Literature DB >> 16415055

The amplitude distribution of release events through a fusion pore.

Stephen W Jones1, David D Friel.   

Abstract

Neurotransmitters, hormones, or dyes may be released from vesicles via a fusion pore, rather than by full fusion of the vesicle with the plasma membrane. If the lifetime of the fusion pore is comparable to the time required for the substance to exit the vesicle, only a fraction of the total vesicle content may be released during a single pore opening. Assuming 1), fusion pore lifetimes are exponentially distributed (tauP), as expected for simple single channel openings, and 2), vesicle contents are lost through the fusion pore with an exponential time course (tauD), we derive an analytical expression for the probability density function of the fraction of vesicle content released (F): dP/dF=A (1-F)(A-1), where A=tauD/tauP. If A>1, the maximum of the distribution is at F=0; if A<1, the maximum is at F=1; if A=1, the distribution is perfectly flat. Thus, the distribution never has a peak in the middle (0<F<1). This should be considered when interpreting the distribution of miniature synaptic currents, or the fraction of FM dye molecules lost during a single fusion pore opening event.

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Year:  2006        PMID: 16415055      PMCID: PMC1367334          DOI: 10.1529/biophysj.105.078881

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  13 in total

1.  Single synaptic vesicles fusing transiently and successively without loss of identity.

Authors:  A M Aravanis; J L Pyle; R W Tsien
Journal:  Nature       Date:  2003-06-05       Impact factor: 49.962

2.  Postfusional control of quantal current shape.

Authors:  Christian Pawlu; Aaron DiAntonio; Manfred Heckmann
Journal:  Neuron       Date:  2004-05-27       Impact factor: 17.173

3.  Spontaneous subthreshold activity at motor nerve endings.

Authors:  P FATT; B KATZ
Journal:  J Physiol       Date:  1952-05       Impact factor: 5.182

4.  Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices.

Authors:  J M Bekkers; G B Richerson; C F Stevens
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

5.  Miniature endplate current rise times less than 100 microseconds from improved dual recordings can be modeled with passive acetylcholine diffusion from a synaptic vesicle.

Authors:  J R Stiles; D Van Helden; T M Bartol; E E Salpeter; M M Salpeter
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

6.  Final steps in exocytosis observed in a cell with giant secretory granules.

Authors:  L J Breckenridge; W Almers
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

7.  Activity-dependent differential transmitter release in mouse adrenal chromaffin cells.

Authors:  Tiberiu Fulop; Stephen Radabaugh; Corey Smith
Journal:  J Neurosci       Date:  2005-08-10       Impact factor: 6.167

8.  Diffusion cannot govern the discharge of neurotransmitter in fast synapses.

Authors:  R Khanin; H Parnas; L Segel
Journal:  Biophys J       Date:  1994-09       Impact factor: 4.033

9.  Dopamine neurons release transmitter via a flickering fusion pore.

Authors:  Roland G W Staal; Eugene V Mosharov; David Sulzer
Journal:  Nat Neurosci       Date:  2004-02-29       Impact factor: 24.884

10.  Two modes of exocytosis at hippocampal synapses revealed by rate of FM1-43 efflux from individual vesicles.

Authors:  David A Richards; Jihong Bai; Edwin R Chapman
Journal:  J Cell Biol       Date:  2005-03-14       Impact factor: 10.539

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  1 in total

1.  Characterization of sequential exocytosis in a human neuroendocrine cell line using evanescent wave microscopy and "virtual trajectory" analysis.

Authors:  Viet Samuel Tran; Sébastien Huet; Isabelle Fanget; Sophie Cribier; Jean-Pierre Henry; Erdem Karatekin
Journal:  Eur Biophys J       Date:  2007-04-18       Impact factor: 1.733

  1 in total

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