Literature DB >> 1151835

Properties of surface and junctional membranes of embryonic cells isolated from blastula stages of Xenopus laevis.

C Slack, A E Warner.   

Abstract

1. Some membrane properties of endoderm and mesoderm cells isolated from late blastula stages of Xenopus laevis have been examined using electrophysiological techniques. 2. Cells were isolated by treatment of whole embryos with Ca-free EDTA containing media, or mechanically by micro-dissection, and cultured in Ca-containing Holtfreter solution (60 mM-NaCl) or Ringer solution (120 mM-NaCl). 3. Membrane potentials lay between -6 and -84 mV; specific membrane resistances ranged from 500 to 29,000 omega cm2; there was no difference between EDTA isolated and mechanically isolated cells. 4. Relative and absolute cation and anion conductances varied from cell to cell. Some cells were anion impermeable; the cation conductance ranged from 35 to 300 mumho/cm2. 5. The resting potential of some cells was largely determined by the concentration gradient and membrane permeability of K ions. In other cells the potential was maintained either by some other ion or by an electrogenic pump. [K]i came to approximately 130 mM in Ringer solution (the value pertaining in the intact embryo) and similar to 60 mM in Holtfreter solution. 6. In most pairs and small clumps of cells ionic current spread from one cell to the next; some single cells and groups of cells were uncoupled from their neighbours. 7. The junctional resistance lay between 10(5) and 10(8) omega; it behaved as a linear resistor in most cell pairs studied. In three pairs the intercellular junction showed rectifying properites. 8. By the late blastula stage of development presumptive endoderm and mesoderm cells form a heterogeneous population with widely varying passive membrane properties. The significance of these findings is discussed in relation to current hypotheses for the formation of spatial patterns during differentiation.

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Year:  1975        PMID: 1151835      PMCID: PMC1309509          DOI: 10.1113/jphysiol.1975.sp010964

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  36 in total

1.  Transmission at the giant motor synapses of the crayfish.

Authors:  E J FURSHPAN; D D POTTER
Journal:  J Physiol       Date:  1959-03-03       Impact factor: 5.182

2.  The effect of sudden changes in ionic concentrations on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1960-09       Impact factor: 5.182

3.  Differentiation of cells of the Rana pipiens gastrula in unconditioned medium.

Authors:  L G BARTH; L J BARTH
Journal:  J Embryol Exp Morphol       Date:  1959-06

4.  The antagonism between Ca and Na ions on the frog's heart.

Authors:  H C LUTTGAU; R NIEDERGERKE
Journal:  J Physiol       Date:  1958-10-31       Impact factor: 5.182

5.  The chloride conductance of frog skeletal muscle.

Authors:  O F HUTTER; D NOBLE
Journal:  J Physiol       Date:  1960-04       Impact factor: 5.182

6.  The pH sensitivity of the chloride conductance of frog skeletal muscle.

Authors:  O F Hutter; A E Warner
Journal:  J Physiol       Date:  1967-04       Impact factor: 5.182

7.  Analysis of non-linearity observed in the current-voltage relation of the tunicate embryo.

Authors:  S I Miyazaki; K Takahashi; K Tsuda; M Yoshii
Journal:  J Physiol       Date:  1974-04       Impact factor: 5.182

8.  The electrical properties of the ectoderm in the amphibian embryo during induction and early development of the nervous system.

Authors:  A E Warner
Journal:  J Physiol       Date:  1973-11       Impact factor: 5.182

9.  Electrical connexions between cells at neural stages of the axolotl.

Authors:  A E Warner
Journal:  J Physiol       Date:  1970-09       Impact factor: 5.182

10.  The distribution of sodium and potassium in amphibian embryos during early development.

Authors:  C Slack; A E Warner; R L Warren
Journal:  J Physiol       Date:  1973-07       Impact factor: 5.182

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  8 in total

1.  Electrical properties of the nexal membrane studied in rat ventricular cell pairs.

Authors:  R Weingart
Journal:  J Physiol       Date:  1986-01       Impact factor: 5.182

2.  Gap junction formation between normal and reaggregated endoderm cells ofXenopus laevis neurulae.

Authors:  K Sugimoto; W J Hage; J G Bluemink
Journal:  Wilehm Roux Arch Dev Biol       Date:  1982-05

3.  Ionic basis of membrane potential in developing ectoderm of the Xenopus blastula.

Authors:  C Baud
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

4.  Low resistance junctions between mesoderm cells during development of trunk muscles.

Authors:  S E Blackshaw; A E Warner
Journal:  J Physiol       Date:  1976-02       Impact factor: 5.182

5.  Developmental changes in the inward current of the action potential of Rohon-Beard neurones.

Authors:  P I Baccaglini; N C Spitzer
Journal:  J Physiol       Date:  1977-09       Impact factor: 5.182

6.  Intracellular pH in early Xenopus embryos: its effect on current flow between blastomeres.

Authors:  L Turin; A E Warner
Journal:  J Physiol       Date:  1980-03       Impact factor: 5.182

7.  Quantitative analysis of low-resistance junctions between cultured cells and correlation with gap-junctional areas.

Authors:  J D Sheridan; M Hammer-Wilson; D Preus; R G Johnson
Journal:  J Cell Biol       Date:  1978-02       Impact factor: 10.539

8.  Functional gap junctions are not required for muscle gene activation by induction in Xenopus embryos.

Authors:  A Warner; J B Gurdon
Journal:  J Cell Biol       Date:  1987-03       Impact factor: 10.539

  8 in total

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