CoChat
Sign Up
Cited by 244

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Motor protein–dependent transport of AMPA receptors into spines during long-term potentiation

Correia, Susana S, Bassani, Silvia, Brown, Tyler C, Lisé, Marie-France, Backos, Donald S, El-Husseini, Alaa, Passafaro, Maria, Esteban, José A·2008·Nature Neuroscience
DOI 10.1038/nn2063
Open this paper in CoChat — free account

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/nn2063

Cites

5 of 5 references verified0 citation errors · 0 not checkable

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.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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

Flagged first, then by citations

Research works printed but not linked: 45

  1. Park, M. et al. Plasticity-induced growth of dendritic spines by exocytic trafficking from recycling endosomes. Neuron 52, 817–830 (2006). · DOI · Paper page
  2. Shi, S.H. et al. Rapid spine delivery and redistribution of AMPA receptors after synaptic NMDA receptor activation. Science 284, 1811–1816 (1999). · DOI · Paper page
  3. Kim, J., Jung, S.C., Clemens, A.M., Petralia, R.S. & Hoffman, D.A. Regulation of dendritic excitability by activity-dependent trafficking of the A-type K+ channel subunit Kv4.2 in hippocampal neurons. Neuron 54, 933–947 (2007). · DOI
  4. Shepherd, J.D. & Huganir, R.L. The cell biology of synaptic plasticity: AMPA receptor trafficking. Annu. Rev. Cell Dev. Biol. 23, 613–643 (2007). · DOI · Paper page
  5. Shi, S., Hayashi, Y., Esteban, J.A. & Malinow, R. Subunit-specific rules governing AMPA receptor trafficking to synapses in hippocampal pyramidal neurons. Cell 105, 331–343 (2001). · DOI · Paper page
  6. Luscher, C. et al. Role of AMPA receptor cycling in synaptic transmission and plasticity. Neuron 24, 649–658 (1999). · DOI · Paper page
  7. Nishimune, A. et al. NSF binding to GluR2 regulates synaptic transmission. Neuron 21, 87–97 (1998). · DOI
  8. Song, I. et al. Interaction of the N-ethylmaleimide–sensitive factor with AMPA receptors. Neuron 21, 393–400 (1998). · DOI
  9. Hayashi, Y. et al. Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction. Science 287, 2262–2267 (2000). · DOI · Paper page
  10. Carlisle, H.J. & Kennedy, M.B. Spine architecture and synaptic plasticity. Trends Neurosci. 28, 182–187 (2005). · DOI
  11. Karcher, R.L., Deacon, S.W. & Gelfand, V.I. Motor-cargo interactions: the key to transport specificity. Trends Cell Biol. 12, 21–27 (2002). · DOI
  12. Osterweil, E., Wells, D.G. & Mooseker, M.S. A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis. J. Cell Biol. 168, 329–338 (2005). · DOI
  13. Lise, M.F. et al. Involvement of myosin Vb in glutamate receptor trafficking. J. Biol. Chem. 281, 3669–3678 (2006). · DOI · Paper page
  14. Triller, A. & Choquet, D. Surface trafficking of receptors between synaptic and extrasynaptic membranes: and yet they do move!. Trends Neurosci. 28, 133–139 (2005). · DOI · Paper page
  15. Mercer, J.A., Seperack, P.K., Strobel, M.C., Copeland, N.G. & Jenkins, N.A. Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature 349, 709–713 (1991). · DOI
  16. Naisbitt, S. et al. Interaction of the postsynaptic density–95/guanylate kinase domain–associated protein complex with a light chain of myosin-V and dynein. J. Neurosci. 20, 4524–4534 (2000). · DOI
  17. Walikonis, R.S. et al. Identification of proteins in the postsynaptic density fraction by mass spectrometry. J. Neurosci. 20, 4069–4080 (2000). · DOI
  18. Yoshimura, A. et al. myosin-Va facilitates the accumulation of mRNA/protein complex in dendritic spines. Curr. Biol. 16, 2345–2351 (2006). · DOI
  19. Pastural, E. et al. Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene. Nat. Genet. 16, 289–292 (1997). · DOI
  20. Sanal, O. et al. An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder). J. Neurol. 247, 570–572 (2000). · DOI
  21. Tabb, J.S., Molyneaux, B.J., Cohen, D.L., Kuznetsov, S.A. & Langford, G.M. Transport of ER vesicles on actin filaments in neurons by myosin V. J. Cell Sci. 111, 3221–3234 (1998). · DOI
  22. Takagishi, Y. et al. The dilute lethal (dl) gene attacks a Ca2+ store in the dendritic spine of Purkinje cells in mice. Neurosci. Lett. 215, 169–172 (1996). · DOI
  23. Petralia, R.S. et al. Glutamate receptor targeting in the postsynaptic spine involves mechanisms that are independent of myosin Va. Eur. J. Neurosci. 13, 1722–1732 (2001). · DOI
  24. Miyata, M. et al. Local calcium release in dendritic spines required for long-term synaptic depression. Neuron 28, 233–244 (2000). · DOI
  25. Schnell, E. & Nicoll, R.A. Hippocampal synaptic transmission and plasticity are preserved in myosin Va mutant mice. J. Neurophysiol. 85, 1498–1501 (2001). · DOI
  26. Wenthold, R.J., Petralia, R.S., Blahos, J., II & Niedzielski, A.S. Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons. J. Neurosci. 16, 1982–1989 (1996). · DOI · Paper page
  27. Ullrich, O., Reinsch, S., Urbe, S., Zerial, M. & Parton, R.G. Rab11 regulates recycling through the pericentriolar recycling endosome. J. Cell Biol. 135, 913–924 (1996). · DOI · Paper page
  28. Brown, J.R., Simonetta, K.R., Sandberg, L.A., Stafford, P. & Langford, G.M. Recombinant globular tail fragment of myosin-V blocks vesicle transport in squid nerve cell extracts. Biol. Bull. 201, 240–241 (2001). · DOI
  29. Lapierre, L.A. et al. myosin vb is associated with plasma membrane recycling systems. Mol. Biol. Cell 12, 1843–1857 (2001). · DOI
  30. Rodriguez, O.C. & Cheney, R.E. Human myosin-Vc is a novel class V myosin expressed in epithelial cells. J. Cell Sci. 115, 991–1004 (2002). · DOI
  31. Zhu, J.J., Esteban, J.A., Hayashi, Y. & Malinow, R. Postnatal synaptic potentiation: delivery of GluR4-containing AMPA receptors by spontaneous activity. Nat. Neurosci. 3, 1098–1106 (2000). · DOI · Paper page
  32. Gerges, N.Z., Brown, T.C., Correia, S.S. & Esteban, J.A. Analysis of Rab protein function in neurotransmitter receptor trafficking at hippocampal synapses. Methods Enzymol. 403, 153–166 (2005). · DOI
  33. Ehrlich, I. & Malinow, R. Postsynaptic density–95 controls AMPA receptor incorporation during long-term potentiation and experience-driven synaptic plasticity. J. Neurosci. 24, 916–927 (2004). · DOI · Paper page
  34. Piccini, A. & Malinow, R. Critical postsynaptic density–95/disc large/zonula occludens–1 interactions by glutamate receptor 1 (GluR1) and GluR2 required at different subcellular sites. J. Neurosci. 22, 5387–5392 (2002). · DOI
  35. Ryu, J. et al. A critical role for myosin IIb in dendritic spine morphology and synaptic function. Neuron 49, 175–182 (2006). · DOI
  36. Brown, T.C., Correia, S.S., Petrok, C.N. & Esteban, J.A. Functional compartmentalization of endosomal trafficking for the synaptic delivery of AMPA receptors during long-term potentiation. J. Neurosci. 27, 13311–13315 (2007). · DOI · Paper page
  37. Seabra, M.C. & Coudrier, E. Rab GTPases and myosin motors in organelle motility. Traffic 5, 393–399 (2004). · DOI
  38. Jordens, I., Marsman, M., Kuijl, C. & Neefjes, J. Rab proteins, connecting transport and vesicle fusion. Traffic 6, 1070–1077 (2005). · DOI
  39. Krementsov, D.N., Krementsova, E.B. & Trybus, K.M. myosin V: regulation by calcium, calmodulin and the tail domain. J. Cell Biol. 164, 877–886 (2004). · DOI
  40. Barral, D.C. et al. Functional redundancy of Rab27 proteins and the pathogenesis of Griscelli syndrome. J. Clin. Invest. 110, 247–257 (2002). · DOI
  41. Cao, T.T., Chang, W., Masters, S.E. & Mooseker, M.S. myosin-Va binds to and mechanochemically couples microtubules to actin filaments. Mol. Biol. Cell 15, 151–161 (2004). · DOI
  42. Ali, M.Y. et al. myosin Va maneuvers through actin intersections and diffuses along microtubules. Proc. Natl. Acad. Sci. USA 104, 4332–4336 (2007). · DOI
  43. Huang, J.D. et al. Direct interaction of microtubule- and actin-based transport motors. Nature 397, 267–270 (1999). · DOI
  44. Mehta, A.D. et al. myosin-V is a processive actin-based motor. Nature 400, 590–593 (1999). · DOI
  45. Dunah, A.W. et al. LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses. Nat. Neurosci. 8, 458–467 (2005). · DOI

Cited by

Sorted by citations

Metadata

Authors
Correia, S. S., Bassani, S., Brown, T. C., Lisé, M.-F., Backos, D. S., El-Husseini, A., Passafaro, M., & Esteban, J. A.
Venue
Nature Neuroscience
Publisher
Springer Science and Business Media LLC
Published
2008-03-02
Volume
11
Issue
4
Pages
457-466
ISSN
  • 1097-6256
  • 1546-1726
DOI
10.1038/nn2063
Cited by
244
References
5
Language
en
Licence
www.springer.com/tdm (tdm)

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