4.5 Article

Differences in mitochondrial movement and morphology in young and mature primary cortical neurons in culture

Journal

NEUROSCIENCE
Volume 141, Issue 2, Pages 727-736

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2006.01.034

Keywords

mitochondria; trafficking; membrane potential; mfn-1; drp-1

Categories

Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM008424] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS049560] Funding Source: NIH RePORTER
  3. NIGMS NIH HHS [T32 GM008424] Funding Source: Medline
  4. NINDS NIH HHS [NS049560] Funding Source: Medline

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Mitochondria have many roles critical to the function of neurons including the generation of ATP and regulation of intracellular Ca2+. Mitochondrial movement is highly dynamic in neurons and is thought to direct mitochondria to specific cellular regions of increased need and to transport damaged or old mitochondria to autophagosomes. Morphology also varies between individual mitochondria and is modulated by fusion and fission proteins such as mitofusin-1 and dynamin-related protein-1, respectively. Although mitochondrial movement and morphology are thought to be modulated to best meet cellular demands,, few regulatory signals have been identified. In this study, we examined how the different cellular environments of synaptically immature and mature rat cortical neurons affect mitochondrial movement, morphology, distribution and function. In younger cells, mitochondria were more mobile, were shorter, occupied a smaller percentage of neuronal processes, and expressed greater mitofusin-1 and lower dynamin-related protein-1 protein levels compared with older cells. However, the number of mitochondria per mu m of neuronal process, mitochondrial membrane potential and the amount of basally sequestered mitochondrial Ca2(+) were similar. Our results suggest that while mitochondria in young neurons are functionally similar to mature neurons, their enhanced motility may permit faster energy dispersal for cellular demands, such as synaptogeriesis. As cells mature, mitochondria in the processes may then elongate and reduce their motility for long-term support of synaptic structures. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.

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