Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Capacitance steps and fusion pores of small and large-dense-core vesicles in nerve terminals

Abstract

The vesicles that package neurotransmitters fall into two distinct classes, large dense-core vesicles (LDCVs) and small synaptic vesicles, the coexistence of which is widespread in nerve terminals1. High resolution capacitance recording reveals unitary steps proportional to vesicle size. Measurements of capacitance steps during LDCV and secretory granule fusion in endocrine and immune cells have provided important insights into exocytosis2,3,4; however, extending these measurements to small synaptic vesicles has proven difficult. Here we report single vesicle capacitance steps in posterior pituitary nerve terminals. These nerve terminals contain neuropeptide-laden LDCVs, as well as microvesicles. Microvesicles are similar to synaptic vesicles in size, morphology5 and molecular composition6,7,8, but their contents are unknown. Capacitance steps of two characteristic sizes, corresponding with microvesicles and LDCVs, were detected in patches of nerve terminal membrane. Both types of vesicles fuse in response to depolarization-induced Ca2+ entry. Both undergo a reversible fusion process commonly referred to as ‘kiss-and-run’, but only rarely. Fusion pores seen during microvesicle kiss-and-run have a conductance of 19 pS, 11 times smaller than LDCV fusion pores. Thus, LDCVs and microvesicles use structurally different intermediates during exocytosis.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Spontaneous single-vesicle capacitance steps in nerve terminals.
Figure 2: Depolarization-induced Ca2+ entry elicits exocytosis of LDCVs and microvesicles.
Figure 3: Kiss-and-run.
Figure 4: Fusion pore analysis for kiss-and-run and non-reversing events.

Similar content being viewed by others

References

  1. De Camilli, P. & Jahn, R. Pathways to regulated exocytosis in neurons. Ann. Rev. Physiol. 52, 625–645 (1990)

    Article  CAS  Google Scholar 

  2. Neher, E. & Marty, A. Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. Proc. Natl Acad. Sci. USA 79, 6712–6716 (1982)

    Article  ADS  CAS  Google Scholar 

  3. Fernandez, J. M., Neher, E. & Gomperts, B. D. Capacitance measurements reveal stepwise fusion events in degranulating mast cells. Nature 312, 453–455 (1984)

    Article  ADS  CAS  Google Scholar 

  4. Lollike, K., Borregaard, N. & Lindau, M. The exocytotic fusion pore of small granules has a conductance similar to an ion channel. J. Cell Biol. 129, 99–104 (1995)

    Article  CAS  Google Scholar 

  5. Morris, J. F., Nordmann, J. J. & Dyball, R. E. J. Structure-function correlation in mammalian neurosecretion. Int. Rev. Exp. Pathol. 18, 1–95 (1978)

    CAS  Google Scholar 

  6. Navone, F. et al. Microvesicles of the neurohypophysis are biochemically related to small synaptic vesicles of presynaptic nerve terminals. J. Cell Biol. 109, 3425–3433 (1989)

    Article  CAS  Google Scholar 

  7. Walch-Solimena, C. et al. Synaptotagmin: a membrane constituent of neuropeptide-containing large dense-core vesicles. J. Neurosci. 13, 3895–3903 (1993)

    Article  CAS  Google Scholar 

  8. Pupier, S. et al. Cysteine string proteins associated with secretory granules of the rat neurohypophysis. J. Neurosci. 17, 2722–2727 (1997)

    Article  CAS  Google Scholar 

  9. Debus, K. & Lindau, M. Resolution of patch capacitance recordings and of fusion pore conductance in small vesicles. Biophys. J. 78, 2983–2997 (2000)

    Article  ADS  CAS  Google Scholar 

  10. Gentet, L. J., Stuart, G. J. & Clements, J. D. Direct measurement of specific membrane capacitance in neurons. Biophys. J. 79, 314–320 (2000)

    Article  CAS  Google Scholar 

  11. Nagasawa, J., Douglas, W. W. & Schulz, R. A. Micropinocytotic origin of coated and smooth microvesicles (‘synaptic vesicles’) in neurosecretory terminals of posterior pituitary glands demonstrated by incorporation of horse-radish peroxidase. Nature 332, 341–342 (1971)

    Article  ADS  Google Scholar 

  12. Morris, J. F. & Nordmann, J. J. Membrane recapture after hormone release from nerve endings in the neural lobe of the rat pituitary gland. Neuroscience 5, 639–649 (1980)

    Article  CAS  Google Scholar 

  13. Hsu, S.-F. & Jackson, M. B. Rapid exocytosis and endocytosis in nerve terminal of the rat posterior pituitary. J. Physiol. 494.2, 539–553 (1996)

    Article  Google Scholar 

  14. Rosenboom, H. & Lindau, M. Exo-endocytosis and closing of the fission pore during endocytosis in single pituitary nerve terminals internally perfused with high calcium concentrations. Proc. Natl Acad. Sci. USA 91, 5267–5271 (1994)

    Article  ADS  CAS  Google Scholar 

  15. Lindau, M. & Almers, W. Structure and function of fusion pores in exocytosis and ectoplasmic membrane fusion. Curr. Opin. Neurobiol. 7, 509–517 (1995)

    Article  CAS  Google Scholar 

  16. Fesce, R., Grohovaz, F., Valtorta, F. & Meldolesi, J. Neurotransmitter release: fusion or ‘kiss-and-run’? Trends Cell Biol. 4, 1–4 (1994)

    Article  CAS  Google Scholar 

  17. Tse, F. W., Iwata, A. & Almers, W. Membrane flux through the pore formed by a fusogenic viral envelope protein during cell fusion. J. Cell Biol. 121, 543–552 (1993)

    Article  CAS  Google Scholar 

  18. Zimmerberg, J., Blumenthal, R., Curran, M., Sarker, D. & Morris, S. Restricted movement of lipid and aqueous dyes through pores formed by influenza hemagglutinin during cell fusion. J. Cell Biol. 127, 1885–1894 (1994)

    Article  CAS  Google Scholar 

  19. Breckenridge, L. J. & Almers, W. Currents through the fusion pore that forms during exocytosis of a secretory granule. Nature 328, 814–817 (1987)

    Article  ADS  CAS  Google Scholar 

  20. Spruce, A. E., Breckenridge, L. J., Lee, A. K. & Almers, W. Properties of the fusion pore that forms during exocytosis of a mast cell secretory granule. Neuron 4, 643–654 (1990)

    Article  CAS  Google Scholar 

  21. Almers, W. et al. Millisecond studies of single membrane fusion events. Ann. NY Acad. Sci. 635, 318–327 (1991)

    Article  ADS  CAS  Google Scholar 

  22. Chow, R. H., von Rüden, L. & Neher, E. Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells. Nature 356, 60–63 (1992)

    Article  ADS  CAS  Google Scholar 

  23. Bruns, D. & Jahn, R. Real-time measurement of transmitter release from single synaptic vesicles. Nature 377, 62–65 (1995)

    Article  ADS  CAS  Google Scholar 

  24. Stiles, J. R., Van Helden, D., Bartol, T. M., Salpeter, E. E. & Salpeter, M. M. Miniature endplate current rise times < 100 μs from improved dual recordings can be modeled with passive acetylcholine diffusion from a synaptic vesicle. Proc. Natl Acad. Sci. USA 93, 5747–5752 (1996)

    Article  ADS  CAS  Google Scholar 

  25. Khanin, R., Parnas, H. & Segel, L. Diffusion cannot govern the discharge of neurotransmitter in fast synapses. Biophys. J. 67, 966–972 (1994)

    Article  ADS  CAS  Google Scholar 

  26. Khanin, R., Parnas, H. & Segel, L. A mechanism for discharge of charged excitatory neurotransmitter. Biophys. J. 72, 507–521 (1997)

    Article  CAS  Google Scholar 

  27. Nanavati, C. & Fernandez, J. M. The secretory granule matrix: a fast acting smart polymer. Science 259, 963–965 (1993)

    Article  ADS  CAS  Google Scholar 

  28. Ales, E. et al. High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism. Nature Cell Biol. 1, 40–44 (1999)

    Article  CAS  Google Scholar 

  29. Verhage, M. et al. Differential release of amino acids, neuropeptides, and catecholamines from isolated nerve terminals. Neuron 6, 517–524 (1991)

    Article  CAS  Google Scholar 

  30. Rae, J. L. & Levis, R. A. A method for exceptionally low noise single channel recordings. Pflügers Arch. Eur. J. Physiol. 420, 618–620 (1992)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank M. Lindau for advice on capacitance measurements, D.L. Armstrong for suggesting the use of oil to reduce noise, and E.R. Chapman, C.-T. Wang, P.Y. Chang, G.P. Ahern and X. Han for helpful comments on the manuscript. We thank R. J. Massey of the UW Electron Microscope Facility for performing electron microscopy. This research was supported by a grant from NIH and a predoctoral fellowship from the AHA to V.A.K.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Meyer B. Jackson.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Cite this article

Klyachko, V., Jackson, M. Capacitance steps and fusion pores of small and large-dense-core vesicles in nerve terminals. Nature 418, 89–92 (2002). https://doi.org/10.1038/nature00852

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature00852

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing