Publications by authors named "Jennifer Beth Nagashima"

Article Synopsis
  • Artificial insemination (AI) is crucial for wildlife conservation, enabling the use of genetic material from animals even after they die, but its effectiveness is hampered by the poor survival rate of frozen sperm.
  • Recent research showed that oviductal extracellular vesicles (oEVs) enhance cat sperm motility and reduce early activation issues, and this study further explores the protein content of dog and cat oEVs.
  • The results indicate that when red wolf and cheetah sperm are thawed with oEVs from dogs and cats respectively, they show better acrosome integrity and improved motility in red wolf sperm, highlighting oEVs as beneficial for enhancing AI success
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Extracellular vesicles (EVs) contain multiple factors that regulate cell and tissue function. However, understanding of their influence on gametes, including communication with the oocyte, remains limited. In the present study, we characterized the proteome of domestic cat (Felis catus) follicular fluid EVs (ffEV).

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Ovarian cancer is the fifth cause of cancer-related mortality in women, with an expected 5-year survival rate of only 47%. High-grade serous carcinoma (HGSC), an epithelial cancer phenotype, is the most common malignant ovarian cancer. It is known that the precursors of HGSC originate from secretory epithelial cells within the Fallopian tube, which first develops as serous tubal intraepithelial carcinoma (STIC).

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The introduction of poly(dimethylsiloxane) (PDMS) and soft lithography in the 90's has revolutionized the field of microfluidics by almost eliminating the need for a clean-room environment for device fabrication. More recently, 3D printing has been introduced to fabricate molds for soft lithography, the only step for which a clean-room environment is still often necessary, to further support the rapid prototyping of PDMS microfluidic devices. However, toxicity of most of the commercial 3D printing resins has been established, and little is known regarding the potential for 3D printed molds to leak components into the PDMS that would, in turn, hamper cells and/or tissues cultured in the devices.

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