Literature DB >> 8246182

Neural induction suppresses early expression of the inward-rectifier K+ channel in the ascidian blastomere.

Y Okamura1, K Takahashi.   

Abstract

1. Early expression of ion channels following neural induction was examined in isolated, cleavage-arrested blastomeres from the ascidian embryo using a two-electrode voltage clamp. Currents were recorded from the isolated, cleavage-arrested blastomere, a4-2, after treatment with serine protease, subtilisin, which induces neural differentiation as consistently as cell contact. 2. The inward-rectifier K+ current increased at the late gastrula stage shortly after the sensitive period for neural induction both in the induced (protease-treated) and uninduced cells. Ca2+ channels, characteristic of epidermal-type differentiation, and delayed-rectifier K+ channels and differentiated-type Na+ channels, characteristic of neural-type differentiation appeared much later than the inward-rectifier K+ channels, at a time corresponding to the tail bud stage of the intact embryo. 3. When cells were treated with subtilisin during the critical period for neural induction, the increase in the inward-rectifier K+ current from the late gastrula stage to the neurula stage was about three times smaller (3.67 +/- 1.74 nA, mean +/- S.D., n = 14) than in untreated cells (11.25 +/- 3.10 nA, n = 26). The same changes in the inward-rectifier K+ channel were also observed in a4 2 blastomeres which were induced by cell contact with an A4-1 blastomere. However, when cells were treated with subtilisin after the critical period for neural induction, the amplitude of the inward-rectifier K+ current was the same as in untreated cells. Thus the expressed level of the inward-rectifier K+ channel was linked to the determination of neural or epidermal cell types. 4. There was no significant difference in the input capacitance of induced and uninduced cells, indicating that the difference in the amplitude of the inward-rectifier K+ currents derived from a difference in the channel density rather than a difference in cell surface area. 5. The expression of the inward-rectifier K+ channel at the late gastrula stage was sensitive to alpha-amanitin, a highly specific transcription inhibitor. In both induced and uninduced cells, injection of alpha-amanitin at the 32-cell stage reduced the current density of the inward-rectifier K+ channel to about 2 nA/nF, corresponding to 13% of that recorded from uninjected cells. By contrast, the expression of the fast-inactivating-type Na+ current, which transiently increased along with the inward-rectifier K+ channel, was resistant to alpha-amanitin injection. 6. The dose of alpha-amanitin injected was controlled by monitoring co-injected fluorescent dye, fura-2.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8246182      PMCID: PMC1175342          DOI: 10.1113/jphysiol.1993.sp019593

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


  32 in total

1.  Differentiation of membrane excitability in isolated cleavage-arrested blastomeres from early ascidian embryos.

Authors:  H Okado; K Takahashi
Journal:  J Physiol       Date:  1990-08       Impact factor: 5.182

2.  Changes in sodium channels during neural differentiation in the isolated blastomere of the ascidian embryo.

Authors:  Y Okamura; M Shidara
Journal:  J Physiol       Date:  1990-12       Impact factor: 5.182

3.  Inactivation kinetics of the sodium channel in the egg and the isolated, neurally differentiated blastomere of the ascidian.

Authors:  Y Okamura; M Shidara
Journal:  J Physiol       Date:  1990-12       Impact factor: 5.182

4.  Electrophysiological and immunohistochemical analysis of muscle differentiation in a mouse mesodermal stem cell line.

Authors:  Y Kubo
Journal:  J Physiol       Date:  1991-10       Impact factor: 5.182

5.  Progressive determination during formation of the anteroposterior axis in Xenopus laevis.

Authors:  H L Sive; K Hattori; H Weintraub
Journal:  Cell       Date:  1989-07-14       Impact factor: 41.582

6.  Animal DNA-dependent RNA polymerases. 11. Mechanism of the inhibition of RNA polymerases B by amatoxins.

Authors:  M Cochet-Meilhac; P Chambon
Journal:  Biochim Biophys Acta       Date:  1974-06-27

7.  Segregation during ascidian embryogenesis of egg cytoplasmic information for tissue-specific enzyme development.

Authors:  J R Whittaker
Journal:  Proc Natl Acad Sci U S A       Date:  1973-07       Impact factor: 11.205

8.  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

9.  Neural differentiation in cleavage-arrested ascidian blastomeres induced by a proteolytic enzyme.

Authors:  H Okado; K Takahashi
Journal:  J Physiol       Date:  1993-04       Impact factor: 5.182

10.  Developmental changes in delayed rectifier K+ currents in the muscular- and neural-type blastomere of ascidian embryos.

Authors:  M Shidara; Y Okamura
Journal:  J Physiol       Date:  1991-11       Impact factor: 5.182

View more
  6 in total

1.  Subfamily-specific posttranscriptional mechanism underlies K(+) channel expression in a developing neuronal blastomere.

Authors:  F Ono; Y Katsuyama; K Nakajo; Y Okamura
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

2.  Cleavage-arrested cell triplets from ascidian embryo differentiate into three cell types depending on cell combination and contact timing.

Authors:  Motoko Tanaka-Kunishima; Kunitaro Takahashi
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

3.  Neuronal expression in cleavage-arrested ascidian blastomeres requires gap junctional uncoupling from neighbouring cells.

Authors:  M Saitoe; T Inazawa; K Takahashi
Journal:  J Physiol       Date:  1996-03-15       Impact factor: 5.182

4.  Basic fibroblast growth factor induction of neuronal ion channel expression in ascidian ectodermal blastomeres.

Authors:  T Inazawa; Y Okamura; K Takahashi
Journal:  J Physiol       Date:  1998-09-01       Impact factor: 5.182

5.  Cross-coupling between voltage-dependent Ca2+ channels and ryanodine receptors in developing ascidian muscle blastomeres.

Authors:  K Nakajo; L Chen; Y Okamura
Journal:  J Physiol       Date:  1999-03-15       Impact factor: 5.182

6.  Hypercholesterolemia suppresses Kir channels in porcine bone marrow progenitor cells in vivo.

Authors:  Emile R Mohler; Yun Fang; Rebecca Gusic Shaffer; Jonni Moore; Robert L Wilensky; Michael Parmacek; Irena Levitan
Journal:  Biochem Biophys Res Commun       Date:  2007-04-30       Impact factor: 3.575

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.