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  Membrane and actin reorganization in electropulse-induced cell fusion

Gerisch, G., Ecke, M., Neujahr, R., Prassler, J., Stengl, A., Hoffmann, M., et al. (2013). Membrane and actin reorganization in electropulse-induced cell fusion. JOURNAL OF CELL SCIENCE, 126(9), 2069-2078. doi:10.1242/jcs.124073.

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Gerisch, Günther1, Autor           
Ecke, Mary1, Autor           
Neujahr, Ralph1, Autor           
Prassler, Jana1, Autor           
Stengl, Andreas1, Autor           
Hoffmann, Max2, Autor
Schwarz, Ulrich S.2, Autor
Neumann, Eberhard2, Autor
Affiliations:
1Gerisch, Günther / Cell Dynamics, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565149              
2external, ou_persistent22              

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Schlagwörter: GREEN FLUORESCENT PROTEIN; ELECTRIC-FIELD PULSE; VESICLE FUSION; CURVATURE; DICTYOSTELIUM; PHASE; CYTOSKELETON; TRANSITION; DIFFUSION; BILAYERSActin polymerization; Cell repair; Diffusion; Electric lipid distortion; Fusion pores; Membrane fusion;
 Zusammenfassung: When cells of Dictyostelium discoideum are exposed to electric pulses they are induced to fuse, yielding motile polykaryotic cells. By combining electron microscopy and direct recording of fluorescent cells, we have studied the emergence of fusion pores in the membranes and the localization of actin to the cell cortex. In response to electric pulsing, the plasma membranes of two contiguous cells are turned into tangles of highly bent and interdigitated membranes. Live-imaging of cells double-labeled for membranes and filamentous actin revealed that actin is induced to polymerize in the fusion zone to temporarily bridge the gaps in the vesiculating membrane. The diffusion of green fluorescent protein (GFP) from one fusion partner to the other was scored using spinning disc confocal microscopy. Fusion pores that allowed intercellular exchange of GFP were formed after a delay, which lasted up to 24 seconds after exposure of the cells to the electric field. These data indicate that the membranes persist in a fusogenic state before pores of about 3 nm diameter are formed.

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Sprache(n): eng - English
 Datum: 2013-05-01
 Publikationsstatus: Erschienen
 Seiten: 10
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: ISI: 000319561700018
DOI: 10.1242/jcs.124073
 Art des Abschluß: -

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Titel: JOURNAL OF CELL SCIENCE
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: BIDDER BUILDING CAMBRIDGE COMMERCIAL PARK COWLEY RD, CAMBRIDGE CB4 4DL, CAMBS, ENGLAND : COMPANY OF BIOLOGISTS LTD
Seiten: - Band / Heft: 126 (9) Artikelnummer: - Start- / Endseite: 2069 - 2078 Identifikator: ISSN: 0021-9533