BMP-2 functions independently of SHH signaling and triggers cell condensation and apoptosis in regenerating axolotl limbs
© Guimond et al; licensee BioMed Central Ltd. 2010
Received: 25 June 2009
Accepted: 12 February 2010
Published: 12 February 2010
Axolotls have the unique ability, among vertebrates, to perfectly regenerate complex body parts, such as limbs, after amputation. In addition, axolotls pattern developing and regenerating autopods from the anterior to posterior axis instead of posterior to anterior like all tetrapods studied to date. Sonic hedgehog is important in establishing this anterior-posterior axis of limbs in all tetrapods including axolotls. Interestingly, its expression is conserved (to the posterior side of limb buds and blastemas) in axolotl limbs as in other tetrapods. It has been suggested that BMP-2 may be the secondary mediator of sonic hedgehog, although there is mounting evidence to the contrary in mice. Since BMP-2 expression is on the anterior portion of developing and regenerating limbs prior to digit patterning, opposite to the expression of sonic hedgehog, we examined whether BMP-2 expression was dependent on sonic hedgehog signaling and whether it affects patterning of the autopod during regeneration.
The expression of BMP-2 and SOX-9 in developing and regenerating axolotl limbs corresponded to the first digits forming in the anterior portion of the autopods. The inhibition of sonic hedgehog signaling with cyclopamine caused hypomorphic limbs (during development and regeneration) but did not affect the expression of BMP-2 and SOX-9. Overexpression of BMP-2 in regenerating limbs caused a loss of digits. Overexpression of Noggin (BMP inhibitor) in regenerating limbs also resulted in a loss of digits. Histological analysis indicated that the loss due to BMP-2 overexpression was the result of increased cell condensation and apoptosis while the loss caused by Noggin was due to a decrease in cell division.
The expression of BMP-2 and its target SOX-9 was independent of sonic hedgehog signaling in developing and regenerating limbs. Their expression correlated with chondrogenesis and the appearance of skeletal elements has described in other tetrapods. Overexpression of BMP-2 did not cause the formation of extra digits, which is consistent with the hypothesis that it is not the secondary signal of sonic hedgehog. However, it did cause the formation of hypomorphic limbs as a result of increased cellular condensation and apoptosis. Taken together, these results suggest that BMP-2 does not have a direct role in patterning regenerating limbs but may be important to trigger condensation prior to ossification and to mediate apoptosis.
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-β superfamily and were first discovered when ectopic cartilage and bone formation were induced by demineralized bone matrix implanted into soft tissues of animals [1, 2]. However, their biological roles go far beyond osteogenesis [3, 4]. BMPs have been extensively studied during the development of the vertebrate limb, which has long been recognized as an excellent experimental system to study the genes and signaling pathways involved in patterning complex structures.
The first stage in which BMPs were assessed in limb development is the establishment of the anterior-posterior limb axis. In amniotes, the posterior region of the forming limb bud is referred to as the zone of polarizing activity (ZPA) and is an organizer of the anterior-posterior patterning of developing limbs . When cells from the ZPA are grafted into the anterior region of a chick limb bud, polydactyly is induced [6, 7]. Previous studies have shown that sonic hedgehog (Shh) is expressed exclusively in the ZPA and that implanting Shh expressing cells, or beads of Shh, in the anterior limb bud is sufficient to reproduce the polydactyly induced with ZPA transplants [5, 8]. On the other hand, knockout mice for Shh display a major deficiency in the anterior-posterior patterning of their autopods which resemble a spike like structure . Thus, Shh appears to be a mediator for the patterning of the anterior-posterior axis of the limb [5, 8, 10]. Because of the restricted expression of Shh to the posterior margin, it remains unclear, however, whether Shh induces the limb polarity directly or through a secondary signal. BMP-2 has received much attention as a downstream target of Shh. Indeed, BMP-2 expression overlaps spatiotemporally with the expression of Shh in the early developing limb bud of mammalian and avian embryos [11–15] and can be induced in chick anterior wing buds by ectopic Shh expression [12, 13]. However, overexpression of BMP-2 alone does not reproduce the polydactyly obtained with Shh overexpression in chick embryos [16, 17]. Moreover, BMP-2 expression is maintained in the limb buds of Shh knockout mice . In addition, the polarity and digit identity is normal in mice with BMP-2 deficient limbs . Hence, these data show that BMP-2 is not essential to relay Shh signaling in developing limbs.
In more advanced limb developmental stages, BMP-2, BMP-4 and BMP-7 are all expressed in the interdigital (ID) tissue [11, 15, 19]. Extirpation experiments of ID tissues have shown that anterior-posterior identity is not a fixed property of digital primordia and that the ID tissues are important for digit patterning . Experiments with inhibitors of BMP signaling in ID tissue suggested that differential levels of BMPs in the ID mesenchyme may be important in directing digit patterning . However, a recent study  with conditional knockout for BMP-2, BMP-4 or BMP-7 showed that these BMPs are not essential as signals from the ID mesenchyme for specifying digit identity but that they mediate ID programmed cell death as previously reported [21, 22]. In the chicken, overexpression of dominant negative type I-A or type I-B BMP receptors (dnBMPR-IA or dnBMPR-IB), in embryonic hind limbs, reduced ID tissue apoptosis and resulted in webbed feet [23, 24]. On the contrary, application of BMP-2 or BMP-7 in the ID tissues accelerated and intensified apoptosis . In ducks  and bats , BMPs are also expressed in the ID tissues of developing digits. However, these animals have webbed autopods and apoptosis is absent in ID tissues, suggesting expression of BMPs could have other roles in digit formation.
One aspect that is clearly affected by the expression of BMP-2 in developing limbs is skeletal development [16, 17, 27–29]. It was shown, in chicks, that BMPs are needed for chondroprogenitor cell determination and/or condensation and subsequent differentiation into chondrocytes . In mice with BMP-2/BMP-4 deficient limbs, differentiation of condensed prechondrocytes into chondrocytes is delayed, indicating that a threshold level of BMPs is required to trigger chondrogenesis . In these mutants, the two posterior digits fail to form as a consequence of the misexpression of the SOX-9 gene. SOX-9, a High Mobility Group (HMG)-domain transcription factor, is the earliest marker of chondrogenesis , and a regulator of the type II collagen gene, which is a major constituent of cartilage [29, 32]. SOX-9 is a known target of BMP-2  and overexpression of BMP-2 in developing chick limbs induces SOX-9 expression which then stimulates cartilage formation .
Among tetrapod vertebrates, urodele amphibians (i.e. axolotls) have a unique developmental pattern of their limbs. Indeed, while amniotes and anurans develop their digits almost simultaneously with a slightly accelerated onset of posterior digit formation (digit 4 being the first digit to condense in mice) [34–36], urodeles show a reversed sequence with a more progressive/successive development of anterior digits followed by posterior digits [36, 37]. Although the order of digit development is different between the aforementioned animals, the end point is the same with similar digit identity in the mature limb . Moreover, even though there is no clearly defined ZPA per se in axolotl and newt, Shh is expressed, as in amniotes, in the posterior mesenchyme of their developing and regenerating limb buds [39–41]. The inhibition of Shh signaling with cyclopamine leads to an anterior-posterior truncation of autopod elements in the developing and regenerating axolotl limbs [42, 43]. In addition, overexpression of Shh in the anterior mesenchyme of regenerating limbs induces polydactyly , showing that as in amniotes, Shh has a morphogenetic property in patterning the anterior-posterior axis in developing and regenerating urodele limbs.
The present study addresses the role of BMP-2 during limb regeneration in axolotl. We report the first cloning of an axolotl full length BMP cDNA (BMP-2). We use cyclopamine, a pharmacological inhibitor of the hedgehog signaling pathway, to show that, as in mouse, BMP-2 is not likely to be the secondary signal of Shh. BMP-2 is expressed in the ID tissues of developing digits in virtually all tetrapod species [11, 15, 19, 24, 26, 45, 46] and the expression of SOX-9 in these digits is linked to BMP-2 expression [29, 30, 47, 48]. The fact that the sequential development/regeneration of digits in axolotl limbs is the opposite of that observed in other tetrapods (anterior digits form first in axolotls instead of the posterior digits), even though Shh expression is expressed on the posterior side of axolotl developing/regenerating limbs, allowed us to assess whether the expression of BMP-2 and SOX-9 correlated with digits appearance (as they condense) or whether their expression correlated with Shh signaling in conditions where it was normal or inhibited. The effect of BMP-2 or Noggin (a general BMP inhibitor) overexpression on regenerating digits was also assessed.
Cloning and analysis of BMP-2
The axolotl full-length cDNA encoding BMP-2 was cloned, sequenced and compared to the sequence of other vertebrates. Several BMP-2 clones were isolated from an axolotl cDNA library. The longest clone of 2228 bp [GenBank: EU339232.1] comprising an open reading frame (ORF) of 1188 bp was selected. The analysis of this ORF, using NCBI-BLAST, showed a highly conserved sequence homology of the BMP-2 ORF with that of other species: 83% identity to human; 83% to mouse; and 67.3% to Xenopus laevis. Moreover, the 3' UTR of the BMP-2 gene was highly conserved with that of other species (data not shown).
The translated ORF of axolotl BMP-2 has a predicted amino acid sequence of 395 amino acids (Additional File 1: Figure S1) that varies by less than 1% in length when compared to that of human, mouse and Xenopus laevis. The amino acid sequence derived from the ORF also showed a highly conserved protein homology between species: 73% with human, 72% with mouse, and 68% with Xenopus laevis and resulted in an expected value (E-value) of less than 1e-164 when blasted in Gen Bank. Seven highly conserved cysteine residues characteristic to all members of the TGF-β super family [49, 50] are also present (Additional File 1: Figure S1 shaded amino acids).
BMP-2 and SOX-9expression during limb development
Whole-mount in situ hybridization was performed on developing forelimbs of axolotl from developmental stages 41 to 53. The nomenclature of Nye et al.  was used to determine the staging and to label the digits of the forelimb. Digit 1 is the anterior most (corresponding to the index side in human) and digit 4 the posterior most.
Effects of blocking Shhsignaling in developing digits
As described above, at stage 47, BMP-2 and Shh expression are on opposite sides of the developing limb bud (Figure 1; first column). It has been clearly demonstrated in mouse that BMP-2 is not essential for digit identity . It was shown (in knockout mice for Shh) that Shh is not essential for chondrogenesis and is dispensable for BMP-2 expression . Based on these observations, we tested, in axolotl, whether BMP-2 expression is independent of Shh signaling. The hedgehog pathway antagonist cyclopamine  was used to determine whether BMP-2 expression is independent of Shh signaling. The expression of BMP-2 and SOX-9 were assessed in limbs of animals treated with 2 different concentrations of cyclopamine that were shown in a previous study to prevent the formation of posterior digits . In the aforementioned study, the digits that remained after cyclopamine treatment were identified as follows: when 2 digits remained after treatment, they were found to be digits 1 and 2, and when only 1 digit remained (the result of a higher concentration of cyclopamine), it was identified as digit 1 . In the present study, cyclopamine treatment was initiated at developmental stage 41 which corresponds to the onset of Shh expression [40, 51]. We confirmed that the expression of Shh at various limb development stages (data not shown) was has it had been reported previously by two other groups [39, 40]. The group of Imokawa et al. also reported that Shh is expressed as late as the 2-3 digit stage  which corresponds to stage 51-52 based on Nye et al. . The expression of BMP-2 and SOX-9 was assessed after 14 (stage 51) and 21 (stage 53) days of treatment to see whether their expression correlated with skeletogenesis even in the absence of Shh signaling. BMP-2 expression was not affected by the presence of cyclopamine prior to stage 51 of limb development (see Additional File 2: Figure S2 for the expression of BMP-2 at stage 45 in control and cyclopamine treated limbs). The expression of SOX-9 was not affected either at stage 45 in cyclopamine treated animals (see Additional File 2: Figure S2).
After 21 days of treatment (Figure 2G-O), control animals had reached stage 53, and at this stage the pattern is complete. Limbs treated with 1 μg/mL of cyclopamine developed only digits 1 and 2 and limbs treated with 2 μg/mL of cyclopamine developed only digit 1. In control animals, the expression of BMP-2 was observed around the digits, and the expression of SOX-9 was in digits 3 and 4. This developmental stage corresponds to the elongation phase of digits in other species [53–55] and as previously mentioned, was not investigated further. In the animals treated with 1 μg/mL (Figure 2H, K, N) or 2 μg/mL of cyclopamine (Figure 2I, L, O) the expression of BMP-2 and SOX-9 in the digits that have formed (digits 1 and 2 for 1 μg/mL treatment and digit 1 for 2 μg/mL treatment) was adjacent, with the expression of BMP-2 surrounding the expression of SOX-9 as in the digits of control animals.
BMP-2 and SOX-9expression during limb regeneration
Effects of blocking Shhsignaling on regenerating digits
Overexpression of BMP-2 and Nogginin regenerating limbs
In vivo experiments were performed on regenerating limbs and were based on the expression pattern of BMP-2 &SOX-9 determined by whole mount in situ hybridisation (Figure 3). BMP-2 and Noggin containing plasmids were electroporated in the posterior-half of the blastema at the LB stages in order to obtain maximal expression of the transgene by the time the regenerates reached Pal; the stage when expression of BMP-2 and SOX-9 is localized in the anterior portion of the limb (Figure 3G &3J). Hence, the electroporation was performed to induce BMP-2 or Noggin at a time and place when no or low endogenous expression of BMP-2 and SOX-9 is detected.
Histological analysis provided some indication as to why BMP-2 and Noggin overexpression caused a loss of digits in regenerating limbs but it did not provide any mechanisms. Therefore, in order to help uncover the mechanism(s) as to how digit loss resulted following BMP-2 and Noggin overexpression, cell division and apoptosis were measured 6 days after electroporation of mRFP, BMP-2 and Noggin. Electroporation was performed at LB stage as described above and cell division was determined by 5-bromo-2-deoxyuridine (BrdU) incorporation (n = 3) and apoptosis was determined by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay (n = 3). BMP-2 overexpression did not seem to cause major changes in cell division (Figure 7B) compared to the controls electroporated with mRFP (Figure 7H) which regenerated normally (Figure 7G). Although BMP-2 overexpression did not cause major changes in cell division, it did cause a marked increase in the number of apoptotic cells (Figure 7C) when compared to control electroporated with mRFP (Figure 7I). On the opposite, Noggin overexpression resulted in a marked reduction in cell division (Figure 7E) and the near absence of apoptotic cells (Figure 7F) compared to BMP-2 overexpression and the control electroporated with mRFP.
Our results show that the expression of BMP-2 and SOX-9 in developing axolotl digits is very similar to the expression observed in other non amphibian species (e.g. mouse & chicken) [11, 15, 19, 24, 26, 29, 30, 45–48]. The expression pattern of these two genes is also reproduced during digit formation in regenerating axolotl limbs. Since SOX-9 is the earliest marker of chondrogenesis and a known target of BMP-2, these results suggest an activation of SOX-9 expression (in cells that will form the digit bones) by BMP-2 expressing cells (in the ID tissue).
As described by previous studies [42, 43], the number of digits that form in cyclopamine treated animals (during development and regeneration) is dose-dependent. In the digits that do form in cyclopamine treated animals, the expression of BMP-2 and SOX-9 as well as chondrogenesis proceed normally. These results suggest that in axolotl just as it was observed in mice , BMP-2 is not likely to be a secondary signal for Shh signaling. This is also supported by the fact that when digits begin to condense in developing and regenerating limbs, BMP-2 and Shh expression are on opposite sides of the limbs (along the anterior-posterior axis) and do not overlap. Hence, these results suggest that, as in mouse, BMP-2 can trigger cell condensation independently of Shh signaling.
Our results strongly suggest that the inhibition of digit regeneration, in the limbs in which BMP-2 was overexpressed, is the result of increased cell condensation and apoptosis. This is also supported by a previous study showing an inhibition of chick limb development in the presence of ectopic BMP-2 . The BMP-2 overexpression experiments and the complementarities of expression of BMP-2 and SOX-9 (in developing and regenerating limbs), support our hypothesis that BMP-2 triggers the condensation of adjacent cells destined to become chondrocytes (e.g. in the digits). Taken together, theses results suggest that the role of BMP-2 during limb regeneration is to trigger cell condensation and may be to control, to some extent, apoptosis. The data obtained with Noggin overexpression also provides further insight on the potential role of BMP signaling in the regeneration process. Noggin is an inhibitor of BMPs (general inhibitor of all BMPs) and therefore the results obtained could potentially affect BMPs other than BMP-2. However, these results indicate that BMP signaling is essential for cellular division and apoptosis during the regeneration process, since both processes are inhibited when Noggin is overexpressed.
The fact that the effects of BMP-2 and Noggin were observed when overexpressed at the LB stage suggest that BMP-2 regulates cellular activities during the redevelopment phase of regeneration that starts approximately at the LB stage or later (see [60, 61] for a more complete description of the different phases of regeneration which are often referred to as: preparation phase which includes the initial stages leading to blastema formation; and redevelopment phase which includes the stages that give rise to the differentiated tissues and the patterning of the regenerated limb). However given that overexpression of BMP-2 and Noggin were performed using electroporation of plasmids, technical limitations do not allow us to draw any conclusion regarding the role of BMP-2 during the preparation phase of regeneration. Given the high level of cell proliferation and tissue reorganisation during the stages prior to the LB stage, it is possible that the electroporated plasmids could have been degraded before affecting the regeneration process or that cells compensated somehow to overcome the ectopic BMP signaling. This is supported by the rapid rate of fading of red fluorescence resulting from the reporter mRFP plasmid, when electroporations were done prior to LB stage. In addition, the fact that Noggin did not affect regeneration when overexpressed prior to LB stage is indicative that BMP signaling may not be essential for cellular proliferation during EB and MB stages.
This work represents the first study on the role of BMPs during the process of limb regeneration in urodele amphibians. Our data demonstrate that the role of BMP-2 is conserved in limb regeneration as in limb development and that its function is related to skeletogenesis, cellular proliferation and apoptosis but not pattern formation, as previously demonstrated by the group of Tabin in mice . The ectopic expression of BMP-2 led to the condensation of cells in regenerating axolotl limbs. The expression of BMP-2 and SOX-9 in addition to our functional analysis data from the ectopic expression of both BMP-2 and Noggin clearly indicate that BMP signaling is essential for the process of limb regeneration especially during the redevelopment phase where re-differentiation of all the different cell types and pattern formation occur.
Animal maintenance and surgery
Axolotl embryos and larvae (3.0 cm to 8.5 cm from snout to tip of the tail) were purchased from the Ambystoma Genetic Stock Center (Lexington, KY, USA). Animals were kept in 20% Holtfreter's solution at a temperature varying from 19-22°C with a photoperiod cycle of 12 hours of light and 12 hours of darkness. Embryos were used for limb development experiments and larvae for limb regeneration experiments. For all manipulations performed, axolotls were anaesthetized in 0.1% MS222 (ethyl 3-aminobenzoate methanesulfonate salt, Sigma-Aldrich, MO, USA) in Holtfreter's solution at pH 7.0. Axolotls were allowed to recover from anaesthesia in 20% Holtfreter's or were euthanized/fixed for subsequent experiments. All animal care and experiments were done in agreement with the Université de Montréal animal care committee's guidelines.
Cloning of axolotl BMP-2full length cDNA
Partial axolotl BMP-2 cDNA of 239 bp was obtained from axolotl larvae total RNA by RT-PCR. The 239 bp cDNA was amplified with primers (see Additional File 4: Figure S4) designed from a partial cDNA sequence of BMP-2/4 like directly submitted to Genbank by Dalglish, G. et al. (Accession number: AY326272). The full length BMP-2 cDNA was subsequently obtained by screening an axolotl cDNA library (Stratagene, CA, USA), following the manufacturer's instructions and using the 239 bp fragment as a probe radioactively labeled with 32P-dCTP (Perkin Elmer, MA, USA).
Whole-mount in situhybridization
Whole-mount in situ hybridization was performed as described in Gardiner et al.  with a few modifications: The axolotls were anaesthetized and euthanized/fixed in 1× MEMFA (10× MEM salt (1 M MOPS pH 7.4, 20 mM EGTA, 10 mM MgSO4), 3,7% formaldehyde in DEPC treated H2O) then transferred to 100% methanol and stored at -20°C until needed. Fragments of 449 bp and 381 bp (for BMP-2 probes), 458 bp and 455 bp (for SOX-9 probes) and 371 bp (for Shh probes) were generated by RT-PCR (see Additional File 4: Figure S4 for primers used) and cloned separately into the pCRII-TOPO cloning vector (Invitrogen, CA, USA). These plasmids were then linearized using the appropriate restriction enzymes and used as template for generating antisense RNA probes. Digoxigenin (DIG) labelled antisense RNA probes were generated using T7 or SP6 RNA polymerase (Invitrogen, CA, USA) and DIG RNA labelling mix (Roche Diagnostics, QC., Canada). Two different probes for BMP-2 were synthesised. The 3' UTR of the BMP-2 gene is highly conserved throughout evolution and it was utilized to make a highly specific probe for BMP-2. Thus, one probe of 381 bp was designed to overlap part of the 3' UTR and the ORF of BMP-2. A second probe of 449 bp was designed in the region overlapping the 5' UTR and the ORF of the gene which confirmed the expression observed with the 381 bp probe (data not shown). The expression pattern of SOX-9 was also determined using two different probes with identical results obtained for both probes (data obtained using the 455 bp probe are not shown). The expression of Shh was assessed with only one probe since the results were identical to the results published by two different groups [39–41]. For tissue permeabilization of developing embryos, the limbs were incubated with 20 μg/mL proteinase K for 15 min on ice and then at 37°C for 5 min. For permeabilization of regenerating tissues, limbs were incubated with 30 μg/mL proteinase K for 1 h on ice and then at 37°C for 45 min. Probes were hybridized 24 h for embryos and 72 h for regenerating animals. Prehybridization and hybridization temperatures were done at: 55°C for the BMP-2 449 bp probe and 60°C for all the other probes. Finally, BM purple (Roche Diagnostics, QC., Canada) was used as the alkaline phosphatase substrate for the colorimetric reaction. Each time point presented were performed at least 3 times.
Whole mount skeletal staining of limbs
Cartilage was stained using the Victoria Blue method . Limbs were fixed in Bouin's fixative solution for 24 h before being rinsed several times with 70% ethanol. Specimens were then rinsed in 3.5% NH4OH for 2 days and subsequently treated with Acid alcohol for 2 h. Specimens were stained with 1% Victoria Blue for 2 h and then rinsed with 70% ethanol. Limbs were dehydrated using a gradient ethanol series of 95% and 100%, then cleared and stored in methyl salicylate.
Electroporated limbs were fixed overnight in Bouin's fixative solution and then rinsed thoroughly with 70% alcohol. Limbs were embedded in paraffin and cut to 10 μm sections. Slides were deparaffinised through 3 baths of toluene for 5 minutes each. Slides were then rehydrated in a graded series of 100%, 90%, 70% and 50% ethanol and then distilled water for 5 minutes each. Masson's trichrome staining method was used to stain cell cytoplasm in red, nuclei in black and collagen in blue .
Cyclopamine powder (Cedarlane, ON., Canada) was dissolved in 100% ethanol at a concentration of 5 mg/mL and stored at -20°C. Cyclopamine was administered by adding it directly to the Holtfreter's solution to the desired concentrations. For each conditions presented in this study, 10 animals were treated with cyclopamine or ethanol (control). For experiments on developing limbs, treatments began at the developmental stage 41 according to Nye et al.  and animals were fixed after 14 and 21 days of treatment (corresponding approximately to stage 51 and 53 in control animals). For regenerating animals, treatments began at the time of limb amputation and animals were fixed when the controls reached the palette stage (see  for stages description) and at completion of regeneration. For limb development as well as limb regenerating experiments, control animals were treated with the same volume of 100% ethanol that was used to dissolve the cyclopamine. Controls were done for both volumes of ethanol (0.2 μL/mL and 0.4 μL/mL) used for the 1 and 2 μg/mL cyclopamine treatment. There was no difference in limb development between these two control conditions (data not shown) and therefore only those corresponding to 2 μg/mL cyclopamine treatment are presented. When the control animals with ethanol were compared with animals bathing in ethanol free solution, there was no difference in limb patterning and gene expression. All solutions were changed daily. Animals were euthanized at the end of the experiment and fixed.
The immortalized human chondrocyte cell line, C28/I2, has been described previously . It was developed from chondrocytes isolated from juvenile human costal cartilage and immortalized by retroviral infection of the SV40 large T antigen . C28/I2 cells were cultured in D-MEM/F12 containing 10% FBS with antibiotics (penstrep, fungizone) and 2 mM L-glutamine.
Transfection was performed using Lipofectamine 2000 (Invitrogen, Carlsbad, CA). BRE2-luc was described previously . C28/I2 cells were seeded at a density of 7.5 × 104 cells in a 12-well plate. The next day, cells were transfected with the following constructs and concentrations: axolotl BMP-2 = 0 or 0.4 μg, Xenopus laevis Noggin = 0 or 0.4 μg, BRE2-luc = 0.35 μg and pCMV-β gal = 0.35 μg. The total DNA concentration was brought up to 1.5 μg using pTYFP (expression vector for mRFP) as filler DNA. Cell lysates were prepared 48 hours later and analyzed for luciferase and β-galactosidase activity as described previously . Data are expressed as a mean ± standard deviation luciferase activity normalized to β-galactosidase activity. Comparison among each condition (n = 3/condition) was tested using Kruskal-Wallis One Way Analysis of Variance on Ranks.
Injections and electroporation of constructs
For injections/electroporation of constructs expressing axolotl BMP-2 or Xenopus laevis Noggin, blastemas were injected with 1-1.5 μL of circular DNA solution through a glass needle with a 0.2-0.4 μm diameter tip, using a cell microinjector PM-1000 (Micro Data Instrument, Inc., NJ, USA). Immediately following injections, constructs were electroporated in blastemas. Thin gold plated rectangular electrodes (3 mm × 5 mm) were placed under (anode) and over (cathode) the blastema. 5 trains (1 train/second) of 20 square wave pulses (200 Hz for 100 ms), at 10 Volts peak to peak, were applied through the electrodes using a S8 stimulator (Grass instruments, MA, USA; Additional File 5: Figure S5). Vectors containing axolotl BMP-2 (5 μg/μL) or Xenopus laevis Noggin (5 μg/μL) were always co-injected with a vector containing the mRFP (2.8 μg/μL) to monitor the spread of the injection over time and space. Control animals were injected with 7.8 μg/μL of mRFP (the vector containing BMP-2 or Noggin was replaced by the same amount of mRFP). BMP-2, Noggin and mRFP expressions were all under the control of the constitutive CMV promoter in the pcDNA1/AMP expression vector (Invitrogen, CA).
BrdU incorporation assay
Regenerating axolotls were injected intra-peritoneally, 6 days after electroporation of plasmids (as described above); with 10 μL of BrdU stock solution using a ratio of 1-2 mL/100 g of body weight according to the manufacturer's instructions (GE Healthcare, # RPN201). Animals were fixed 12 hours after injection in 4% paraformaldehyde in 0.7× PBS for 24 hours at 4°C. Samples were paraffin embedded, deparaffinized and rehydrated as for histology. For immuno-histochemistry, slides were washed 4 × 15 minutes in PBST (1× PBS with 0,1% Tween 20). They were incubated with 0.8% Pepsin in 0,2N HCl for 10 minutes at 37°C to promote denaturation of DNA. Slides were then washed 3 × 10 minutes in PBST, and incubated in a blocking solution (2% bovine serum albumin, 1% DMSO, 10% sheep serum and 0,1% Triton X-100) at room temperature for one hour. Slides were then incubated overnight at 4°C with an anti-BrdU mouse monoclonal antibody (BrdU Ab-3, Labvision/Neomarkers, Fremont, CA.) diluted 1:50 in blocking solution. PBST washes (4 × 15 minutes) were done before incubating with an anti-mouse secondary antibody coupled to horseradish peroxidase, dilution 1:250, for 2 hours at room temperature (GE Healthcare). Slides were washed again 4 × 15 minutes in PBST before being incubated in DAB (Zymed, Invitrogen CA) for signal detection. Slides were counterstained with methyl green for 6 minutes (Dako, Mississauga, ON) before being serially dehydrated 2 × 2 minutes each in 90% EtOH, 100% EtOH and 100% Xylene. Slides were mounted with Permount (Fisher scientific, Ottawa, ON). Immunohistochemical detection for BrdU incorporation was done on three different samples for each condition tested.
TUNEL assay was adapted from Vlaskalin et al.  with minor modifications. Tissue sections were deparaffinised and rehydrated as for histology. In a humidified chamber, sections were incubated for 20 minutes in TBS (Tris-buffered saline: 100 mM Tris-HCL pH 7.5 + 150 mM NaCl), containing 20 μg/ml proteinase K at RT and rinsed 3 × 1 minute in TBS. Slides were rinsed in TBS, equilibrated in 1× TdT buffer for 5 minutes and incubated in TdT buffer containing 75 U/ml TdT and 2 μM digoxygenin-dUTP for 1 h at 37°C. End labelling was stopped by transferring the sections into 1× TBS/1 mM EDTA for 10 minutes at RT, followed by 2 × 2 minutes rinses in TBS. Sections were equilibrated for 5 minutes in TBS and incubated in blocking solution [2% sheep serum in TBS] for 1 h at RT. Tissues were incubated overnight at 4°C in blocking solution containing 1:1500 dilution of anti-DIG-AP. The following day, sections were rinsed in PBS and equilibrated 5 minutes in AP buffer. The chromogenic reaction was carried out in AP buffer containing 100 mg/ml NBT and 50 mg/ml BCIP. The reaction was monitored for up to 15 minutes and stopped by several washes in 1× PBS.
Pictures of whole mounts, Victoria blue staining, and mRFP fluorescence were taken by a digital infinity 2 camera (Lumenera corporation, ON., Canada) through a Leica MZ-16F binocular (Leica Microsystems Ltd., Switzerland). Images of fluorescence in regenerating limbs were merged with white light images using Photoshop 7.0.1 (Adobe Systems Inc., CA, USA).
The authors would like to thank Cara Hutchison and Mireille Pilote for the use of their plasmids containing the fragments for the two Sox-9 probes used in this paper. We would also like to acknowledge the help of Éric Villiard and Samuel Gatien in preparing the photographs presented in the various figures. The authors would also like to thank Dr Antonio Nanci, from the department of Stomatology at the Université de Montréal, for help with the histology and Dr Marko Horb from the Institut de Recherche Clinique de Montréal, for providing the Xenopus laevis Noggin plasmid. This work was funded by a grant from the National Sciences and Engineering Research Council of Canada (NSERC) to SR. J-CG was supported by a Ph.D. scholarship from NSERC, P-LM and JB were supported by an undergraduate studentship from the Network for Oral Research Training and Health of the Canadian Institutes of Health Research and ML was supported by a Ph.D. scholarship from the Réseau de Recherche en Santé buccodentaire et osseuse of the Fond de la Recherche en Santé du Québec.
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