Mitochondria


  线粒体是真核细胞的重要细胞器,是动物细胞生成ATP的主要地点。它们内部基本上是空的,但具有复杂的膜结构。线粒体基质的三羧酸循环酶系通过底物脱氢氧化生成NADH。NADH通过线粒体内膜呼吸链氧化,与此同时合成ATP。合成的ATP进入细胞质后参与细胞的各种需能过程。线粒体的遗传基因(DNA)跟人的细胞核的DNA有质的不同,线粒体独立自主地复制繁衍,跟它寄主的细胞的繁衍没有关系。如果线粒体DNA发生突变,则细胞不能产生足够的ATP而导致细胞功能减退甚至坏死,从而使临床上表现为复杂多样的症状。即线粒体病。正是由于线粒体的特殊性及在人体细胞中的重要作用使得它一直是科学家关注的焦点。牛津大学的科学家在日前出版的英国《自然》杂志上报告说,他们从两种恐鸟的亚化石骨骼中提取出线粒体进行测序,绘出了线粒体基因组图谱。这对于研究线粒体的起源和功能都是一大贡献,下面我们搜集了有关线粒体及线粒体病的最新报道和文献200多篇奉献给大家,更多的文献请查阅cmbi的综述查询和相关栏目:

cell-mitochondrial- import machinery- preprotein-conducting channels with binding sites for presequences

cell-mitochondrial-Contact sites between the outer and inner membrane of mitochondria—role in protein transport

cell-mitochondrial-Delivery of nascent polypeptides to the mitochondrial surface

cell-mitochondrial-Functions of outer membrane receptors in mitochondrial protein import

cell-mitochondrial-Import and assembly of proteins into mitochondria

cell-mitochondrial-Insertion of proteins into the inner membrane of mitochondria

cell-mitochondrial-Membrane protein degradation by AAA proteases

cell-mitochondrial--Mitochondrial processing peptidases

cell-mitochondrial-Molecular chaperones as essential mediators of mitochondrial biogenesis

cell-mitochondrial-Protein import into and across the mitochondrial inner membrane

cell-Mitochondria, the killer organelles and their weapons

cell-Mitochondrial mutations may drive Y chromosome evolution

cell-mitochondrial specific stress respone

ns-clin Mitochondrial-EImpairment of brain mitochondrial function by reactive nitrogen species

ns-clin Mitochondrial-EInteractions of oxidative stress with thiamine homeostasis promote neurodegeneration

ns-clin Mitochondrial-EMitochondrial contributions to tissue damage in stroke

ns-clin Mitochondrial-EMitochondrial dysfunction in acute hyperammonemia

ns-clin Mitochondrial-EMitochondrial dysfunction in progressive supranuclear palsy

ns-clin Mitochondrial-EMitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease

ns-clin Mitochondrial-EMitochondrial involvement in amyotrophic lateral sclerosis

ns-clin Mitochondrial-EMitochondrial involvement in Parkinson's disease

ns-clin Mitochondrial-Energy metabolism, stress hormones and neural recovery from cerebral ischemia

ns-clin Mitochondrial-EOptic nerve degeneration and mitochondrial dysfunction

ns-clin Mitochondrial-EPeripheral benzodiazepine receptors and mitochondrial function

ns-clin Mitochondrial-ESpinocerebellar ataxias due to mitochondrial defects

ns-clin Mitochondrial-Neurolathyrism-mitochondrial dysfunction in excitotoxicity mediated by-oxalyl aminoalanine

cell-mitochondrial protein-

cell-mitochondrial protein-Contact sites between the outer and inner membrane of mitochondria-role in protein transport

cell-mitochondrial protein-Delivery of nascent polypeptides to the mitochondrial surface

cell-mitochondrial protein-Functions of outer membrane receptors in mitochondrial protein import

cell-mitochondrial protein-Import and assembly of proteins into mitochondria of mammalian cells

cell-mitochondrial protein-Insertion of proteins into the inner membrane of mitochondria

cell-mitochondrial protein-Membrane protein degradation by AAA proteases in mitochondria

cell-mitochondrial protein-Mitochondrial processing peptidases

cell-mitochondrial protein-Molecular chaperones as essential mediators of mitochondrial biogenesis

cell-mitochondrial protein-Origins and consequences of mitochondrial decline in nucleated erythrocytes

cell-mitochondrial protein-Protein import into and across the mitochondrial inner membrane

cell-mitochondrial protein-The mitochondrial import machinery-preprotein-conducting channels with binding sites

cell-mitochondrial specific stress response in mammalian cells

proteome-cv-Applied Proteomics-Mitochondrial Proteins and Effect on Function

ageing-Can Antioxidant Diet Supplementation Protect against Age-related Mitochondrial Damage

ageing-Therapeutics against Mitochondrial Oxidative Stress in Animal Models of Aging

ageing-Prevention of Mitochondrial Oxidative Damage Using Targeted Antioxidants

ageing-Mitochondrial DNA Deletion Mutations and Sarcopenia

ageing-Mitochondrial Decay in the Aging Rat Heart

ageing-Mitochondrial Damage in Aging and Apoptosis

ageing-Melatonin Reduces Oxidant Damage and Promotes Mitochondrial Respiration

biochem-Biogenesis of the mitochondrial TOM complex

ageing-Delaying Brain Mitochondrial Decay and Aging with Mitochondrial Antioxidants and Metabolites

cell-mitochondrial-Regulated and unregulated mitochondrial permeability transition pores

cv-Cardioprotection-Enhanced Mitochondrial PKC-MAPK Interactions and Differential MAPK Activation in PKC-Induced Cardioprotection

cell-apoptosis-Does nitric oxide modulate mitochondrial energy generation and apoptosis

cv-Preconditioning-Mitochondrial ATP-Sensitive Potassium Channels Inhibit Apoptosis Induced by Oxidative Stress in Cardiac Cells

cv-Preconditioning-Ischemic and Pharmacological Preconditioning in Girardi Cells and C2C12 Myotubes Induce Mitochondrial Uncoupling

cv-Preconditioning-Evidence for mitochondrial KATP channels as effectors of human myocardial preconditioning

cv-Preconditioning-Direct activation of mitochondrial KATP channels mimics preconditioning but protein kinase C activation is less effective

biochem-Mitochondrial ATP Formation

cv-Cardioprotection-Selective Pharmacological Agents Implicate Mitochondrial but Not Sarcolemmal KATP Channels in Ischemic Cardioprotection

cv-Cardioprotection-Opioid-Induced Second Window of Cardioprotection-Potential Role of Mitochondrial KATP Channels

cv-Cardioprotection-Modulation of Mitochondrial ATP-Dependent K+ Channels by Protein Kinase

cv-Cardioprotection-Mitochondrial ATP-Sensitive Potassium Channels Attenuate Matrix Ca2+ Overload During Simulated Ischemia and Reperfusion-Possible Mechanism of Cardioprotection

cv-Cardioprotection-Mitochondrial ATP-Dependent Potassium Channels-Novel Effectors of Cardioprotection

cv-Cardioprotection-Increased Mitochondrial KATP Channel Activity During Chronic Myocardial Hypoxia-Is Cardioprotection Mediated by Improved Bioenergetics

cv-Cardioprotection-Enhanced Mitochondrial PKC-MAPK Interactions and Differential MAPK Activation in PKC-Induced Cardioprotection

cv-Cardioprotection-Cardioprotective Effect of Diazoxide and Its Interaction With Mitochondrial ATP-Sensitive K+ Channels-Possible Mechanism of Cardioprotection

cv-Cardioprotection-Enhanced Mitochondrial PKC-MAPK Interactions and Differential MAPK Activation in PKC-Induced Cardioprotection

proteome-Yeast mitochondrial biogenesis-a model system for humans

proteome-Applied Proteomics-Mitochondrial Proteins and Effect on Function

cv-Preconditioning-tylcholine, Bradykinin, Opioids, and Phenylephrine, but not Adenosine, Trigger Preconditioning by Generating Free Radicals and Opening Mitochondrial KATP Channels

proteome-Survey of human mitochondrial diseases using new genomic-proteomic tools

biochem-Mitochondrial ATP Formation

cv-remodeling-Mitochondrial DNA Damage and Dysfunction Associated With Oxidative Stress in Failing Hearts

tgf-novel mitochondrial septin-like protein, ARTS, mediates apoptosis dependent on its P-loop motif

respir-Mitochondrial Disease-A Pulmonary and Critical-Care Medicine Perspective

physiol-NO-Modulation of liver mitochondrial NOS is implicated in thyroid-dependent regulation of O2 uptake

blood-leukemia-Receptor-and mitochondrial-mediated apoptosis in acute leukemia

obesity-Mitochondrial uncoupling as a target for drug development for the treatment of obesity

Mutation analysis in mitochondrial fatty acid oxidation defects

molecular med-Mitochondrial DNA mutations in the pathogenesis of human disease

mitochondrial-A critical appraisal of the mitochondrial coenzyme Q pool

mitochondrial-Making mitochondrial mutants

Mitochondrial disorders-genetics, counseling, prenatal diagnosis and reproductive options

Mitochondrial disease-The Pathophysiology of Mitochondrial Biogenesis

Mitochondrial diseases-Respiratory chain complex I deficiency

Mitochondrial diseases-Mitochondrial DNA mutations in human disease

Mitochondrial diseases-Mitochondria, oxygen free radicals, and apoptosis

Mitochondrial diseases-Mitochondria and degenerative disorders

Mitochondrial diseases-Epidemiology and treatment of mitochondrial disorders

Mitochondrial diseases-Diseases caused by nuclear genes affecting mtDNA stability

Mitochondrial diseases-disease models for mitochondrial disease

Mitochondrial diseases-Cytochrome c oxidase deficiency

Mitochondrial diseases-Clinical spectrum and diagnosis of mitochondrial disorders

Mitochondrial diseases-Beyond the Magic Circle

Mitochondrial disease-Homoplasmic Mitochondrial DNA Diseases as the Paradigm to Understand the Tissue Specificity

mitochondrial disease-A nuclear modifier for a mitochondrial DNA disorder

microarrays-Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarrays

biotech-determination of complete human mitochondrial DNA sequences in single cells

genome-mitochondrial genome-mutation, selection and recombination

genome-Major genomic mitochondrial lineages delineate early human expansions

Diabetes-cell-nature insight-Mitochondrial function in normal and diabetic-cells

diabetes-cell-Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes

biochem-Nuclear and mitochondrial apoptotic pathways of p53

cv-physiol-Plasticity in Skeletal, Cardiac, and Smooth Muscle-Effects of contractile activity on mitochondrial transcription factor A expression in skeletal muscle

cv-physiol-Plasticity in Skeletal, Cardiac, and Smooth muscle-Contractile activity-induced mitochondrial biogenesis in skeletal muscle

cv-physiol-NO-Bioenergetics in cardiac hypertrophy-mitochondrial respiration as a pathological target of NO

cv-myocardial ischemia-Effects of myocardial ischemia and reperfusion on mitochondrial function and susceptibility to oxidative stress

bi-db-Update of AMmtDB-a database of multi-aligned Metazoa mitochondrial DNA sequences

bi-db-MitoNuc-a database of nuclear genes coding for mitochondrial proteins. Update 2002

cv-cell-Mitochondrial Coupling Factor 6 Is Present on the Surface of Human Vascular Endothelial Cells

cv-cell-Mitochondrial coupling factor 6 as a potent endogenous vasoconstrictor

cv-cardiomyopathy-The emerging concept of mitochondrial cardiomyopathies

cell-transport machinery for the import of preproteins across the outer mitochondrial membrane

cell-Mitochondrial DNA Depletion, Oxidative Stress, and Mutation-Mechanisms 0f Dysfunction from Nucleoside Reverse Transcriptase Inhibitors

cell-A Mitochondrial Division Apparatus Takes Shape

gt-Gene therapy by mitochondrial transfer

ageing--Mitochondrial DNA mutations, oxidative stress, and aging

Breakthroughs and Views-Mitochondrial Processing Peptidase- Multiple-Site Recognition of Precursor Proteins

Plasticity in Skeletal, Cardiac, and Smooth Muscle- mitochondrial biogenesis in skeletal muscle

Drug and mitochondria -Mitochondrial DNA metabolism targeting drugs

Drug and mitochondria -Mitochondrial contributions to cancer cell physiology

Drug and mitochondria -Human mitochondrial DNA diseases

Drug and mitochondria -Gene therapy by mitochondrial transfer

Drug and mitochondria Pharmacology of Nucleoside and Nucleotide Reverse Transcriptase Inhibitor-Induced Mitochondrial Toxicity

How do mitochondrial genes get into the nucleus

mp-Mitochondrial respiratory chain disorders II- neurodegenerative disorders and nuclear gene defectsm

mp-Mitochondrial respiratory chain disorders I- mitochondrial DNA defects

mp-Mitochondrial diseases

mp-Controlling the mitochondrial gatekeeper for effective chemotherapy

mp-MITOCHONDRIAL DISORDERS

MITOCHONDRIAL DISORDERS

Mitochondrial disorders- genetics, counseling, prenatal diagnosis and reproductive options

Mitochondrial diseases-Respiratory chain complex I deficiency

Mitochondrial diseases-Mouse models for mitochondrial disease

Mitochondrial diseases-Mitochondrial DNA mutations in human disease

Mitochondrial diseases-Mitochondria, oxygen free radicals, and apoptosis

Mitochondrial diseases-Mitochondria and degenerative disorders

Mitochondrial diseases-Epidemiology and treatment of mitochondrial disorders

Mitochondrial diseases-Diseases caused by nuclear genes affecting mtDNA stability

Mitochondrial diseases-Cytochrome c oxidase deficiency

Mitochondrial diseases-Clinical spectrum and diagnosis of mitochondrial disorders

Mitochondrial diseases

Drug and DNA delivery to mitochondria -Mitochondrial DNA metabolism targeting drugs

Drug and DNA delivery to mitochondria -Mitochondrial contributions to cancer cell physiology

Drug and DNA delivery to mitochondria -Human mitochondrial DNA diseases

Drug and DNA delivery to mitochondria -Gene therapy by mitochondrial transfer

mitochondrial apoptosome- a killer

skeletal muscle -Mitochondrial uncoupling protein 3 (UCP3) in skeletal muscle

Mitochondrial genome instability in human cancers

mitochondrial -What do mitochondrial diseases teach us about normal mitochondrial functions

mitochondrial -Regulation of mitochondrial respiration by nitric oxide inhibition of cytochrome c oxidase

Mitochondrial efficiency- lessons learned from transgenic mice

Mitochondrial defects and hearing loss

mitochondrial - investigation of mitochondrial dysfunction, regulation and pharmacology

cell-Breaking the mitochondrial barrier

mitochondrial-Effects of mutations in mitochondrial cytochrome b in yeast and man

Programmed cell death- The mitochondrial factor

mitochondrial biogenesis and function- a regulatory cross-talk between two genomes

UCP-Mitochondrial proton leak

UCP-Mitochondrial proton leak and the uncoupling protein 1 homologues

Mitochondrial genomics flies high

cardiac failure -Mitochondrial pathology in cardiac failure

bi-PLMItRNA, a database for mitochondrial tRNA genes and tRNAs in photosynthetic eukaryotes

Transmitochondrial mice- Proof of principle and promises

cholesterol-Steroidogenic acute regulatory protein and the intramitochondrial translocation of cholesterol

mitochondrial-Breaking the mitochondrial barrier

mitochondrial barrier -Breaking the mitochondrial barrier

cardiac failure-Mitochondrial pathology in cardiac failure

Role of Mitochondrial Oxidant Generation in Endothelial Cell Responses to Hypoxia

Mitochondrial PKC and MAPK Form Signaling Modules in the Murine Heart -Enhanced Mitochondrial PKC-MAPK Interactions and Differential MAPK Activation in PKC-Induced Cardioprotection

Cigarette Smoke Exposure and Hypercholesterolemia Increase Mitochondrial Damage in Cardiovascular Tissues

Mitochondrial Preference for Short Chain Fatty Acid Oxidation During Coronary Artery Constriction

Characteristics and Superoxide-Induced Activation of Reconstituted Myocardial Mitochondrial ATP-Sensitive Potassium Channels

Mitochondrial Coupling Factor 6 Is Present on the Surface of Human Vascular Endothelial Cells and Is Released by Shear Stress

Mitochondrial Disease and Stroke

Mitochondrial ATP-Sensitive Potassium Channels Attenuate Matrix Ca2+ Overload During Simulated Ischemia and Reperfusion -Possible Mechanism of Cardioprotection

Ischemic and Pharmacological Preconditioning in Girardi Cells and C2C12 Myotubes Induce Mitochondrial Uncoupling

Mitochondrial Abnormalities in Tumor Necrosis Factor-–Induced Heart Failure Are Associated With Impaired DNA Repair Activity

Heat Shock Protein 70 Gene Transfection Protects Mitochondrial and Ventricular Function Against Ischemia-Reperfusion Injury

Phosphorylation of Mitochondrial Elongation Factor Tu in Ischemic Myocardium

Acetylcholine, Bradykinin, Opioids, and Phenylephrine, but not Adenosine, Trigger Preconditioning by Generating Free Radicals and Opening Mitochondrial KATP Channels

Effects of propionyl--carnitine on isolated mitochondrial function in the reperfused diabetic rat heart

Downregulation of Protein Kinase C Inhibits Activation of Mitochondrial KATP Channels by Diazoxide

Mitochondrial DNA deletion associated with the reduction of adenine nucleotides in human atrium and atrial fibrillation

Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle

Novel biomarkers of the metabolism of caffeic acid derivatives in vivo Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle

Changes in mitochondrial and microsomal lipid peroxidation and fatty acid profiles in adrenal glands, testes, and livers from α-tocopherol-deficient rats

Protection by thiols of the mitochondrial complexes from 4-hydroxy-2-nonenal

DNA repair and aging in mouse liver: 8-oxodG glycosylase activity increase in mitochondrial but not in nuclear extracts

Combined and Individual Mitochondrial HSP60 and HSP10 Expression in Cardiac Myocytes Protects Mitochondrial Function and Prevents Apoptotic Cell Deaths Induced by Simulated Ischemia-Reoxygenation

Morphine Mimics Preconditioning via Free Radical Signals and Mitochondrial KATP Channels in Myocytes

Morphine Mimics Preconditioning via Free Radical Signals and Mitochondrial KATP Channels in Myocytes

Mitochondrial DNA Damage and Dysfunction Associated With Oxidative Stress in Failing Hearts After Myocardial Infarction

Direct activation of mitochondrial KATP channels mimics preconditioning but protein kinase C activation is less effective in middle-aged rat hearts

Mitochondrial pathology in cardiac failure

Inhibition of heart mitochondrial lipid peroxidation by non-toxic concentrations of carvedilol and its analog BM-910228

Free radicals alter maximal diaphragmatic mitochondrial oxygen consumption in endotoxin-induced sepsis

Direct activation of mitochondrial KATP channels mimics preconditioning but protein kinase C activation is less effective in middle-aged rat hearts

Mitochondrial pathology in cardiac failure

Direct activation of mitochondrial KATP channels mimics preconditioning but protein kinase C activation is less effective in middle-aged rat hearts

Mitochondrial pathology in cardiac failure

 

 

更新于2002-11-3