By grafting beads soaked in growth factors or specific inhibitors of signaling pathways into developing embryos it is possible to directly test their effects in vivo. In this protocol beads are grafted into the limb bud to determine the effects of these molecules on gene expression and signal transduction.
Using chicken embryos it is possible to test directly the effects of either growth factors or specific inhibitors of signaling pathways on gene expression and activation of signal transduction pathways. This technique allows the delivery of signaling molecules at precisely defined developmental stages for specific times. After this embryos can be harvested and gene expression examined, for example by in situ hybridization, or activation of signal transduction pathways observed with immunostaining.
In this video heparin beads soaked in FGF18 or AG 1-X2 beads soaked in U0126, a MEK inhibitor, are grafted into the limb bud in ovo. This shows that FGF18 induces expression of MyoD and ERK phosphorylation and both endogenous and FGF18 induced MyoD expression is inhibited by U0126. Beads soaked in a retinoic acid antagonist can potentiate premature MyoD induction by FGF18.
This approach can be used with a wide range of different growth factors and inhibitors and is easily adapted to other tissues in the developing embryo.
Avian embryos have provided a powerful tool for the study of development for many years1. One of their most useful characteristics is that they are relatively easy to manipulate. External development makes it possible to open the egg to access the embryo and perform various micromanipulations including examples such as the classic quail-chick chimera system for studying cell fate2,3, the injection of retroviruses for overexpression in specific tissues during development4,5 and explant culture to identify developmental signaling sources6. More recently chimeras generated between unlabeled hosts with grafts from a transgenic chicken line expressing GFP has shown that the combination of classical grafting and genetic modification can provide important insights into development7,8.
The ease with which the avian embryo can be manipulated has made it an excellent model for studying limb development9. Application of specific growth factors to developing limbs in vivo has been instrumental in identifying factors that alter limb patterning10,11 and continues to provide insights into this process12. This approach has also been used to study the factors that regulate muscle development and has uncovered roles for numerous signals such as Wnts13, BMPs14 and HGF15.
Recently this technique has been used to investigate the signals controlling myogenic gene expression in the limb bud and has shown that interactions between FGF18 and retinoic acid can control the timing of MyoD expression16. Using a combination of growth factors and small molecules that can be loaded onto beads and then grafted directly into specific tissues at defined developmental stages gives the opportunity to intervene at almost any time and region during development. This has been used to investigate many processes including somite patterning17,18, neural specification19, neural crest migration20 and axis extension21.
Here we describe a method for grafting beads soaked in either growth factors or inhibitors into developing chicken limbs. This has been used to determine the effects of these signals on myogenesis by analyzing muscle specific gene expression with in situ hybridization. We describe grafts using either heparin soaked beads, which are used for growth factors, or AG 1-X2 beads for small hydrophobic molecules such as retinoic acid or small molecule inhibitors of specific signaling pathways. However other beads are also available which have been used to deliver both FGFs22 and Shh23.
Ethics Statement: All these experiments follow the animal care and ethical guidelines of the University of Nottingham.
1. Preparation of Heparin Beads for Grafting
2. Preparation of AG 1-X2 Beads for Grafting
3. Preparing Tungsten Needles
4. Preparing Embryos for Bead Grafts
At HH stage 21 MyoD is not expressed in developing limb myoblasts although staining can be seen in the myotome of the developing somites (Figure 1A). Figure 1B shows in situ hybridization for MyoD 6 hr following an FGF18 bead graft. MyoD is induced in myoblasts close to the bead while there is no expression in the contralateral limb. Co-grafting a bead soaked in U0126, a specific inhibitor of MEK, blocks FGF18 induction of MyoD (Figure 1C). Similarly grafting a U0126 bead at HH stage 21 and looking for MyoD expression after 24 hr reduces the endogenous expression of MyoD compared with the untreated contralateral limb (Figure 1D, E).
In limb buds at HH stage 19 FGF18 does not induce MyoD (Figure 1F). However co-grafting of beads soaked in FGF18 and the retinoic acid antagonist BMS493 can overcome this and ectopic MyoD is detected (Figure 1G)
To confirm that FGF18 is acting through MEK embryos were harvested 1 hr after bead graft and immunostained for phosphorylated ERK, the target of MEK. Figure 1H shows a brightfield image of an FGF18 bead 1 hr after grafting while Figure 1I shows that FGF18 induces rapid phosphorylation of ERK around the grafted bead. Figure 1J shows an overlay of these images. Control beads soaked in 0.1% BSA do not induce ERK phosphorylation (Figure 1K, L, M)
Figure 1. MyoD expression in limbs is regulated by FGF18 and retinoic acid through ERK phosphorylation. Unmanipulated control limbs at HH stage 21 do not express MyoD (A) but premature expression is detected 6 hr after grafting an FGF18 bead (B). Co-grafting FGF18 and U0126 beads blocks this induction (C). Endogenous MyoD expression is seen at HH stage 21 (D) but this is blocked by grafting beads soaked in U0126 (E). In earlier limb buds premature MyoD expression is not induced by FGF18 (F) but is induced by co-grafting beads soaked in FGF18 and the retinoic acid antagonist BMS493 (G). FGF18 beads grafted into HH21 limbs induce ERK phosphorylation after 1 hr: brightfield (H), fluorescent (I) and merged (J) images of an HH21 limb immunostained for anti-phosphoERK. Control beads soaked in BSA do not induce ERK phosphorylation: (K), fluorescent (L) and merged (M) images of an HH21 limb immunostained for anti-phosphoERK. This figure has been modified from Mok et al, 201416. Black asterisks: heparin beads; white asterisks: AG 1-X2 beads; arrows show ectopic MyoD expression in limb buds. Please click here to view a larger version of this figure.
The use of bead grafts applied directly to developing tissues in ovo is a powerful tool to dissect the role of growth factor signaling during development giving unparalleled control over the developmental stage at which they are applied and the duration of exposure.
The choice of bead for each type of molecule is important. Small hydrophobic molecules, such as the inhibitors described here and retinoic acid, usually bind well to derivatized AG 1-X2 beads although it is necessary to test the effectiveness of each inhibitor on these beads empirically. Similarly, for growth factors it may be necessary to test different types of bead. Some beads are transparent and so can be hard to visualize during the manipulations but a short treatment with phenol red followed by a rinse in PBS will label them for long enough to perform the graft.
When preparing beads, particularly those which have been soaked with inhibitors, it is important to protect them from light as far as possible. During their initial treatment and during manipulation they should be covered and only removed when beads are being transferred. It is best to use freshly thawed aliquots as some of these reagents are unstable and can give misleading negative results if not stored properly. It is also important not to leave them soaking in phenol red for too long before grafting as this can reduce the effectiveness of the bead.
The concentrations used for these bead grafts, of both growth factors and drugs, are often very high; FGF18 beads are soaked in a concentration of 0.5 mg/ml and beads for small molecule inhibitors are often soaked at a concentration of 100 µM. Although this is much higher than the concentrations typically used to treat cells in solution this is necessary as the amounts of growth factors and drugs absorbed by beads and then released are hard to measure directly but presumably generate lower levels than this in vivo. As a result a range of concentrations must be tested for each molecule used to determine an effective dose.
This technique is also applicable to a wide range of other tissues, such as somites24, during development and can be used on embryos in ovo or in cultures, such as EC culture25. It is also possible to grow cultured cells which secrete specific growth factors as pellets which can then be grafted into developing embryos in the same way26.
The combination of accessibility, ease of manipulation and low cost makes chicken embryos an excellent model of development. As transgenic technologies are increasingly applied to avian species and genetically modified lines of both chickens7 and quails27 become available the combination of classical embryo grafting techniques with these modified birds is already providing novel insights into development8,28.
The authors have nothing to disclose.
This work was partly funded by a University of Nottingham Early Career award to DS. RM is funded by the Higher Committee for Education Development of Iraq.
Heparin acrylic beads | Sigma | H5263 | The acrylic-heparin beads used have been discontinued. However a replacement product is available, Heparin agarose beads, cat no H6508. These are transparent so harder to work with but can be stained with phenol red in the same way as AG 1-X2 beads, |
AG 1-X2 beads | Bio-Rad | 140-1231 | |
Affi Gel blue beads | Bio-Rad | 153-7301; 153-7302 | These beads have been used with a range of growth factors including Shh and FGFs and can be used to replace heparin beads |
FGF18 | Peprotech | 100-28 | Resuspend in PBS with 0/1% BSA, prepare single use aliquots of 0.5-1ul and store at -80°C. Batches and suppliers can vary so different concentrations should be tested to determine an effective dose. |
U0126 | Cell Signalling | 9903 | Make to 20mM stock in DMSO and store in single use aliquots at -80°C. Protect from light. |
BMS-493 | Tocris Biosciences | 3509 | Resuspend in DMSO and store in single use aliquots at -80°C. Protect from light. |
Black Indian ink | Windsor and Newton | 5012572003384 (30ml) | While alternatives to this product are available care should be taken as some inks are toxic to embryos |
Tungsten wire, 0.1mm dia. 99.95% | Alfa Aesar | 10404 | |
Penicillin / streptomycin | Sigma | P0781 | Dilute 100X in PBS/ink and PBS/FCS |