The Journal of General Physiology
Cell MicroControls
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow PDF (Full Text)
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JGP
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alvarez de Toledo, G.
Right arrow Articles by Fernandez, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alvarez de Toledo, G.
Right arrow Articles by Fernandez, J. M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

The Journal of General Physiology, Vol 95, 397-409, Copyright © 1990 by The Rockefeller University Press


ARTICLES

Compound versus multigranular exocytosis in peritoneal mast cells

G Alvarez de Toledo and JM Fernandez
Department of Physiology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6085.

We have used the whole-cell patch-pipette technique to measure the step increases in the cell membrane capacitance (equivalent to the membrane area) caused by the fusion of secretory granules in degranulating murine mast cells. We have observed that up to 30% of the total membrane expansion caused by degranulation results from large fusion events that cannot be explained by the fusion of single secretory granules. These large events are observed mainly in the initial phase of a degranulation. We have developed a simple mathematical model for a mast cell to test whether these large events are caused by a stimulus- induced, granule-to-granule fusion that occurs before their exocytosis (multigranular exocytosis). Our results suggest that the large fusion events are caused by the exocytosis of granule aggregates that existed before stimulation and that are located at the cell's periphery. We propose a novel mechanism by which granule aggregates can be formed at the periphery of the cell. This mechanism relies on the ability of a transiently fused granule ("flicker") to fuse with more internally located granules in a sequential manner. This pattern may result in the formation of larger peripheral granules that later on can fuse with the membrane. The formation of peripheral granule aggregates may potentiate a subsequent secretory response.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Neurosci.Home page
G. Matthews and P. Sterling
Evidence That Vesicles Undergo Compound Fusion on the Synaptic Ribbon
J. Neurosci., May 21, 2008; 28(21): 5403 - 5411.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
N. Tiwari, C.-C. Wang, C. Brochetta, G. Ke, F. Vita, Z. Qi, J. Rivera, M. R. Soranzo, G. Zabucchi, W. Hong, et al.
VAMP-8 segregates mast cell-preformed mediator exocytosis from cytokine trafficking pathways
Blood, April 1, 2008; 111(7): 3665 - 3674.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
A. G. Garcia, A. M. Garcia-De-Diego, L. Gandia, R. Borges, and J. Garcia-Sancho
Calcium signaling and exocytosis in adrenal chromaffin cells.
Physiol Rev, October 1, 2006; 86(4): 1093 - 1131.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
G. R. V. Hammond, S. K. Dove, A. Nicol, J. A. Pinxteren, D. Zicha, and G. Schiavo
Elimination of plasma membrane phosphatidylinositol (4,5)-bisphosphate is required for exocytosis from mast cells
J. Cell Sci., May 15, 2006; 119(10): 2084 - 2094.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. Kishimoto, T.-T. Liu, H. Hatakeyama, T. Nemoto, N. Takahashi, and H. Kasai
Sequential compound exocytosis of large dense-core vesicles in PC12 cells studied with TEPIQ (two-photon extracellular polar-tracer imaging-based quantification) analysis
J. Physiol., November 1, 2005; 568(3): 905 - 915.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
E. P. Kwan and H. Y. Gaisano
Glucagon-Like Peptide 1 Regulates Sequential and Compound Exocytosis in Pancreatic Islet {beta}-Cells
Diabetes, September 1, 2005; 54(9): 2734 - 2743.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
C. Amatore, S. Arbault, I. Bonifas, Y. Bouret, M. Erard, A. G. Ewing, and L. A. Sombers
Correlation between Vesicle Quantal Size and Fusion Pore Release in Chromaffin Cell Exocytosis
Biophys. J., June 1, 2005; 88(6): 4411 - 4420.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
M. W. Allersma, L. Wang, D. Axelrod, and R. W. Holz
Visualization of Regulated Exocytosis with a Granule-Membrane Probe Using Total Internal Reflection Microscopy
Mol. Biol. Cell, October 1, 2004; 15(10): 4658 - 4668.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
N. Takahashi, H. Hatakeyama, H. Okado, A. Miwa, T. Kishimoto, T. Kojima, T. Abe, and H. Kasai
Sequential exocytosis of insulin granules is associated with redistribution of SNAP25
J. Cell Biol., April 26, 2004; 165(2): 255 - 262.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
S. Martin-Verdeaux, I. Pombo, B. Iannascoli, M. Roa, N. Varin-Blank, J. Rivera, and U. Blank
Evidence of a role for Munc18-2 and microtubules in mast cell granule exocytosis
J. Cell Sci., January 15, 2003; 116(2): 325 - 334.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
J. D. Machado, A. Morales, J. F. Gomez, and R. Borges
cAMP Modulates Exocytotic Kinetics and Increases Quantal Size in Chromaffin Cells
Mol. Pharmacol., September 1, 2001; 60(3): 514 - 520.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
E. N. Pothos, K. E. Larsen, D. E. Krantz, Y.-j. Liu, J. W. Haycock, W. Setlik, M. D. Gershon, R. H. Edwards, and D. Sulzer
Synaptic Vesicle Transporter Expression Regulates Vesicle Phenotype and Quantal Size
J. Neurosci., October 1, 2000; 20(19): 7297 - 7306.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
F. Paumet, J. Le Mao, S. Martin, T. Galli, B. David, U. Blank, and M. Roa
Soluble NSF Attachment Protein Receptors (SNAREs) in RBL-2H3 Mast Cells: Functional Role of Syntaxin 4 in Exocytosis and Identification of a Vesicle-Associated Membrane Protein 8-Containing Secretory Compartment
J. Immunol., June 1, 2000; 164(11): 5850 - 5857.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
B. Niemeyer and T. Schwarz
SNAP-24, a Drosophila SNAP-25 homologue on granule membranes, is a putative mediator of secretion and granule-granule fusion in salivary glands
J. Cell Sci., January 11, 2000; 113(22): 4055 - 4064.
[Abstract] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
M. J. Tuvim, R. Adachi, J. F. Chocano, R. H. Moore, R. M. Lampert, E. Zera, E. Romero, B. J. Knoll, and B. F. Dickey
Rab3D, a Small GTPase, Is Localized on Mast Cell Secretory Granules and Translocates to the Plasma Membrane upon Exocytosis
Am. J. Respir. Cell Mol. Biol., January 1, 1999; 20(1): 79 - 89.
[Abstract] [Full Text]


Home page
J. Neurosci.Home page
E. N. Pothos, S. Przedborski, V. Davila, Y. Schmitz, and D. Sulzer
D2-Like Dopamine Autoreceptor Activation Reduces Quantal Size in PC12 Cells
J. Neurosci., August 1, 1998; 18(15): 5575 - 5585.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. F. Oberhauser and J. M. Fernandez
A fusion pore phenotype in mast cells of the ruby-eye mouse
PNAS, December 10, 1996; 93(25): 14349 - 14354.
[Abstract] [Full Text] [PDF]



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents