Which Low-Abundance Proteins are Present in the Human Milieu of Gamete/Embryo Maternal Interaction?

• Published in: International journal of molecular sciences Vol. 20; no. 21; p. 5305
• Main Authors: Canha-Gouveia, Analuce, Paradela, A, Ramos-Fernández, António, Prieto-Sánchez, Maria Teresa, Sánchez-Ferrer, Maria Luisa, Corrales, Fernando, Coy, Pilar
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 24-10-2019; MDPI
• Subjects: Abundance; Adult; Blood Proteins - analysis; Chromatography, High Pressure Liquid; Cluster Analysis; Clustering; Comparative analysis; Comparative studies; Culture media; Embryos; Fallopian Tubes - metabolism; Female; Fertilization; Fluids; human reproductive fluids; Humans; Hypotheses; Implantation; In vitro fertilization; low abundance proteins; Neonates; Peptides; Plasma; Pregnancy; Principal Component Analysis; Principal components analysis; Proteins; Proteome - analysis; Reproductive system; salpingectomy; Secretome; Spectrometry, Mass, Electrospray Ionization; Sperm-Ovum Interactions; Uterus; Uterus - metabolism; human reproductive fluids; low abundance proteins; salpingectomy
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms20215305

The improvement of the embryo culture media is of high relevance due to its influence on successful implantation rates, pregnancy, neonatal outcomes, and potential effects in adult life. The ideal conditions for embryo development are those naturally occurring in the female reproductive tract, i.e., the oviductal and uterine fluids. To shed light on the differences between chemical and natural media, we performed the first comparative study of the low abundance proteins in plasma, uterine, and oviductal fluid collected, simultaneously, from healthy and fertile women that underwent a salpingectomy. The rationale for this design derives from the fact that high-abundant proteins in these fluids are usually those coming from blood serum and frequently mask the detection of low abundant proteins with a potentially significant role in specific processes related to the embryo-maternal interaction. The proteomic analysis by 1D-nano LC ESI-MSMS detected several proteins in higher amounts in oviductal fluid when compared to uterine and plasma samples (RL3, GSTA1, EZRI, DPYSL3, GARS, HSP90A). Such oviductal fluid proteins could be a target to improve fertilization rates and early embryo development if used in the culture media. In conclusion, this study presents a high-throughput analysis of female reproductive tract fluids and contributes to the knowledge of oviductal and uterine secretome.