Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-26T13:16:24.111Z Has data issue: false hasContentIssue false

Time-dependent expression of ryanodine receptors in sea urchin eggs, zygotes and early embryos

Published online by Cambridge University Press:  28 July 2021

G. Percivale
Affiliation:
CNR Institute of Biophysics, Via De Marini 6, 16149 Genoa, Italy
C. Angelini
Affiliation:
Laboratory of Developmental Neurobiology, Department of Earth, Environment and Life Sciences, University of Genoa, Viale Benedetto XV 5, 16132 Genoa, Italy
C. Falugi
Affiliation:
Laboratory of Developmental Neurobiology, Department of Earth, Environment and Life Sciences, University of Genoa, Viale Benedetto XV 5, 16132 Genoa, Italy
C. Picco*
Affiliation:
CNR Institute of Biophysics, Via De Marini 6, 16149 Genoa, Italy
G. Prestipino
Affiliation:
CNR Institute of Biophysics, Via De Marini 6, 16149 Genoa, Italy
*
Author for correspondence: Cristiana Picco. IBF CNR, Via de Marini 6, 16149 Genova, Italy. E-mail [email protected]

Summary

In this work, the presence of calcium-dependent calcium channels and their receptors (RyR) has been investigated in Paracentrotus lividus eggs and early embryos, from unfertilized egg to four-blastomere stages. Electrophysiological recordings of RyR single-channel current fluctuations showed that RyRs are functional during the first developmental events with a maximum at zygote stage, c. 40 min after fertilization, corresponding to the first cleavage. The nature of vertebrate-like RyRs active at this stage was established by specific activation/blockade experiments.

Type
Research Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Buratti, R, Prestipino, G, Menegazzi, P, Treves, S and Zorzato, F (1995). Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin. Biochem Biophys Res Commun 213, 1082–90.CrossRefGoogle ScholarPubMed
Colquhoun, D and Sakmann, B (1985). Fast events in single-channel currents activated by acetylcholine and its analogues at the frog muscle endplate. J Physiol 369, 501–57.CrossRefGoogle Scholar
Dale, B, Yazaki, I and Tosti, E (1997). Polarized distribution of L-type calcium channels in early sea urchin embryos. Am J Physiol 273(3 Pt 1), C8225.CrossRefGoogle ScholarPubMed
Galeotti, N, Quattrone, A, Vivoli, E, Bartolini, A and Ghelardini, C (2008). Type 1 and type 3 ryanodine receptors are selectively involved in muscarinic antinociception in mice: An antisense study. Neuroscience 153, 814–22.Google Scholar
Galione, A and Churchill, GC (2002). Interaction between calcium release pathways: Multiple messengers and multiple stores. Cell Calcium 32(5–6), 343–54.CrossRefGoogle Scholar
Galione, A, Lee, HC and Busa, WB (1991). Ca2+-induced Ca2+ release in sea urchin egg homogenates: Modulation by cyclic ADP-ribose. Science 261, 348–52.CrossRefGoogle Scholar
Galione, A White, A, Willmott, N, Turner, M, Potter, BVL and Watson, SP (1993a). cGMP mobilizes intracellular Ca2+ in sea urchin eggs by stimulating cyclic ADP-ribose synthesis. Nature 365(6445), 456–9.CrossRefGoogle ScholarPubMed
Galione, A, Galione, A, McDougall, A, Busa, WB, Willmott, N, Gillot, I and Whitaker, M (1993b). Redundant mechanisms of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs. Science 261(5119), 348–52.Google ScholarPubMed
Harrison, PK, Falugi, C, Angelini, C and Whitaker, MJ (2002). Muscarinic signalling affects intracellular calcium concentration during the first cell cycle of sea urchin embryos. Cell Calcium 31, 289–97.Google ScholarPubMed
Lindsay, AR, Tinker, A and Williams, AJ (1994). How does ryanodine modify ion handling in the sheep cardiac sarcoplasmic reticulum Ca2+-release channel? J Gen Physiol 104, 425–47.Google Scholar
Liu, QH, Zheng, YM, Korde, AS, Yadav, VR, Rathore, R, Wess, J and Wang, YX (2009). Membrane depolarization causes a direct activation of G protein-coupled receptors leading to local Ca2+ release in smooth muscle. Proc Natl Acad Sci USA 106, 11418–23.CrossRefGoogle ScholarPubMed
Lokuta, AJ, Darszon, A, Beltrán, C and Valdivia, HH (1998). Detection and functional characterization of ryanodine receptors from sea urchin eggs. J Physiol 510, 155–64.CrossRefGoogle ScholarPubMed
McPherson, SM, McPherson, PS, Mathews, L, Campbell, KP and Longo, FJ (1992). Cortical localization of a calcium release channel in sea urchin eggs. J Cell Biol 116, 1111–21.Google ScholarPubMed
Mueller, P, Rudin, DO, Tien, HT and Wescott, WC (1962). Reconstitution of excitable cell membrane structure in vitro . Circulation 26, 1167–71.CrossRefGoogle Scholar
Pérez, CF, Marengo, JJ, Bull, R and Hidalgo, C (1998). Cyclic ADP-ribose activates caffeine-sensitive calcium channels from sea urchin egg microsomes. Am J Physiol 274, C4309.CrossRefGoogle ScholarPubMed
Rousseau, E, Smith, JS and Meissner, G (1987). Ryanodyne modifies conductance and gating behaviour of single Ca2+ release channel. Am J Physiol 253, 364–8.Google Scholar
Whitaker, M (2006). Calcium at fertilization and in early development. Physiol Rev 86, 2588.Google ScholarPubMed
Whitaker, M and Larman, MG (2001). Calcium and mitosis. Semin Cell Dev Biol 12, 53–8.Google ScholarPubMed
Wolniak, SM, Hepler, PK and Jackson, WT (1983). Ionic changes in the mitotic apparatus at the metaphase/anaphase transition. J Cell Biol 96, 598605.CrossRefGoogle ScholarPubMed
Ziman, AP, Ward, CW, Rodney, GG, Lederer, WJ and Bloch, RJ (2010). Quantitative measurement of Ca2+ in the sarcoplasmic reticulum lumen of mammalian skeletal muscle. Biophys J 99, 2705–14.Google Scholar
Supplementary material: PDF

Percivale et al. supplementary material

Percivale et al. supplementary material

Download Percivale et al. supplementary material(PDF)
PDF 802.9 KB