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

被引:106
作者
Chang, D. T. W. [1 ]
Reynolds, I. J. [1 ]
机构
[1] Univ Pittsburgh, Dept Pharmacol, Pittsburgh, PA 15261 USA
关键词
mitochondria; trafficking; membrane potential; mfn-1; drp-1;
D O I
10.1016/j.neuroscience.2006.01.034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:727 / 736
页数:10
相关论文
共 55 条
[31]   NEURONAL CA2+ - GETTING IT UP AND KEEPING IT UP [J].
MILLER, RJ .
TRENDS IN NEUROSCIENCES, 1992, 15 (09) :317-319
[32]   AXONAL-TRANSPORT OF MITOCHONDRIA ALONG MICROTUBULES AND F-ACTIN IN LIVING VERTEBRATE NEURONS [J].
MORRIS, RL ;
HOLLENBECK, PJ .
JOURNAL OF CELL BIOLOGY, 1995, 131 (05) :1315-1326
[33]   Dnm1p GTPase-mediated mitochondrial fission is a multi-step process requiring the novel integral membrane component Fis1p [J].
Mozdy, AD ;
McCaffery, JM ;
Shaw, JM .
JOURNAL OF CELL BIOLOGY, 2000, 151 (02) :367-379
[34]   Interaction theory of mammalian mitochondria [J].
Nakada, K ;
Inoue, K ;
Hayashi, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 288 (04) :743-746
[35]   KIF1B, A NOVEL MICROTUBULE PLUS END-DIRECTED MONOMERIC MOTOR PROTEIN FOR TRANSPORT OF MITOCHONDRIA [J].
NANGAKU, M ;
SATOYOSHITAKE, R ;
OKADA, Y ;
NODA, Y ;
TAKEMURA, R ;
YAMAZAKI, H ;
HIROKAWA, N .
CELL, 1994, 79 (07) :1209-1220
[36]  
Overly CC, 1996, J CELL SCI, V109, P971
[37]   Mitochondria-specific function of the dynamin family protein DLP1 is mediated by its C-terminal domains [J].
Pitts, KR ;
McNiven, MA ;
Yoon, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :50286-50294
[38]   The dynamin-like protein DLP1 is essential for normal distribution and morphology of the endoplasmic reticulum and mitochondria in mammalian cells [J].
Pitts, KR ;
Yoon, Y ;
Krueger, EW ;
McNiven, MA .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (12) :4403-4417
[39]   Impairing the bioenergetic status and the biogenesis of mitochondria triggers mitophagy in yeast [J].
Priault, M ;
Salin, B ;
Schaeffer, J ;
Vallette, FM ;
di Rago, JP ;
Martinou, JC .
CELL DEATH AND DIFFERENTIATION, 2005, 12 (12) :1613-1621
[40]  
Rintoul GL, 2003, J NEUROSCI, V23, P7881