Biological research conducted in deep-underground environments is limited due to the lack of scientific infrastructure to accommodate the investigations, and only a few studies have utilized complex whole organism models. In this study, lake whitefish (Coregonus clupeaformis) embryogenesis was examined in two different unique laboratory environments; at the Earth's surface and 2 km deep underground shielded from cosmic radiation. Established developmental endpoints and morphometric analysis were utilized to investigate differences between lake whitefish embryos reared in these two laboratories. No significant differences were observed between the surface and underground laboratories with respect to the timing of hatch or percent survival. However, a significant increase in body length and body weight of up to 10% was observed in embryos reared underground. These findings have been interpreted and discussed in the context of the novel research challenges faced in an inherently difficult to control deep-underground environment. This study represents one of the few investigations with an established whole organism model deep-underground and provides an opportunity to discuss the highly unique technical and logistical challenges of conducting biological experiments in this novel field of scientific research.
The lens of the eye is one of the most radiosensitive tissues. Although the exact mechanism of radiation-induced cataract development remains unknown, altered proliferation, migration, and adhesion have been proposed as factors. Lens epithelial cells were exposed to X-rays (0.1–2 Gy) and radiation effects were examined after 12 h and 7 day. Proliferation was quantified using an MTT assay, migration was measured using a Boyden chamber and wound-healing assay, and adhesion was assessed on three extracellular matrices. Transcriptional changes were also examined using RT-qPCR for a panel of genes related to these processes. In general, a nonlinear radiation response was observed, with the greatest effects occurring at a dose of 0.25 Gy. At this dose, a reduction in proliferation occurred 12 h post irradiation (82.06 ± 2.66%), followed by an increase at 7 day (116.16 ± 3.64%). Cell migration was increased at 0.25 Gy, with rates 121.66 ± 6.49% and 232.78 ± 22.22% greater than controls at 12 h and 7 day respectively. Cell adhesion was consistently reduced above doses of 0.25 Gy. Transcriptional alterations were identified at these same doses in multiple genes related to proliferation, migration, and adhesion. Overall, this research began to elucidate the functional changes that occur in lens cells following radiation exposure, thereby providing a better mechanistic understanding of radiation-induced cataract development.
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