A microneedle puncture of the fibroblast or sea urchin egg surface rapidly evokes a localized exocytotic reaction that may be required for the rapid resealing that follows this breach in plasma membrane integrity (Steinhardt, R.A,. G. Bi, and J.M. Alderton. 1994. Science (Wash. DC). 263:390–393). How this exocytotic reaction facilitates the resealing process is unknown. We found that starfish oocytes and sea urchin eggs rapidly reseal much larger disruptions than those produced with a microneedle. When an ∼40 by 10 μm surface patch was torn off, entry of fluorescein stachyose (FS; 1,000 mol wt) or fluorescein dextran (FDx; 10,000 mol wt) from extracellular sea water (SW) was not detected by confocal microscopy. Moreover, only a brief (∼5–10 s) rise in cytosolic Ca2+ was detected at the wound site. Several lines of evidence indicate that intracellular membranes are the primary source of the membrane recruited for this massive resealing event. When we injected FS-containing SW deep into the cells, a vesicle formed immediately, entrapping within its confines most of the FS. DiI staining and EM confirmed that the barrier delimiting injected SW was a membrane bilayer. The threshold for vesicle formation was ∼3 mM Ca2+ (SW is ∼10 mM Ca2+). The capacity of intracellular membranes for sealing off SW was further demonstrated by extruding egg cytoplasm from a micropipet into SW. A boundary immediately formed around such cytoplasm, entrapping FDx or FS dissolved in it. This entrapment did not occur in Ca2+-free SW (CFSW). When egg cytoplasm stratified by centrifugation was exposed to SW, only the yolk platelet–rich domain formed a membrane, suggesting that the yolk platelet is a critical element in this response and that the ER is not required. We propose that plasma membrane disruption evokes Ca2+ regulated vesicle–vesicle (including endocytic compartments but possibly excluding ER) fusion reactions. The function in resealing of this cytoplasmic fusion reaction is to form a replacement bilayer patch. This patch is added to the discontinuous surface bilayer by exocytotic fusion events.
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6 October 1997
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October 06 1997
Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca2+-dependent Vesicle–Vesicle Fusion Events
Mark Terasaki,
Mark Terasaki
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
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Katsuya Miyake,
Katsuya Miyake
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
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Paul L. McNeil
Paul L. McNeil
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
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Mark Terasaki
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
Katsuya Miyake
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
Paul L. McNeil
*Department of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06032; ‡The Marine Biological Laboratory, Woods Hole, Massachusetts 02543; §Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892; ‖Fukushima Medical College, Second Department of Anatomy, Fukushima 960-12 Japan; and ¶The Medical College of Georgia, Department of Cellular Biology and Anatomy, Augusta, Georgia 30912
Address correspondence to Mark Terasaki Tel.: (860) 679-2695. Fax: (860) 679-1661. E-mail: [email protected] or Paul McNeil Tel.: (706) 721-3065. Fax: (706) 721-8732. E-mail: [email protected].
Quicktime movies of most of the figures are available at http://www.uchc.edu/∼terasaki/resealing.html
Received:
May 13 1997
Revision Received:
July 28 1997
Online ISSN: 1540-8140
Print ISSN: 0021-9525
1997
J Cell Biol (1997) 139 (1): 63–74.
Article history
Received:
May 13 1997
Revision Received:
July 28 1997
Citation
Mark Terasaki, Katsuya Miyake, Paul L. McNeil; Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca2+-dependent Vesicle–Vesicle Fusion Events . J Cell Biol 6 October 1997; 139 (1): 63–74. doi: https://doi.org/10.1083/jcb.139.1.63
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