Skip to main content
Log in

Dominant-Negative Myosin Va Impairs Retrograde but Not Anterograde Axonal Transport of Large Dense Core Vesicles

  • Original Research
  • Published:
Cellular and Molecular Neurobiology Aims and scope Submit manuscript

Abstract

Axonal transport of peptide and hormone-containing large dense core vesicles (LDCVs) is known to be a microtubule-dependent process. Here, we suggest a role for the actin-based motor protein myosin Va specifically in retrograde axonal transport of LDCVs. Using live-cell imaging of transfected hippocampal neurons grown in culture, we measured the speed, transport direction, and the number of LDCVs that were labeled with ectopically expressed neuropeptide Y fused to EGFP. Upon expression of a dominant-negative tail construct of myosin Va, a general reduction of movement in both dendrites and axons was observed. In axons, it was particularly interesting that the retrograde speed of LDCVs was significantly impaired, although anterograde transport remained unchanged. Moreover, particles labeled with the dominant-negative construct often moved in the retrograde direction but rarely in the anterograde direction. We suggest a model where myosin Va acts as an actin-dependent vesicle motor that facilitates retrograde axonal transport.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Abbreviations

AIS:

Axon initial segment

EGFP:

Enhanced green fluorescent protein

LDCV:

Large dense core vesicle

mGFP/mRFP:

Monomeric green/red fluorescent protein

NPY:

Neuropeptide Y

SEM:

Standard error of the mean

SG:

Secretory granule

DIV:

Days in vitro

References

  • Adachi N, Kohara K, Tsumoto T (2005) Difference in trafficking of brain-derived neurotrophic factor between axons and dendrites of cortical neurons, revealed by live-cell imaging. BMC Neurosci 6:42

    Article  PubMed  Google Scholar 

  • Alami NH, Jung P, Brown A (2009) Myosin Va increases the efficiency of neurofilament transport by decreasing the duration of long-term pauses. J Neurosci 29:6625–6634

    Article  CAS  PubMed  Google Scholar 

  • Ali MY, Krementsova EB, Kennedy GG, Mahaffy R, Pollard TD, Trybus KM, Warshaw DM (2007) Myosin Va maneuvers through actin intersections and diffuses along microtubules. Proc Natl Acad Sci USA 104:4332–4336

    Article  CAS  PubMed  Google Scholar 

  • Baas PW, Deitch JS, Black MM, Banker GA (1988) Polarity orientation of microtubules in hippocampal neurons: uniformity in the axon and nonuniformity in the dendrite. Proc Natl Acad Sci USA 85:8335–8339

    Article  CAS  PubMed  Google Scholar 

  • Bittins CM, Eichler TW, Gerdes HH (2009) Expression of the dominant-negative tail of myosin Va enhances exocytosis of large dense core vesicles in neurons. Cell Mol Neurobiol 29:597–608

    Article  CAS  PubMed  Google Scholar 

  • Bridgman PC (1999) Myosin Va movements in normal and dilute-lethal axons provide support for a dual filament motor complex. J Cell Biol 146:1045–1060

    Article  CAS  PubMed  Google Scholar 

  • Bridgman PC (2004) Myosin-dependent transport in neurons. J Neurobiol 58:164–174

    Article  CAS  PubMed  Google Scholar 

  • Brigadski T, Hartmann M, Lessmann V (2005) Differential vesicular targeting and time course of synaptic secretion of the mammalian neurotrophins. J Neurosci 25:7601–7614

    Article  CAS  PubMed  Google Scholar 

  • Brown JR, Stafford P, Langford GM (2004) Short-range axonal/dendritic transport by myosin-V: a model for vesicle delivery to the synapse. J Neurobiol 58:175–188

    Article  CAS  PubMed  Google Scholar 

  • Burack MA, Silverman MA, Banker G (2000) The role of selective transport in neuronal protein sorting. Neuron 26:465–472

    Article  CAS  PubMed  Google Scholar 

  • Burgess TL, Kelly RB (1987) Constitutive and regulated secretion of proteins. Annu Rev Cell Biol 3:243–293

    Article  CAS  PubMed  Google Scholar 

  • Correia SS, Bassani S, Brown TC, Lise MF, Backos DS, El-Husseini A, Passafaro M, Esteban JA (2008) Motor protein-dependent transport of AMPA receptors into spines during long-term potentiation. Nat Neurosci 11:457–466

    Article  CAS  PubMed  Google Scholar 

  • Cui B, Wu C, Chen L, Ramirez A, Bearer EL, Li WP, Mobley WC, Chu S (2007) One at a time, live tracking of NGF axonal transport using quantum dots. Proc Nat Acad Sci USA 104:13666–13671

    Article  CAS  PubMed  Google Scholar 

  • de Wit J, Toonen RF, Verhaagen J, Verhage M (2006) Vesicular trafficking of semaphorin 3A is activity-dependent and differs between axons and dendrites. Traffic (Copenhagen, Denmark) 7:1060–1077

    Article  Google Scholar 

  • Desnos C, Huet S, Fanget I, Chapuis C, Bottiger C, Racine V, Sibarita JB, Henry JP, Darchen F (2007) Myosin Va mediates docking of secretory granules at the plasma membrane. J Neurosci 27:10636–10645

    Article  CAS  PubMed  Google Scholar 

  • Eichler TW, Kogel T, Bukoreshtliev NV, Gerdes HH (2006) The role of myosin Va in secretory granule trafficking and exocytosis. Biochem Soc Trans 34:671–674

    Article  CAS  PubMed  Google Scholar 

  • Frischknecht R, Fejtova A, Viesti M, Stephan A, Sonderegger P (2008) Activity-induced synaptic capture and exocytosis of the neuronal serine protease neurotrypsin. J Neurosci 28:1568–1579

    Article  CAS  PubMed  Google Scholar 

  • Glombik MM, Gerdes HH (2000) Signal-mediated sorting of neuropeptides and prohormones: secretory granule biogenesis revisited. Biochimie 82:315–326

    Article  CAS  PubMed  Google Scholar 

  • Goslin K, Banker GA (1998) Rat hippocampal neurons in low-density culture. In: Banker GA, Goslin K (eds) Culturing nerve cells, 2nd edn. MIT Press, Cambridge, MA, pp 339–370

    Google Scholar 

  • Gross SP, Vershinin M, Shubeita GT (2007) Cargo transport: two motors are sometimes better than one. Curr Biol 17:R478–R486

    Article  CAS  PubMed  Google Scholar 

  • Hartmann M, Heumann R, Lessmann V (2001) Synaptic secretion of BDNF after high-frequency stimulation of glutamatergic synapses. EMBO J 20:5887–5897

    Article  CAS  PubMed  Google Scholar 

  • Hill DB, Plaza MJ, Bonin K, Holzwarth G (2004) Fast vesicle transport in PC12 neurites: velocities and forces. Eur Biophys J 33:623–632

    Article  CAS  PubMed  Google Scholar 

  • Hirokawa N, Takemura R (2005) Molecular motors and mechanisms of directional transport in neurons. Nat Rev 6:201–214

    Article  CAS  Google Scholar 

  • Hodi Z, Nemeth AL, Radnai L, Hetenyi C, Schlett K, Bodor A, Perczel A, Nyitray L (2006) Alternatively spliced exon B of myosin Va is essential for binding the tail-associated light chain shared by dynein. Biochemistry 45:12582–12595

    Article  CAS  PubMed  Google Scholar 

  • Huttner WB, Ohashi M, Kehlenbach RH, Barr FA, Bauerfeind R, Braunling O, Corbeil D, Hannah M, Pasolli HA, Schmidt A et al (1995) Biogenesis of neurosecretory vesicles. Cold Spring Harb Sym Quant Biol 60:315–327

    CAS  Google Scholar 

  • Kim T, Gondre-Lewis MC, Arnaoutova I, Loh YP (2006) Dense-core secretory granule biogenesis. Physiology (Bethesda, MD) 21:124–133

    CAS  Google Scholar 

  • Kural C, Kim H, Syed S, Goshima G, Gelfand VI, Selvin PR (2005) Kinesin and dynein move a peroxisome in vivo: a tug-of-war or coordinated movement? Science (New York, NY) 308:1469–1472

    CAS  Google Scholar 

  • Kwinter DM, Lo K, Mafi P, Silverman MA (2009) Dynactin regulates bidirectional transport of dense-core vesicles in the axon and dendrites of cultured hippocampal neurons. Neuroscience 162:1001–1010

    Article  CAS  PubMed  Google Scholar 

  • Lalli G, Gschmeissner S, Schiavo G (2003) Myosin Va and microtubule-based motors are required for fast axonal retrograde transport of tetanus toxin in motor neurons. J Cell Sci 116:4639–4650

    Article  CAS  PubMed  Google Scholar 

  • Levi V, Serpinskaya AS, Gratton E, Gelfand V (2006) Organelle transport along microtubules in Xenopus melanophores: evidence for cooperation between multiple motors. Biophys J 90:318–327

    Article  CAS  PubMed  Google Scholar 

  • Lochner JE, Honigman LS, Grant WF, Gessford SK, Hansen AB, Silverman MA, Scalettar BA (2006) Activity-dependent release of tissue plasminogen activator from the dendritic spines of hippocampal neurons revealed by live-cell imaging. J Neurobiol 66:564–577

    Article  CAS  PubMed  Google Scholar 

  • Mercer JA, Seperack PK, Strobel MC, Copeland NG, Jenkins NA (1991) Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature 349:709–713

    Article  CAS  PubMed  Google Scholar 

  • Overly CC, Rieff HI, Hollenbeck PJ (1996) Organelle motility and metabolism in axons vs dendrites of cultured hippocampal neurons. J Cell Sci 109(Pt 5):971–980

    CAS  PubMed  Google Scholar 

  • Park JJ, Cawley NX, Loh YP (2008) A bi-directional carboxypeptidase E-driven transport mechanism controls BDNF vesicle homeostasis in hippocampal neurons. Mol Cell Neurosci 39:63–73

    Article  CAS  PubMed  Google Scholar 

  • Pastural E, Barrat FJ, Dufourcq-Lagelouse R, Certain S, Sanal O, Jabado N, Seger R, Griscelli C, Fischer A, de Saint Basile G (1997) Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene. Nat Genet 16:289–292

    Article  CAS  PubMed  Google Scholar 

  • Rose SD, Lejen T, Casaletti L, Larson RE, Pene TD, Trifaro JM (2003) Myosins II and V in chromaffin cells: myosin V is a chromaffin vesicle molecular motor involved in secretion. J Neurochem 85:287–298

    Article  CAS  PubMed  Google Scholar 

  • Roy S, Winton MJ, Black MM, Trojanowski JQ, Lee VM (2007) Rapid and intermittent cotransport of slow component-b proteins. J Neurosci 27:3131–3138

    Article  CAS  PubMed  Google Scholar 

  • Rudolf R, Salm T, Rustom A, Gerdes HH (2001) Dynamics of immature secretory granules: role of cytoskeletal elements during transport, cortical restriction, and F-actin-dependent tethering. Mol Biol Cell 12:1353–1365

    CAS  PubMed  Google Scholar 

  • Rudolf R, Kogel T, Kuznetsov SA, Salm T, Schlicker O, Hellwig A, Hammer JA 3rd, Gerdes HH (2003) Myosin Va facilitates the distribution of secretory granules in the F-actin rich cortex of PC12 cells. J Cell Sci 116:1339–1348

    Article  CAS  PubMed  Google Scholar 

  • Seperack PK, Mercer JA, Strobel MC, Copeland NG, Jenkins NA (1995) Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner. EMBO J 14:2326–2332

    CAS  PubMed  Google Scholar 

  • Shakiryanova D, Tully A, Levitan ES (2006) Activity-dependent synaptic capture of transiting peptidergic vesicles. Nat Neurosci 9:896–900

    Article  CAS  PubMed  Google Scholar 

  • Song AH, Wang D, Chen G, Li Y, Luo J, Duan S, Poo MM (2009) A selective filter for cytoplasmic transport at the axon initial segment. Cell 136:1148–1160

    Article  CAS  PubMed  Google Scholar 

  • Tabb JS, Molyneaux BJ, Cohen DL, Kuznetsov SA, Langford GM (1998) Transport of ER vesicles on actin filaments in neurons by myosin V. J Cell Sci 111(Pt 21):3221–3234

    CAS  PubMed  Google Scholar 

  • Tooze SA (1998) Biogenesis of secretory granules in the trans-Golgi network of neuroendocrine and endocrine cells. Biochim Biophys Acta 1404:231–244

    Article  CAS  PubMed  Google Scholar 

  • Tooze SA, Huttner WB (1990) Cell-free protein sorting to the regulated and constitutive secretory pathways. Cell 60:837–847

    Article  CAS  PubMed  Google Scholar 

  • Varadi A, Tsuboi T, Rutter GA (2005) Myosin Va transports dense core secretory vesicles in pancreatic MIN6 beta-cells. Mol Biol Cell 16:2670–2680

    Article  CAS  PubMed  Google Scholar 

  • Wagner W, Fodor E, Ginsburg A, Hammer JA 3rd (2006) The binding of DYNLL2 to myosin Va requires alternatively spliced exon B and stabilizes a portion of the myosin’s coiled-coil domain. Biochemistry 45:11564–11577

    Article  CAS  PubMed  Google Scholar 

  • Welte MA (2004) Bidirectional transport along microtubules. Curr Biol 14:R525–R537

    Article  CAS  PubMed  Google Scholar 

  • Wu X, Bowers B, Wei Q, Kocher B, Hammer JA 3rd (1997) Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor. J Cell Sci 110(Pt 7):847–859

    CAS  PubMed  Google Scholar 

  • Wu X, Bowers B, Rao K, Wei Q, Hammer JA 3rd (1998) Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo. J Cell Biol 143:1899–1918

    Article  CAS  PubMed  Google Scholar 

  • Wu X, Wang F, Rao K, Sellers JR, Hammer JA 3rd (2002) Rab27a is an essential component of melanosome receptor for myosin Va. Mol Biol Cell 13:1735–1749

    Article  CAS  PubMed  Google Scholar 

  • Wu YJ, Kruttgen A, Moller JC, Shine D, Chan JR, Shooter EM, Cosgaya JM (2004) Nerve growth factor, brain-derived neurotrophic factor, and neurotrophin-3 are sorted to dense-core vesicles and released via the regulated pathway in primary rat cortical neurons. J Neurosci Res 75:825–834

    Article  CAS  PubMed  Google Scholar 

  • Yoshimura A, Fujii R, Watanabe Y, Okabe S, Fukui K, Takumi T (2006) Myosin-Va facilitates the accumulation of mRNA/protein complex in dendritic spines. Curr Biol 16:2345–2351

    Article  CAS  PubMed  Google Scholar 

  • Yoshizaki T, Imamura T, Babendure JL, Lu JC, Sonoda N, Olefsky JM (2007) Myosin 5a is an insulin-stimulated Akt2 (protein kinase Bbeta) substrate modulating GLUT4 vesicle translocation. Mol Cell Biol 27:5172–5183

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The imaging was performed at the Molecular Imaging Center (FUGE, Norwegian Research Council), University of Bergen. The authors are grateful to W. Almers for providing NPY-EGFP and NPY-mRFP and to the University of Bergen for financial support including research fellowships. H.-H. G. acknowledges grants from the Meltzer Foundation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hans-Hermann Gerdes.

Additional information

Claudia Margarethe Bittins and Tilo Wolf Eichler have contributed equally.

Electronic Supplementary Material

Below is the link to the electronic supplementary material.

NPY-EGFP labeled LDCVs in living neurons at 12 DIV. Cells were transfected with NPY-EGFP and a vector encoding mCherry (not shown). Images were taken at 1 Hz for a duration of 100 s. Scale bar 50 µm (AVI 3300 kb)

MyosinVa-tail-mCherry in living neurons at 12 DIV. Cells were double transfected with NPY-EGFP (not shown) and myosinVa-tail-mCherry. Images were taken at 1 Hz for a duration of 100 s. Scale bar 50 µm (AVI 6414 kb)

Dual-color time lapse recording of a neuron at 12 DIV, transfected with NPY-EGFP (green) and myosinVa-tail-mCherry (red) showing cotransport of the two proteins. Images were taken at 1 Hz for a duration of 100 s. Scale bar, 50 µm (AVI 2794 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bittins, C.M., Eichler, T.W., Hammer, J.A. et al. Dominant-Negative Myosin Va Impairs Retrograde but Not Anterograde Axonal Transport of Large Dense Core Vesicles. Cell Mol Neurobiol 30, 369–379 (2010). https://doi.org/10.1007/s10571-009-9459-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10571-009-9459-2

Keywords

Navigation