The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Microtubules provide directional cues for polarized axonal transport through interaction with kinesin motor head
Open accessAbstract
Post-Golgi carriers of various newly synthesized axonal membrane proteins, which possess kinesin (KIF5)-driven highly processive motility, were transported from the TGN directly to axons. We found that KIF5 has a preference to the microtubules in the initial segment of axon. Low dose paclitaxel treatment caused missorting of KIF5, as well as axonal membrane proteins to the tips of dendrites. Microtubules in the initial segment of axons showed a remarkably high affinity to EB1–YFP, which was known to bind the tips of growing microtubules. These findings revealed unique features of the microtubule cytoskeletons in the initial segment, and suggested that they provide directional information for polarized axonal transport.
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
Rat hippocampal neurons in dispersed cell culture.
Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110
Direct observation of single kinesin molecules moving along microtubules
Vale, R. D., Funatsu, T., Pierce, D. W., Romberg, L., Harada, Y., & Yanagida, T. (1996) · Nature · doi:10.1038/380451a0 · Cited by 711
Kinesin׳s tail domain is an inhibitory regulator of the motor domain
Coy, D. L., Hancock, W. O., Wagenbach, M., & Howard, J. (1999) · Nature Cell Biology · doi:10.1038/13001 · Cited by 329
Hirokawa, N., Funakoshi, T., Sato-Harada, R., & Kanai, Y. (1996) · The Journal of cell biology · doi:10.1083/jcb.132.4.667 · Cited by 179
Self-citationCargo binding and regulatory sites in the tail of fungal conventional kinesin
Seiler, S., Kirchner, J., Horn, C., Kallipolitou, A., Woehlke, G., & Schliwa, M. (2000) · Nature Cell Biology · doi:10.1038/35014022 · Cited by 147
Cited by
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
Self-citationHirokawa, N., Niwa, S., & Tanaka, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.039 · Cited by 1,138
Self-citationMicrotubule assembly, organization and dynamics in axons and dendrites
Conde, C., & Cáceres, A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2631 · Cited by 1,086
Microtubule Acetylation Promotes Kinesin-1 Binding and Transport
Reed, N. A., Cai, D., Blasius, T. L., Jih, G. T., Meyhofer, E., Gaertig, J., & Verhey, K. J. (2006) · Current Biology · doi:10.1016/j.cub.2006.09.014 · Cited by 919
Axonal 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
Neuronal polarity: from extracellular signals to intracellular mechanisms.
Arimura, N., & Kaibuchi, K. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2056 · Cited by 655
Traffic control: regulation of kinesin motors
Verhey, K. J., & Hammond, J. W. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2782 · Cited by 546
Microtubule stabilization specifies initial neuronal polarization
Witte, H., Neukirchen, D., & Bradke, F. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200707042 · Cited by 564
MEC-17 is an α-tubulin acetyltransferase
Akella, J. S., Wloga, D., Kim, J., Starostina, N. G., Lyons-Abbott, S., Morrissette, N. S., Dougan, S. T., Kipreos, E. T., & Gaertig, J. (2010) · Nature · doi:10.1038/nature09324 · Cited by 489
The axon initial segment and the maintenance of neuronal polarity
Rasband, M. N. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2852 · Cited by 442
A selective filter for cytoplasmic transport at the axon initial segment
Song, A.-H., Wang, D., Chen, G., Li, Y., Luo, J., Duan, S., & Poo, M.-M. (2009) · Cell · doi:10.1016/j.cell.2009.01.016 · Cited by 322
Mixed microtubules steer dynein-driven cargo transport into dendrites
Kapitein, L. C., Schlager, M. A., Kuijpers, M., Wulf, P. S., van Spronsen, M., MacKintosh, F. C., & Hoogenraad, C. C. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.052 · Cited by 320
Differentiation between oppositely oriented microtubules controls polarized neuronal transport
Tas, R. P., Chazeau, A., Cloin, B. M. C., Lambers, M. L. A., Hoogenraad, C. C., & Kapitein, L. C. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.018 · Cited by 306
Single molecule imaging reveals differences in microtubule track selection between Kinesin motors
Cai, D., McEwen, D. P., Martens, J. R., Meyhofer, E., & Verhey, K. J. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000216 · Cited by 300
Posttranslational modifications of tubulin and the polarized transport of kinesin-1 in neurons
Hammond, J. W., Huang, C.-F., Kaech, S., Jacobson, C., Banker, G., & Verhey, K. J. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-01-0044 · Cited by 281
Guardia, C. M., Farías, G. G., Jia, R., Pu, J., & Bonifacino, J. S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.062 · Cited by 269
CRMP-2 Is Involved in Kinesin-1-Dependent Transport of the Sra-1/WAVE1 Complex and Axon Formation
Kawano, Y., Yoshimura, T., Tsuboi, D., Kawabata, S., Kaneko-Kawano, T., Shirataki, H., Takenawa, T., & Kaibuchi, K. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.22.9920-9935.2005 · Cited by 241
van Beuningen, S. F. B., Will, L., Harterink, M., Chazeau, A., van Battum, E. Y., Frias, C. P., Franker, M. A. M., Katrukha, E. A., Stucchi, R., Vocking, K., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.11.012 · Cited by 225
The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders
Lasser, M., Tiber, J., & Lowery, L. A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00165 · Cited by 201
Anterograde Transport of TrkB in Axons Is Mediated by Direct Interaction with Slp1 and Rab27
Arimura, N., Kimura, T., Nakamuta, S., Taya, S., Funahashi, Y., Hattori, A., Shimada, A., Ménager, C., Kawabata, S., Fujii, K., et al. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.03.005 · Cited by 192
AnkyrinG is required to maintain axo-dendritic polarity in vivo
Sobotzik, J.-M., Sie, J. M., Politi, C., Del Turco, D., Bennett, V., Deller, T., & Schultz, C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909267106 · Cited by 185
Multiple roles for the actin cytoskeleton during regulated exocytosis
Porat-Shliom, N., Milberg, O., Masedunskas, A., & Weigert, R. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1156-5 · Cited by 181
MAP7 family proteins regulate kinesin-1 recruitment and activation
Hooikaas, P. J., Martin, M., Mühlethaler, T., Kuijntjes, G.-J., Peeters, C. A. E., Katrukha, E. A., Ferrari, L., Stucchi, R., Verhagen, D. G. F., van Riel, W. E., et al. (2019) · Journal of Cell Biology · doi:10.1083/jcb.201808065 · Cited by 166
Nakata, T., Niwa, S., Okada, Y., Perez, F., & Hirokawa, N. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201104034 · Cited by 156
Self-citationKinesin-binding-triggered conformation switching of microtubules contributes to polarized transport
Shima, T., Morikawa, M., Kaneshiro, J., Kambara, T., Kamimura, S., Yagi, T., Iwamoto, H., Uemura, S., Shigematsu, H., Shirouzu, M., et al. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201711178 · Cited by 125
Self-citationJenkins, B., Decker, H., Bentley, M., Luisi, J., & Banker, G. (2012) · Journal of Cell Biology · doi:10.1083/jcb.201205070 · Cited by 77
Ayloo, S., Guedes-Dias, P., Ghiretti, A. E., & Holzbaur, E. L. F. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-01-0068 · Cited by 41
Causes, costs and consequences of kinesin motors communicating through the microtubule lattice
Verhey, K. J., & Ohi, R. (2023) · Journal of Cell Science · doi:10.1242/jcs.260735 · Cited by 37
Regulation of plasma membrane expansion during axon formation
Quiroga, S., Bisbal, M., & Cáceres, A. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22553 · Cited by 31
Yoshida, M. W., Hakozaki, M., & Goshima, G. (2023) · Nature Plants · doi:10.1038/s41477-023-01397-x · Cited by 20
Modification of the neck-linker of KIF18A alters Microtubule subpopulation preference
Queen, K. A., Cario, A., Berger, C. L., & Stumpff, J. (2024) · Molecular Biology of the Cell · doi:10.1091/mbc.e23-05-0167 · Cited by 5
Metadata
- Authors
- Nakata, T., & Hirokawa, N.
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2003-09-15
- Volume
- 162
- Issue
- 6
- Pages
- 1045-1055
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2160996171
- Cited by
- 313
- References
- 5
- FWCI
- 3.46
- 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.