TY - JOUR
T1 - Large-scale production of human blastoids amenable to modeling blastocyst development and maternal-fetal cross talk
AU - Yu, Leqian
AU - Logsdon, Deirdre
AU - Pinzon-Arteaga, Carlos A.
AU - Duan, Jialei
AU - Ezashi, Toshihiko
AU - Wei, Yulei
AU - Ribeiro Orsi, Ana Elisa
AU - Oura, Seiya
AU - Liu, Lizhong
AU - Wang, Lei
AU - Liu, Kun
AU - Ding, Xiaoyun
AU - Zhan, Linfeng
AU - Zhang, Junfei
AU - Nahar, Asrafun
AU - Stobbe, Caitlen
AU - Katz-Jaffe, Mandy
AU - Schoolcraft, William B.
AU - Tan, Tao
AU - Hon, Gary C.
AU - Yuan, Ye
AU - Wu, Jun
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/9/7
Y1 - 2023/9/7
N2 - Recent advances in human blastoids have opened new avenues for modeling early human development and implantation. One limitation of our first protocol for human blastoid generation was relatively low efficiency. We now report an optimized protocol for the efficient generation of large quantities of high-fidelity human blastoids from naive pluripotent stem cells. This enabled proteomics analysis that identified phosphosite-specific signatures potentially involved in the derivation and/or maintenance of the signaling states in human blastoids. Additionally, we uncovered endometrial stromal effects in promoting trophoblast cell survival, proliferation, and syncytialization during co-culture with blastoids and blastocysts. Side-by-side single-cell RNA sequencing revealed similarities and differences in transcriptome profiles between pre-implantation blastoids and blastocysts, as well as post-implantation cultures, and uncovered a population resembling early migratory trophoblasts during co-culture with endometrial stromal cells. Our optimized protocol will facilitate broader use of human blastoids as an accessible, perturbable, scalable, and tractable model for human blastocysts.
AB - Recent advances in human blastoids have opened new avenues for modeling early human development and implantation. One limitation of our first protocol for human blastoid generation was relatively low efficiency. We now report an optimized protocol for the efficient generation of large quantities of high-fidelity human blastoids from naive pluripotent stem cells. This enabled proteomics analysis that identified phosphosite-specific signatures potentially involved in the derivation and/or maintenance of the signaling states in human blastoids. Additionally, we uncovered endometrial stromal effects in promoting trophoblast cell survival, proliferation, and syncytialization during co-culture with blastoids and blastocysts. Side-by-side single-cell RNA sequencing revealed similarities and differences in transcriptome profiles between pre-implantation blastoids and blastocysts, as well as post-implantation cultures, and uncovered a population resembling early migratory trophoblasts during co-culture with endometrial stromal cells. Our optimized protocol will facilitate broader use of human blastoids as an accessible, perturbable, scalable, and tractable model for human blastocysts.
KW - endometrial stromal cells
KW - human blastocyst-like structures
KW - human blastocysts
KW - human blastoids
KW - human integrated stem cell embryo model
KW - human peri-implantation development
KW - naive human embryonic stem cells
KW - naive human induced pluripotent stem cells
KW - syncytiotrophoblast
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UR - http://www.scopus.com/inward/citedby.url?scp=85168995919&partnerID=8YFLogxK
U2 - 10.1016/j.stem.2023.08.002
DO - 10.1016/j.stem.2023.08.002
M3 - Article
C2 - 37683605
AN - SCOPUS:85168995919
SN - 1934-5909
VL - 30
SP - 1246-1261.e9
JO - Cell Stem Cell
JF - Cell Stem Cell
IS - 9
ER -