Generating human blastoids modeling blastocyst-stage embryos and implantation

• Published in: Nature protocols Vol. 18; no. 5; pp. 1584 - 1620
• Main Authors: Heidari Khoei, Heidar, Javali, Alok, Kagawa, Harunobu, Sommer, Theresa Maria, Sestini, Giovanni, David, Laurent, Slovakova, Jana, Novatchkova, Maria, Scholte op Reimer, Yvonne, Rivron, Nicolas
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01-05-2023; Nature Publishing Group
• Subjects: 631/136/532/2117; 631/1647/1407/651; 631/61/2035; 631/61/2320; 631/80/86/820; Adult; Analytical Chemistry; Biological Techniques; Biomedical and Life Sciences; Blastocyst; Blastocysts; Cell culture; Computational Biology/Bioinformatics; Cryopreservation; Culture; Developmental stages; Embryo Implantation; Embryo, Mammalian; Embryogenesis; Embryonic Development; Embryos; Endometrium; Female; Humans; Implantation; In vitro fertilization; Life Sciences; Microarrays; Modelling; Morphology; Organic Chemistry; Organoids; Pluripotency; Pregnancy; Protocol; Stem cells
• ISSN: 1754-2189; 1750-2799; 1750-2799
• DOI: 10.1038/s41596-023-00802-1

Human early development sets the stage for embryonic and adult life but remains difficult to investigate. A solution came from the ability of stem cells to organize into structures resembling preimplantation embryos—blastocysts—that we termed blastoids. This embryo model is available in unlimited numbers and could thus support scientific and medical advances. However, its predictive power depends on how faithfully it recapitulates the blastocyst. Here, we describe how we formed human blastoids that (1) efficiently achieve the morphology of the blastocyst and (2) form lineages according to the pace and sequence of blastocyst development, (3) ultimately forming cells that transcriptionally reflect the blastocyst (preimplantation stage). We employ three different commercially available 96- and 24-well microwell plates with results similar to our custom-made ones, and show that blastoids form in clinical in vitro fertilization medium and can be cryopreserved for shipping. Finally, we explain how blastoids replicate the directional process of implantation into endometrial organoids, specifically when these are hormonally stimulated. It takes 4 d for human blastoids to form and 10 d to prepare the endometrial implantation assay, and we have cultured blastoids up to 6 d (time-equivalent of day 13). On the basis of our experience, we anticipate that a person with ~1 year of human pluripotent stem cell culture experience and of organoid culture should be able to perform the protocol. Altogether, blastoids offer an opportunity to establish scientific and biomedical discovery programs for early pregnancy, and an ethical alternative to the use of embryos.
The authors present a protocol for the generation of human blastoids—structures morphologically and transcriptionally resembling complete blastocysts—from pluripotent stem cells and for their use in modeling implantation into hormonally stimulated endometrial cells.