HKUST Library Institutional Repository Banner

HKUST Institutional Repository >
Biology >
BIOL Journal/Magazine Articles >

Please use this identifier to cite or link to this item:
Title: Visualization, characterization and modulation of Ca2+ signaling during the development of slow muscle cells in intact zebrafish embryos
Authors: Cheung, Chris Y.
Webb, Sarah E.
Love, Donald R.
Miller, Andrew L.
Keywords: Ca2+ imaging
Slow muscle cells
Transgenic zebrafish
Issue Date: Feb-2011
Citation: International journal of developmental biology, February 2011, v. 55, p. 153-174
Abstract: Intact zebrafish embryos were used as an in vivo animal model to investigate the role of Ca2+ signaling during the differentiation of slow muscle cells (SMCs) within forming skeletal muscle. Transgenic zebrafish were generated using an α-actin promoter that targeted apoaequorin expression specifically to muscle cells. Two distinct Ca2+ signaling periods (CSPs) were visualized in the developing SMCs: between ~17.5-19.5 hours post-fertilization (hpf) and after ~23 hpf, separated by a ~3.5 hour Ca2+ signaling quiet period. Further spatial characterization of these Ca2+ signals using confocal fluorescent microscopy and calcium green-1 dextran as a reporter, indicated that the earlier CSP displayed distinct nuclear and cytoplasmic components, whereas the later CSP was predominantly cytoplasmic. Both CSPs consisted of a series of oscillating Ca2+ waves generated at distinct frequencies, while the earlier CSP also displayed a slow rise then fall in the Ca2+ baseline-level. Imaging of cyclopamine- and forskolin-treated wild-type, or smo-/- mutant embryos, where SMCs do not form, confirmed the specific cell population generating the signals. Treating embryos with antagonists indicated that both IP3Rs and RyRs are responsible for generating the temporal characteristics of the Ca2+ signaling signature, and that the latter plays a necessary role in SMC differentiation and subsequent myotome patterning. Together, these data support and extend the proposition that specific spatiotemporal patterns of spontaneous Ca2+ signals might be used for different as well as combinatorial regulation of both nuclear and cytosolic signal transduction cascades, resulting in myofibrillogenesis in SMCs as well as myotome patterning.
Rights: © Copyright 2011 UBC Press.
Appears in Collections:BIOL Journal/Magazine Articles

Files in This Item:

File Description SizeFormat
Miller_A298_new.pdfpre-published version1625KbAdobe PDFView/Open

Find published version via OpenURL Link Resolver

All items in this Repository are protected by copyright, with all rights reserved.