4.5 Article

Differential Size Distribution and Estrogen Receptor Cargo of Oviductal Extracellular Vesicles at Various Stages of Estrous Cycle in Mice

期刊

REPRODUCTIVE SCIENCES
卷 29, 期 10, 页码 2847-2858

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s43032-022-00862-w

关键词

Extracellular vesicles; Exosomes; Oviduct; Oviductal extracellular vesicles; Estrogen receptor; Vesicles size; Estrus

资金

  1. Health Sci&Tech Plan Project of Zhejiang Province [2019KY363]
  2. Sci&Tech Program Project of Zhejiang Province [2018C37126]
  3. Zhejiang Provincial Natural Science Foundation [LY22H040011]
  4. Special Project for the Research Institutions of Zhejiang Province [C11920D-04]
  5. Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents

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This study investigated the changes in size and protein cargo of oviductal extracellular vesicles (OEVs) during the different stages of the estrous cycle in mice. The results showed that the size distribution and protein cargo of OEVs varied at different stages of the estrous cycle. Additionally, OEVs were found in the cilia and microvilli of epithelial cells, with the highest number observed during the proestrus stage. These findings contribute to a better understanding of the physiological characteristics of OEVs and their potential clinical applications.
Oviductal extracellular vesicles (OEVs) play an important role in fertilization and embryo development. However, it remains largely unknown whether the size and protein cargo of OEVs change during the estrous cycle in mice. This study analyzed the changes in the size distribution and protein cargo of OEVs at four stages of the estrous cycle in mice. The distribution widths of OEVs according to the estrous cycle stage were as follows: proestrus, 20-690 nm in diameter, with two peaks at 50 and 250 nm; estrus, 22-420 nm in diameter, with two peaks at 40 and 200 nm; metestrus, 30-70 nm diameter, with a single peak at 40 nm; and diestrus, 10-26 nm diameter, with a single peak at 20 nm. The estrogen receptor (ER) level in OEVs at the proestrus stage differed significantly from that at estrus (P = 0.013) and diestrus (P = 0.005). The levels of CD9 and Hsc70 fluctuated across the four stages, although with no significant differences. Furthermore, OEVs were observed among the cilia and microvilli of epithelial cells at the proestrus, estrus, and diestrus stages, but not at the metestrus stage. The number of observed OEVs was the highest at the proestrus stage, followed by the estrus, and the diestrus stage. Endosomes were also observed at the estrus and diestrus stages. The change of the OEV size and ER cargo is associated with the estrous cycle in mice. Our findings increase the understanding of the physiological characteristics of OEVs, which may have clinical applications.

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