The Extracellular Vesicles Proteome of Endometrial Cells Simulating the Receptive Menstrual Phase Differs from That of Endometrial Cells Simulating the Non-Receptive Menstrual Phase.
Amber Rose HartNorhayati Liaqat Ali KhanKeerthie DissanayakeKasun GodakumaraAneta AndronowskaSaji EapenPaul Roy HeathAlireza FazeliPublished in: Biomolecules (2023)
Successful embryo implantation into a receptive endometrium requires mutual endometrial-embryo communication. Recently, the function of extracellular vehicles (EVs) in cell-to-cell interaction in embryo-maternal interactions has been investigated. We explored isolated endometrial-derived EVs, using RL95-2 cells as a model of a receptive endometrium, influenced by the menstrual cycle hormones estrogen (E2; proliferative phase), progesterone (P4; secretory phase), and estrogen plus progesterone (E2P4; the receptive phase). EV sized particles were isolated by differential centrifugation and size exclusion chromatography. Nanoparticle tracking analysis was used to examine the different concentrations and sizes of particles and EV proteomic analysis was performed using shotgun label-free mass spectrometry. Our results showed that although endometrial derived EVs were secreted in numbers independent of hormonal stimulation, EV sizes were statistically modified by it. Proteomics analysis showed that hormone treatment changes affect the endometrial EV's proteome, with proteins enhanced within the EV E2P4 group shown to be involved in different processes, such as embryo implantation, endometrial receptivity, and embryo development, supporting the concept of a communication system between the embryo and the maternal endometrium via EVs.
Keyphrases
- pregnancy outcomes
- induced apoptosis
- mass spectrometry
- endometrial cancer
- cell cycle arrest
- label free
- estrogen receptor
- cell therapy
- endoplasmic reticulum stress
- single cell
- liquid chromatography
- oxidative stress
- stem cells
- high performance liquid chromatography
- type diabetes
- skeletal muscle
- ms ms
- body mass index
- high resolution
- bone marrow
- birth weight
- physical activity
- high speed
- mesenchymal stem cells
- weight loss
- single molecule