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Miguel Paul Conde-Hinojosa Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0003-4689-1390
Jaime Gallegos-Sánchez Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0001-6062-805X
Glafiro Torres-Hernández Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0002-0479-1191
Juan Salazar-Ortiz Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0002-0435-8160
Fernando Clemente-Sánchez Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0001-5052-7888
César Cortez-Romero Colegio de Postgraduados image/svg+xml https://orcid.org/0000-0001-7213-9034

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Resumen

Objective: To describe the involvement of the interferon tau gene in the maternal recognition of pregnancy in sheep.


Design/Methodology/Approach: A search and analysis of the scientific documents retrieved from the Web of Science and Scopus databases related to the functions of the interferon tau gene in the maternal recognition of pregnancy in sheep were conducted.


Results: The interferon tau gene (IFNτ) participates in maternal recognition of pregnancy to avoid possible rejection of the embryo, and supports the secretion of progesterone involved in preparing the endometrium for implantation; it also inhibits myometrial motility to maintain pregnancy. IFNτ stimulates the transcription of so-called interferon-stimulated genes (ISGs), which are the effectors of cell-autonomous antiviral defense.  One of the representative members of ISGs is the interferon 15-stimulated gene (ISG15) which regulates endometrial receptivity at implantation, as well as survival, growth and development of the conceptus.


Study Limitations/Implications: Most embryonic losses occur between fertilization and maternal recognition of pregnancy. Understanding this issue is essential to understanding the possible causes of early pregnancy losses.


Findings/Conclusions: Considerable progress has been made in the discovery of how the IFNτ and ISG15 genes act in maternal recognition of gestation in sheep

Abstract | EARLY ACCESS 17 Downloads

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