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Imaging patterns of calcium transients during neural induction in Xenopus laevis embryos
Author(s) -
Catherine Leclerc,
Sarah E. Webb,
Christiane Daguzan,
Marc Moreau,
Andrew L. Miller
Publication year - 2000
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.113.19.3519
Subject(s) - biology , ectoderm , gastrulation , xenopus , endoderm , calcium , microbiology and biotechnology , noggin , aequorin , embryo , mesoderm , calcium imaging , voltage dependent calcium channel , calcium channel , neural development , anatomy , embryogenesis , medicine , endocrinology , cellular differentiation , genetics , embryonic stem cell , gene , intracellular , bone morphogenetic protein
Through the injection of f-aequorin (a calcium-sensitive bioluminescent reporter) into the dorsal micromeres of 8-cell stage Xenopus laevis embryos, and the use of a Photon Imaging Microscope, distinct patterns of calcium signalling were visualised during the gastrulation period. We present results to show that localised domains of elevated calcium were observed exclusively in the anterior dorsal part of the ectoderm, and that these transients increased in number and amplitude between stages 9 to 11, just prior to the onset of neural induction. During this time, however, no increase in cytosolic free calcium was observed in the ventral ectoderm, mesoderm or endoderm. The origin and role of these dorsal calcium-signalling patterns were also investigated. Calcium transients require the presence of functional L-type voltage-sensitive calcium channels. Inhibition of channel activation from stages 8 to 14 with the specific antagonist R(+)BayK 8644 led to a complete inhibition of the calcium transients during gastrulation and resulted in severe defects in the subsequent formation of the anterior nervous system. BayK treatment also led to a reduction in the expression of Zic3 and geminin in whole embryos, and of NCAM in noggin-treated animal caps. The possible role of calcium transients in regulating developmental gene expression is discussed.

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