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関連する概念動画

Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

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...
Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
Mitochondrial Membranes01:45

Mitochondrial Membranes

A single mitochondrion is a bean-shaped organelle enclosed by a double-membrane system. The outer membrane of mitochondria is smooth and contains many porins - the integral membrane transporters. Porins enable free diffusion of ions and small uncharged molecules through the outer mitochondrial membrane but limit the transport of molecules larger than 5000 Daltons. Further, the outer mitochondrial membrane forms a unique structure called membrane contact sites with other subcellular organelles,...
Mitochondrial Membranes01:45

Mitochondrial Membranes

A single mitochondrion is a bean-shaped organelle enclosed by a double-membrane system. The outer membrane of mitochondria is smooth and contains many porins - the integral membrane transporters. Porins enable free diffusion of ions and small uncharged molecules through the outer mitochondrial membrane but limit the transport of molecules larger than 5000 Daltons. Further, the outer mitochondrial membrane forms a unique structure called membrane contact sites with other subcellular organelles,...
Mitochondria01:37

Mitochondria

Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...

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関連する実験動画

Updated: May 23, 2026

Using Live Cell STED Imaging to Visualize Mitochondrial Inner Membrane Ultrastructure in Neuronal Cell Models
08:48

Using Live Cell STED Imaging to Visualize Mitochondrial Inner Membrane Ultrastructure in Neuronal Cell Models

Published on: June 30, 2023

ミトコンドリア系疾患は,ミトコンドリア系疾患である.

Anthony H V Schapira1

  • 1Department of Clinical Neurosciences, Institute of Neurology, University College London, London, UK. a.schapira@medsch.ucl.ac.uk

Lancet (London, England)
|April 10, 2012
PubMed
まとめ

ミトコンドリア機能障害は,遺伝子の変異によって引き起こされ,神経変性疾患を含む様々な疾患に寄与します. ミトコンドリアをターゲットにすることで,これらの疾患に対する新たな治療の道が開けます.

科学分野:

  • 細胞生物学 細胞生物学
  • 遺伝学 遺伝学とは
  • 医学 医学 医学 医学 医学

背景:

  • ミトコンドリアは,細胞のエネルギー生産 (バイオエネルギー) とプログラム細胞死 (アポトーシス) に不可欠です.
  • ミトコンドリア疾患は,ミトコンドリアDNA (mtDNA) またはミトコンドリアタンパク質をコードする核遺伝子の変異から生じる.
  • これらの疾患は複数のシステムに影響を及ぼしたり,組織特異的であり,視神経,聴覚系,臓などの臓器に影響を与える可能性があります.

研究 の 目的:

  • ヒトの疾患におけるミトコンドリア機能障害の重要性を強調する.
  • 病気の病原性におけるミトコンドリアダイナミクス,特に分裂融合の役割を強調する.
  • 様々な疾患に対するミトコンドリアを標的とした治療の可能性を調査する.

主な方法:

  • ミトコンドリアDNAと核遺伝子に影響を与える遺伝子変異のレビュー.
  • 病気におけるミトコンドリア動力学 (分裂-融合) の役割の分析.
  • ミトコンドリアを標的とした現在のおよび新興の治療法の検討.

主要な成果:

  • mtDNAの維持と機能に影響を与える核遺伝子の変異は,いくつかの疾患に関連しています.

さらに関連する動画

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry
06:53

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry

Published on: November 23, 2011

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle
09:40

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle

Published on: January 19, 2017

関連する実験動画

Last Updated: May 23, 2026

Using Live Cell STED Imaging to Visualize Mitochondrial Inner Membrane Ultrastructure in Neuronal Cell Models
08:48

Using Live Cell STED Imaging to Visualize Mitochondrial Inner Membrane Ultrastructure in Neuronal Cell Models

Published on: June 30, 2023

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry
06:53

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry

Published on: November 23, 2011

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle
09:40

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle

Published on: January 19, 2017

  • ミトコンドリアの異常は,パーキンソン病やアルツハイマー病などの進行性神経退行性疾患に関連しています.
  • ミトコンドリアの分裂-融合プロセスは,ヒトの病気の研究の重要な分野である.
  • 結論:

    • ミトコンドリア機能障害は,幅広いヒト疾患の重要な要因です.
    • 小分子を含むミトコンドリアを標的とした治療戦略,転写調節,遺伝子操作は有望である.
    • ミトコンドリアのダイナミクスに関するさらなる研究と,標的を絞った介入は,さまざまな疾患に対する効果的な治療法につながる可能性があります.