Notochord-derived hedgehog is essential for tail regeneration in Xenopus tadpole
© Taniguchi et al.; licensee BioMed Central Ltd. 2014
Received: 27 March 2014
Accepted: 12 June 2014
Published: 18 June 2014
Appendage regeneration in amphibians is regulated by the combinatorial actions of signaling molecules. The requirement of molecules secreted from specific tissues is reflected by the observation that the whole process of regeneration can be inhibited if a certain tissue is removed from the amputated stump. Interestingly, urodeles and anurans show different tissue dependencies during tail regeneration. The spinal cord is essential for tail regeneration in urodele but not in anuran larva, whereas the notochord but not the spinal cord is essential for tail regeneration in anuran tadpoles. Sonic hedgehog is one of the signaling molecules responsible for such phenomenon in axolotl, as hedgehog signaling is essential for overall tail regeneration and sonic hedgehog is exclusively expressed in the spinal cord. In order to know whether hedgehog signaling is involved in the molecular mechanism underlying the inconsistent tissue dependency for tail regeneration between anurans and urodeles, we investigated expression of hedgehog signal-related genes in the regenerating tail of Xenopus tadpole and examined the effect of the hedgehog signal inhibitor, cyclopamine, on the tail regeneration.
In Xenopus, sonic hedgehog is expressed exclusively in the notochord but not in the spinal cord of the regenerate. Overall regeneration was severely impaired in cyclopamine-treated tadpoles. Notochord maturation in the regenerate, including cell alignment and vacuolation, and myofiber formation were inhibited. Proliferation of spinal cord cells in the neural ampulla and of mesenchymal cells was also impaired.
As in the axolotl, hedgehog signaling is required for multiple steps in tail regeneration in the Xenopus tadpole, although the location of the Shh source is quite different between the two species. This difference in Shh localization is the likely basis for the differing tissue requirement for tail regeneration between urodeles and anurans.
Regeneration of amphibian appendages, including the tail, represents a valuable model system to analyze molecular mechanisms underlying cell growth, cell differentiation, morphogenesis and pattern formation in epimorphic regeneration (reviewed in [1–5]). Multiple signaling molecules have critical roles both in anuran and urodele tail regeneration. For example, larval tail regeneration in Xenopus is regulated by bone morphogenetic protein (BMP), Notch, fibroblast growth factors (FGFs), transforming growth factor (TGF)–β, canonical Wnt and non-canonical Wnt [6–12]. Hedgehog signaling is required for axolotl tail regeneration . A significant role of FGFs and Wnts has been suggested by their expression patterns during tail regeneration in adult or larval salamander [14–17]. Therefore, a considerable number of signaling mechanisms are thought to be shared between anurans and urodeles during tail regeneration.
The requirement for signaling molecules in regeneration should be related, at least in part, to the phenomenon of the tissue dependency in appendage regeneration, which has been shown by ablating or destroying a specific tissue in the amputated stump [17–20]. The tissue dependency in tail regeneration is quite different between anurans and urodeles, although both species expressed overlapping set of genes for signaling molecules during tail regeneration. Urodele tail regeneration is completely dependent on the presence of the spinal cord , which is now known to be the source of FGFs and sonic hedgehog (Shh), while an ablation of the spinal cord results in a normal or partially defective regenerating tail in anuran larvae [12, 18, 19]. As hedgehog signalling is essential for overall tail regeneration in urodele , the exclusive expression of shh in the spinal cord is likely to be one of major reasons for the requirement of the spinal cord in urodele tail regeneration. It is interesting to know whether hedgehog signal is essential for the tail regeneration in anuran larvae, especially since the presence of the spinal cord is not required for anuran tail regeneration.
In this work we showed that tail regeneration in Xenopus larva is dependent on hedgehog signaling as in axolotl and that shh is expressed in the notochord but not in the spinal cord in the regenerating tadpole tail. Our results suggest that the different tissue specificity of shh expression is the major cause leading to the differences in the tissue dependency between anurans and urodeles.
Expression of genes related to hedgehog signal during tail regeneration
RT-PCR showed that two patched genes (ptc-1 and ptc-2), smoothened (smo) and three gli genes (gli-1, gli-2 and gli-3) were also expressed in the regenerating tail (Figure 1A). Whole mount in situ hybridization revealed that ptc-1 and ptc-2 were expressed in the regenerating spinal cord (Figure 1D, E). Hybridization signal in other tissues, for example, notochord and muscle, was indistinguishable from the background staining. Expression of gli genes was not detected in any tissues by in situ hybridization (data not shown). These results support a possibility that hedgehog signal regulates growth and/or differentiation of regenerating tissues, including the spinal cord in Xenopus.
Cyclopamine treatment suppresses tail regeneration in Xenopus
Effect of cyclopamine on length of regenerating tail
CP + PM
CP + PM
Effect of cyclopamine on length of regenerating notochord
CP + PM
CP + PM
TUNEL staining showed apoptotic cells in the distal region of the amputated tail at day 1 to day 3 in both cyclopamine-treated and control tadpoles (Additional file 1: Figure S1). The signals were found mainly in epidermis but rarely in notochord, spinal cord and mesenchymal region. It appeared that cyclopamine do not cause a significant change of the apoptotic cell number in this condition.
Gene expression in the regenerating tail was analyzed by RT-PCR (Figure 2K). Cyclopamine treatment resulted in down-regulation of several component genes for hedgehog signaling cascade, including ptc-1, ptc-2, gli-1 and smo, indicating that these genes are targets of hedgehog signaling, although the expression level of shh was not affected. The down-regulation of ptc-1 is consistent with the reduced expression of ptc-1 in cyclopamine-treated axolotl tails . The cyclopamine treatment down-regulated expression of myoD representing muscle tissue and slightly affected sox-2 representing nerve tissues, although it did not affect bra-3 representing the notochord or genes expressed in a broad range of regenerating tissues, such as msx-1 and wnt-5a. Formation of normal wound epidermis was observed morphologically and confirmed by the unaffected expression of ES-1, a marker for the wound epidermis  (Figure 2K).
Cyclopamine inhibits notochord differentiation
Effect of Cyclopamine on proliferation of regenerating cells
% BrdU+ cells
number of sections
Cyclopamine affects spinal cord regeneration
The spinal cord grows posteriorly in close proximity to the regenerating notochord during tail regeneration. Immunostaining with an anti-NCAM antibody showed an impaired growth of the spinal cord in the cyclopamine-treated regenerated tail (Figure 3F). Expression of sox2, which is abundant in the regenerating spinal cord, is slightly reduced by the cyclopamine treatment (Figure 2K). A sagittal section showed that the neural ampulla of the regenerated spinal cord was small or not formed in the cyclopamine-treated tail (Figures 3C, 4C). Cyclopamine treatment significantly reduced the proliferation rate of cells in the neural ampulla region (Figure 4C, G, Table 3) but not in the proximal region of the spinal cord (data not shown).
Cyclopamine inhibits muscle regeneration
Cyclopamine treatment greatly impaired the myofiber formation in the regenerated tail (Figure 3G-K). It suppressed up-regulation of myoD during tail regeneration (Figure 2K). It is known that Pax7-expressing myogenic cells migrate and proliferate to form new muscle tissue after tail amputation [5, 24]. A few myogenic cells labeled with anti-Pax7 antibody were found in the regenerating tail treated with cyclopamine (Figure 3M), while many more Pax7 positive cells are in the control tadpole (Figure 3L). This is consistent with the result of RT-PCR showing that expression of pax7 was down-regulated by cyclopamine treatment (Figure 2K). The proliferation rate of mesenchymal cells was reduced by cyclopamine in the region distal to the damaged muscle where Pax7-positive myogenic cells reside (Figure 4D-G, Table 3). We conclude that the hedgehog signal is required for muscle regeneration in the larval tail.
Cyclopamine inhibits tail regeneration of Xenopustadpole
In this study we showed that cyclopamine treatment resulted in a wide range of cellular defects including proliferation and differentiation during Xenopus tail regeneration. Muscle regeneration was especially inhibited. The fact that the number of Pax-7 positive myogenic cells and myofibers were significantly reduced is consistent with a previous report in which cyclopamine-treatment during axolotl tail regeneration results in a reduced number of Pax7-positive cells in regenerating blastema . Our results suggest that the proliferation of the myogenic cells requires hedgehog signaling. The Pax-7 positive cells in the regenerating tail are derived from the satellite cells residing in the remaining muscle of the Xenopus tadpole tail [5, 24, 25]. As the promotive effect of Shh on proliferation and differentiation of the satellite cells has been reported in mouse and chicken [26, 27], our results suggest that vertebrate muscle regeneration is regulated by a common mechanism involving hedgehog signaling.
We found a different effect of cyclopamine on the spinal cord regeneration between axolotl and Xenopus. Cyclopamine treatment does not affect proliferation of the regenerating spinal cord cells in axolotl tail regeneration . On the other hand, it reduced the proliferation rate of cells in the neural ampulla region of the Xenopus spinal cord. Expression of ptc-1 and ptc-2 in the regenerating spinal cord (see Figure 1D, E) suggests a direct influence of hedgehog signal on spinal cord growth.
Cyclopamine treatment affected late steps of the notochord regeneration including the alignment of the immature cells and their terminal differentiation, although it did not affect the early step including the proliferation of the immature notochord cells. This result may be consistent with a previous report that shh is required for maintenance but not formation of the embryonic mouse notochord . As the regenerating notochord cells express the hedgehog ligand, Shh, the hedgehog signal may regulate differentiation of notochord cells in an autocrine manner. Alternatively, Shh secreted by the notochord may regulate notochord regeneration indirectly by affecting other tissues, for example, the spinal cord that has been shown to be required for correct regeneration of the notochord . The precise role of hedgehog signaling in the notochord cells will be determined using defined experimental systems, for example, culturing isolated notochord cells.
Localized expression of shhcauses the different tissue dependency in tail regeneration
Despite the differences in the affected tissues by cyclopamine treatment, this study together with previous reports show that hedgehog signaling is essential for the overall tail regeneration both in urodele and anuran . The critical difference between Xenopus and axolotl is in the tissue-specific expression of shh in regenerating tail: shh is expressed exclusively in spinal cord in axolotl while it is expressed exclusively or predominantly in notochord in Xenopus. Genes for other signaling molecules, including FGFs, Wnts and BMPs, are also required for tail regeneration in Xenopus and are expressed in a broader range of tissues in contrast to shh[7, 12, 23]. The different location of shh expressing cells is likely to be a main reason underlying the different tissue dependency for tail regeneration between urodele and anuran. shh is expressed in both the ventral spinal cord, namely the floor plate, and the notochord in vertebrate embryos. The original spinal cord in the Xenopus tadpole tail has a floor plate that expresses shh, while the regenerated one has no identifiable floor plate . Therefore, the absence of shh expression in the regenerated spinal cord reflects the incomplete regeneration of the Xenopus spinal cord. Notochord, the main source of Shh in the regenerating Xenopus tadpole tail, is not formed in the regenerated tail of axolotl larva . Regenerating tail in urodele larva forms cartilaginous tissue in place of the notochord, reflecting the normal developmental process in which notochord is replaced by cartilaginous vertebrae. On the other hand cartilage is never formed in the anuran tadpole tail. The difference in tissue-specific expression of shh between axolotl and Xenopus is, therefore, caused by the incomplete spinal cord regeneration in Xenopus and the absence of regenerated notochord in axolotl.
In this study we clearly showed that overall regeneration of the Xenopus tadpole tail is inhibited by cyclopamine, a specific inhibitor for hedgehog signaling, consistent with a previous report using axolotl larva. We also showed that shh is exclusively or predominantly expressed in regenerating notochord but not in spinal cord in Xenopus, while it is expressed exclusively in spinal cord in axolotl. Our findings together with the previous report explain why the tissue dependency for tail regeneration is different between anuran and urodele larvae.
Surgery and animals
Xenopus laevis larvae were maintained at 22°C in 0.1% NaCl. The developmental stages were determined according to Nieuwkoop and Faber . The stage 49 tadpoles were used for the tail amputation described previously . The animals were handled in with a protocol approved by the animal care and use committee in University of Hyogo.
Treatment with chemicals
Stock solutions (5 mM) of Cyclopamine (Enzo Life Science) and Tomatidine hydrochloride (Enzo Life Science) were prepared with ethanol and added into the feeding water at final concentration of 2.5 μM. Pumorphamine (Calbiochem) was dissolved in dimethyl sulfoxide at 10 mM and used at 0.25 μM. The concentrations used were determined empirically. Tadpoles were transferred into the water containing the chemicals immediately after amputation and the feeding water was replaced every day. Length of regenerated tail was measured from the center of the amputation plane to the distal epidermal tip. Length of regenerated notochord was measured using the different batch of tadpoles.
Histological and immunological analyses
Histological analysis for staining with hematoxylin and eosin was performed as described previously . Procedure for whole mount immunostaining was also described previously . For frozen sections a tadpole were fixed in 7.4% formaldehyde, infiltrated in 18% sucrose, embedded in OCT compound and frozen at -80°C. Cryosection was made with cryostat (Leica CM3050S) and treated with a primary antibody and followed with Alexa Fluor 594-labeled secondary antibody (Molecular probes). Monoclonal antibodies 4d (anti-N-CAM) , 12/101  and anti-PAX7  were obtained from the Developmental Studies Hybridoma Bank at the University of Iowa (Iowa City, IA, USA).
Labeling of proliferating cells using bromodeoxyuridine (BrdU) was performed as described previously . BrdU-labeled cells were detected with horseradish peroxidase-labeled secondary antibody and diaminobenzidine (DAB) coloring.
Apoptotic cells were detected by whole mount TUNEL staining using the In Situ Cell Death Detection Kit, POD (Roche Applied Science) according to manufacture’s protocol.
Reverse transcription-polymerase chain reaction (RT-PCR)
The procedure for RNA extraction, cDNA synthesis and polymerase chain reaction was described previously . The reaction conditions were empirically determined in each case within the linear range of amplification. Primers, annealing temperature and cycle number were as described in Additional file 2: Table S1.
In situ hybridization
Procedures for whole mount and section in situ hybridizations were described previously [11, 23]. Bluescript plasmids encoding Xenopus laevis shh (xl096o20), patched-1 (xl008p21), patched-2 (xl045b21), gli-1 (xl088k18), gli-2 (xl063k18) and gli-3 (xl074e23) were characterized using the NIBB/NIG/NBRP Xenopus laevis EST database . Complementary DNAs for Xenopus bhh was amplified from cDNA of the taildud embryo using primers (US: 5′-TGGAAGCTGGATTTGACTGGGTCTAC-3′; DS: 5′-GCTATACCAGTGAATGCCCATCTGCT-3′) and cloned into the PCR II-TOPO VECTOR (Life technologies) according to the manufacture’s protocol.
We thank Hidekazu Yasudi and Yuriko Nakahata for providing preliminary data for this study. We also thank Drs. Akira Tazaki, Josh Currie and Elly Tanaka for critical reading of the manuscript. This work is supported by JSPS KAKENHI Grant numbers 21570232, 24570239 to MM.
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