Literature DB >> 18666204

Mitochondrial biogenesis in the axons of vertebrate peripheral neurons.

Mandana Amiri1, Peter J Hollenbeck.   

Abstract

Mitochondria are widely distributed via regulated transport in neurons, but their sites of biogenesis remain uncertain. Most mitochondrial proteins are encoded in the nuclear genome, and evidence has suggested that mitochondrial DNA (mtDNA) replication occurs mainly or entirely in the cell body. However, it has also become clear that nuclear-encoded mitochondrial proteins can be translated in the axon and that components of the mitochondrial replication machinery reside there as well. We assessed directly whether mtDNA replication can occur in the axons of chick peripheral neurons labeled with 5-bromo-2'-deoxyuridine (BrdU). In axons that were physically separated from the cell body or had disrupted organelle transport between the cell bodies and axons, a significant fraction of mtDNA synthesis continued. We also detected the mitochondrial fission protein Drp1 in neurons by immunofluorescence or expression of GFP-Drp1. Its presence and distribution on the majority of axonal mitochondria indicated that a substantial number had undergone recent division in the axon. Because the morphology of mitochondria is maintained by the balance of fission and fusion events, we either inhibited Drp1 expression by RNAi or overexpressed the fusion protein Mfn1. Both methods resulted in significantly longer mitochondria in axons, including many at a great distance from the cell body. These data indicate that mitochondria can replicate their DNA, divide, and fuse locally within the axon; thus, the biogenesis of mitochondria is not limited to the cell body. Copyright (c) 2008 Wiley Periodicals, Inc.

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Year:  2008        PMID: 18666204      PMCID: PMC2538952          DOI: 10.1002/dneu.20668

Source DB:  PubMed          Journal:  Dev Neurobiol        ISSN: 1932-8451            Impact factor:   3.964


  69 in total

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2.  An integrated theory of aging as the result of mitochondrial-DNA mutation in differentiated cells.

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Authors:  W Neupert
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Authors:  N J Gross; G S Getz; M Rabinowitz
Journal:  J Biol Chem       Date:  1969-03-25       Impact factor: 5.157

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8.  Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.

Authors:  N G Larsson; A Oldfors; E Holme; D A Clayton
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  72 in total

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Review 4.  Mitochondrial trafficking in neurons.

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5.  Mitochondrial biogenesis and fission in axons in cell culture and animal models of diabetic neuropathy.

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7.  The Organization of Mitochondrial Quality Control and Life Cycle in the Nervous System In Vivo in the Absence of PINK1.

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Review 8.  Sigma-1 Receptors Fine-Tune the Neuronal Networks.

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10.  Disruption of mitochondrial DNA replication in Drosophila increases mitochondrial fast axonal transport in vivo.

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