Publications by authors named "Yat Sen Wong"

Article Synopsis
  • Mare endometrosis is a problem that makes it hard for horses to have babies because it causes inflammation and damage to the reproductive system.
  • Scientists tested if special cells, called mesenchymal stem cells (MSCs), could help by using tiny packages they release called extracellular vesicles (EVs) with important information inside (miRNAs).
  • They found that treating MSCs with a specific signal (TGFβ-1) for only 4 hours made them better at fighting the damage, while longer treatment (24 hours) caused more problems, which could help create new treatments for mares with endometrial fibrosis.
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Endometrosis in mares is a disease resulting from chronic inflammation characterized by peri glandular fibrosis. There is no effective treatment so far, which opens the door for exploring the use of stem cells as a candidate. Transforming growth factor beta (TGFβ) is crucial for the establishment and progression of fibrosis in mare's endometrosis.

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Pre-implantation embryos release extracellular vesicles containing different molecules, including DNA. The presence of embryonic DNA in E-EVs released into the culture medium during in vitro embryo production could be useful for genetic diagnosis. However, the vesicles containing DNA might be derived from embryos suffering from apoptosis, i.

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The embryo-maternal interaction occurs during the early stages of embryo development and is essential for the implantation and full-term development of the embryo. In bovines, the secretion of interferon Tau (IFNT) during elongation is the main signal for pregnancy recognition, but its expression starts around the blastocyst stage. Embryos release extracellular vesicles (EVs) as an alternative mechanism of embryo-maternal communication.

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Equine endometrial and adipose mesenchymal stem cells (eMSCs and aMSCs, respectively) were isolated from the same donors of thoroughbred mares. The cells displayed characteristic features of MSCs, including trilineage mesodermal and also neurogenic differentiation. We evaluated the influence of cellular origin on their transcriptome profile.

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