Literature DB >> 2390415

Uptake and release of 63Ni2+ by Xenopus embryos during early cleavage stages.

F W Sunderman1, F J Mongillo, M C Plowman, S M Brennan.   

Abstract

Uptake and release of 63Ni was studied in dejellied Xenopus laevis embryos exposed to 63Ni2+ (0.3-30 mumol/l) for 0.5-h intervals during the period 1-4.5 h post-fertilization (i.e. from first cleavage to early blastula stage). At first cleavage, the mean uptake of 63Ni by embryos was 12-17 times that by non-fertilized eggs, suggesting that conversion of the vitelline envelope to the fertilization envelope enhanced integumental permeability to 63Ni2+. 63Ni uptake by embryos at the 1-2-cell stage averaged 1.8-2.5 times that at the early blastula stage. An average of 5% of total 63Ni in washed embryos was recovered in isolated fertilization envelopes, indicating that 63Ni2+ passed through the envelope into internal compartments. Progressive increases of 63Ni uptake were seen with increasing exposure levels; after exposure during 1-1.5 h post-fertilization to the highest concentration of 63Ni2+ (30 mumol/l), 63Ni uptake averaged 11.4 (SD +/- 5.1) pmol/embryo. Rapid efflux of 63Ni was noted after 63Ni2(+)-exposed embryos were transferred to nickel-free medium; mean 63Ni contents at 0.25 h and 2 h post-exposure diminished to 50% and 15% of the initial values, regardless of the exposure level. The finding that Xenopus embryos are permeable to 63Ni2+ during early cleavage stages provides a convenient experimental system to investigate the embryotoxicity and teratogenicity of nickel.

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Year:  1990        PMID: 2390415     DOI: 10.1007/bf01141362

Source DB:  PubMed          Journal:  Biol Met        ISSN: 0933-5854


  18 in total

1.  Accumulation and efflux of nickel from cultured pneumocytes.

Authors:  K Saito; D B Menzel
Journal:  Tohoku J Exp Med       Date:  1986-03       Impact factor: 1.848

2.  Proteases released from Xenopus laevis eggs at activation and their role in envelope conversion.

Authors:  L L Lindsay; J L Hedrick
Journal:  Dev Biol       Date:  1989-09       Impact factor: 3.582

3.  Methods for nuclear transplantation in amphibia.

Authors:  J B Gurdon
Journal:  Methods Cell Biol       Date:  1977       Impact factor: 1.441

4.  Testing the statistical certainty of a response to increasing doses of a drug.

Authors:  J W Tukey; J L Ciminera; J F Heyse
Journal:  Biometrics       Date:  1985-03       Impact factor: 2.571

5.  Protein blotting method for detection of nickel-binding proteins.

Authors:  S M Lin; S M Hopfer; S M Brennan; F W Sunderman
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1989-09

Review 6.  Toxicity and carcinogenicity of nickel compounds.

Authors:  T P Coogan; D M Latta; E T Snow; M Costa
Journal:  Crit Rev Toxicol       Date:  1989       Impact factor: 5.635

7.  Nickel inhibition of calcium release from subsarcolemmal calcium stores of molluscan smooth muscle.

Authors:  Z Wang; C P Bianchi; S R Narayan
Journal:  J Pharmacol Exp Ther       Date:  1984-06       Impact factor: 4.030

8.  Reversible inhibition of acetylcholine contracture of molluscan smooth muscle by heavy metals: correlation to Ca++ and metal content.

Authors:  R B Raffa; C P Bianchi; S R Narayan
Journal:  J Pharmacol Exp Ther       Date:  1987-10       Impact factor: 4.030

9.  Effect of nickel chloride and cadmium acetate on the development of preimplantation mouse embryos in vitro.

Authors:  R Storeng; J Jonsen
Journal:  Toxicology       Date:  1980       Impact factor: 4.221

Review 10.  Embryonic induction--molecular prospects.

Authors:  J B Gurdon
Journal:  Development       Date:  1987-03       Impact factor: 6.868

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