Congress Abstracts - Society for Developmental Biology
Congress Abstracts - Society for Developmental Biology
Congress Abstracts - Society for Developmental Biology
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Program/Abstract # 573<br />
Fluoride induces apoptosis in Sertoli cells in vitro<br />
Erkan, Melike (Istanbul Univ, Turkey)<br />
Fluorine is potent toxicant, widely distributed through drinking water and food. Fluorine is not freely found in nature, it combines with<br />
almost all metals and nonmetals, except oxygen and the noble gases. Fluoride is found in drinking water and foods threat to the<br />
environment and human health. Although several hypotheses have been proposed, the exact mechanism of fluoride has not been<br />
clearly defined. Fluoride accumulation leads to a large number of hematological, hepatic, renal and neurological disorders. Although<br />
research has been carried out on the effects of fluoride on the reproductive organs and reproductive system impairment in animal<br />
models, the results are controversial. Increasing exposure of fluorides on daily basis might have a potential negative impact on male<br />
fertility, including spermatogenesis and sperm fertilizing ability. However, the effects of fluoride on reproductive organs are not fully<br />
understood. The present study was aimed at determining the direct effects of sodium fluoride on Sertoli cell viability, proliferation,<br />
cytotoxicity and apoptosis/necrosis rate in vitro. In this study, sodium fluoride was exposed to TM4 Sertoli cells <strong>for</strong> 24, 48 and 72<br />
hours at 2 ppm and 16 ppm doses. After incubation, the treated cells were used <strong>for</strong> measurement of cell viability, proliferation, lactate<br />
dehydrogenase assay and propidium iodide and Hoechst stain <strong>for</strong> apoptosis/necrosis rate. The results indicated that cell viability and<br />
cell proliferation are decreased, while lactate dehydrogenase levels and apoptosis/necrosis rate are increased. These findings suggest<br />
that direct exposure to fluoride could induce cytotoxicity and resulting in the apoptosis of Sertoli cells.<br />
Program/Abstract # 574<br />
Telomere biology in the switching of reproductive modes in planarian Dugesia ryukyuensis<br />
Nodono, Hanae (Keio Univ, Japan); Aboobaker, Aziz (Ox<strong>for</strong>d, UK); Matsumoto, Midori (Keio Univ, Japan)<br />
Eukaryotic chromosomes get shorter as cells divide and cells senesce when telomeres shorten to a critical length, which is<br />
hypothesized to be a contributory factor to ageing and mortality in sexually reproducing organisms. However, some eukaryotes can<br />
reproduce both sexually and asexually. It is unclear whether reproductive mode and ageing correlates or not. To ask this question, we<br />
focus on freshwater planarians. They reproduce either asexually, by fission, or sexually, by cross-fertilization. Several planarians use<br />
exclusively one mode of reproduction; others might alternate between them. Schmidtea mediterranea is one of the <strong>for</strong>mer species,<br />
comprised of obligate asexuals and sexuals. Recently, it was showed that asexuals recover age-related telomere shortening through<br />
fission, whereas sexual worms only achieve telomere elongation through sexual reproduction. This difference correlated with the<br />
expression level of an active splice<strong>for</strong>m of the telomere reverse transcriptase subunit (Smed-tert). Our model species Dugesia<br />
ryukyuensis is comprised of populations with different reproductive strategies: exclusively innately asexual, exclusively innately<br />
sexual, and seasonally switching. Moreover asexuals can be sexualized by feeding them with minced sexuals. In this report, we<br />
compared telomere biology of these strains. In contrast to S. mediterranea, D. ryukyuensis sexual worms showed a slight telomere<br />
shortening. Then a tert homolog (Dr-tert) was identified and characterized. Though two alternate splice sites were identified like<br />
Smed-tert, all strains expressed high-level of active iso<strong>for</strong>m, which correlated with their telomere length dynamics and telomerase<br />
activity. These results suggest the existence of immortal sexually reproducing animals that can maintain their telomere length.<br />
Program/Abstract # 575<br />
Effect of maternal glucocorticoid exposure on mouse embryonic development<br />
Lee, Ji-Yeon Lee; Yun, Hyo Jung; Kim, Jongsoo; Kim, Myoung Hee (Yonsei Univ Coll of Med, Rep of Korea)<br />
Prenatal stress is known to cause intrauterine growth retardation and physiological dysfunctions in various aspects. In addition, many<br />
of the diseases associated with prenatal stress exhibit a sex bias. Perturbations and vulnerability to prenatal stress are often more<br />
profound <strong>for</strong> the male fetus, however, the mechanisms responsible <strong>for</strong> this relationship are not clear. We previously have shown that<br />
administration of dexamethasone at gestational day 7.5~9.5, a critical time point on early placenta development, induces placental<br />
defects as well as embryonic growth restriction. In the present study, we further examined the dexamethasone-induced morphological<br />
changes during fetal growth and investigated the influence of prenatal glucocorticoid exposure on sex-specific gene expression and<br />
male gonad development. Compared with the control group, 30% of the experimental group exhibited homeotic trans<strong>for</strong>mation and<br />
other alterations of the axial skeleton. Moreover, embryos exposed to dexamethasone showed smaller rib cages and varying degrees of<br />
xiphoid process protrusion. Here we will present these skeletal mal<strong>for</strong>mations and morphological development of the testes in male<br />
mouse fetuses treated in utero with dexamethasone.<br />
Program/Abstract # 576<br />
The Effect of Methylmercury on Neural Gene Expression in Zebra Finch Development<br />
Murray, Jessica R.; Ramos, Claire; Cristol, Dan; Saha, Margaret (College of William and Mary, USA)<br />
Mercury is a highly toxic pollutant that adversely affects neural development. Preliminary data reveal that male juvenile zebra finch<br />
(Taeniopygia guttata) learn a less complex and lower pitched song after developmental exposure to methylmercury. Zebra Finches are<br />
the most commonly used laboratory songbird species, yet their embryological development has been poorly characterized. Most<br />
studies to date apply Hamburger and Hamilton stages derived from chicken development, however significant differences exist<br />
between development of the two species. Here we provide the first detailed description of embryological development in zebra finch<br />
under standard artificial incubation. Once the embryology was characterized, expression of key song learning genes (e.g., FoxP2) in<br />
Zebra Finch embryos whose parents had been raised on a diet containing low, biologically relevant levels of mercury was<br />
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