Spatially ordered embryo-like structures self-assembled from blastocyst-derived stem cells can be generated to mimic embryogenesis in vitro. However, the assembly system and developmental potential of such structures needs to be further studied. Here, we devise a nonadherent-suspension-shaking system to generate self-assembled embryo-like structures (ETX-embryoids) using mouse embryonic, trophoblast and extra-embryonic endoderm stem cells. When cultured together, the three cell types aggregate and sort into lineage-specific compartments. Signaling among these compartments results in molecular and morphogenic events that closely mimic those observed in wild-type embryos. These ETX-embryoids exhibit lumenogenesis, asymmetric patterns of gene expression for markers of mesoderm and primordial germ cell precursors, and formation of anterior visceral endoderm-like tissues. After transplantation into the pseudopregnant mouse uterus, ETX-embryoids efficiently initiate implantation and trigger the formation of decidual tissues. The ability of the three cell types to self-assemble into an embryo-like structure in vitro provides a powerful model system for studying embryogenesis.
The mammalian zygote undergoes a series of changes, including zygotic genome activation and lineage specification, that are each critical for generating a blastocyst. The blastocyst is comprised of an inner cell mass (ICM) within the trophectoderm (TE), with the ICM including the epiblast (EPI), and primitive endoderm (PE)1,2. During implantation, the blastocyst undergoes a morphogenetic transformation in which the original vesicular structure is reorganized into an elongated structure at E6.5. This elongated structure is made up of: (1) the ectoplacental cone, (2) the EPI, (3) the extra-embryonic ectoderm (ExE), (4) a layer of visceral endoderm (VE) that envelopes both the EPI and ExE, and (5) the parietal yolk sac, Reichert’s membrane, and trophoblast giant cell (TGC) layer, which together surround the entire conceptus3,4,5,6. During gastrulation (i.e., the formation of a gastrula from a blastula), communication between these embryonic tissues causes the EPI cells to polarize, adopt a rosette-like configuration, and undergo lumenogenesis. This is followed by development of the trophectoderm into the ExE, which forms a second cavity7,8. Both the embryonic and extra-embryonic cavities unite to form a single pro-amniotic cavity, and the embryo breaks symmetry to initiate the specification of mesoderm and primordial germ cells9. The VE is a particularly important source of signals for embryonic patterning5. Precursor cells of the anterior VE (AVE) arise at the distal tip of the embryo (termed the distal VE, DVE) and then migrate to the anterior side of the embryo. The AVE is crucial for anterior-posterior patterning, as it is a source of antagonists for posteriorizing signals, such as Nodal and Wnt10,11,12. By the end of gastrulation, the three primary germ layers have been formed, including the ectoderm, mesoderm and definitive endoderm, from which all fetal tissues will develop.
Stem cells have been derived from the three cell lineages of the mouse blastocysts, namely, embryonic stem cells (ESCs) from the EPI13, extra-embryonic endoderm stem cells (XENCs) from the PE14, and trophoblast stem cells (TSCs) from the TE15. Each of these stem cell types can be maintained indefinitely in culture. ESCs can differentiate into cells from all three germ layers13,16, and can be induced to form embryoid bodies (EBs) or micro-patterned colonies. These are valuable tools for studying embryonic development, but EBs do not fully recapitulate the spatial-temporal events of embryogenesis, nor do they acquire the cellular architecture of a post-implantation embryo17,18,19,20. Recently, ESCs and TSCs were combined in a three-dimensional (3D)-scaffold to produce ETS-embryoids that undergo embryogenic process similar to normal embryogenesis9. However, these embryo-like structures lack PE-derived cells, which may play critical roles during later stages of embryogenesis5,21. Here, we mimic embryogenesis in vitro by culturing together the three types of blastocyst-derived stem cells (ESCs, TSCs, and XENCs; we refer to this combination as ETX) using a nonadherent-suspension-shaking system. We hypothesize that if these cell types were cultured together under suitable conditions, they would engage in both homo- and heterotypic interactions necessary for embryo formation. Indeed, interactions between these stem cells in this suspension system recapitulate many of the molecular and morphogenic events of early mouse embryogenesis, resulting in the generation of what we call ETX-embryoids.
Forming self-assembled structures under nonadherent-suspension-shaking culture system
Individual cells in tissues and organs are able to recognize, adhere to, and communicate with each other through binding between cell surface molecules. The three types of blastocyst-derived stem cells (ESCs, TSCs, and XENCs) are no exception, as they each express lineage-specific cell surface proteins22,23. We hypothesized that if the three blastocyst-specific stem cell types were cultured together under suitable conditions they would be able to aggregate, sort into specific cellular compartments, and then recapitulate the signaling and morphogenic events necessary for mouse embryogenesis. To establish these conditions, we used ESC and TSC reporter lines (DsRed-ESCs and EGFP-TSCs) (Supplementary Fig. 1a, b) to trace their spatial location in aggregated structures, and compared different methods, including hanging drop culture24, microporous culture25,26, microinjection method, and nonadherent-suspension-shaking culture (Supplementary Fig. 1c–f). The last method was proved to be the most suitable for promoting cell–cell contacts, cell–cell self-recognition, and cellular aggregation into ordered structures. Thus, the nonadherent-suspension-shaking culture method was used for further studies.
To investigate how different types of stem cells assemble together, we designed an experimental strategy (Fig. 1a). We first examined combinations of two cell types. When ESCs and TSCs were cultured together, they formed a cylindrical structure similar to the recently reported ETS-embryoid9 (Supplementary Fig. 1g, h). The TSC/XENC combination did not form a specific structure, whereas ESCs and XENCs self-assembled into a structure, in which a XENC-derived cell layer surrounded an ESC sphere (EXE-embryoid) (Fig. 1b and Supplementary Fig. 1i). A similar to result of EPI-explants in vitro cultured from the EPI-part wrapped with the VE of E5 embryos27,28 (Fig. 1c).
When the three stem cell types were combined, they generated embryonic-like structures (ETX-embryoids) that had spatial relationships between the cell types that resembled post-implantation embryos. In these ETX-embryoids, ESC-derived cells were on one side, TSC-derived cells were on the other side, and XENC-derived cells enveloped the ESC- and TSC-derived structures (Fig. 1d, e and Supplementary Fig. 1j–m). Localization of the ESC-, TSC- and XENC-derived cells was further confirmed via immunostaining, using antibodies specific for the lineage markers Gata4, Oct4, Cdx2, and Eomes (Fig. 1b–e and Supplementary Fig. 1h, i, k–m). Eomes is expressed in the ExE and embryonic VE, and is robustly induced at the onset of gastrulation29. Labeling wild-type embryos for Eomes showed the ExE developed from the TE, and the VE developed from the PE (Fig. 1f, g). Lineage marker gene expression levels for single cells isolated from ESC-, TSC-, and XENC-specific compartments confirmed their spatial localization in ETX-embryoids at 84 h (Fig. 1h). The volume of ESC and TSC compartments in 72 h ETX-embryoids was comparable to that seen for E5.75 embryos (Fig. 1i).
We found that the initial number of cells, the cell ratios, and the medium composition affected the efficiency of formation for these reconstructed embryos (Supplementary Fig. 2a, e–h). When we visually assessed ETS-embryoids, we identified both regular and irregular structures (Supplementary Fig. 2b, c). We observed higher efficiency (35%) and better morphology of ETS-embryoids using a mixture of 1 × 105 ESCs and 1 × 105 TSCs in a 3.5-cm dish when shaken at 60 revolutions per minute (Supplementary Fig. 2a, d). A previous study reported that ETS-embryoids must be cultured in a medium that includes FGF4 for TSC self-renewal and proliferation9,15. Here, we found that the addition of small molecules, such as LIF, 2i (CHIR99021 and PD0325901), and FGF4, which inhibit ESC and TSC differentiation respectively, affected the formation of the reconstructed embryos (Supplementary Fig. 2e–h). Therefore, we did not include these factors in our culture system for subsequent self-assembly experiments.
We next examined the reproducibility by which these EXE-, ETS-, and ETX-embryoids could be reconstructed. The EXE-embryoids were most efficiently assembled, with > 90% exhibiting regular structures (i.e., the ESC compartment surrounded by XENC-derived cells) (Fig. 1b and Supplementary Fig. 1i). For ETX-embryoids, an initial ratio of 1 × 105 ESCs, 1 × 105 TSCs, and 2 × 105 XENCs in a 3.5-cm dish generated the highest percentage (~23%) of regular ETX-embryoids (Supplementary Fig. 3a–e).
Altogether, these results demonstrate that in vitro self-recognition and self-assembly of the three types of blastocyst-derived stem cells can lead to the formation of embryo-like structures in which the spatial distributions of the stem cell-derived tissues resemble the distribution of the ExE, EPI and VE in E5.5 embryos.
Lumenogenesis in EXE-embryoids
Next, we determined whether the reconstructed embryoids develop in a progressive sequence of spatial and temporal morphogenetic steps consistent with normal embryogenesis and examined the occurrence of events such as polarization, lumenogenesis, asymmetrical gene expression, mesoderm and PGC-like cell specification, and DVE/AVE-like tissue formation4,5.
We first examined the development of EXE-embryoids, which initially formed after 12 h of shaking culture (Supplementary Fig. 4a). Labeling EXE-embryoids for Podocalyxin (PCX), E-Cadherin and aPKC, which accumulate on the apical sides of EPI cells during natural pro-amniotic cavity formation8,9, we detected cavity formation at 48 h (Fig. 2a, d, g, h, i). This lumen or cavity enlarged with prolonged culture time (Fig. 2i and Supplementary Fig. 4b, c). Localization of the cell adhesion protein E-Cadherin revealed that the nuclei in the ESC compartment were aligned with the cavity. These morphogenetic steps are similar to those seen during the development of EPI-explants27,28 (Fig. 2b, e). However, we did not observe similar experimental phenomena in EBs (Fig. 2c, f). Using the previously determined optimal number of ESCs and XENCs (ESCs, 1 × 105 and XENCs, 1 × 105) and ESCs alone (2 × 105) as controls, we found a higher number of EXE-embryoids formed compared with EBs, resulting in EBs that were larger in volume than EXE-embryoids. The average volume of EXE-embryoids at 60 h was comparable to the volume of EPI-explants cultured in vitro for 24 h (Supplementary Fig. 4d–h).
For wild-type embryos at the implantation stage of development, Laminins secreted primarily by the VE create a basal membrane niche, which helps establish EPI tissue polarity8,30. Immunostaining for Laminins revealed that EXE-embryoids and EPI-explants, but not EBs, were enveloped by a basal membrane (Fig. 2d–f), suggesting that Laminins play a role in the polarity and cavitation of EXE-embryoids. Lamc1 encodes for the Laminin γ1 subunit and is necessary for basement membrane formation31,32. To test the role of Laminins in the formation of EXE-embryoids, we derived Lamc1 knockout (Lamc1-/-) ESCs and XENCs to generate EXE-embryoids (Supplementary Fig. 5a). Loss of lamc1 from ESCs or XENCs did not affect the formation and cavitation of EXE-embryoids. However, EXE-embryoids were not formed when Lamc1-/- ESCs and Lamc1-/- XENCs were used (Supplementary Fig. 5b–f). This suggests that the basal membrane created by Laminins plays an important role in the development of reconstructed embryos. This is consistent with the role of Laminins in providing a signal for EPI reorganization8,31.
We also examined cleaved caspase-3 expression in EXE-embryoids assembled from wild-type XENCs and p53-/- ESCs (Supplementary Fig. 5g, h), as well as apoptosis events in EXE-embryoids, EPI-explants and EBs (Fig. 2a–c). We found that apoptosis was not required for lumen formation, as previously reported for developing embryos8. Taken together, these results indicate that ESCs and XENCs can self-assemble in vitro into structures that mimic embryogenesis, including the formation of a basal membrane, the induction of cellular polarity and lumenogenesis.
Pro-amniotic cavity formation during ETX-embryogenesis
We generated ETX-embryoids using EGFP-TSCs and selected regular ETX-embryoids for these experiments (Fig. 3a, b and Supplementary Fig. 3d, e). Immunostaining for Oct4 indicated that ETX-embryoids at 84 h were similar to E4.5 embryos that had been cultured in vitro for 60 h. For both types of embryos, their centers lacked DAPI fluorescence, suggesting cavity formation (Fig. 3a, d and Supplementary Fig. 6a). To obtain insight into the polarization and cavitation of ETX-embryoids, we examined the distribution of E-Cadherin in ETX-embryoids at different developmental time points, and compared this to E5.75 embryos (Fig. 3c, e and Supplementary Fig. 6b). To further confirm cavity formation, we labeled embryos for PCX, which accumulated along the apical side of cells in the ESC compartment by 60 h, and in the TSC compartment by 72 h. By 84 h, PCX lined a central common cavity. These results suggested that a small cavity could be first formed in ESC compartments and then in TSC compartments, and later, these cavities united to form a single large common cavity in ETX-embryoids (Fig. 3f). This was also supported by analyzing PCX distribution in the ESC and TSC compartments of ETX-embryoids as the cavities progressively enlarged (Fig. 3k and Supplementary Fig. 6c). Lumenogenesis in ETX-embryoids is similar to pro-amniotic cavity formation that occurs during natural embryogenesis5,8.
Similar immunohistochemical analyses revealed that ETS-embryoids failed to acquire morphological features under the same condition (Supplementary Fig. 7a, b). This suggests that interactions between the ESC and TSC compartments are not sufficient to initiate cavitation in ETS-embryoids. This failure of cavity formation may be due to lack of basal membrane niche created by Laminins8,9. Thus, we further examined the distribution of Laminins in ETS-embryoids, and found that secreted Laminins were not sufficient to assemble a basal membrane that enveloped the reconstructed embryos. In 84 h ETX-embryoids, the distribution of Laminins were similar to those seen in wild-type embryos at E5.75 (Fig. 3g, h and Supplementary Fig. 7c). Further, caspase-3 localization indicated that apoptotic cells were distributed throughout the lineages and not exclusively at the center of the ESC- or TSC-derived tissues (Fig. 3i, j), suggesting that apoptosis is not essential for cavity formation8.
ETX-embryogenesis requires Nodal signaling
In wild-type embryos, Nodal signaling is required throughout early post-implantation stages33,34,35, and inhibition of the Nodal pathway in ETS-embryoids affects the development and cavitation of the TSC compartment9. To examine the role of Nodal signaling during ETX-embryogenesis, we generated ETX-embryoids in the presence of the TGF-beta receptor inhibitor SB431542, which was added when the cells were first mixed under culture conditions. Inhibition of Nodal signaling affected the cavity formation of the TSC compartment in ETX-embryoids (Fig. 4a–c). To further confirm the role of Nodal signaling, we designed sgRNAs to knockout Nodal in ESCs (Nodal-/- ESCs) (Fig. 4d). These cells were then used to generate ETX-embryoids. In 90% of ETX-embryoids assembled using Nodal-/- ESCs, the TSC compartment failed to cavitate, consistent with the SB431542 results. In these experiments, small effects on the ESC compartment (e.g., smaller cavities) were sometimes observed (Fig. 4c, e, f). Altogether, these experiments suggest that Nodal signaling from the ESC compartment is required for development of the TSC compartment in ETX-embryoids.
Regionalization of VE during ETX-embryogenesis
Before mouse embryos initiate gastrulation, asymmetric patterns of gene expression are seen in the VE. This directs the migration of cells from the DVE to form the AVE at E6.536,37. Signaling molecules from the AVE, such as Lefty1 and Cer1, inhibit Nodal signaling in the underlying EPI, leading to asymmetric patterns of gene expression and formation of the anteroposterior axis2,38,39.
To determine whether XENC-derived tissue in ETX-embryoids mimics DVE/AVE formation in wild-type embryos, we used XENCs that express a Lefty1-mCherry reporter to monitor Lefty1 expression. A small number of cells on one side of the XENC-derived layer expressed Lefty1-mCherry in 23% ETX-embryoids under culture from 72 to 84 h (Fig. 5a–e and Supplementary Fig. 8a–c). This was confirmed by quantitative assessment of Lefty1-mCherry positive cell number in ETX-embryoids (Fig. 5f). We detected that the mCherry positive cells in DVE-like tissue of the ETX-embryoids at 72 h migrated to the anterior side of the embryoids after further culture for 12 h in a ratio of 53% (Supplementary Fig. 8d). This is similar to the distribution of DVE/AVE in wild-type embryos (E5.5-6.5). In EXE-embryoids, however, the distribution of Lefty1-mCherry positive cells in XENC-derived tissue was random (Fig. 5h and Supplementary Fig. 8e). We further confirmed that the mCherry positive cells were DVE/AVE-like tissue cells by measuring the expression of specific lineage markers via single-cell PCR. Partial least square-discriminate analysis (PLS-DA)40 and box-plots revealed that DVE/AVE markers such as Foxa1, Cer1, Otx2 and Sfrp5 were upregulated in the mCherry positive XENC-derived cells (Fig. 5g, i). Markers of posterior VE (Bmp2, Fgf5) were upregulated in the mCherry negative XEN cells at 84 h compared with mCherry negative cells at 24 h (Fig. 5j). These results suggest that regionalized DVE/AVE-like tissue formed in ETX-embryoids.
Asymmetric expression of genes specific for mesoderm and PGC precursors
A crucial event in mouse embryogenesis is the breaking of symmetry in gene expression. This plays a major role in embryonic patterning, resulting in the formation of regionalized mesoderm and the specification of PGCs in the EPI36,41.
We next sought to determine whether mesoderm induction and PGC specification occurred in ETX-embryoids. Blimp1 (also known as Prdm1) is the key regulator of PGC specification and is expressed in PGC precursors as they emerge from the most proximal posterior portion of the EPI, as well as in the VE41,42,43. Blimp1-positive cells also initially express many genes involved in embryonic development, particularly mesoderm induction44. To identify cells resembling mesoderm cells and PGC precursors, we used a Blimp1-mVenus and Stella-ECFP (BVSC) double-transgenic ESC line45,46 to generate ETX-embryoids. Notably, in contrast to EXE-embryoids, ETX-embryoids showed asymmetric expression of Blimp1-mVenus, which was confined to a domain in the ESC compartments extending from the boundary of the ESC and TSC compartments at 84 h, but ECFP was not detected (Fig. 6a, c and Supplementary Fig. 9a–c). This phenomenon resembled the events in chimeric embryos at E6.5 (Fig. 6b and Supplementary Fig. 9d) after injection of BVSC-ESCs into embryos at the 8-cell stage47, as well patterns seen in previous reports46. We did not detect Stella-ECFP PGCs in BVSC chimeric embryos before E7.5, consistent with the absence of Stella-GFP observed in embryos between E5.5-E7.5, which has been reported previously48.
To examine changes in gene expression patterns in different compartments at different stages, we analyzed the gene expression levels in single cells from the three compartments at 0, 24, and 84 h using single-cell qPCR. PLS-DA components suggested that the three types of stem cells differentiated along with the development of the ETX-embryoids (Fig. 6d). Exit from the naive pluripotent state is required to generate the pro-amniotic cavity in mouse embryos49. Therefore, we analyzed patterns of gene expression for cells from the ESC compartment of ETX-embryoids at 24 and 84 h. Naive ESC markers, such as Nanog, Klf4, and Sox2, were downregulated (Fig. 6e) and EPI markers, such as Fgf5, Fgf4, Fgfr1, Gdf3, and Cripto, were upregulated (Fig. 6f), consistent with the gene expression patterns in the EPI cells of wild-type embryos during gastrulation49.
Next, we compared the gene expression patterns of Blimp1-mVenus-positive (BV+) and Blimp1-mVenus-negative (BV−) cells in ETX-embryoids at 84 h. As expected, PGC markers, such as Blimp1, Prdm14, Stella and Tfap2c, were higher in mVenus-positive cells, whereas there was a trend toward Dnmt3b down-regulation (Fig. 6g). Markers known to be elevated in the region opposite to the mesoderm in E6.5 embryos, such as Pou3f1 and Slc7a3, tended to be upregulated in mVenus-negative cells isolated from the region opposite to that of BV+ cells (Fig. 6i). BV+ cells also initially express mesoderm genes44. Interestingly, we found the mesoderm markers, such as Flk1, Hhex, and Hand1, were upregulated in BV+ cells (Supplementary Fig. 9f). We further confirmed mesoderm formation by immunostaining for Cripto, a mesoderm marker, which asymmetric expressed at the posterior side in the ESC compartment (Fig. 6h and Supplementary Fig. 9e). Single-cell qPCR revealed that anterior EPI markers (Fgf4, Mixl1) were upregulated in 84 h BV+ cells compared to 84 h BV− cells (Supplementary Fig. 9g). These results indicate that the formation of regionalized mesoderm and specification of PGC precursor-like cells occurred in ETX-embryoids.
ETX-embryoids initiate implantation
We further analyzed the expression of genes related to blastocyst activation and embryo implantation50,51. Markers known to be elevated during implantation and post-implantation, such as Alk2, Erk2, Gata3, Cb1, Cb2, ErBb1, ErBb4, and Igf2, were upregulated in cells isolated from TSC compartment in ETX-embryoids compared to those of TSCs (Supplementary Fig. 10a, b), suggesting that they may be able to initiate implantation after transfer into the uterus of a pseudopregnant female.
To test this possibility, we transferred 36 h ETX-embryoids into the uteri of 2.5 and 3.5 dpc pseudopregnant mice. We observed a higher percentage of implantation sites when using 3.5 dpc mice, so this method was used for further study. The highest percentage of implantation sites was observed for ETX-embryoids compared with ETS- and EXE-embryoids (Fig. 7a, b, d and Supplementary Fig. 12a). The average size of decidual tissues for the three types of reconstructed embryos was comparable, although the individual sizes were variable (Fig. 7c). The identity of these decidual tissues was confirmed via in situ hybridization for Dtprp (Fig. 7e). Coordinated uterine-embryonic axis formation and decidual remodeling are hallmarks of mammalian post-implantation embryo development52. Haemotoxylin and eosin (H.E.) staining indicated that ETX-embryoids established the uterine-embryonic axis (Fig. 7f, g, h, i and Supplementary Fig. 11a–d). We further examined the expression of implantation markers at the implantation sites, such as Cyclooxygenase-2 (COX2)53 and Placental Lactogen-I (PL1)54,55, which marks trophoblast giant cells, as well as Cytokeratin (CK) in the luminal epithelium (LE) (Fig. 7i, j). The expression patterns of these genes at the implantation sites were similar to those seen in E6.5 wild-type embryos (Fig. 7h, j). In addition, the results of CK and PL1 co-immunostaining showed that CK had no signal around the ETX-embryoid at 72 h (Fig. 7k), combined with previous H.E. staining results (Fig. 7g), which suggested clearance of uterine luminal epithelial cells56 (Supplementary Fig. 11i). These results indicated that the ETX-embryoids recapitulate key events of uterine implantation, such as discrete decidualization, vascular anastomosis, patterned Dtprp expression in the decidua, and clearance of uterine luminal epithelium.
For transferred ETX-embryoids, E5.5 embryo-like structures were detected in the decidual tissues at 48 h after transplantation through H.E. staining (Fig. 7f, g). These structures were surrounded by a basement membrane of Laminins (Fig. 7l), which is crucial for early developmental events32. No such structures were seen for ETS- or EXE-embryoids (Fig. 7m). However, at later time points (72 and 84 h), we failed to detect ETX-embryoids with a normal developmental morphology (Fig. 7n and Supplementary Fig. 11c, d), suggesting that ETX-embryoids were degraded after implantation initiation. This did not result from immune rejection, as similar results were seen using NOG immune-deficient mice as the recipients (Supplementary Fig. 11e, f). We characterized the cytoarchitecture of these ETX-embryoids by isolating them from deciduae 3 days after transplantation and subjecting them to histochemical and PCR analyses. A total of 17 structures were detected from nine recipient mice. Many identifiable tissues could be identified in ETX-embryoids, but most ETX-embryoids had structural defects (Supplementary Fig. 12b–g). Immunostaining for Gata4 and Laminin confirmed that the implantation sites contained XENC-derived tissues that secreted Laminins (Supplementary Fig. 12h). Comparing ETX-embryoids and wild-type embryos labeled for Laminins and Gata4 (Supplementary Fig. 11g, h), we found that implanted ETX-embryoids lack a structure similar to the outer layer surrounding the entire conceptus, which forms a safe environment for the developing embryo. Altogether, these results indicate that ETX-embryoids can initiate implantation response after transplantation into a pseudopregnant mouse, although they exhibited limited developmental potential.
In this study, we found that the three types of blastocyst-derived stem cells have a remarkable ability to self-assemble into a structure (ETX-embryoids) that has embryonic architectural features when cultured under nonadherent-suspension-shaking conditions (Fig. 8). Resulting embryo-like structures represent a powerful model system for studying embryogenesis and post-implantation morphogenesis. ETX-embryoids undergo a series of molecular and morphogenic transitions similar to those seen for wild-type embryos, such as lumenogenesis, the formation of DVE/AVE-like tissues, and the induction of mesoderm and PGC precursors. We also demonstrate that XENC-derived tissues play critical roles in polarization and lumenogenesis events in EXE- and ETX-embryoids. In addition, the length of time from initiation of ETX-embryoid assembly to PGC specification (when Blimp1 expressed) is close to that observed for wild-type embryos (E4.5 to E6.5). This suggests that the ETX-embryoid assembly system closely mimics embryogenesis in vitro, enabling exploration of the molecular mechanisms driving these events. Using this system, we plan to investigate the signaling pathways mediating both homo- and heterotypic interactions between these stem cell types that are required for this spatially ordered assembly, as well as the pathways underlying interactions between the different stem cell-derived tissues.
EBs or micro-patterned colonies derived from ESCs have previously been shown to polarize and to carry out lumenogenesis, but they do not execute many of the spatial and temporal events observed in embryogenesis due to the lack of signals from extra-embryonic tissues17,18,19. Combining ESCs and TSCs in a 3D ECM-scaffold can generate ETS-embryoids whose morphogenesis is similar to that of wild-type embryos, including the induction of asymmetric patterns of gene expression for markers of mesoderm and PGC without signals from the DVE or AVE9. However, we have shown that ETS-embryoids, when cultured in simpler culture conditions (see the Method section), do not recapitulate embryogenesis. Our EXE-embryoids formed rosette-like structures and cavities, but did not break symmetry, whereas ETX-embryoids showed events similar to early post-implantation development, even the formation of DVE and AVE-like tissues. Therefore, our studies indicated that XENC-derived tissues play important roles in embryogenesis, and interactions among the three compartments are required for the in vitro development and patterning of self-assembled embryos. Further investigations are needed to better understand the mechanisms governing interactions among the three compartments, and how XENC-derived tissues contribute to development.
ETX-embryoids successfully mimicked early events of natural embryogenesis, even initiating implantation to trigger decidual tissues with typical local vascular permeability and breach of uterine luminal epithelium. However, ETX-embryoids exhibited limited developmental potential after implantation initiation. This could be because ETX-embryoids lack structures such as the parietal yolk sac and Reichert’s membrane that function to protect the embryo and to passively filter nutrients3,57,58. Normally during gastrulation, the trophoblast-derived giant cell layer and the parietal endoderm, together with the Reichert’s membrane, surround the entire conceptus5,54. Methods to further improve the in vitro assembly system so as to add more complex structures such as these are clear targets of future studies.
All animal procedures and all of the mouse work were approved by the Animal Care and Use Committee of China Agriculture University (Permit Number: SKLAB-2016-01-04). CD1 and 129 mice were obtained from Beijing Vital River Laboratory Animal Technology Co., Ltd. Actin-GFP mice were obtained from Shaorong Gao’s Laboratory in Tongji University. All mice were maintained in specific pathogen-free (SPF) conditions with a 12-h dark / 12-h light cycle between 06:00 and 18:00 in a temperature controlled room (22 ± 2 °C) with free access to water and food.
Stem cell lines and cell culture
G4 and G4-ACTB-DsRed-MST ESCs were obtained from Dr. Andras Nagy, Kristina Vintersten and Marina Gertsenstein’s Laboratory in Mount Sinai Hospital & the Samuel Lunemfeld Research Institute. Blimp1-mVenus and Stella-ECFP (BVSC) double-transgenic ESC line, expressing membrane-targeted Venus (mVenus) under the control of Prdm1 (Blimp1) regulatory elements and enhanced CFP (ECFP) under the control of Dppa3 (Stella/Pgc7), were obtained from Dr. Mitinori Saitou45,46.
For generation of Lefty1-mCherry mouse XEN cell line, the Lefty1 promoter and fluorescent protein were used to integrated into XEN cells by the Sleeping Beauty transposon system, which consists of two components: the transposon vector modified from pT2/LTR7-GFP (addgene#62541) and the transposase vector (pCMV(CAT)T7-SB100, addgene #34879). PT2/LTR7-GFP was added with “puro” castle, which could express puromycin N-acetyltransferase and GFP CDS region was replaced by mCherry. DNA fragment, which was amplified from pT2/LTR7-GFP by primer PT2-F (GTTTGGACAAACCACAACTAGAATG) & R (TCTAAAGCCATGACATCATTTTCTG), coupled with “puro” castle and mCherry CDS region to acquire the vector named PT2-Puro-mCherry using NEBuilder®HiFi DNA Assembly Master Mix (NEW ENGLAND BioLabs). The promoter sequence of the Lefty1 gene was amplified from the DNA of mouse ES cells using Lefty1-F (GTCCGGTGGGGAATCACATT) & R (AAAGGGTCTTGAGTCTGCGG). Then the promoter sequence of the Lefty1 gene was added to PT2-Puro-mCherry by NEBuilder®HiFi DNA Assembly Master Mix (NEW ENGLAND BioLabs), in which PT2-Puro-mCherry was linearized by EcoRI and the overlap sequence containing EcoRI sequence was added to the promoter sequence of the Lefty1 gene. The vector was named PT2-Puro-mCherry-Lefty1. Then PT2-Puro-mCherry-Lefty1 and pCMV(CAT)T7-SB100 were transfected into mouse XEN cells and screened by 2 μg per mL puromycin for subsequent analyses.
For generation of Lamc1 (laminin, gamma 1) knockout cell lines, two sgRNA sequence targeting (GGAGTACTGCGTGCAGACTGGGG and GCTTTGCCACCAGGTGGTGTCGG) Lamc1’s exon1 were used for constructing a dual sgRNA vector. Fragments containing two sgRNA sequences amplified from PUC-U6-sgRNA-Kana (from Huang Xingxu lab) using primers (Lamc1sg1-F: atgcgtctcacaccggagtactgcgtgcagactggttttagagctagaaatagcaag and Lamc1sg2-R: atgcgtctcgaaacacaccacctggtggcaaagcggtgtttcgtcctttccacaag). The PCR product was digested with BsmbI and ligated with linearized PX330-GFP. The Vectors has been transfected into ESCs and XENCs using Lipofectamine 3000 (L3000001, Thermo Fisher Scientific), respectively. Then GFP-positive cells were sorted using flow cytometry and diluted for monoclonal growth. DNA was extracted from the obtained monoclonal cells and subjected to PCR amplification and sequencing. Knockout-positive cells were selected for follow-up experiments.
For generation of Nodal knockout cell lines, gRNA sequence targeting (GCCCTCGTCACCGTCCCCTCTGG) Nodal’s exon1 were used for constructing sgRNA vector. Primers for Nodal sgRNA (Nodal-sgF: caccgccctcgtcaccgtcccctc and Nodal-sgR: aaacgaggggacggtgacgagggc) were annealed and the annealed product was ligated to linearized PX330-GFP by BbsI. The Vectors has been transfected into ESCs using Lipofectamine 3000 and GFP-positive cells were sorted using flow cytometry and diluted for monoclonal growth. DNA was extracted from the obtained monoclonal cells and subjected to PCR amplification and sequencing. Knockout-positive cells were selected for follow-up experiments.
For generation of p53 knockout ESC line, the sgRNA sequence for p53 mutation was cloned into the PX330-GFP vector (addgene, #48138) using CRISPR-Cas9 system59. The vector was transfected into G4 ESCs by Lipofectamine 3000 (L3000001, Thermo Fisher Scientific). Three days after transfection, GFP-positive cells were sorted and plated on 6-well plate. Colonies were picked, and the knockout regions were amplified by PCR using primers (F: CATCCAGGCGGGAAATAGAGAC; R: CCTGACTGTGTGTAAACTAGGC) and sequenced. By aligning with the wild-type sequence, homozygous knockout cell colonies were identified and selected for further study.
ESCs were cultured in Dulbecco's Modified Eagle Medium (DMEM) (11960069, Thermo Fisher Scientific) with 15% (v/v) FBS (Gibco, ES cell qualified), 2 mM GlutaMAX (35050061, Thermo Fisher Scientific), 0.1 mM β-mercaptoethanol (21985-023, Thermo Fisher Scientific), 0.1 mM MEM non-essential amino acids (11140050, Thermo Fisher Scientific), 1 mM sodium pyruvate (11360070, Thermo Fisher Scientific), 1% penicillin–streptomycin (15140122, Thermo Fisher Scientific), 1000 IU LIF (130-099-895, Miltenyi Biotec), 1 µM PD0325901 (4423, Tocris), and 3 µM CHIR99021 (4192, Tocris). ESCs were cultured at 37 °C and 5% CO2 on gelatinized and feeder-covered tissue culture grade well plates, and passaged when 80% confluency is achieved.
TSCs were derived from E3.5 blastocysts flushed from the uterus of 5-weeks-old female CD1 mouse15,60. The blastocysts were cultured on mitotically inactivated mouse MEF cells (feeder cells) with TSC culture medium: advanced RPMI 1640 (11875-093, Thermo Fisher Scientific) supplemented with 20% (v/v) FBS (Gibco, ES cell qualified), 2 mM GlutaMAX (35050061, Thermo Fisher Scientific), 0.1 mM β-mercaptoethanol (21985-023, Thermo Fisher Scientific), 1 mM sodium pyruvate (11360070, Thermo Fisher Scientific), 1% (v/v) penicillin–streptomycin (15140122, Thermo Fisher Scientific), 25 ng per mL recombinant human FGF4 (235-F4-025, R&D) and 1 µg per mL heparin (07980, Stem Cell). Until the outgrowth formed on day 4, they were subsequently disaggregated by incubated in 0.1% trypsin-EDTA for 5 min in the incubator. Add fresh mouse 70% embryonic fibroblast-conditioned medium containing FGF4 and heparin to stop the reaction and return to the incubator. Replace the medium every other day until TS cell colonies can be observed, and change medium with TSC culture medium to maintain the cells. TSC expressing EGFP (TSC-EGFP) cell lines were derived from wild-type TSCs which were transfected with the PB-UBC-EGFP vector by JetPrime (114-15, Polyplus transfection). TSCs were cultured at 37°C and 5% CO2 on gelatinized and feeder-covered tissue culture grade well plate and passaged when 80% confluency is achieved. Culture medium was changed daily.
XENCs were derived from E3.5 blastocysts flushed from the uterus of 5-weeks-old female 129 mouse using modified XENC conditions61. Mouse blastocysts were cultured on feeder cells until they formed an outgrowth on day 4 that was subsequently disaggregated by incubated in 0.1% trypsin-EDTA for 5 min in the incubator. Add fresh mouse ES cell medium without PD0325901 and CHIR99021 to stop the reaction, and replace the medium every other day until XEN cell colonies can be observed. XEN cell colonies was maintained with standard XEN medium: advanced RPMI 1640 (11875-093, Thermo Fisher Scientific) supplemented with 15% (v/v) FBS (Gibco) and 0.1 mM β-mercaptoethanol (21985-023, Thermo Fisher Scientific), 1% penicillin–streptomycin (15140122, Thermo Fisher Scientific). XENC-EGFP cell line was derived directly from Actin-EGFP mouse blastocyst. For feeder-free culture, XENCs were maintained on tissue culture grade well plate coated with gelatin. XEN cells were cultured at 37 °C and 5% CO2. Passaged once they reached 90% confluency. Culture medium was changed daily.
Generation of self-assembled embryos
ESCs, which reached 80% confluency, were washed once with PBS (14190-094, Gibco) and were incubated for 5 min at 37 °C in TrypLE (12605010, Thermo Fisher Scientific). TSCs and XENCs were dissociated to single cells by incubation with 0.1% trypsin-EDTA (25300054, Thermo Fisher Scientific) at 37 °C. Cells were pelleted by centrifugation at 1000 rpm for 5 min. The pellet was re-suspended in reconstructed embryo medium by pipetting to single cells. The cells were counted automatically with automated cell counter.
For ETX-embryoids, mix ESCs, TSCs, and XNECs at cell number of 1 × 105, 1 × 105, and 2 × 105, respectively (for ETS-embryoids, mix ESCs and TSCs at cell number of 1 × 105 and 1 × 105, respectively; for EXE-embryoids, mix ESCs, and XENCs at cell number of 1 × 105 and 1 × 105, respectively) with 2 mL of reconstructed embryo medium per 35 mm non-treated cell culture dish. Move the dish on the horizontal rotators at 37 °C, 5% CO2, and 100% humidity. The rotation rate is at 60 rpm per min. The reconstructed embryo medium includes 39% advanced RPMI 1640 (11875-093, Thermo Fisher Scientific) and 39% DMEM (11960069, Thermo Fisher Scientific) supplement with 17.5% FBS (Gibco, ES cell qualified), 2 mM GlutaMAX (35050061, Thermo Fisher Scientific), 0.1 mM β-mercaptoethanol (21985-023, Thermo Fisher Scientific), 0.1 mM MEM non-essential amino acids (11140050, Thermo Fisher Scientific), 1 mM sodium pyruvate (11360070, Thermo Fisher Scientific), 1% penicillin–streptomycin (15140122, Thermo Fisher Scientific). Changed medium with 2 mL fresh reconstructed embryo medium every day.
EXE-embryoids formed consistently and efficiently, the functional experiments can be performed without selection of regular or irregular structures. For the functional experiments of ETX-embryoids and ETS-embryoids, we selected the regular structures based on their morphology, and the appropriate proportions and positions of ESC and TSC compartments by indication of TSC-EGFP under stereo fluorescence microscope.
Wild-type embryo recovery and in vitro culture
Blastocysts were recovered from E4.5 superovulated pregnant female mice by uterine flushing with M2 (MR-015-D, Millipore). Culturing embryos in IVC medium after removal of the mural trophectoderm in vitro on 8-well μ-Slides (80826, Ibidi)62. For recovery of E5.5, E5.75, and E6.5 embryos, dissection of the decidua from the uterus describe as the reported protocol63. For EPI-explants from CD1 mice were dissected on day E5.0 as previous reported28 and cultured with ETX-embryoids medium in vitro.
Mouse embryos and reconstructed embryos were fixed with 4% paraformaldehyde (DingGuo, AR-0211) at 4 °C for 20 min and washed three times with a wash buffer (PBS containing 0.1% Tween-20). Then, the embryos were permeabilized with 0.5% Triton X-100 (H5142, Promega) for 30 min at room temperature and were incubated with primary antibodies in blocking buffer (3% BSA, 0.3% Triton X-100) overnight at 4 °C. After being washed to remove unbound primary antibodies, cells were incubated with secondary antibody in blocking buffer overnight at 4 °C. Cell nucleus were stained with DAPI, followed by twice washes with washing buffer, then were mounted in Fluoroshield Mounting Medium with DAPI (104140, abcam). Images were captured with a Nikon A1 confocal microscope.
Imaging with processing and analysis
Images for mouse embryos and reconstructed embryos were acquired using a Nikon A1 confocal microscope with a 20 × or 40 × objective. All analyses were carried out using open-source image analysis software ‘‘Fiji’’. Tissues’ volume and cell numbers for reconstructed embryos and wild-type embryos were estimated and immunofluorescence intensity measurements for PCX distribution analysis was also performed using Fiji software9.
High-throughput single-cell qPCR and data processing
For single-cell isolation, certain cells at different developmental stages (0, 24, and 84 h) were collected from two types of ETX-embryoids, which were reconstructed with Lefty1-mCherry XENC (LC-ETX-embryoids) and BVSC ESC (BVSC-ETX-embryoids) reporter cell lines, respectively. To isolate the single cells, we only select the LC-ETX-embryoids with DVE/AVE-like tissues identified by asymmetry expression of the mCherry proteins, and select the BVSC-ETX-embryoids with asymmetry expression of the mVenus proteins in the ESC compartment near the boundary between the ESC- and TSC compartments. For LC-ETX-embryoids, 0, 24, and 84 h LC negative ESC-derived cells (LC- XEN) as well as 84 h positive ESCs (BVSC+ ES) from the opposite side of LC- XEN were collected. For BVSC-ETX-embryoids, 0, 24, and 84 h BV negative ESC-derived cells (BVSC- ES) as well as 84 h positive ESCs (BVSC+ ES) from the opposite side of BVSC- ES were collected. In addition, single cells from TSC compartments in the ETX-embryoids assembled with BVSC-ESCs at 0, 24, and 84 h were collected based on EGFP reporter.
For single-cell separation, all ETX-embryoids were incubated in 0.1% trypsin-EDTA (Invitrogen, Carlsbad, USA) for 5 min at 37 °C and then transferred into M2 medium (MR-015-D, Millipore). After gentle repeated mouth pipetting for several times, single cells were isolated with a finely pulled glass tip. On average, 30–40 cells were collected for each type. Each cell was washed three times in Dulbecco’s phosphate-buffered saline (Invitrogen, Carlsbad, USA) containing 0.1% BSA (Sigma-Aldrich, MO, USA), and placed into reverse transcription-polymerase chain reaction (RT-PCR) master mix for lysis, sequence-specific reverse transcription, and pre-amplification, as described as previous report64.
For design and validation of primers, genes which regulate cell lineage differentiation (mainly from E3.5 to E6.5 stage) and participate in dominant signaling pathway (e.g., Wnt, Nodal signaling pathway) were selected, according to the embryogenesis of mouse. The mRNA sequences for each interested gene were retrieved from NCBI and only common regions were used for genes with different transcripts. Gene-specific qRT-primers were designed with Primer3 software within the length of 100–250 bp. All primers had been tested using cDNA of mouse embryos (mixture of E5.5 and E6.5) for amplification efficiency and specificity (listed in Supplementary Data 1).
Single-cell sequence-specific pre-amplification similar to previous report65. A total of 96 primer sets were pooled to a final concentration of 0.1 μM for each primer. Individual cells isolated from embryos were transferred into sterile microtubes loaded with 5 μL of RT-PCR master mix containing 2.5 μL of CellsDirect reaction mix (Invitrogen, Carlsbad, USA), 0.5 μL of primer pool, 0.1 μL of RT/Taq enzyme (Invitrogen, Carlsbad, USA), and 1.9 μL of nuclease free water (Invitrogen, Carlsbad, USA) in each tube. Tubes were immediately frozen on dry ice. After brief centrifugation at 4 °C, tubes were immediately placed in PCR machine. Cell lyses and sequence-specific reverse transcriptions were performed at 50 °C for 1 h. Afterwards, reverse transcriptase inactivation and Taq polymerase activation were achieved by heating to 95 °C for 3 min. Subsequently, in the same tube, cDNA went through 20 cycles of sequence-specific amplification by denaturing at 95 °C for 15 s, and annealing and elongation at 60 °C for 15 min. To avoid evaporation, the resulting products were stored at −80 °C.
For high-throughput microfluidic single-cell quantitative PCR, all preamplified cDNA products were validated by real-time PCR system (ABI 7500) using endogenous control gene Actinb, only threshold crossing (Ct) value within 9 to 12 were selected for subsequent experiment. Amplified single-cell samples were analyzed with SsoFast EvaGreen Supermix with Low ROX (Bio-Rad, California, USA) and individual qPCR primers in 96 × 96 dynamic arrays on a Biomark System (Fluidigm, San Francisco, USA). Ct values calculation were conducted with the BioMark Real-Time PCR Analysis software (Fluidigm, San Francisco, USA).
For Single-Cell Data Processing and Visualization, all raw Ct values obtained from the BioMark System were converted into Log2 relative expression levels by subtracting the values from the assumed background Ct value of 26. Samples with low or absent expression of endogenous control genes (Actinb and Gapdh) were excluded from subsequent analysis. PLS-DA was applied to the expression data to discriminate cell groups in different ETX-embryoids with R package mixOmics66. Hierarchical clustering was performed using Euclidean distances, and dendrograms were displayed along the rowscaled heatmaps using the fluidigmSC package. Box-plots and violin plots were generated with the origin 8.6 and R software.
BVSC ESC-Chimeric embryo production
We produced the BVSC ESC-Chimeric embryos by 8-cell embryo injection method by Piezo Micromanipulation67. To ensure the host embryos were injected before compaction, we collected the embryos at two-cell stage and cultured in vitro. To obtain two-cell stage embryos, 5-weeks-old female mice were superovulated by intraperitoneal injection of five international units (IU) of PMSG, followed by 5 IU HCG 46–48 h later, and mated with male mice. Two-cell stage embryos were collected by flushing the oviduct with M2 at E1.5. Embryos were washed in M2 (MR-015-D, Millipore) and then transferred into 10 μL KSOM (MR-020P-5F, Millipore) drops covered with mineral oil on a tissue culture dish. The embryos were maintained at 37 °C with 5% CO2 in an incubator.
About 15 ES cells were injected into 8-cell stage embryos by Piezo Micromanipulation67,68. Eight-weeks-old CD1 females mated with vasectomized males were used as pseudopregnant mice. Injected blastocysts were transferred into the uterus of pseudopregnant females at 2.5 days post coitum (dpc). Embryos at the morula stage with injected ESCs were transferred into the oviduct of 0.5 dpc recipients. And we transferred 14-16 embryos per recipient. At E6.5, we collected the chimeric embryos from deciduae as described above.
Embryo transfer and implantation evaluation
Eight-weeks-old CD1 females mated with vasectomized males were used as pseudopregnant mice. For reconstructed embryos, 36 h reconstructed spheres (ETX-, ETS-, and EXE-embryoids) were transferred into the uteri horns of pseudopregnant recipient CD1 female mice at 2.5 dpc or 3.5 dpc. Sixteen to twenty embryos were transferred per recipient. Implantation sites on Day 6.5 were identified and counted by intravenous injection of 100 μL 1% Chicago Sky Blue solution. The length and radius of each decidua was measured using image analysis software, and the volume was calculated from these measurements as V = πr2l.
HE staining and immunostaining of implantation sites
To examine the development potential of self-assembled embryos, we collected decidua from diverse stage, including 48, 72, and 84 h after transplantation. These reconstructed (ETX, EXE, and ETS) embryos samples were fixed with 4% paraformaldehyde for overnight at 4 °C, dehydrated with gradient alcohols, transferred into xylene and embedded in Paraffin. We used E5.5, E6.0, and E6.5 wild-type embryos as control. Samples were sliced to 5 μm thickness, stained with hematoxylin and eosin, and observed under a microscope. Deparaffinized rehydrated samples were subjected to heat-induced epitope retrieval in citrate buffer at around 95 °C by a microwave oven for 10 min, following cooled down to room temperature and rinsed twice in PBS with 3 min by twice. Permeabilization was performed with 0.5% Triton X-100 in PBS for 20 min at room temperature. After permeabilizing, specimens were washed in PBS for three times (3 min each). Then samples were blocked for 30 min with 5% bovine serum albumin (BSA) in PBS and incubated with primary antibodies against Rabbit anti-CK (ab9377, Abcam), Rabbit anti-COX2 (ab15191, Abcam), Rabbit anti-Laminin (L9393, Sigma), Goat anti-Gata4 (sc-1237, Santa Cruz), or Mouse anti-PL1(sc-376436, Santa Cruz) at 4 °C overnight. The following day, slices were washed three times in PBS for 5 min and incubated with secondary antibody for 30 min at 37 °C. Secondary antibodies were labeled with Alexa Fluorophore 488 or 594 (Invitrogen). Subsequently, sections were rinsed six times in PBS with 5 min each and mounted with Fluoroshield mounting medium with DAPI (ab104140, Abcam). Slides were kept at −20 °C until observed. Images were captured with a Leica fluorescent microscope.
In situ hybridization
In situ hybridization with digoxygenin (DIG) was performed on cryosections52. Mouse-specific cRNA probes for Dtprp were used for hybridization. Sections hybridized with sense probes served as negative controls. Frozen sections (8–10 μm) were adhered to poly-l-lysine coated slides (Citotest Labware Manufacturing Co., Ltd, Jiang Su, China) and stored at −80 °C until used. Sections were placed on a slide warmer (37 °C) for 2 min and then rehydrated in PBS, post-fixed in 4% PFA for 15 min at 4 °C, treated with proteinase K (15 μg per mL for 5 min at room temperature), 0.25% acetylated for 10 min and hybridized with DIG-labeled probes overnight at 65 °C. Two 65 °C post-hybridization washes were carried out followed by two washes in 1 × MABT, and 30 min RNase treatment (20 μg per mL) at 37 °C. Sections were blocked for 1 h, and incubated overnight in block with anti-DIG antibody (1:2500, Sigma-Aldrich). After washing, color was developed using NBT/BCIP until a brown precipitate was visible. Slides were counterstained with nuclear fast red, dehydrated and cleared in xylene, and mounted in cytoseal mounting medium. Photographs were taken promptly before fading of the INT/BCIP precipitate occurred.
Genotype identification of the transferred self-assembled embryos
Genomic DNA was extracted from DsRed-ESCs, EGFP-TSCs, and ETX-embryoids isolated from decidua tissues using a TIANamp Micro DNA Kit (DP316, Tiangen) according to the manufacturer’s instructions. The diagnostic primer set EGFP (5ʹ-AGGACGTCATCAAGGAGTTC-3ʹ, 5ʹ-CAGCCCATAGTCTTCTTCTG-3ʹ) and DsRed (5ʹ-GTGCTTCAGCCGCTACCC-3ʹ, 5ʹ-AGTTCACCTTGATGCCGTTCT-3ʹ) were used to identify the region of the cells and the samples by PCR. The thermal profile was 95 °C for 5 min, 35 cycles of 95 °C for 30 s, 60 °C for 30 s, and 72 °C for 20 or 40 s, and a final cycle at 72 °C for 5 min.
Statistical analyses were processed on GraphPad Prism 7.0 software (GraphPad Software, La Jolla, CA) for Windows (including single-cell Log2 expression data). Data had been checked for normal distribution and equal variances with F-test before each parametric statistical test was performed. Where appropriate, two-tailed Student’s t-tests were performed with Welch’s correction if variance between groups was not equal. Error bars represent standard error of s.e.m or s.d. as specified. Figure legends indicate the number of independent experiments performed in each analysis. Each experiment had been repeated for reproducibility.
Tissue volume (Figs. 1i and 7c, and Supplementary Fig. 4h), percentage and number calculation (Figs. 2h, 2i, 3k, 4c, 4f, 5e, 5f, 7b, 7m, and 7n; Supplementary Figs. 2d, 3c, 4g, 8d, 11f, 12a and 12g) was determined using Excel. The significance analysis was performed using t-test by GraphPad Prism. Bar graphs were drawn by Excel and GraphPad Prism, and scatterplots were plotted using GraphPad Prism.
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
The data supporting the findings of this study are available from the corresponding author on reasonable request. Source data for single-cell quantitative PCR experiments (Figs. 1h, 5g, 5i, 5j, 6d–g and 6i; Supplementary Fig. 9f, 9g, 10a, and 10b) and the gene list with corresponding sequences (Supplementary Fig. 10a) have been provided in Supplementary Data 1. Qualifications of the data (Figs. 1i, 2h, 2i, 3k, 4c, 4f, 5e, and 5f; Supplementary Figs. 2d, 3c, 4g, 4h, 8d, and 12f) and embryo transplantation data (Figs. 7b, 7c, 7m, and 7n; Supplementary Fig. 11f, 12a) have been provided in Source Data.
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We thank Andras Nagy, Kristina Vintersten, and Marina Gertsenstein G4 and G4-ACTB-DsRed-MST ESCs; Mitinori Saitou for BVSC ESC line; Shaorong Gao for Actin-GFP mice. We thank Ivan Bedzhov (Max Planck Institute for Molecular Biomedicine, Germany) for suggestion of Oct4 immunostaining for mouse embryos. This work was supported by China National Basic Research Program (2016YFA0100202), National Natural Science Foundation of China (31571497, 31601941, and 31772601), Plan 111 (B12008) and Research Programs from the State Key Laboratories for Agrobiotechnology, China Agricultural University (2017SKLAB1-2 and 2018SKLAB6-20).