Hiroo Sasaki, Iori Sasaki, Jennifer Nichols, Ayaka Yanagid
{"title":"Generation of Blastoids from Human Naïve Pluripotent Stem Cells.","authors":"Hiroo Sasaki, Iori Sasaki, Jennifer Nichols, Ayaka Yanagid","doi":"10.1007/7651_2025_642","DOIUrl":null,"url":null,"abstract":"<p><p>Human embryo research is essential for understanding the development of human embryos and their unique features that cannot be investigated in mouse embryos. Natural development of human embryos remains challenging to study both in vivo and in vitro owing to ethical concerns, technical difficulties, and limited availability of embryos for research purposes. Until recently, access to human embryo research, especially the implantation period, was limited. However, optimization of a stem cell-based model known as a blastoid has opened a new era for human embryo research. In contrast with mouse embryonic stem cells, human naïve pluripotent stem cells retain extended cell lineage plasticity. They can differentiate into hypoblast and trophectoderm while retaining characteristic resembling the naïve epiblast in the inner cell mass region. Taking this unique differentiation potential and inherent propagation capacity as pluripotent stem cells, human blastoids are generated by the self-organization of naïve pluripotent stem cells. They resemble human blastocyst structures, consisting of the three founder cell lineages that closely resemble the gene expression profile of human blastocysts. This protocol for generating blastoids solely from naïve human pluripotent stem cells utilizing simple, efficient, and scalable procedures is a robust tool for advancing aspects of human embryo research.</p>","PeriodicalId":18490,"journal":{"name":"Methods in molecular biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/7651_2025_642","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Human embryo research is essential for understanding the development of human embryos and their unique features that cannot be investigated in mouse embryos. Natural development of human embryos remains challenging to study both in vivo and in vitro owing to ethical concerns, technical difficulties, and limited availability of embryos for research purposes. Until recently, access to human embryo research, especially the implantation period, was limited. However, optimization of a stem cell-based model known as a blastoid has opened a new era for human embryo research. In contrast with mouse embryonic stem cells, human naïve pluripotent stem cells retain extended cell lineage plasticity. They can differentiate into hypoblast and trophectoderm while retaining characteristic resembling the naïve epiblast in the inner cell mass region. Taking this unique differentiation potential and inherent propagation capacity as pluripotent stem cells, human blastoids are generated by the self-organization of naïve pluripotent stem cells. They resemble human blastocyst structures, consisting of the three founder cell lineages that closely resemble the gene expression profile of human blastocysts. This protocol for generating blastoids solely from naïve human pluripotent stem cells utilizing simple, efficient, and scalable procedures is a robust tool for advancing aspects of human embryo research.
期刊介绍:
For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.