Expression of apo-aequorin during embryonic development; how much is needed for calcium imaging?
Abstract
Aequorin is a bioluminescent calcium indicator consisting of a 21 kDa protein (apo-aequorin) that is covalently linked to a lipophilic cofactor (coelenterazine). The aequorin gene can be expressed in a variety of cell lines and tissues, allowing non-invasive calcium imaging of specific cell types. In the present paper, we describe the possibilities and limitations of calcium imaging with genetically introduced apo-aequorin during embryonic development. By injecting aequorin into sea urchin, Drosophila and zebrafish eggs, we found that higher aequorin concentrations are needed in smaller eggs. Our results suggest that for measuring resting levels of free cytosolic calcium, one needs aequorin concentrations of at least 40 microM in sea urchin eggs, 2 microM in Drosophila eggs, and only 0.11 microM in zebrafish eggs. A simple assay was used to determine the absolute concentrations of expressed apo-aequorin and the percentage of aequorin formation in vivo. The use of this assay is illustrated by expression of the aequorin gene in Drosophila oocytes. These oocytes form up to 1 microM apo-aequorin. In our hands, only 0.3% of this apo-aequorin combined with coelenterazine entering from the medium to form aequorin, which was not enough for calcium imaging of the oocytes, but did allow in vivo imaging of the ovaries. From these studies, we conclude that coelenterazine entry into the cell is the rate limiting step in aequorin formation. Based on the rate of coelenterazine uptake in Dro…
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Bioluminescence has met with only limited success in the zebrafish system.
“In addition, bioluminescence has met with only limited success in the zebrafish system (Creton et al., 1997; Kaneko and Cahill, 2005”
From Transparent Adult Zebrafish as a Tool for In Vivo Transplantation Analysis (2008) · cites this paper as Creton et al., 1997
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Transparent Adult Zebrafish as a Tool for In Vivo Transplantation Analysis
White, R. M., Sessa, A., Burke, C., Bowman, T., LeBlanc, J., Ceol, C., Bourque, C., Dovey, M., Goessling, W., Burns, C. E., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.11.002 · Cited by 1,408 · see citing works
- Authors
- Créton, R., Steele, M. E., & Jaffe, L. F.
- Affiliations
- Marine Biological Laboratory (US)
- Corresponding author
- Créton, Robbert
- ORCID
- Créton, Robbert
- Venue
- Cell Calcium
- Publisher
- Elsevier BV
- Published
- 1997-12
- Volume
- 22
- Issue
- 6
- Pages
- 439-446
- ISSN
- 0143-4160 (ISSN-L)
- OpenAlex
- W2076129711
- Cited by
- 18
- References
- 0
- Citations by year
- 2018: 1 · 2013: 2
- FWCI
- 0.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell Calcium (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › bioluminescence and chemiluminescence research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Advanced Fluorescence Microscopy Techniques
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence Properties of Advanced Materials
- Keywords
- aequorin, coelenterazine, calcium imaging, embryonic development, intracellular calcium, sea urchin eggs, Drosophila oocyte, zebrafish eggs, in vivo calcium imaging, embryonic gene expression, Drosophila ovary
- MeSH terms
- Aequorin, Animals, Apoproteins, Calcium, Calcium-Binding Proteins, Drosophila, Indicators and Reagents, Recombinant Proteins, Sea Urchins, Zebrafish, Animals, Genetically Modified, Embryonic Development, Cell Size
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