Evidence for Functional Roles of MicroRNAs in Lineage Specification During Mouse and Human Preimplantation Development

被引:0
作者
Biondic, Savana [1 ,2 ]
Petropoulos, Sophie [1 ,2 ,3 ]
机构
[1] Ctr Hosp Univ Montreal, Ctr Rech, Axe Immunopathol, Montreal, PQ, Canada
[2] Univ Montreal, Fac Med, Mol Biol Program, Montreal, PQ, Canada
[3] Karolinska Inst, Dept Clin Sci Intervent & Technol, Div Obstet & Gynecol, Stockholm, Sweden
基金
加拿大健康研究院;
关键词
microRNAs; blastocyst; preimplantation development; lineage specification; trophectoderm; inner cell mass; epiblast; primitive endoderm; differentiation; stem cells; EMBRYONIC STEM-CELLS; SELF-RENEWAL; DNA METHYLATION; MIRNA; EXPRESSION; FAMILY; DIFFERENTIATION; PLURIPOTENCY; NAIVE; BIOGENESIS;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proper formation of the blastocyst, including the specification of the first embryonic cellular lineages, is required to ensure healthy embryo development and can significantly impact the success of assisted reproductive technologies (ARTs). However, the regulatory role of microRNAs in early development, particularly in the context of preimplantation lineage specification, remains largely unknown. Taking a cross-species approach, this review aims to summarize the expression dynamics and functional significance of microRNAs in the differentiation and maintenance of lineage identity in both the mouse and the human. Findings are consolidated from studies conducted using in vitro embryonic stem cell models representing the epiblast, trophectoderm, and primitive endoderm lineages (modeled by naive embryonic stem cells, trophoblast stem cells, and extraembryonic endoderm stem cells, respectively) to provide insight on what may be occurring in the embryo. Additionally, studies directly conducted in both mouse and human embryos are discussed, emphasizing similarities to the stem cell models and the gaps in our understanding, which will hopefully lead to further investigation of these areas. By unraveling the intricate mechanisms by which microRNAs regulate the specification and maintenance of cellular lineages in the blastocyst, we can leverage this knowledge to further optimize stem cell-based models such as the blastoids, enhance embryo competence, and develop methods of non-invasive embryo selection, which can potentially increase the success rates of assisted reproductive technologies and improve the experiences of those receiving fertility treatments.
引用
收藏
页码:481 / 494
页数:14
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