Modeling mitochondrial dysfunctions in the brain : From mice to men

The biologist Lewis Thomas once wrote: "my mitochondria comprise a very large proportion of me. I cannot do the calculation, but I suppose there is almost as much of them in sheer dry bulk as there is the rest of me". As humans, or indeed as any mammal, bird, or insect, we contain a specific molecular makeup that is driven by vast numbers of these miniscule powerhouses residing in most of our cells (mature red blood cells notwithstanding), quietly replicating, living independent lives and containing their own DNA. Everything we do, from running a marathon to breathing, is driven by these small batteries, and yet there is evidence that these molecular energy sources were originally bacteria, possibly parasitic, incorporated into our cells through symbiosis. Dysfunctions in these organelles can lead to debilitating, and sometimes fatal, diseases of almost all the bodies' major organs. Mitochondrial dysfunction has been implicated in a wide variety of human disorders either as a primary cause or as a secondary consequence. To better understand the role of mitochondrial dysfunction in human disease, a multitude of pharmacologically induced and genetically manipulated animal models have been developed showing to a greater or lesser extent the clinical symptoms observed in patients with known and unknown causes of the disease. This review will focus on diseases of the brain and spinal cord in which mitochondrial dysfunction has been proven or is suspected and on animal models that are currently used to study the etiology, pathogenesis and treatment of these diseases.

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Main Authors: Breuer, Megan E., Willems, Peter H.G.M., Russel, Frans G.M., Koopman, Werner J.H., Smeitink, Jan A.M.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Life Science,
Online Access:https://research.wur.nl/en/publications/modeling-mitochondrial-dysfunctions-in-the-brain-from-mice-to-men
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spelling dig-wur-nl-wurpubs-6242252024-05-14 Breuer, Megan E. Willems, Peter H.G.M. Russel, Frans G.M. Koopman, Werner J.H. Smeitink, Jan A.M. Article/Letter to editor Journal of Inherited Metabolic Disease 35 (2012) 2 ISSN: 0141-8955 Modeling mitochondrial dysfunctions in the brain : From mice to men 2012 The biologist Lewis Thomas once wrote: "my mitochondria comprise a very large proportion of me. I cannot do the calculation, but I suppose there is almost as much of them in sheer dry bulk as there is the rest of me". As humans, or indeed as any mammal, bird, or insect, we contain a specific molecular makeup that is driven by vast numbers of these miniscule powerhouses residing in most of our cells (mature red blood cells notwithstanding), quietly replicating, living independent lives and containing their own DNA. Everything we do, from running a marathon to breathing, is driven by these small batteries, and yet there is evidence that these molecular energy sources were originally bacteria, possibly parasitic, incorporated into our cells through symbiosis. Dysfunctions in these organelles can lead to debilitating, and sometimes fatal, diseases of almost all the bodies' major organs. Mitochondrial dysfunction has been implicated in a wide variety of human disorders either as a primary cause or as a secondary consequence. To better understand the role of mitochondrial dysfunction in human disease, a multitude of pharmacologically induced and genetically manipulated animal models have been developed showing to a greater or lesser extent the clinical symptoms observed in patients with known and unknown causes of the disease. This review will focus on diseases of the brain and spinal cord in which mitochondrial dysfunction has been proven or is suspected and on animal models that are currently used to study the etiology, pathogenesis and treatment of these diseases. en text/html https://research.wur.nl/en/publications/modeling-mitochondrial-dysfunctions-in-the-brain-from-mice-to-men 10.1007/s10545-011-9375-8 https://edepot.wur.nl/646025 Life Science https://creativecommons.org/licenses/by-nc/4.0/ Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Life Science
Life Science
spellingShingle Life Science
Life Science
Breuer, Megan E.
Willems, Peter H.G.M.
Russel, Frans G.M.
Koopman, Werner J.H.
Smeitink, Jan A.M.
Modeling mitochondrial dysfunctions in the brain : From mice to men
description The biologist Lewis Thomas once wrote: "my mitochondria comprise a very large proportion of me. I cannot do the calculation, but I suppose there is almost as much of them in sheer dry bulk as there is the rest of me". As humans, or indeed as any mammal, bird, or insect, we contain a specific molecular makeup that is driven by vast numbers of these miniscule powerhouses residing in most of our cells (mature red blood cells notwithstanding), quietly replicating, living independent lives and containing their own DNA. Everything we do, from running a marathon to breathing, is driven by these small batteries, and yet there is evidence that these molecular energy sources were originally bacteria, possibly parasitic, incorporated into our cells through symbiosis. Dysfunctions in these organelles can lead to debilitating, and sometimes fatal, diseases of almost all the bodies' major organs. Mitochondrial dysfunction has been implicated in a wide variety of human disorders either as a primary cause or as a secondary consequence. To better understand the role of mitochondrial dysfunction in human disease, a multitude of pharmacologically induced and genetically manipulated animal models have been developed showing to a greater or lesser extent the clinical symptoms observed in patients with known and unknown causes of the disease. This review will focus on diseases of the brain and spinal cord in which mitochondrial dysfunction has been proven or is suspected and on animal models that are currently used to study the etiology, pathogenesis and treatment of these diseases.
format Article/Letter to editor
topic_facet Life Science
author Breuer, Megan E.
Willems, Peter H.G.M.
Russel, Frans G.M.
Koopman, Werner J.H.
Smeitink, Jan A.M.
author_facet Breuer, Megan E.
Willems, Peter H.G.M.
Russel, Frans G.M.
Koopman, Werner J.H.
Smeitink, Jan A.M.
author_sort Breuer, Megan E.
title Modeling mitochondrial dysfunctions in the brain : From mice to men
title_short Modeling mitochondrial dysfunctions in the brain : From mice to men
title_full Modeling mitochondrial dysfunctions in the brain : From mice to men
title_fullStr Modeling mitochondrial dysfunctions in the brain : From mice to men
title_full_unstemmed Modeling mitochondrial dysfunctions in the brain : From mice to men
title_sort modeling mitochondrial dysfunctions in the brain : from mice to men
url https://research.wur.nl/en/publications/modeling-mitochondrial-dysfunctions-in-the-brain-from-mice-to-men
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