The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
The axonal transport of mitochondria
Open accessAbstract
Vigorous transport of cytoplasmic components along axons over substantial distances is crucial for the maintenance of neuron structure and function. The transport of mitochondria, which serves to distribute mitochondrial functions in a dynamic and non-uniform fashion, has attracted special interest in recent years following the discovery of functional connections among microtubules, motor proteins and mitochondria, and their influences on neurodegenerative diseases. Although the motor proteins that drive mitochondrial movement are now well characterized, the mechanisms by which anterograde and retrograde movement are coordinated with one another and with stationary axonal mitochondria are not yet understood. In this Commentary, we review why mitochondria move and how they move, focusing particularly on recent studies of transport regulation, which implicate control of motor activity by specific cell-signaling pathways, regulation of motor access to transport tracks and static microtubule–mitochondrion linkers. A detailed mechanism for modulating anterograde mitochondrial transport has been identified that involves Miro, a mitochondrial Ca2+-binding GTPase, which with associated proteins, can bind and control kinesin-1. Elements of the Miro complex also have important roles in mitochondrial fission–fusion dynamics, highlighting questions about the interdependence of biogenesis, transport, dynamics, maintenance and degradation.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility
VALE, R., REESE, T., & SHEETZ, M. (1985) · Cell · doi:10.1016/s0092-8674(85)80099-4 · Cited by 1,993 · cited 1×
“…and biochemical studies indicate that kinesin-1 is the primary anterograde mitochondrial motor (Barkus et al., 2008; Pilling et al., 2006; Vale et al., 1985), but there is evidence from studies of tissue culture cells that the kinesin-3 motors Kif1b and Klp6 also can transport…”
BackgroundThe Molecular Motor Toolbox for Intracellular Transport
Vale, R. D. (2003) · Cell · doi:10.1016/s0092-8674(03)00111-9 · Cited by 1,982
Kinesin superfamily motor proteins and intracellular transport
Hirokawa, N., Noda, Y., Tanaka, Y., & Niwa, S. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2774 · Cited by 1,859 · cited 2×
“myosin VI), whereas kinesins move organelles toward microtubule plus ends, and dyneins move them toward minus ends (Hirokawa et al., 2009; Lister et al., 2004; Trybus, 2008; Vale, 2003).”
BackgroundMutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
Züchner, S., Mersiyanova, I. V., Muglia, M., Bissar-Tadmouri, N., Rochelle, J., Dadali, E. L., Zappia, M., Nelis, E., Patitucci, A., Senderek, J., et al. (2004) · Nature Genetics · doi:10.1038/ng1341 · Cited by 1,572
Differential Regulation of Dynein and Kinesin Motor Proteins by Tau
Dixit, R., Ross, J. L., Goldman, Y. E., & Holzbaur, E. L. F. (2008) · Science · doi:10.1126/science.1152993 · Cited by 1,012
Tanaka, Y., Kanai, Y., Okada, Y., Nonaka, S., Takeda, S., Harada, A., & Hirokawa, N. (1998) · Cell · doi:10.1016/s0092-8674(00)81459-2 · Cited by 654
Kamal, A., Almenar-Queralt, A., LeBlanc, J. F., Roberts, E. A., & Goldstein, L. S. B. (2001) · Nature · doi:10.1038/414643a · Cited by 583
Motor coordination via a tug-of-war mechanism drives bidirectional vesicle transport
Hendricks, A. G., Perlson, E., Ross, J. L., Schroeder, H. W., Tokito, M., & Holzbaur, E. L. F. (2010) · Current Biology · doi:10.1016/j.cub.2010.02.058 · Cited by 423
Hurd, D. D., & Saxton, W. M. (1996) · Genetics · doi:10.1093/genetics/144.3.1075 · Cited by 379
Self-citationMartin, M., Iyadurai, S. J., Gassman, A., Gindhart, J. G., Hays, T. S., & Saxton, W. M. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.11.3717 · Cited by 365
Self-citation
Research works printed but not linked: 156
- Adams, 1982, Organelle movement in axons depends on ATP, Nature, 297, 327, 10.1038/297327a0 · DOI
- Akhmanova, 2010, Linking molecular motors to membrane cargo, Curr. Opin. Cell Biol., 22, 479, 10.1016/j.ceb.2010.04.008 · DOI
- Ally, 2009, Opposite-polarity motors activate one another to trigger cargo transport in live cells, J. Cell Biol., 187, 1071, 10.1083/jcb.200908075 · DOI
- Amiri, 2008, Mitochondrial biogenesis in the axons of vertebrate peripheral neurons, Dev. Neurobiol., 68, 1348, 10.1002/dneu.20668 · DOI
- Aoyama, 2009, Cayman ataxia protein caytaxin is transported by kinesin along neurites through binding to kinesin light chains, J. Cell Sci., 122, 4177, 10.1242/jcs.048579 · DOI
- Baloh, 2007, Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations, J. Neurosci., 27, 422, 10.1523/JNEUROSCI.4798-06.2007 · DOI · Paper page
- Baqri, 2009, Disruption of mitochondrial DNA replication in Drosophila increases mitochondrial fast axonal transport in vivo, PLoS ONE, 4, e7874, 10.1371/journal.pone.0007874 · DOI
- Barkus, 2008, Identification of an axonal kinesin-3 motor for fast anterograde vesicle transport that facilitates retrograde transport of neuropeptides, Mol. Biol. Cell, 19, 274, 10.1091/mbc.e07-03-0261 · DOI
- Bartlett, 1984, An electron microscopic study of the development of axons and dendrites by hippocampal neurons in culture. I. Cells which develop without intercellular contacts, J. Neurosci., 4, 1944, 10.1523/JNEUROSCI.04-08-01944.1984 · DOI · Paper page
- Bearer, 1999, Association of actin filaments with axonal microtubule tracts, J. Neurocytol., 28, 85, 10.1023/A:1007025421849 · DOI
- Berg, 2001, A millennial myosin census, Mol. Biol. Cell, 12, 780, 10.1091/mbc.12.4.780 · DOI · Paper page
- Blackstone, 2011, Hereditary spastic paraplegias: membrane traffic and the motor pathway, Nature Rev. Neurosci., 12, 31, 10.1038/nrn2946 · DOI · Paper page
- Bloom, 1993, GTP gamma S inhibits organelle transport along axonal microtubules, J. Cell Biol., 120, 467, 10.1083/jcb.120.2.467 · DOI
- Brady, 1984, Gelsolin inhibition of fast axonal transport indicates a requirement for actin microfilaments, Nature, 310, 56, 10.1038/310056a0 · DOI
- Brady, 1985, Video microscopy of fast axonal transport in extruded axoplasm: a new model for study of molecular mechanisms, Cell Motil., 5, 81, 10.1002/cm.970050203 · DOI
- Brady, 1990, A monoclonal antibody against kinesin inhibits both anterograde and retrograde fast axonal transport in squid axoplasm, Proc. Natl. Acad. Sci. USA, 87, 1061, 10.1073/pnas.87.3.1061 · DOI
- Brickley, 2011, N-acetylglucosamine transferase is an integral component of a kinesin-directed mitochondrial trafficking complex, Biochim. Biophys. Acta, 1813, 269, 10.1016/j.bbamcr.2010.10.011 · DOI
- Bridgman, 2004, Myosin-dependent transport in neurons, J. Neurobiol., 58, 164, 10.1002/neu.10320 · DOI
- Byrd, 2001, UNC-16, a JNK-signaling scaffold protein, regulates vesicle transport in C. elegans, Neuron, 32, 787, 10.1016/S0896-6273(01)00532-3 · DOI
- Cai, 2009, Mitochondrial transport and docking in axons, Exp. Neurol., 218, 257, 10.1016/j.expneurol.2009.03.024 · DOI
- Cai, 2005, Syntabulin-mediated anterograde transport of mitochondria along neuronal processes, J. Cell Biol., 170, 959, 10.1083/jcb.200506042 · DOI
- Cai, 2007, Syntabulin-kinesin-1 family member 5B-mediated axonal transport contributes to activity-dependent presynaptic assembly, J. Neurosci., 27, 7284, 10.1523/JNEUROSCI.0731-07.2007 · DOI
- Cai, 2001, The docking of kinesins, KIF5B and KIF5C, to Ran-binding protein 2 (RanBP2) is mediated via a novel RanBP2 domain, J. Biol. Chem., 276, 41594, 10.1074/jbc.M104514200 · DOI
- Carter, 2011, Crystal structure of the dynein motor domain, Science, 331, 1159, 10.1126/science.1202393 · DOI · Paper page
- Chada, 2003, Mitochondrial movement and positioning in axons: the role of growth factor signaling, J. Exp. Biol., 206, 1985, 10.1242/jeb.00263 · DOI
- Chada, 2004, Nerve growth factor signaling regulates motility and docking of axonal mitochondria, Curr. Biol., 14, 1272, 10.1016/j.cub.2004.07.027 · DOI · Paper page
- Chang, 2006, Mitochondrial trafficking to synapses in cultured primary cortical neurons, J. Neurosci., 26, 7035, 10.1523/JNEUROSCI.1012-06.2006 · DOI · Paper page
- Chen, 2009, Mitochondrial dynamics–fusion, fission, movement, and mitophagy–in neurodegenerative diseases, Hum. Mol. Genet., 18, R169, 10.1093/hmg/ddp326 · DOI · Paper page
- Chen, 2009, Dynein light chain LC8 regulates syntaphilin-mediated mitochondrial docking in axons, J. Neurosci., 29, 9429, 10.1523/JNEUROSCI.1472-09.2009 · DOI
- Chevalier-Larsen, 2006, Axonal transport and neurodegenerative disease, Biochim. Biophys. Acta, 1762, 1094, 10.1016/j.bbadis.2006.04.002 · DOI · Paper page
- Cho, 2010, Mitochondrial dynamics in cell death and neurodegeneration, Cell. Mol. Life Sci., 67, 3435, 10.1007/s00018-010-0435-2 · DOI · Paper page
- Cho, 2007, Association of the kinesin-binding domain of RanBP2 to KIF5B and KIF5C determines mitochondria localization and function, Traffic, 8, 1722, 10.1111/j.1600-0854.2007.00647.x · DOI
- Crimella, 2011, Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2, Clin. Genet.
- Das, 2003, Regional and developmental regulation of syntaphilin expression in the brain: a candidate molecular element of synaptic functional differentiation, Brain Res. Mol. Brain Res., 116, 38, 10.1016/S0169-328X(03)00212-2 · DOI
- de Duve, 2007, The origin of eukaryotes: a reappraisal, Nat. Rev. Genet., 8, 395, 10.1038/nrg2071 · DOI · Paper page
- De Vos, 2000, Tumor necrosis factor induces hyperphosphorylation of kinesin light chain and inhibits kinesin-mediated transport of mitochondria, J. Cell Biol., 149, 1207, 10.1083/jcb.149.6.1207 · DOI
- De Vos, 2008, Role of axonal transport in neurodegenerative diseases, Annu. Rev. Neurosci., 31, 151, 10.1146/annurev.neuro.31.061307.090711 · DOI · Paper page
- Ebneth, 1998, Overexpression of tau protein inhibits kinesin-dependent trafficking of vesicles, mitochondria, and endoplasmic reticulum: implications for Alzheimer's disease, J. Cell Biol., 143, 777, 10.1083/jcb.143.3.777 · DOI · Paper page
- Fahim, 1985, AVEC-DIC and electron microscopic analyses of axonally transported particles in cold-blocked squid giant axons, J. Neurocytol., 14, 689, 10.1007/BF01170822 · DOI
- Fath, 1988, Two classes of actin microfilaments are associated with the inner cytoskeleton of axons, J. Cell Biol., 107, 613, 10.1083/jcb.107.2.613 · DOI
- Fransson, 2006, The atypical Rho GTPases Miro-1 and Miro-2 have essential roles in mitochondrial trafficking, Biochem. Biophys. Res. Commun., 344, 500, 10.1016/j.bbrc.2006.03.163 · DOI · Paper page
- Frederick, 2007, Moving mitochondria: establishing distribution of an essential organelle, Traffic, 8, 1668, 10.1111/j.1600-0854.2007.00644.x · DOI · Paper page
- Gill, 1991, Dynactin, a conserved, ubiquitously expressed component of an activator of vesicle motility mediated by cytoplasmic dynein, J. Cell Biol., 115, 1639, 10.1083/jcb.115.6.1639 · DOI · Paper page
- Gioio, 2001, Local synthesis of nuclear-encoded mitochondrial proteins in the presynaptic nerve terminal, J. Neurosci. Res., 64, 447, 10.1002/jnr.1096 · DOI
- Glater, 2006, Axonal transport of mitochondria requires milton to recruit kinesin heavy chain and is light chain independent, J. Cell Biol., 173, 545, 10.1083/jcb.200601067 · DOI · Paper page
- Goldstein, 2008, Axonal transport and the delivery of pre-synaptic components, Curr. Opin. Neurobiol., 18, 495, 10.1016/j.conb.2008.10.003 · DOI
- Górska-Andrzejak, 2003, Mitochondria are redistributed in Drosophila photoreceptors lacking milton, a kinesin-associated protein, J. Comp. Neurol., 463, 372, 10.1002/cne.10750 · DOI
- Grafstein, 1980, Intracellular transport in neurons, Physiol. Rev., 60, 1167, 10.1152/physrev.1980.60.4.1167 · DOI · Paper page
- Gross, 2004, Hither and yon: a review of bi-directional microtubule-based transport, Phys. Biol., 1, R1, 10.1088/1478-3967/1/2/R01 · DOI · Paper page
- Gross, 2002, Interactions and regulation of molecular motors in Xenopus melanophores, J. Cell Biol., 156, 855, 10.1083/jcb.200105055 · DOI · Paper page
- Guo, 2005, The GTPase dMiro is required for axonal transport of mitochondria to Drosophila synapses, Neuron, 47, 379, 10.1016/j.neuron.2005.06.027 · DOI · Paper page
- Habermann, 2001, Immunolocalization of cytoplasmic dynein and dynactin subunits in cultured macrophages: enrichment on early endocytic organelles, J. Cell Sci., 114, 229, 10.1242/jcs.114.1.229 · DOI
- Haghnia, 2007, Dynactin is required for coordinated bidirectional motility, but not for dynein membrane attachment, Mol. Biol. Cell, 18, 2081, 10.1091/mbc.e06-08-0695 · DOI
- Hillefors, 2007, Axon viability and mitochondrial function are dependent on local protein synthesis in sympathetic neurons, Cell. Mol. Neurobiol., 27, 701, 10.1007/s10571-007-9148-y · DOI
- Hirokawa, 1991, Kinesin associates with anterogradely transported membranous organelles in vivo, J. Cell Biol., 114, 295, 10.1083/jcb.114.2.295 · DOI · Paper page
- Hollenbeck, 1993, Products of endocytosis and autophagy are retrieved from axons by regulated retrograde organelle transport, J. Cell Biol., 121, 305, 10.1083/jcb.121.2.305 · DOI · Paper page
- Hollenbeck, 2005, The axonal transport of mitochondria, J. Cell Sci., 118, 5411, 10.1242/jcs.02745 · DOI · Paper page
- Hollenbeck, 1985, Effects of the uncoupling agents FCCP and CCCP on the saltatory movements of cytoplasmic organelles, Cell Biol. Int. Rep., 9, 193, 10.1016/0309-1651(85)90094-3 · DOI · Paper page
- Holzbaur, 2010, Axonal transport: CDKs as traffic signals for motor-ists along the axon?, Curr. Biol., 20, R641, 10.1016/j.cub.2010.06.016 · DOI
- Iyer, 2003, Roles of the tetratricopeptide repeat domain in O-GlcNAc transferase targeting and protein substrate specificity, J. Biol. Chem., 278, 24608, 10.1074/jbc.M300036200 · DOI
- Jordan, 2000, Signaling networks: the origins of cellular multitasking, Cell, 103, 193, 10.1016/S0092-8674(00)00112-4 · DOI · Paper page
- Kang, 2008, Docking of axonal mitochondria by syntaphilin controls their mobility and affects short-term facilitation, Cell, 132, 137, 10.1016/j.cell.2007.11.024 · DOI · Paper page
- Karcher, 2002, Motor-cargo interactions: the key to transport specificity, Trends Cell Biol., 12, 21, 10.1016/S0962-8924(01)02184-5 · DOI
- Karki, 1995, Affinity chromatography demonstrates a direct binding between cytoplasmic dynein and the dynactin complex, J. Biol. Chem., 270, 28806, 10.1074/jbc.270.48.28806 · DOI · Paper page
- Khodjakov, 1998, A specific light chain of kinesin associates with mitochondria in cultured cells, Mol. Biol. Cell, 9, 333, 10.1091/mbc.9.2.333 · DOI
- Koutsopoulos, 2010, Human Miltons associate with mitochondria and induce microtubule-dependent remodeling of mitochondrial networks, Biochim. Biophys. Acta, 1803, 564, 10.1016/j.bbamcr.2010.03.006 · DOI
- Kural, 2005, Kinesin and dynein move a peroxisome in vivo: a tug-of-war or coordinated movement?, Science, 308, 1469, 10.1126/science.1108408 · DOI · Paper page
- Kuznetsov, 1992, Actin-dependent organelle movement in squid axoplasm, Nature, 356, 722, 10.1038/356722a0 · DOI · Paper page
- Labrousse, 1999, C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane, Mol. Cell, 4, 815, 10.1016/S1097-2765(00)80391-3 · DOI · Paper page
- Lackner, 2009, The molecular mechanism and cellular functions of mitochondrial division, Biochim. Biophys. Acta, 1792, 1138, 10.1016/j.bbadis.2008.11.011 · DOI
- Lalli, 2002, Analysis of retrograde transport in motor neurons reveals common endocytic carriers for tetanus toxin and neurotrophin receptor p75NTR, J. Cell Biol., 156, 233, 10.1083/jcb.200106142 · DOI
- Langford, 2002, Myosin-V, a versatile motor for short-range vesicle transport, Traffic, 3, 859, 10.1034/j.1600-0854.2002.31202.x · DOI
- Lao, 2000, Syntaphilin: a syntaxin-1 clamp that controls SNARE assembly, Neuron, 25, 191, 10.1016/S0896-6273(00)80882-X · DOI
- Lee, 2003, Organization and translation of mRNA in sympathetic neurons, J. Cell Sci., 116, 4467, 10.1242/jcs.00745 · DOI
- Li, 2009, HUMMR, a hypoxia- and HIF-1alpha-inducible protein, alters mitochondrial distribution and transport, J. Cell Biol., 185, 1065, 10.1083/jcb.200811033 · DOI
- Li, 2004, The importance of dendritic mitochondria in the morphogenesis and plasticity of spines and synapses, Cell, 119, 873, 10.1016/j.cell.2004.11.003 · DOI · Paper page
- Ligon, 2000, Role of microtubules and actin filaments in the movement of mitochondria in the axons and dendrites of cultured hippocampal neurons, J. Comp. Neurol., 427, 351, 10.1002/1096-9861(20001120)427:3<351::AID-CNE3>3.0.CO;2-R · DOI
- Ligon, 2004, A direct interaction between cytoplasmic dynein and kinesin I may coordinate motor activity, J. Biol. Chem., 279, 19201, 10.1074/jbc.M313472200 · DOI
- Ling, 2004, Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein, Proc. Natl. Acad. Sci. USA, 101, 17428, 10.1073/pnas.0408114101 · DOI
- Lister, 2004, Myosin VI: a multifunctional motor, Biochem. Soc. Trans., 32, 685, 10.1042/BST0320685 · DOI
- Liu, 2009, Mitochondrial ‘kiss-and-run’: interplay between mitochondrial motility and fusion-fission dynamics, EMBO J., 28, 3074, 10.1038/emboj.2009.255 · DOI · Paper page
- Logroscino, 1980, Electron microscopic study of the early changes proximal to a constriction in myelinated nerve, Int. Orthop., 4, 121, 10.1007/BF00271095 · DOI
- Ma, 2009, KIF5B motor adaptor syntabulin maintains synaptic transmission in sympathetic neurons, J. Neurosci., 29, 13019, 10.1523/JNEUROSCI.2517-09.2009 · DOI
- MacAskill, 2010, Control of mitochondrial transport and localization in neurons, Trends Cell Biol., 20, 102, 10.1016/j.tcb.2009.11.002 · DOI · Paper page
- MacAskill, 2009, GTPase dependent recruitment of Grif-1 by Miro1 regulates mitochondrial trafficking in hippocampal neurons, Mol. Cell. Neurosci., 40, 301, 10.1016/j.mcn.2008.10.016 · DOI
- MacAskill, 2009, Miro1 is a calcium sensor for glutamate receptor-dependent localization of mitochondria at synapses, Neuron, 61, 541, 10.1016/j.neuron.2009.01.030 · DOI · Paper page
- Malaiyandi, 2005, Zn2+ inhibits mitochondrial movement in neurons by phosphatidylinositol 3-kinase activation, J. Neurosci., 25, 9507, 10.1523/JNEUROSCI.0868-05.2005 · DOI
- Mandelkow, 2004, MARK/PAR1 kinase is a regulator of microtubule-dependent transport in axons, J. Cell Biol., 167, 99, 10.1083/jcb.200401085 · DOI · Paper page
- Martin, 1998, Protein synthesizing units in presynaptic and postsynaptic domains of squid neurons, J. Cell Sci., 111, 3157, 10.1242/jcs.111.21.3157 · DOI
- Mavlyutov, 2002, Identification of RanBP2- and kinesin-mediated transport pathways with restricted neuronal and subcellular localization, Traffic, 3, 630, 10.1034/j.1600-0854.2002.30905.x · DOI
- Miller, 2004, Axonal mitochondrial transport and potential are correlated, J. Cell Sci., 117, 2791, 10.1242/jcs.01130 · DOI · Paper page
- Mironov, 2006, Spontaneous and evoked neuronal activities regulate movements of single neuronal mitochondria, Synapse, 59, 403, 10.1002/syn.20256 · DOI
- Misgeld, 2007, Imaging axonal transport of mitochondria in vivo, Nat. Methods, 4, 559, 10.1038/nmeth1055 · DOI · Paper page
- Misko, 2010, Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex, J. Neurosci., 30, 4232, 10.1523/JNEUROSCI.6248-09.2010 · DOI · Paper page
- Morfini, 2002, Glycogen synthase kinase 3 phosphorylates kinesin light chains and negatively regulates kinesin-based motility, EMBO J., 21, 281, 10.1093/emboj/21.3.281 · DOI · Paper page
- Morfini, 2004, A novel CDK5-dependent pathway for regulating GSK3 activity and kinesin-driven motility in neurons, EMBO J., 23, 2235, 10.1038/sj.emboj.7600237 · DOI · Paper page
- Morfini, 2006, JNK mediates pathogenic effects of polyglutamine-expanded androgen receptor on fast axonal transport, Nat. Neurosci., 9, 907, 10.1038/nn1717 · DOI
- Morfini, 2009, Axonal transport defects in neurodegenerative diseases, J. Neurosci., 29, 12776, 10.1523/JNEUROSCI.3463-09.2009 · DOI · Paper page
- Morfini, 2009, Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin, Nat. Neurosci., 12, 864, 10.1038/nn.2346 · DOI · Paper page
- Morris, 1993, The regulation of bidirectional mitochondrial transport is coordinated with axonal outgrowth, J. Cell Sci., 104, 917, 10.1242/jcs.104.3.917 · DOI · Paper page
- Morris, 1995, Axonal transport of mitochondria along microtubules and F-actin in living vertebrate neurons, J. Cell Biol., 131, 1315, 10.1083/jcb.131.5.1315 · DOI · Paper page
- Nangaku, 1994, KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria, Cell, 79, 1209, 10.1016/0092-8674(94)90012-4 · DOI · Paper page
- Ohno, 2011, Myelination and axonal electrical activity modulate the distribution and motility of mitochondria at CNS nodes of Ranvier, J. Neurosci., 31, 7249, 10.1523/JNEUROSCI.0095-11.2011 · DOI
- Parton, 1992, Axonal and dendritic endocytic pathways in cultured neurons, J. Cell Biol., 119, 123, 10.1083/jcb.119.1.123 · DOI · Paper page
- Paschal, 1992, Homology of the 74-kD cytoplasmic dynein subunit with a flagellar dynein polypeptide suggests an intracellular targeting function, J. Cell Biol., 118, 1133, 10.1083/jcb.118.5.1133 · DOI
- Pathak, 2010, Evidence that myosin activity opposes microtubule-based axonal transport of mitochondria, J. Neurosci., 30, 8984, 10.1523/JNEUROSCI.1621-10.2010 · DOI
- Peraza-Reyes, 2010, Mitochondrial manoeuvres: latest insights and hypotheses on mitochondrial partitioning during mitosis in Saccharomyces cerevisiae, Bioessays, 32, 1040, 10.1002/bies.201000083 · DOI
- Perlson, 2010, Retrograde axonal transport: pathways to cell death?, Trends Neurosci., 33, 335, 10.1016/j.tins.2010.03.006 · DOI · Paper page
- Pigino, 2009, Disruption of fast axonal transport is a pathogenic mechanism for intraneuronal amyloid beta, Proc. Natl. Acad. Sci. USA, 106, 5907, 10.1073/pnas.0901229106 · DOI
- Pilling, 2006, Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons, Mol. Biol. Cell, 17, 2057, 10.1091/mbc.e05-06-0526 · DOI · Paper page
- Popov, 2005, Mitochondria form a filamentous reticular network in hippocampal dendrites but are present as discrete bodies in axons: a three-dimensional ultrastructural study, J. Comp. Neurol., 492, 50, 10.1002/cne.20682 · DOI
- Rao, 2001, Visualization of neuropeptide expression, transport, and exocytosis in Drosophila melanogaster, J. Neurobiol., 49, 159, 10.1002/neu.1072 · DOI
- Rapali, 2011, Directed evolution reveals the binding motif preference of the LC8/DYNLL hub protein and predicts large numbers of novel binders in the human proteome, PLoS ONE, 6, e18818, 10.1371/journal.pone.0018818 · DOI
- Ratner, 1998, A role for cyclin-dependent kinase(s) in the modulation of fast anterograde axonal transport: effects defined by olomoucine and the APC tumor suppressor protein, J. Neurosci., 18, 7717, 10.1523/JNEUROSCI.18-19-07717.1998 · DOI
- Rayment, 1993, Three-dimensional structure of myosin subfragment-1: a molecular motor, Science, 261, 50, 10.1126/science.8316857 · DOI · Paper page
- Reed, 2006, Microtubule acetylation promotes kinesin-1 binding and transport, Curr. Biol., 16, 2166, 10.1016/j.cub.2006.09.014 · DOI · Paper page
- Reis, 2009, The Miro GTPases: at the heart of the mitochondrial transport machinery, FEBS Lett., 583, 1391, 10.1016/j.febslet.2009.04.015 · DOI
- Rice, 1999, A structural change in the kinesin motor protein that drives motility, Nature, 402, 778, 10.1038/45483 · DOI · Paper page
- Rintoul, 2010, Mitochondrial trafficking and morphology in neuronal injury, Biochim. Biophys. Acta, 1802, 143, 10.1016/j.bbadis.2009.09.005 · DOI
- Rintoul, 2003, Glutamate decreases mitochondrial size and movement in primary forebrain neurons, J. Neurosci., 23, 7881, 10.1523/JNEUROSCI.23-21-07881.2003 · DOI · Paper page
- Rogers, 1998, Myosin cooperates with microtubule motors during organelle transport in melanophores, Curr. Biol., 8, 161, 10.1016/S0960-9822(98)70063-6 · DOI
- Ruthel, 2003, Response of mitochondrial traffic to axon determination and differential branch growth, J. Neurosci., 23, 8618, 10.1523/JNEUROSCI.23-24-08618.2003 · DOI
- Santama, 2004, Distribution and functions of kinectin isoforms, J. Cell Sci., 117, 4537, 10.1242/jcs.01326 · DOI
- Saotome, 2008, Bidirectional Ca2+-dependent control of mitochondrial dynamics by the Miro GTPase, Proc. Natl. Acad. Sci. USA, 105, 20728, 10.1073/pnas.0808953105 · DOI · Paper page
- Schnapp, 1989, Dynein is the motor for retrograde axonal transport of organelles, Proc. Natl. Acad. Sci. USA, 86, 1548, 10.1073/pnas.86.5.1548 · DOI · Paper page
- Shidara, 2010, Defects in mitochondrial axonal transport and membrane potential without increased reactive oxygen species production in a Drosophila model of Friedreich ataxia, J. Neurosci., 30, 11369, 10.1523/JNEUROSCI.0529-10.2010 · DOI
- Smirnova, 2001, Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells, Mol. Biol. Cell, 12, 2245, 10.1091/mbc.12.8.2245 · DOI
- Smith, 2006, Mapping the GRIF-1 binding domain of the kinesin, KIF5C, substantiates a role for GRIF-1 as an adaptor protein in the anterograde trafficking of cargoes, J. Biol. Chem., 281, 27216, 10.1074/jbc.M600522200 · DOI
- Sotelo-Silveira, 2006, RNA trafficking in axons, Traffic, 7, 508, 10.1111/j.1600-0854.2006.00405.x · DOI
- Stamer, 2002, Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress, J. Cell Biol., 156, 1051, 10.1083/jcb.200108057 · DOI · Paper page
- Steffen, 1997, The involvement of the intermediate chain of cytoplasmic dynein in binding the motor complex to membranous organelles of Xenopus oocytes, Mol. Biol. Cell, 8, 2077, 10.1091/mbc.8.10.2077 · DOI
- Stowers, 2002, Axonal transport of mitochondria to synapses depends on milton, a novel Drosophila protein, Neuron, 36, 1063, 10.1016/S0896-6273(02)01094-2 · DOI
- Su, 2004, Syntabulin is a microtubule-associated protein implicated in syntaxin transport in neurons, Nat. Cell Biol., 6, 941, 10.1038/ncb1169 · DOI
- Tanaka, 2011, KLP6: a newly identified kinesin that regulates the morphology and transport of mitochondria in neuronal cells, J. Cell Sci., 124, 2457, 10.1242/jcs.086470 · DOI
- Tatsuta, 2008, Quality control of mitochondria: protection against neurodegeneration and ageing, EMBO J., 27, 306, 10.1038/sj.emboj.7601972 · DOI
- Taylor, 2009, Axonal mRNA in uninjured and regenerating cortical mammalian axons, J. Neurosci., 29, 4697, 10.1523/JNEUROSCI.6130-08.2009 · DOI · Paper page
- Trybus, 2008, Myosin V from head to tail, Cell. Mol. Life Sci., 65, 1378, 10.1007/s00018-008-7507-6 · DOI
- Tsukita, 1980, The movement of membranous organelles in axons. Electron microscopic identification of anterogradely and retrogradely transported organelles, J. Cell Biol., 84, 513, 10.1083/jcb.84.3.513 · DOI · Paper page
- Twig, 2010, Biophysical properties of mitochondrial fusion events in pancreatic beta-cells and cardiac cells unravel potential control mechanisms of its selectivity, Am. J. Physiol. Cell Physiol., 299, C477, 10.1152/ajpcell.00427.2009 · DOI
- Uchida, 2009, Tight functional coupling of kinesin-1A and dynein motors in the bidirectional transport of neurofilaments, Mol. Biol. Cell, 20, 4997, 10.1091/mbc.e09-04-0304 · DOI
- Vale, 2000, The way things move: looking under the hood of molecular motor proteins, Science, 288, 88, 10.1126/science.288.5463.88 · DOI · Paper page
- Varadi, 2004, Cytoplasmic dynein regulates the subcellular distribution of mitochondria by controlling the recruitment of the fission factor dynamin-related protein-1, J. Cell Sci., 117, 4389, 10.1242/jcs.01299 · DOI
- Vaughan, 1995, Cytoplasmic dynein binds dynactin through a direct interaction between the intermediate chains and p150Glued, J. Cell Biol., 131, 1507, 10.1083/jcb.131.6.1507 · DOI · Paper page
- Verburg, 2008, Mitochondrial membrane potential in axons increases with local nerve growth factor or semaphorin signaling, J. Neurosci., 28, 8306, 10.1523/JNEUROSCI.2614-08.2008 · DOI
- Verhey, 2009, Traffic control: regulation of kinesin motors, Nat. Rev. Mol. Cell Biol., 10, 765, 10.1038/nrm2782 · DOI · Paper page
- Vershinin, 2007, Multiple-motor based transport and its regulation by Tau, Proc. Natl. Acad. Sci. USA, 104, 87, 10.1073/pnas.0607919104 · DOI · Paper page
- Vershinin, 2008, Tuning microtubule-based transport through filamentous MAPs: the problem of dynein, Traffic, 9, 882, 10.1111/j.1600-0854.2008.00741.x · DOI · Paper page
- Verstreken, 2005, Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions, Neuron, 47, 365, 10.1016/j.neuron.2005.06.018 · DOI · Paper page
- Wang, 2009, The mechanism of Ca2+ -dependent regulation of kinesin-mediated mitochondrial motility, Cell, 136, 163, 10.1016/j.cell.2008.11.046 · DOI · Paper page
- Weihofen, 2009, Pink1 forms a multiprotein complex with Miro and Milton, linking Pink1 function to mitochondrial trafficking, Biochemistry, 48, 2045, 10.1021/bi8019178 · DOI · Paper page
- Wickstead, 2006, A “holistic” kinesin phylogeny reveals new kinesin families and predicts protein functions, Mol. Biol. Cell, 17, 1734, 10.1091/mbc.e05-11-1090 · DOI
- Wickstead, 2007, Dyneins across eukaryotes: a comparative genomic analysis, Traffic, 8, 1708, 10.1111/j.1600-0854.2007.00646.x · DOI
- Yi, 2004, Control of mitochondrial motility and distribution by the calcium signal: a homeostatic circuit, J. Cell Biol., 167, 661, 10.1083/jcb.200406038 · DOI · Paper page
- Zhang, 2010, Activity-dependent regulation of mitochondrial motility by calcium and Na/K-ATPase at nodes of Ranvier of myelinated nerves, J. Neurosci., 30, 3555, 10.1523/JNEUROSCI.4551-09.2010 · DOI
- Zinsmaier, 2009, Mitochondrial transport dynamics in axons and dendrites, Results Probl. Cell Differ., 48, 361, 10.1007/400_2009_20 · DOI
- Züchner, 2006, Mechanisms of disease: a molecular genetic update on hereditary axonal neuropathies, Nat. Clin. Pract. Neurol., 2, 45, 10.1038/ncpneuro0071 · DOI
Cited by
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Mitochondria: In Sickness and in Health
Nunnari, J., & Suomalainen, A. (2012) · Cell · doi:10.1016/j.cell.2012.02.035 · Cited by 3,479
Kinesin superfamily motor proteins and intracellular transport
Hirokawa, N., Noda, Y., Tanaka, Y., & Niwa, S. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2774 · Cited by 1,859
Functions and dysfunctions of mitochondrial dynamics
Detmer, S. A., & Chan, D. C. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2275 · Cited by 1,369
Hirokawa, N., Niwa, S., & Tanaka, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.039 · Cited by 1,138
Mitochondria in neuroplasticity and neurological disorders
Mattson, M. P., Gleichmann, M., & Cheng, A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.010 · Cited by 1,081
Mitochondrial Fusion and Fission in Mammals
Chan, D. C. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104638 · Cited by 972
Mitochondrial dynamics and mitochondrial quality control
Ni, H.-M., Williams, J. A., & Ding, W.-X. (2015) · Redox Biology · doi:10.1016/j.redox.2014.11.006 · Cited by 931
The Mechanism of Ca2+-Dependent Regulation of Kinesin-Mediated Mitochondrial Motility
Wang, X., & Schwarz, T. L. (2009) · Cell · doi:10.1016/j.cell.2008.11.046 · Cited by 871
The Machines that Divide and Fuse Mitochondria
Hoppins, S., Lackner, L., & Nunnari, J. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.071905.090048 · Cited by 790
Mitochondrial Defects and Oxidative Stress in Alzheimer Disease and Parkinson Disease
Yan, M. H., Wang, X., & Zhu, X. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.11.014 · Cited by 718
Zempel, H., Thies, E., Mandelkow, E., & Mandelkow, E.-M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2357-10.2010 · Cited by 686
“As shown previously (Stamer et al., 2002; Hollenbeck and Saxton, 2005; Thies and Mandelkow, 2007), such mitochondrial traffic jams cause a local drop of energy (ATP) and consequently spine destruction through the perturbation of the actin network and loss of synaptic components (Whiteman et al.,…”
BackgroundAxonal transport: cargo-specific mechanisms of motility and regulation
Maday, S., Twelvetrees, A. E., Moughamian, A. J., & Holzbaur, E. L. F. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.019 · Cited by 683
Mitochondrial Dysfunction and Oxidative Stress in Alzheimer’s Disease
Misrani, A., Tabassum, S., & Yang, L. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.617588 · Cited by 654
Mitochondrial bioenergetics and structural network organization
Benard, G., Bellance, N., James, D., Parrone, P., Fernandez, H., Letellier, T., & Rossignol, R. (2007) · Journal of Cell Science · doi:10.1242/jcs.03381 · Cited by 618
Kang, J.-S., Tian, J.-H., Pan, P.-Y., Zald, P., Li, C., Deng, C., & Sheng, Z.-H. (2008) · Cell · doi:10.1016/j.cell.2007.11.024 · Cited by 598
Bidirectional Ca 2+ -dependent control of mitochondrial dynamics by the Miro GTPase
Saotome, M., Safiulina, D., Szabadkai, G., Das, S., Fransson, Å., Aspenstrom, P., Rizzuto, R., & Hajnóczky, G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808953105 · Cited by 538
Mitochondrial Trafficking in Neurons
Schwarz, T. L. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a011304 · Cited by 525
Amyloid Beta and Phosphorylated Tau-Induced Defective Autophagy and Mitophagy in Alzheimer’s Disease
Reddy, P. H., & Oliver, D. M. (2019) · Cells · doi:10.3390/cells8050488 · Cited by 496
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms
Salinas, S., Proukakis, C., Crosby, A., & Warner, T. T. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70258-8 · Cited by 474
Mitochondrial changes within axons in multiple sclerosis
Mahad, D. J., Ziabreva, I., Campbell, G., Lax, N., White, K., Hanson, P. S., Lassmann, H., & Turnbull, D. M. (2009) · Brain · doi:10.1093/brain/awp046 · Cited by 454
TRAK/Milton motor-adaptor proteins steer mitochondrial trafficking to axons and dendrites
van Spronsen, M., Mikhaylova, M., Lipka, J., Schlager, M. A., van den Heuvel, D. J., Kuijpers, M., Wulf, P. S., Keijzer, N., Demmers, J., Kapitein, L. C., et al. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.027 · Cited by 450
There's Something Wrong with my MAM; the ER–Mitochondria Axis and Neurodegenerative Diseases
Paillusson, S., Stoica, R., Gomez-Suaga, P., Lau, D. H. W., Mueller, S., Miller, T., & Miller, C. C. J. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.01.008 · Cited by 439
p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
Okatsu, K., Saisho, K., Shimanuki, M., Nakada, K., Shitara, H., Sou, Y., Kimura, M., Sato, S., Hattori, N., Komatsu, M., et al. (2010) · Genes to Cells · doi:10.1111/j.1365-2443.2010.01426.x · Cited by 397
“Indeed, mitochondria are delivered to areas of the axon where metabolic demand is high, such as synapses, active growth cones and branches (Hollenbeck & Saxton 2005).”
BackgroundLiu, S., Sawada, T., Lee, S., Yu, W., Silverio, G., Alapatt, P., Millan, I., Shen, A., Saxton, W., Kanao, T., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002537 · Cited by 371
Self-citationMitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity
Bertholet, A. M., Delerue, T., Millet, A. M., Moulis, M. F., David, C., Daloyau, M., Arnauné-Pelloquin, L., Davezac, N., Mils, V., Miquel, M. C., et al. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.10.011 · Cited by 363
Thies, E., & Mandelkow, E.-M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4674-06.2007 · Cited by 293
Recent advances in our understanding of neurodegeneration
Jellinger, K. A. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0240-y · Cited by 274
Boldogh, I. R., & Pon, L. A. (2007) · Trends in Cell Biology · doi:10.1016/j.tcb.2007.07.008 · Cited by 270
Mitochondria and Calcium in Alzheimer’s Disease: From Cell Signaling to Neuronal Cell Death
Calvo-Rodriguez, M., & Bacskai, B. J. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.10.004 · Cited by 254
Chen, Y., & Sheng, Z.-H. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201302040 · Cited by 250
Abnormal Mitochondrial Dynamics in the Pathogenesis of Alzheimer's Disease
Zhu, X., Perry, G., Smith, M. A., & Wang, X. (2012) · Journal of Alzheimer's Disease · doi:10.3233/jad-2012-129005 · Cited by 242
Soluble forms of tau are toxic in Alzheimer's disease
Kopeikina, K., Hyman, B., & Spires-Jones, T. (2012) · Translational Neuroscience · doi:10.2478/s13380-012-0032-y · Cited by 232
The Interplay of Axonal Energy Homeostasis and Mitochondrial Trafficking and Anchoring
Sheng, Z.-H. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.01.005 · Cited by 221
Drosophila Miro Is Required for Both Anterograde and Retrograde Axonal Mitochondrial Transport
Russo, G. J., Louie, K., Wellington, A., Macleod, G. T., Hu, F., Panchumarthi, S., & Zinsmaier, K. E. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5417-08.2009 · Cited by 217
Shahpasand, K., Uemura, I., Saito, T., Asano, T., Hata, K., Shibata, K., Toyoshima, Y., Hasegawa, M., & Hisanaga, S.-I. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5927-11.2012 · Cited by 206
Cigarette smoke-induced mitochondrial fragmentation and dysfunction in human airway smooth muscle
Aravamudan, B., Kiel, A., Freeman, M., Delmotte, P., Thompson, M., Vassallo, R., Sieck, G. C., Pabelick, C. M., & Prakash, Y. S. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00155.2013 · Cited by 192
Role of mitochondrial homeostasis and dynamics in Alzheimer's disease
Selfridge, J. E., E, L., Lu, J., & Swerdlow, R. H. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.057 · Cited by 175
Inter and Intracellular mitochondrial trafficking in health and disease
Shanmughapriya, S., Langford, D., & Natarajaseenivasan, K. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101128 · Cited by 171
Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders
Plotegher, N., & Duchen, M. R. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.12.003 · Cited by 161
PINK1 function in health and disease
Deas, E., Plun‐Favreau, H., & Wood, N. W. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900024 · Cited by 154
Mitochondrial matrix Ca 2 + as an intrinsic signal regulating mitochondrial motility in axons
Chang, K. T., Niescier, R. F., & Min, K.-T. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106862108 · Cited by 153
Mechanically-induced membrane poration causes axonal beading and localized cytoskeletal damage
Kilinc, D., Gallo, G., & Barbee, K. A. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.04.025 · Cited by 144
Iijima-Ando, K., Sekiya, M., Maruko-Otake, A., Ohtake, Y., Suzuki, E., Lu, B., & Iijima, K. M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002918 · Cited by 142
Canty, J. T., Hensley, A., Aslan, M., Jack, A., & Yildiz, A. (2023) · Nature Communications · doi:10.1038/s41467-023-36945-8 · Cited by 131
Cytochrome c oxidase deficiency: Patients and animal models
Diaz, F. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.07.013 · Cited by 127
Kim, Y., Zheng, X., Ansari, Z., Bunnell, M. C., Herdy, J. R., Traxler, L., Lee, H., Paquola, A. C. M., Blithikioti, C., Ku, M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.105 · Cited by 117
Kevenaar, J. T., Bianchi, S., van Spronsen, M., Olieric, N., Lipka, J., Frias, C. P., Mikhaylova, M., Harterink, M., Keijzer, N., Wulf, P. S., et al. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.048 · Cited by 110
Physical Exercise and Brain Mitochondrial Fitness: The Possible Role Against Alzheimer's Disease
Bernardo, T. C., Marques‐Aleixo, I., Beleza, J., Oliveira, P. J., Ascensão, A., & Magalhães, J. (2016) · Brain Pathology · doi:10.1111/bpa.12403 · Cited by 108
Are Tangles as Toxic as They Look?
Spires-Jones, T. L., Kopeikina, K. J., Koffie, R. M., de Calignon, A., & Hyman, B. T. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9566-7 · Cited by 104
A PGAM5–KEAP1–Nrf2 complex is required for stress-induced mitochondrial retrograde trafficking
O'Mealey, G. B., Plafker, K. S., Berry, W. L., Janknecht, R., Chan, J. Y., & Plafker, S. M. (2017) · Journal of Cell Science · doi:10.1242/jcs.203216 · Cited by 99
Civitarese, A. E., MacLean, P. S., Carling, S., Kerr-Bayles, L., McMillan, R. P., Pierce, A., Becker, T. C., Moro, C., Finlayson, J., Lefort, N., et al. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.04.004 · Cited by 95
Axonal energy metabolism, and the effects in aging and neurodegenerative diseases
Yang, S., Park, J. H., & Lu, H.-C. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00634-3 · Cited by 94
Kreft, M., Bak, L. K., Waagepetersen, H. S., & Schousboe, A. (2012) · ASN Neuro · doi:10.1042/an20120007 · Cited by 88
Mitochondrial Abnormalities in Alzheimer’s Disease
Silva, D. F., Selfridge, J. E., Lu, J., E, L., Cardoso, S. M., & Swerdlow, R. H. (2012) · Advances in Pharmacology · doi:10.1016/b978-0-12-394816-8.00003-9 · Cited by 86
Microtubule motors transport phagosomes in the RPE, and lack of KLC1 leads to AMD-like pathogenesis
Jiang, M., Esteve-Rudd, J., Lopes, V. S., Diemer, T., Lillo, C., Rump, A., & Williams, D. S. (2015) · Journal of Cell Biology · doi:10.1083/jcb.201410112 · Cited by 85
Ping, H. A., Kraft, L. M., Chen, W., Nilles, A. E., & Lackner, L. L. (2016) · Journal of Cell Biology · doi:10.1083/jcb.201511021 · Cited by 82
Mitochondrial calcium at the synapse
Datta, S., & Jaiswal, M. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.04.006 · Cited by 73
Minireview: Mitochondrial Energetics and Insulin Resistance
Civitarese, A. E., & Ravussin, E. (2008) · Endocrinology · doi:10.1210/en.2007-1444 · Cited by 70
An Unbalanced Synaptic Transmission: Cause or Consequence of the Amyloid Oligomers Neurotoxicity?
Sciaccaluga, M., Megaro, A., Bellomo, G., Ruffolo, G., Romoli, M., Palma, E., & Costa, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115991 · Cited by 70
Role of MAP1B in axonal retrograde transport of mitochondria
Jiménez-Mateos, E.-M., González-Billault, C., Dawson, H. N., Vitek, M. P., & Avila, J. (2006) · Biochemical Journal · doi:10.1042/bj20060205 · Cited by 70
A cryo-ET survey of microtubules and intracellular compartments in mammalian axons
Foster, H. E., Ventura Santos, C., & Carter, A. P. (2022) · Journal of Cell Biology · doi:10.1083/jcb.202103154 · Cited by 69
Roy, D., & Tedeschi, A. (2021) · Cells · doi:10.3390/cells10051078 · Cited by 68
Axonopathy in Huntington's disease
Li, J.-Y., & Conforti, L. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2012.08.010 · Cited by 55
Structure-Function Analysis of the Yeast Mitochondrial Rho GTPase, Gem1p
Koshiba, T., Holman, H. A., Kubara, K., Yasukawa, K., Kawabata, S.-I., Okamoto, K., Macfarlane, J., & Shaw, J. M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.180034 · Cited by 50
Mitochondrial dynamics in aging and disease
Bereiter-Hahn, J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394625-6.00004-0 · Cited by 48
Morel, M., Authelet, M., Dedecker, R., & Brion, J. P. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.02.077 · Cited by 46
Giovarelli, M., Zecchini, S., Martini, E., Garrè, M., Barozzi, S., Ripolone, M., Napoli, L., Coazzoli, M., Vantaggiato, C., Roux-Biejat, P., et al. (2020) · Cell Death & Differentiation · doi:10.1038/s41418-020-0510-7 · Cited by 41
Axonal Organelles as Molecular Platforms for Axon Growth and Regeneration after Injury
Petrova, V., Nieuwenhuis, B., Fawcett, J. W., & Eva, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041798 · Cited by 32
Metadata
- Authors
- Saxton, W. M., & Hollenbeck, P. J.
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2012-01-01
- Volume
- 125
- Issue
- Pt 9
- Pages
- 2095-104
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W2055572268
- Cited by
- 1,185
- References
- 14
- FWCI
- 37.87
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.