maria Schropp1, Carola Eberhagen1, Alisha Simmons1, Wolfgang Beisker1, Michaela Aichler2, Hans Zischka3.   

Abstract

Prompted by pronounced structural differences between rat liver and rat hepatocellular carcinoma mitochondria, we suspected these mitochondrial populations to differ massively in their molecular composition. Aiming to reveal these mitochondrial differences, we came across the issue on how to normalize such comparisons and decided to focus on the absolute number of mitochondria. To this end, fluorescently stained mitochondria were quantified by flow cytometry. For rat liver mitochondria, this approach resulted in mitochondrial protein contents comparable to earlier reports using alternative methods. We determined similar protein contents for rat liver, heart and kidney mitochondria. In contrast, however, lower protein contents were determined for rat brain mitochondria and for mitochondria from the rat hepatocellular carcinoma cell line McA 7777. This result challenges mitochondrial comparisons that rely on equal protein amounts as a typical normalization method. Exemplarily, we therefore compared the activity and susceptibility toward inhibition of complex II of rat liver and hepatocellular carcinoma mitochondria and obtained significant discrepancies by either normalizing to protein amount or to absolute mitochondrial number. Importantly, the latter normalization, in contrast to the former, demonstrated a lower complex II activity and higher susceptibility toward inhibition in hepatocellular carcinoma mitochondria compared to liver mitochondria. These findings demonstrate that solely normalizing to protein amount may obscure essential molecular differences between mitochondrial populations.
Copyright © 2014 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

Entities:  

Keywords:  Metabolic shift; Mitochondria; Mitochondrial number; Mitochondrial protein content; Respiratory complex II

Mesh:

Substances:

Year:  2014        PMID: 24969531     DOI: 10.1016/j.mito.2014.06.005

Source DB:  PubMed          Journal:  Mitochondrion        ISSN: 1567-7249            Impact factor:   4.160


  5 in total

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Journal:  Am J Physiol Renal Physiol       Date:  2019-12-02

2.  Data on chow, liver tissue and mitochondrial fatty acid compositions as well as mitochondrial proteome changes after feeding mice a western diet for 6-24 weeks.

Authors:  Claudia Einer; Simon Hohenester; Ralf Wimmer; Lena Wottke; Renate Artmann; Sabine Schulz; Christian Gosmann; Alisha Simmons; Christin Leitzinger; Carola Eberhagen; Sabine Borchard; Sabine Schmitt; Stefanie M Hauck; Christine von Toerne; Martin Jastroch; Ellen Walheim; Christian Rust; Alexander L Gerbes; Bastian Popper; Doris Mayr; Max Schnurr; Angelika M Vollmar; Gerald Denk; Hans Zischka
Journal:  Data Brief       Date:  2017-09-18

3.  Press-pulse: a novel therapeutic strategy for the metabolic management of cancer.

Authors:  Thomas N Seyfried; George Yu; Joseph C Maroon; Dominic P D'Agostino
Journal:  Nutr Metab (Lond)       Date:  2017-02-23       Impact factor: 4.169

4.  A High-Calorie Diet Aggravates Mitochondrial Dysfunction and Triggers Severe Liver Damage in Wilson Disease Rats.

Authors:  Claudia Einer; Christin Leitzinger; Josef Lichtmannegger; Carola Eberhagen; Tamara Rieder; Sabine Borchard; Ralf Wimmer; Gerald Denk; Bastian Popper; Frauke Neff; Elena V Polishchuk; Roman S Polishchuk; Stefanie M Hauck; Christine von Toerne; Jennifer-Christin Müller; Uwe Karst; Bipin S Baral; Alan A DiSpirito; Andreas E Kremer; Jeremy Semrau; Karl Heinz Weiss; Simon Hohenester; Hans Zischka
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2018-12-23

5.  Mitochondria in smooth muscle cells of viscera.

Authors:  Giorgio Gabella
Journal:  J Smooth Muscle Res       Date:  2018
  5 in total

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