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New clues about mitochondrial 'growth spurts'
March 02, 2009
Mitochondria are restless, continually merging and splitting. But contrary to conventional wisdom, the size of these organelles depends on more than fusion and fission, as Berman et al. show. Mitochondrial growth and degradation are also part of the equation. The study will appear online March 2, 2009 (www.jcb.org) and in the March 9, 2009 print issue of The Journal of Cell Biology (JCB). Fission is necessary to produce new mitochondria, such as those that power synaptic activity in healthy neurons. Fusion is also important. It goes awry in one form of Charcot-Marie-Tooth disease, in which peripheral nerves deteriorate, and in other neurodegenerative diseases. How cells manage mitochondrial size and number remains unclear. Berman et al. found a clue when they started refining measurements of mitochondrial dynamics. The team labeled the organelles with a red fluorescent protein and a light-activated green fluorescent protein. By switching on the green marker with a laser and then looking for the mixing of colors, the researchers could distinguish mitochondrial mergers from near misses. To their surprise, they found that in healthy neurons, fission occurs up to six times more often than fusion. So why aren't the cells cluttered with tiny mitochondria? Because the organelles grow longer, the researchers determined. This size increase offsets the higher fission rate. The researchers also surmised that to "balance the books," another process has to be operating-mitochondrial degradation. Together, fusion, fission, growth, and breakdown determine mitochondrial size and shape, Berman et al. propose. Orchestrating many of these changes is the protein Bcl-xL. The team found that it spurred mitochondrial elongation and sped up fission and fusion. Without Bcl-xL, mitochondria became stumpy and seemingly less energy efficient. Bcl-xL belongs to the Bcl-2 protein family, whose members can protect mitochondria or shatter them to drive apoptosis. Berman et al.'s results suggest that Bcl-xL manages the number, size, and energy-producing capacity of mitochondria long before the cell is faced with a life-or-death decision. Still a mystery, the scientists say, is how Bcl-xL sparks mitochondrial growth. Rockefeller University Press

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Living Well With Mitochondrial Disease: A Handbook for Patients, Parents, and Families
by Cristy Balcells (Author)
LIVING WELL WITH MITOCHONDRIAL DISEASE helps make sense of mitochondrial disease (Mito), an overwhelming and complex group of diagnoses that has grown exponentially in recent years. The most common of all metabolic disorders, thought to be more common than cystic fibrosis and broader-reaching than most genetic diseases, Mito can affect babies, children, and teens from birth or at any point during their development. Previously healthy adults, as well as adults with a history of unexplained fatigue, are increasingly receiving a Mito diagnosis. Some children with autism spectrum disorders who have medical issues such as digestive difficulties and fatigue are also being identified as having a mitochondrial disorder. This guide is the first book about Mito written for patients and their...
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The Mitochondrial Curiosities of Marcels 1 to 19
by Jocelyn Brown (Author)
Biology is not Dree’s thing. Equally heinous are English, Social Studies, her sister and mother, not to mention Edmonton in general. Toronto is where she belongs specifically the upcoming Renegade Craft Fair where, finally, her crafts will be appreciated.Escape is imminent: on her 15th birthday, she will get the special fund her father promised, and the day after that she’ll be on Westjet Flight 233 to Toronto. Instead, her dad has a fatal heart attack, and all she finds are clues leading to the ominous Alberta Psychiatric Hospital where her parents once worked. As Dree tries to unearth a mystery, and to knit herself a passing mark in science, she keeps searching for the money, and for a way to grieve her father.Told in a fresh, frank voice, The Mitochondrial Curiosities of Marcels...
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Mitochondrial Signaling in Health and Disease (Oxidative Stress and Disease)
by Sten Orrenius (Editor), Lester Packer (Editor), Enrique Cadenas (Editor)
Mitochondria have traditionally been associated with metabolic functions; however recent research has uncovered a central role for these organelles in cell signaling, cell survival, and cell death. Mitochondrial dysfunction is a factor in a myriad of pathophysiological conditions, including age-related neurodegenerative disorders, cancer, metabolic syndrome, and cardiovascular disease. Mitochondrial Signaling in Health and Disease examines themes essential for the maintenance of the mitochondrial redox (reduction-oxidation) energy axis. With contributions from an impressive cadre of internationally recognized scientists, the book discusses coordinated mitochondrial functions that regulate cell function by discrete signaling pathways. Topics discussed include: Electron transport and...
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Mitochondrial Disorders Caused by Nuclear Genes
by Lee-Jun C. Wong (Editor)
Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are encoded by both mitochondrial and nuclear genomes and are essential in all cells. In addition, the biogenesis, structure and function of mitochondria, including DNA replication, transcription, and translation, all require nuclear encoded genes. Since mitochondria are present in every cell, every tissue, mitochondrial disorder usually affects multiple organs.
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Mitochondrial DNA: Methods and Protocols (Methods in Molecular Biology)
by Jeffrey A. Stuart (Editor)
Since the publication of the first edition, the number of unique heritable mtDNA mutations recognized as being associated with bioenergetic dysfunction, cell death and disease has grown. Likewise, our understanding of the basic biology of somatic mtDNA mutations continues to improve. In Mitochondrial DNA: Methods and Protocols, Second Edition, specialists from eight countries share their expertise, providing detailed protocols for studying many aspects of mtDNA. The volume is divided into three sections, which cover the transduction of information from mtDNA to functionally active respiratory complexes, mitochondrial reactive oxygen species (ROS) production as well as mtDNA damage and its repair, and the identification and quantification of heteroplasmic mtDNA mutations. Written in the...
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Human Mitochondrial DNA and the Evolution of Homo sapiens (Nucleic Acids and Molecular Biology)
by Hans-Jürgen Bandelt (Editor), Martin Richards (Editor), Vincent Macaulay (Editor)
Mitochondrial DNA is one of the most closely explored genetic systems, because it can tell us so much about the human past. This book takes a unique perspective, presenting the disparate strands that must be tied together to exploit this system. From molecular biology to anthropology, statistics to ancient DNA, this first volume of three presents a comprehensive global picture and a critical appraisal of human mitochondrial DNA variation.
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Mitochondrial Bioenergetics: Methods and Protocols (Methods in Molecular Biology)
by Carlos M. Palmeira (Editor), António J. Moreno (Editor)
Increasing interest in mitochondrial bioenergetics is being driven by the impact of drug and environmental chemical-induced disturbances of mitochondrial function as well as hereditary deficiencies and the progressive deterioration of bioenergetic performance with age. These initiatives have fostered the investigation of genetic and environmental influences on bioenergetics. In Mitochondrial Bioenergetics: Methods and Protocols, researchers in the field detail the practical principles and assays designed to derive quantitative assessment of each set of parameters that reflect different aspects of mitochondrial bioenergetics. Written in the highly successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary...
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The Official Parent's Sourcebook on Mitochondrial Myopathies: A Revised and Updated Directory for the Internet Age
by Icon Health Publications (Author)
This sourcebook has been created for parents who have decided to make education and Internet-based research an integral part of the treatment process. Although it gives information useful to doctors, caregivers and other health professionals, it also tells parents where and how to look for information covering virtually all topics related to mitochondrial myopathies, from the essentials to the most advanced areas of research. The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research. Selected readings from various agencies are reproduced to give you some of the latest official information available to date on mitochondrial myopathies. Following an introductory chapter, the sourcebook is...
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Drug-Induced Mitochondrial Dysfunction
by James A. Dykens (Editor), Yvonne Will (Editor)
This is the definitive, one-stop resource on preclinical drug evaluation for potential mitochondrial toxicity, addressing the issue upfront in the drug development process. It discusses mitochondrial impairment to organs, skeletal muscle, and nervous systems and details methodologies used to assess mitochondria function. It covers both in vitro and in vivo methods for analysis and includes the latest models. This is the authoritative reference on drug-induced mitochondrial dysfunction for safety assessment professionals in the pharmaceutical industry and for pharmacologists and toxicologists in both drug and environmental health sciences.
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Mitochondrial Medicine: Mitochondrial Metabolism, Diseases, Diagnosis and Therapy
by Anna Gvozdjáková (Editor)
Mitochondrial Medicine is a relatively new area where several disciplines from basic science to clinical medicine converge. Mitochondrial medicine deals with diseases that are related to mitochondrial dysfunction due to a number of causes from free radical damage to genetic mutation. A primary feature of mitochondrial dysfunction is impaired cellular bioenergetics. This book is based upon extensive data gathered over 30 years of clinical and experimental research. Internationally recognized authors share their experience and state-of-the-art knowledge in various fields of their expertise such as mitochondrial cardiology, neurology, diabetology, nephrology, immunology, rheumatology, reproductive medicine, sports medicine, and chronobiology, and guide readers through the disease process,...
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