Proximal visceral endoderm and extraembryonic ectoderm regulate the formation of primordial germ cell precursors
© de Sousa Lopes et al; licensee BioMed Central Ltd. 2007
Received: 16 May 2007
Accepted: 20 December 2007
Published: 20 December 2007
The extraembryonic tissues, visceral endoderm (VE) and extraembryonic ectoderm (ExE) are known to be important for the induction of primordial germ cells (PGCs) in mice via activation of the bone morphogenetic protein (BMP) signalling pathway. We investigated whether the VE and ExE have a direct role in the specification of PGCs, or in an earlier event, namely the induction of the PGC precursors in the proximal posterior epiblast cells.
We cultured embryonic day (E) 5.75 to E7.0 mouse embryos in an explant-assay with or without extraembryonic tissues. The reconstituted pieces of embryonic and extraembryonic tissues were assessed for the formation of both PGC precursors and specified PGCs. For this, Blimp1:gfp and Stella:gfp transgenic mouse lines were used to distinguish between PGC precursors and specified PGC, respectively. We observed that the VE regulates formation of an appropriate number of PGC precursors between E6.25–E7.25, but it is not essential for the subsequent specification of PGCs from the precursor cells. Furthermore, we show that the ExE has a different role from that of the VE, which is to restrict localization of PGC precursors to the posterior part of the embryo.
We show that the VE and ExE have distinct roles in the induction of PGC precursors, namely the formation of a normal number of PGC precursors, and their appropriate localization during early development. However, these tissues do not have a direct role during the final stages of specification of the founder population of PGCs.
In the postimplantation mammalian embryo, germ cells are the first embryonic lineage to become fate-restricted. This was thought to occur during gastrulation at embryonic day 7.25 (E7.25) in the mouse, when a population of about 40 founder primordial germ cells (PGCs) present at the base of allantois are detected. These PGCs exhibit expression of several genes including Dppa3 (or Stella or PGC7) and Akp2 (or tissue non-specific alkaline phosphatase, TNAP) (reviewed by ). This view has recently been challenged by the unexpected observation of a distinct PGC precursor population present in the embryo already at E6.25–E7.25 . The PGC precursors express Prdm1 (or Blimp1) and are present in the proximal-posterior epiblast as a row of cells adjacent to the extraembryonic ectoderm. The population of PGC precursors increases from about 6 cells at E6.25 to about 40 cells by the time of specification around E7.25. The initial 6 Blimp1-positive cells may be derived from epiblast cells already present in the posterior part of the embryo; the rest probably derives from epiblast cells scattered throughout the proximal epiblast, but moving to the posterior part of the embryo during gastrulation [3, 4].
The visceral endoderm (VE) and the extraembryonic ectoderm (ExE) play an important role in the emergence of PGCs. This was demonstrated by the observation that epiblast cells isolated from E6.0 embryos failed to develop any specified TNAP-positive PGCs, unless they were cultured either on feeder STO cells, or in the presence of both VE and ExE [5–7]. The discovery of the existence of a population of PGC precursors compelled us to investigate whether the VE and ExE were directly involved in the specification of PGCs. For this purpose, we used two recently generated transgenic mouse lines, Blimp1:gfp and Stella:gfp, which allowed us to distinguish between PGC precursors (Blimp1-positive) and specified PGCs (Blimp1-positive and Stella-positive) [2, 8]. We demonstrate that the proximal VE and ExE contribute respectively to the generation of the appropriate number of PGC precursors in their correct location between E6.25–E7.25. More importantly, proximal VE and ExE were not only necessary for the induction of PGC precursors, but also sufficient to induce PGC fate in distal epiblast cells.
The VE is required for the formation of Blimp1-positive PGC precursor cells
The ExE prevents ectopic induction of Blimp1-positive PGC precursors
We also studied whether the ExE was involved in formation of PGC precursors or in the subsequent commitment of PGC precursors to PGCs. For this we examined the number of PGC (and PGC precursors) in E5.75–E6.0 Blimp1:gfp, Stella:gfp and ΔPEOct4:gfp explanted embryos cultured in the absence of ExE (Fig. 1A,G–J). After 1 day of culture, similar to whole Blimp1:gfp embryo explants, Blimp1(GFP)-positive cells were observed only in the VE of -ExE explants (white arrow in Fig. 1E,G). However, after 3 days of culture of -ExE explants (n = 13/16), Blimp1(GFP) was also downregulated in the VE, but the epiblast-derivative was entirely Blimp1(GFP)-positive (red arrow in Fig. 1H). Note that the dimensions of the epiblast-derivative in both whole and -ExE explants are similar (cartoon in Fig. 1F,H).
When Stella:gfp or ΔPEOct4:gfp E5.75–E6.0 embryos were cultured for 3 days, no GFP expression (indicative of specified PGCs [8, 9]) was observed in whole (Fig. 1I,J) and -ExE explants (bottom left inserts in Fig. 1I,J), suggesting that specification of PGCs had not yet occurred in vitro. After 4 days of culture, the Blimp1(GFP)-positive cluster in the explanted whole embryos gave rise to TNAP-positive PGCs (Fig. 1K), whereas the Blimp1(GFP)-expressing cells in -ExE explants remained TNAP-negative (data not shown). This suggested that the Blimp1(GFP)-positive cells that populated the epiblast in the -ExE explants are either no genuine PGC precursors, or if they are PGC precursors, they may need additional signals to commit to the PGC lineage. In any case, these experiments demonstrate that the ExE is (directly or indirectly) important for the restriction of Blimp1(GFP) induction in the epiblast by the VE.
VE is necessary for the formation of PGC precursors but not for the subsequent PGC-specification event
The absence of Blimp1(GFP)-positive PGC precursor cells in E5.75–E6.0 Blimp1:gfp -VE explants could be a secondary effect due to defects in the initiation of morphogenetic movements associated with gastrulation. Therefore, we cultured slightly older gastrulating embryos (E6.75–E7.0), which have a distinct Blimp1(GFP)-positive cluster of ±20 PGC precursors (Fig. 2A and ) after having removed the still Blimp1(GFP)-positive VE (-VE). After 3 days in culture, the number of PGCs (Stella-positive and TNAP-positive) observed in Blimp1:gfp E6.75–E7.0 -VE explants was reduced compared to explants from whole embryos, but more importantly, the number of Blimp1(GFP)-expressing cells was also correspondingly reduced by half (±40 cells in the whole embryo explant compared to ±20 cells in the -VE explant) (Fig. 2B–J). Note that some of the Blimp1(GFP)-positive cells were small and probably entering apoptosis (contained fragmented DAPI-positive nucleus). These smaller cells failed to upregulate Stella, but were positive for TNAP (including a TNAP-positive cytoplasmic spot) (Fig. 2B,E,F,I,J). In agreement, we observed higher levels of apoptosis using the TUNEL-assay in the -VE explants when compared to whole explants (data not shown).
Notably, the PGC precursors present in the -VE explants undergo specification to PGCs, even though the PGC precursor cluster was rather reduced in size (Fig. 2B–J), indicating that the size of the cluster is not important for specification. Also unexpected was the fact that some of those PGCs acquired a migratory phenotype and were moving out of the PGC-cluster, similarly to PGCs generated from whole E6.5 embryo-explants (asterisks in Fig. 2C,F) and therefore do not seem to require signals from the VE to do so.
Epiblast cells need to be posterior to become PGCs
The ectopic expression of Blimp(GFP) in the -ExE explants derived from E5.75–E6.0 Blimp1:gfp embryos raised the possibility that the ExE may be critical for regionalizing the embryo at E5.75–E6.0, so that the Blimp1-positive PGC precursors can only emerge posteriorly. To investigate this in more detail, we cut E5.75–E6.0 transgenic Cerl:gfp embryos  longitudinally though the long left-right (L-R) axis (Fig. 3A,B). Cerberus-like (Cerl) is an anterior visceral endoderm (AVE) marker  and therefore in Cerl:gfp transgenic embryos GFP expression is present exclusively in the anterior region, allowing clear identification of the embryonic axes (Fig. 3B,C).
The two embryo-halves, each containing epiblast, VE and ExE, were cultured separately for 4 days. After culture, both embryo halves were stained for alkaline phosphatase-activity to assess the presence of TNAP-positive specified PGCs. Notably, the explants-pairs that contained PGCs only exhibited them in one of the explant-halves (Fig. 3D,E) invariably the posterior part (Cerl(GFP)-negative). Only one explant-pair (n = 1/30) showed PGCs in both explant-halves (Fig. 3E). Our data indicates that the anterior VE and anterior ExE were not able to support the formation of PGCs and may even play an active role in repressing Blimp1 expression.
Proximal VE and ExE are sufficient to induce PGC formation de novo in distal epiblast cells at E6.75
To exclude the possibility that the induced PGCs resulted from contamination of proximal epiblast cells present in the ExE, we made reconstituted-embryos using ROSA26:LacZ distal epiblast and wild type VE and ExE. These reconstituted-embryos showed that the newly induced TNAP-positive PGCs are LacZ-positive, demonstrating that the PGCs indeed originated from the ROSA26:LacZ distal epiblast (Fig. 4H–J).
PGC precursors still need a specific niche to undergo PGC specification
Regionalization of the embryo by ExE (and VE) regulates the formation of PGC precursors posteriorly
At E5.5, the anterior and posterior ExE exhibit already different characteristics important for the correct patterning (and migration) of the AVE and the subsequent patterning (and migration) of the epiblast [13, 14]. At E5.75, the ExE may no longer influence the migration of the AVE, but it still plays a crucial role in regionalizing the epiblast, allowing gastrulation to take place. Indeed, Elf5 mutants, which contain no ExE, showed defects in embryonic patterning and failure to undergo gastrulation, despite the fact that the AVE is well specified . In agreement, our data also suggests that ExE plays a critical role at E5.75–E6.0 in regionalizing the epiblast with respect to where the PGC precursors can emerge.
The anterior ExE (and AVE) does not support development of PGCs and may even inhibit the formation of Blimp1-positive cells. However, it is well known that cells lying throughout the perimeter of the proximal epiblast at E6.0 can potentially give rise 40 hour later to PGCs in the posterior part of the embryo . These proximal cells move to the posterior part of the embryo due to the characteristic morphogenetic movements occurring during gastrulation. This directional movement allows some of these cells either to avoid signals from the anterior part of the embryo or to receive the necessary signals in the posterior part to become PGC progenitors.
Induction of PGC precursors (by the VE and ExE) occurs gradually between E6.25–E7.25
The VE at E5.75 shows asymmetric expression of several secreted factors, including Cerl and Lefty1 in the AVE, important for the formation of the anteroposterior axis [16, 17]. By contrast, there is little evidence for a direct role of the posterior part of the VE in embryonic patterning.
Our data suggests that the proximal-posterior VE plays a role in the generation of the full population of PGC precursors in the posterior part of the embryo. The role of the proximal-posterior VE could be that of promoting proliferation of the initial pool of PGC progenitors and therefore removing the VE would block cell division of the PGC progenitors, resulting in a smaller PGC population. Alternatively, as the VE is required for general cell survival in culture, we cannot exclude the possibility that normal numbers of PGC precursors were formed but died and could not be traced. However, we favor the possibility that when the VE is removed no more PGC precursors emerge but the ones allocated are able to undergo specification, although due to limitation of the culture system used some degenerate. Therefore, we propose that the proximal-posterior VE (together with the ExE) is actively recruiting additional PGC precursors from epiblast cells between E6.25–E7.25. This model also explains our observations that an E6.5 embryo is able to generate a PGC cluster de novo, when its original cluster is removed and that E6.5 distal epiblast cells when placed proximally (near a PGC precursor existing cluster) are still able to adopt a PGC fate (data not shown).
Are neighbouring somatic cells providing PGC precursors with the molecular niche needed for specification?
The results presented show that cross talk between the posterior epiblast, the proximal VE and ExE is needed for the emergence of Blimp1-positive PGC precursors. In addition, we also show that Blimp1-positive PGC precursors do not autonomously undergo specification to PGCs. It is likely that extra inductive signals present locally trigger the specification of Blimp1-positive PGC precursors. The proposed extra inductive signals most probably originate from the extraembryonic mesoderm (ExM) surrounding the PGC progenitor cluster and not the VE and ExE. In contrast to our ideas, Yoshimizu and colleagues (2001) observed that E6.75 dissociated epiblast cells could give rise to PGCs , however they cultured those epiblast cells in the presence of feeder cells, which could be providing the necessary signals for specification.
One of the candidate secreted molecules exclusively expressed by the ExM, and not by PGCs, at E7.5 is BMP4 . In addition, a necessary event during PGC specification is the downregulation of E-cadherin , followed by the acquisition of a motile phenotype. Both FGF and WNT signalling pathways are known to regulate gastrulation and can downregulate E-cadherin [20–24]. Further research will demonstrate whether the BMP, WNT or FGF signalling pathways are directly involved in PGC specification.
The recent evidence for a population of PGCs progenitors in the mouse embryo has compelled us to re-evaluate the role of the extraembryonic tissues in the formation of PGCs. Using transgenic mouse models in combination with an explant-assay, we determined that the extraembryonic tissues, VE and ExE, as part of their patterning role during gastrulation, are also responsible for the correct induction of PGC progenitors. However, the VE and ExE do not seem to be directly involved in the specification to PGCs as expected. We support the idea that not only the VE, but also the ExE is regionalized and that it is the cross talk in the proximal-posterior part of the embryo that allows the development of PGC progenitors at E6.25–E7.25. To date, little importance has been given to the posterior VE, in contrast to the AVE. The ExE and VE seem to play different roles, but both important for the normal development of PGC progenitors. Finally, being a PGC progenitor is not sufficient to become a specified PGC and signals probably secreted from the ExM should prove to induce PGC specification.
Animals, isolation of embryos and culture of explants
All experiments involving animals were approved by the Home Office, UK. Wild type mice and transgenic Blimp1:gfp, Stella:gfp, ΔPEOct4:gfp and Cerl:gfp mice were on a mixed C57BL/6 and CBA background, ROSA26:LacZ mice were C57BL/6. Noon of the day of vaginal plug was designated E0.5. Embryos were isolated at E5.75–E6.0 and E6.75–E7.0 in cold Dulbecco's minimal medium (DMEM, Invitrogen) supplemented with 7.5% fetal calf serum (FCS) and 10 mM HEPES. Blimp1:gfp embryos were selected from non-transgenic littermates under an Olympus IX71 inverted microscope (London, UK). If necessary, the VE was removed as described previously . Embryos were cut (1) longitudinally through the long L-R axis; (2) transversely at several heights in the presence of absence of the VE; or (3) parts of one or several different embryos were recombined using tungsten needles. Thereafter, they were cultured in DMEM+15% FCS at 37°C and 5% CO2 on air either on fibronectin (20 μg/ml) coated glass coverslips in 4 well culture plates (NUNC) or in suspension in 3 cm bacteriologic dishes. The two methods were used to obtain explants attached to a coverslip or to maintain the explants in suspension, respectively. The two methods gave similar results in terms of PGC development. Explants derived from E5.75–E6.0 embryos were cultured for maximal 4 days and explants derived from E6.75–E7.0 embryos for maximal 3 days. Fresh embryos and explants were imaged using an Olympus IX71 (London, UK) inverted microscope.
Immunofluorescence staining of explants on coverslips was performed essentially as described . The primary antibodies used were rat anti-GFP (1:500, Nacalai Tesque) and rabbit anti-PGC7/Stella (1:2000); and the secondary antibodies used were from Molecular Probes. Explants were imaged using an Olympus IX71 (London, UK) inverted microscope or a Bio-Rad Radiance 2000 confocal microscope (CA, USA).
Cytological stainings and histology
Some of the explants (grown in suspension or on coverslips) were used for detection of alkaline phosphatase-activity. Briefly, the explants were washed three times in PBS, kept 1 hour in 70% EtOH at 4°C, washed three times with distilled water and treated with an aqueous solution containing 1% veronal (Sigma), 0.12% MgCl2, 0.02 mg/ml α-naphtyl phosphate (Sigma) and 1 mg/ml Fast Red TR (Sigma).
Recombinates of wild type and ROSA26:LacZ embryos were fixed in 4% paraformaldehyde in PBS, stained for LacZ using standard procedures, embedded in Technovit 8100 (Heraeus Kulzer), sectioned (6 μm) and stained for alkaline phosphatase-activity using ASMX/Fast Red TR (Sigma) following manufacturer's instructions. Explants were imaged using an Olympus IX71 (London, UK) inverted microscope.
List of abbreviations
anterior visceral endoderm
bone morphogenetic protein
green fluorescent protein
primordial germ cells
tissue non-specific alkaline phosphatase
We thank J.A. Belo and M. Zernicka-Goetz for the use of Cerl:gfp transgenic mice, T. Nakano for anti-PGC7/Stella, M.E. Torres-Padilla for discussion, J. Deschamps and A. McLaren for reading the manuscript and C. Mummery for the use of lab space. This work was supported by the Netherlands Organization for Scientific Research (NWO, TALENT 809.67.024) to S.C.S.L., the Japan Society for Promotion of Science to K.H. and the Wellcome Trust (062801).
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