image: To assess whether TBLCs possess the ability to form blastoids, 5, 10, 25, and 50 cells of mCMG-TBLCs were aggregated per microwell of the AggrewellTM 400 in the reported medium for generating EPS-blastoid (iBlastoid medium). After 5 days of culture, some of the microwells initiating with 5 and 10 cells turned out to be empty because of cell death. Nevertheless, most of the remaining cell clumps with different initiating cell numbers started to form a cavity. The cavities gradually grew bigger to form a blastocyst-like structure in another 2 days. view more
Credit: ©Science China Press
This study is led by Dr. Man Zhang (Guangzhou Laboratory, Guangzhou Medical University). Previous studies showed that the efficiency of the blastocyst-like structures (blastoids) formation from extended pluripotent cells (EPS) was pretty low (15%). Besides, EPS-blastoids contained few TE cells and a considerable amount of mesoderm-like cells. In order to increase the efficiency of blastoid generation, spliceosomal repression-induced totipotent blastomere-like cells (TBLCs) were used to generate blastoids. It was reported that TBLCs have similar transcriptomes to 2C-4C embryos. The team found that blastoids were observed in nearly 80% of micro-wells when aggregated in the iBlastoid medium, which is much higher than the efficiency of EPS-blastoid formation. “This is an unexpected promotion,” Man Zhang said. immunofluorescence staining revealed that around 71% of TBLC-blastoids expressed the markers of early cell lineages with a similar location to natural embryos.
Meanwhile, Dr. Pengfei Zhang together with the lab director Man Zhang sought to determine whether a single TBLC could give rise to blastocyst-like structures. As it’s critical to generate blastoid from a single cell for high-throughput screening of the effects of gene manipulation in early embryogenesis. Accordingly, 9.3% of microwells (multiplied 18.6% by 50%) from a single TBLC can form blastocyst-like structures that expressed all 3 lineage markers in a similar pattern to that of natural blastocysts.
In addition, scRNA-seq revealed that TBLC-blastoids shared a similar lineage composition and cell transcriptome to blastocysts. Compared to the blastoids generated from other reported cell types (EPS, ETS and TPS), TBLC-blastoids contained more TE lineage cells but fewer PrE-like cells. Besides TSC-like and PrESC-like cell lines were established from TBLC-blastoids.
The researchers also evaluated whether TBLC-blastoid can develop beyond implantation and recapitulate some aspects of post-implantation development both in vitro and in vivo. TBLC-blastoids cultured in vitro in the IVC medium can transit to the egg-cylinder stage. When transplanted into the uterus of pseudopregnant mice, TBLC blastoids can induce deciduae in vivo. They obtained an E7.5 embryo-like structure from the deciduae. However, they were unable to develop normally in vivo. The authors indicate that the abnormal gene expression profile of extra-embryonic lineages (TE and PrE) of blastoids might be the major cause of their abnormal in vivo development. Further studies to optimize the medium to obtain an adequate proportion and faithful PrE and TE cells in TBLC-blastoids are necessary to generate fully functional synthetic embryos.
See the article:
Highly efficient generation of blastocyst-like structures from spliceosomes repressed mouse totipotent blastomere-like cells
https://doi.org/10.1007/s11427-022-2209-3
Journal
Science China Life Sciences