Literature DB >> 6438112

Characterization of electric field-induced fusion in erythrocyte ghost membranes.

A E Sowers.   

Abstract

Fusion has been reported to occur in a variety of membrane systems in response to the application of certain electric currents to the medium (Zimmermann, U., 1982, Biochim. Biophys. Acta., 694:227-277). The application of a weak but continuous alternating current causes the membranes in suspension to become rearranged into the "pearl-chain" formation. Fusion can then be induced by one or more strong direct current pulses that cause pore formation. This results in the conversion of individual membranes in the "pearl-chain" formation to a single membrane with one or more hourglass constrictions that form lumens which connect the cytoplasmic compartments. As the diameter of the lumens increases, the overall membrane shape grows to one large sphere. To further characterize electric field-induced fusion, experiments were conducted using the erythrocyte ghost as a model membrane, and a new combination of electrical circuit and fusion chamber that is simpler and improved over previous systems. All odd-shaped ghosts (collapsed or partly collapsed spherical shapes, echinocytes, discocytes, and stomatocytes) in 30 mM phosphate buffer was first converted to spherocytes and then fused with increasing yields by increasing the number of pulses. After fusion, the lateral diffusion of a fluorescent lipid soluble label (Dil) from labeled to unlabeled membranes was observed to occur both with and without the appearance in phase-contrast optics of distinct communication (lumens) between cytoplasmic compartments of the fused membranes. Connections between cytoplasmic compartments, however, were unmistakable with the instant transfer of a fluorescent water-soluble label (fluorescein isothiocyanate-dextran) from labeled to unlabeled cytoplasmic compartments upon fusion. Although pulses still resulted in the lateral diffusion of Dil to unlabeled membranes, the presence of glycerol in the medium strongly reduced the yield of lumens observable by phase-contrast optics in fusion events. The presence of glycerol also inhibited the conversion of membranes to spherocytes, but did not inhibit the lateral diffusion of Dil from labeled to unlabeled membranes.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6438112      PMCID: PMC2113536          DOI: 10.1083/jcb.99.6.1989

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  9 in total

1.  Three-dimensional model of purple membrane obtained by electron microscopy.

Authors:  R Henderson; P N Unwin
Journal:  Nature       Date:  1975-09-04       Impact factor: 49.962

2.  Lateral mobility of human erythrocyte integral membrane proteins.

Authors:  V Fowler; D Branton
Journal:  Nature       Date:  1977-07-07       Impact factor: 49.962

3.  Fusion of mitochondrial inner membranes by electric fields produces inside-out vesicles. Visualization by freeze-fracture electron microscopy.

Authors:  A E Sowers
Journal:  Biochim Biophys Acta       Date:  1983-11-23

4.  Electric field effects on lipid membrane structure.

Authors:  G Stulen
Journal:  Biochim Biophys Acta       Date:  1981-02-06

Review 5.  Electric field-mediated fusion and related electrical phenomena.

Authors:  U Zimmermann
Journal:  Biochim Biophys Acta       Date:  1982-11-30

Review 6.  Electric field-induced cell-to-cell fusion.

Authors:  U Zimmermann; J Vienken
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

7.  Modulation of membrane protein lateral mobility by polyphosphates and polyamines.

Authors:  M Schindler; D E Koppel; M P Sheetz
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

8.  The resealing process of lipid bilayers after reversible electrical breakdown.

Authors:  R Benz; U Zimmermann
Journal:  Biochim Biophys Acta       Date:  1981-01-08

9.  The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons.

Authors:  L D Frye; M Edidin
Journal:  J Cell Sci       Date:  1970-09       Impact factor: 5.285

  9 in total
  23 in total

1.  Determination of electric field threshold for electrofusion of erythrocyte ghosts. Comparison of pulse-first and contact-first protocols.

Authors:  Y Wu; J G Montes; R A Sjodin
Journal:  Biophys J       Date:  1992-03       Impact factor: 4.033

2.  Evidence that the spectrin network and a nonosmotic force control the fusion product morphology in electrofused erythrocyte ghosts.

Authors:  L V Chernomordik; A E Sowers
Journal:  Biophys J       Date:  1991-11       Impact factor: 4.033

3.  Electroporation: an arsenal of application.

Authors:  Ti-Fei Yuan
Journal:  Cytotechnology       Date:  2007-06-16       Impact factor: 2.058

4.  Changes in membrane structure induced by electroporation as revealed by rapid-freezing electron microscopy.

Authors:  D C Chang; T S Reese
Journal:  Biophys J       Date:  1990-07       Impact factor: 4.033

5.  Electroporation-induced formation of individual calcium entry sites in the cell body and processes of adherent cells.

Authors:  M N Teruel; T Meyer
Journal:  Biophys J       Date:  1997-10       Impact factor: 4.033

6.  Effects of pH on cell fusion induced by electric fields.

Authors:  D C Chang; J R Hunt; P Q Gao
Journal:  Cell Biophys       Date:  1989-06

7.  The long-lived fusogenic state induced in erythrocyte ghosts by electric pulses is not laterally mobile.

Authors:  A E Sowers
Journal:  Biophys J       Date:  1987-12       Impact factor: 4.033

8.  Kinetics of ultrastructural changes during electrically induced fusion of human erythrocytes.

Authors:  D A Stenger; S W Hui
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

9.  Fusion events and nonfusion contents mixing events induced in erythrocyte ghosts by an electric pulse.

Authors:  A E Sowers
Journal:  Biophys J       Date:  1988-10       Impact factor: 4.033

10.  Characterization of PEG-mediated electrofusion of human erythrocytes.

Authors:  L H Li; S W Hui
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.