Maternal exposure to estradiol and endocrine disrupting compounds alters the sensitivity of sea urchin embryos and the expression of an orphan steroid receptor
Abstract
Endocrine disrupting compounds (EDCs) are known to affect reproduction and development in marine invertebrates. In previous work, we have shown that developing sea urchin embryos were sensitive to estradiol and estrogenic EDCs at environmentally relevant concentrations in a tamoxifen-sensitive manner (Roepke et al. 2005. Aquat Toxicol 71:155-173). In this study, we report the effects of maternal exposure to EDCs on embryo sensitivity and regulation of an orphan steroid receptor in sea urchin eggs. Maternal exposures were conducted by injecting female Strongylocentrotus purpuratus sea urchins initiating oogenesis with two concentrations of estradiol, octylphenol, tributyltin and o, p-DDD for 8 weeks with an induced spawning before and after the injection cycle. Developing embryos were less sensitive to estradiol following maternal exposure to estradiol, octylphenol and DDD. The steroidogenesis inhibitor, spironolactone, and the aromatase inhibitor, formestane, affected normal sea urchin development with EC50 values of 18 and 2 microM, respectively. Binding of estradiol was demonstrated in homogenates supernatants of sea urchin embryos by filtration centrifugation and column chromatography, but saturation was not reached until 4-6 hr and was highly variable. Analysis of eggs from pre- and post-injection spawns using real-time Q-PCR for the mRNA of an orphan steroid receptor, SpSHR2, shows that receptor mRNA increased in eggs with estradiol, octylphenol and tributyltin but decreased with DDD. RIA showed that estradiol may be present during gastrulation. In summary, maternal exposure to estradiol and EDCs alters embryo sensitivity and regulates the expression of an orphan steroid receptor in the egg.
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Sp-Shr2 has been shown to bind estradiol.
“a previously cloned NR, Sp-Shr2 (NR2B/C-like, SPU_00817; Kontrogianni-Konstantopoulos et al., 1996), has recently been shown to bind estradiol (Roepke et al., 2006).”
From The chemical defensome: Environmental sensing and response genes in the Strongylocentrotus purpuratus genome (2006) · cites this paper as Roepke et al., 2006
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References 36 · Cited by 18
- Authors
- Roepke, T. A., Chang, E. S., & Cherr, G. N.
- Affiliations
- Oregon Health & Science University (US)
- University of California, Davis (US)
- Corresponding author
- Cherr, Gary N.
- Venue
- Journal of Experimental Zoology Part A Comparative Experimental Biology
- Publisher
- Wiley
- Published
- 2006-10-01
- Volume
- 305A
- Issue
- 10
- Pages
- 830-841
- ISSN
- 1548-8969 (ISSN-L)
- 1552-499X
- OpenAlex
- W2076682200
- Cited by
- 18
- References
- 36
- Citations by year
- 2025: 1 · 2023: 1 · 2018: 1 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 1 · 2012: 1
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Experimental Zoology Part A Comparative Experimental Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Eli Lilly and Company
- National Institute of Environmental Health Sciences (T 32 ES07059, T32ES007059)
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Effects and risks of endocrine disrupting chemicals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Reproductive biology and impacts on aquatic species
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Environmental Toxicology and Ecotoxicology
- Keywords
- endocrine disruptors, maternal exposure, estradiol, sea urchin embryo, Strongylocentrotus purpuratus, octylphenol, tributyltin, mitotane, spironolactone, formestane, aromatase inhibition, steroidogenesis inhibition, gastrulation, estrogen receptor binding
- MeSH terms
- Animals, Embryo, Nonmammalian, Estradiol, Estrogen Antagonists, Female, RNA, Messenger, Sea Urchins, Transcription Factors, Receptors, Cytoplasmic and Nuclear, Gene Expression Regulation, Developmental, Maternal Exposure, Embryonic Development, Endocrine Disruptors
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