Abstract
The anuran amphibian Xenopus laevis can regenerate its limbs for a limited time during the larval stage, while limbs are still developing. Using this regeneration model, we evaluated the proximo-distal blastema cell identity when endogenous retinoids were increased by CYP26 inhibition or when RAR-specific agonists altered RA signaling. Simultaneous proximo-distal and antero-posterior limb duplications were generated and the RAR-specific agonist can modify blastema identity after amputation, because chemical activation of RARβ produced bilateral hindlimb duplications that resulted in a drastic duplication phenotype of regenerating limbs.
Similar content being viewed by others
Introduction
The ability to regenerate lost or damaged body parts is a widespread phenomenon in invertebrates but is exceptional in vertebrates. Only animals capable of asexual reproduction by budding are able to re-establish post-embryonically a new set of axes1. Regeneration implies not only the replacement of the lost structures, but also the integration of positional information that specifies the correct spatial patterns. During development, the appendicular skeleton is positioned at specific antero-posterior places with respect to the main body axis and maintains left-right asymmetry with equal size proportion. The mechanisms that establish internal organ asymmetries versus external bilateral symmetry are mostly unknown2.
Proximo-distal (P-D) and antero-posterior (A-P) limb duplications in regenerating amphibian limbs were first obtained by Niazi and Saxena in 1978 and Maden in 1982 by using exogenously applied retinol (vitamin A) or derived retinoids3,4. They revealed for the first time a role of vitamin A derivates in the change of positional information and proximalization of blastema and showed that the responses are time, stage and concentration-dependent. Retinoic acid (RA) is a metabolic product of retinol that binds and activates nuclear retinoic acid receptors (RARs), which regulate the transcription of specific genes. Retinol dehydrogenases metabolize the retinol obtained from the diet as carotenoids and retinyl esters to retinaldehyde, which is then metabolized by retinaldehyde dehydrogenases to RA. Once RA binds and activates heterodimers formed by RARs and RXRs, it is catabolized in the cytoplasm by CYP26 enzymes yielding polar metabolites that are inactive or less active than RA5. Therefore, the balance between its synthesis and its degradation controls intracellular levels of active RA. Studies in Xenopus laevis indicate that at-RA and 9-cis-RA are not present at detectable levels in embryos6, while 4-oxo-RA is detected at high levels, binds avidly to and activates RARβ receptor and has strong teratogenic activity7.
The role of RA on blastema proximalization and regeneration has been studied mainly by exogenous administration of retinoids3,4. However, the effect of excess endogenous retinoids on limb regeneration is unknown. Based on this, in the present work CYP26 enzymatic activity was inhibited in amputated limbs by using a pharmacological CYP26 inhibitor. Results show that this inhibitor was able to induce simultaneous P-D and A-P limb duplications during limb regeneration of Xenopus larvae, while in developing limbs it promoted apoptosis leading to severe hypomorphic phenotypes. In addition, to determine which retinoic acid receptors (RARs) are involved in this process, specific chemical agonists of RARs were assayed. Using nano-molar concentrations of a RARβ2 agonist induced the most striking A-P and P-D duplications described to date.
Results
Inhibition of CYP26 induces P-D and A-P duplications
To explore the effect of increased endogenous retinoids available to RARs we applied R115866 a specific and strong CYP26 enzyme inhibitor8. Unilateral amputations were performed leaving the proximal stump spanning the first third of E51-51.5 hindlimbs9. After an interval of 8 h for recovery, the epithelized wounds were exposed to 2 μM of R115866 during 72 h. Under this condition a frequency of 49% was obtained of what we named incomplete simultaneous duplications, that is, P-D and A-P duplications within the same regenerate without the formation of any distinguishable new pelvic bone (Table 1). This kind of duplication is basically equal to that reported in regenerating limb buds of Xenopus laevis treated with vitamin A10. The other 44% were complete simultaneous duplications; those including the formation of a new pelvic girdle with a well-formed glenoid cavity, articulated with the head-bone of the new stylopod. In all cases of simultaneous duplications a mirror-duplicated autopod was formed distally (Fig. 1A–C). The development of the contralateral uncut hindlimbs and both forelimbs were also affected showing hypomorphic malformations. Interestingly, despite displaying severely shortened or even the absence of autopod bones, they developed what seem to be interdigital membranes (Fig. 1D–F).
Based on previous results, the effect of CYP26 enzyme inhibitor was evaluated in another important limb regeneration animal model, the urodele amphibian Ambystoma mexicanum. More prolonged treatments with 2 μM of R115866 over 5 days were necessary to induce complete P-D duplications in juvenile axolotls, which included the formation of a secondary shoulder girdle (data not shown). However, although the concentrations of R115866 were either reduced or increased ten-fold or the treatment prolonged, A-P or simultaneous duplications were never obtained. It is important to mention that preliminary assays with the imidazole derivate liarozole, a first generation CYP26 inhibitor, at doses as high as 250 μM, failed to generate duplications in Xenopus larvae and juvenile axolotls.
Over-activation of RARβ induces bilateral hindlimb duplication
The effects of the specific commercially available RAR agonists such as adapalene, AC55649, AM-580 and CD437 were then explored. The most consistent and striking effects were obtained with AC55649, a strong RARβ2 receptor agonist that displays 100-fold selectivity over other retinoid receptors11. Under the same experimental conditions as described above we determined that exposing regenerates for 18 h to just 100 nM of AC-55649 was sufficient to induce what we named bilateral limb (B-L) duplications. With this concentration, approximately 65% (n = 45) of larvae survived the treatment and practically all began to form a pair of bilaterally symmetric limb buds (Table 1; Fig. 2A, A′). Skeletal staining showed a pair of legs emerging from a complete and symmetric new pelvis, which consistently maintained the same position regarding the A-P, P-D and dorso-ventral (D-P) axes of the femur bone from which it emerged (Fig. 2B, B′, B”). The pelvic bones were well formed, symmetric and emerged dorsally attached to the distal stump of the original femur (Fig. 2C, D, E). The original femoral blood vessel that runs down the ventral side of the thigh divided and continued toward the ventral side of both new hindlimbs (Fig. 2F, G). In Xenopus the opening of the cloaca is located between the thighs under the pelvis and in front of the ventral fin fold; in the present experiments, no formation of a cloaca or fin-fold tissue was observed in B-L duplication. Furthermore, it has been reported that near of the midline, notochord cells are sources of molecules that are involved in tissue patterning and that amputated tails of frogs treated with retinoids develop an overgrowth of notochord cells at the base of the limb duplicates12; such overgrowth of notochord cells was not observed in this study (Fig. 2H). Contralateral developing hindlimbs and forelimbs also showed severe hypomorphic malformations (data not shown).
Interestingly, treatments with R115866 and AC-55649 provoked death of larvae at the onset of metamorphosis at around stage 62, a stage when the levels of T3 and T4 thyroid hormones peak, meanwhile all control larvae were metamorphosed.
Discussion
The role of endogenous RA in limb regeneration has been studied in conditions of RA deficiency using alcohol and aldehyde dehydrogenase enzyme inhibitors; these treatments impair limb regeneration13,14. In contrast, in the present study we uncovered the effects of excess endogenous retinoids by using a CYP26 enzyme inhibitor, which consists in simultaneous P-D and A-P limb duplications and complete simultaneous duplications at higher frequency than in experiments applying exogenous vitamin A (see Table 1)10,15. With this inhibitor, an excess of endogenous retinoids was possibly generated in tissues with active synthesis-degradation of RA other than limbs. In this case, a systemic increase of endogenous retinoids may affect the blastema. However, it is known that blastema produces RA16, up-regulates the protein CRABP2, expresses Cyp26b and Raldh2 genes17 and RA signaling is active in the apical wound epithelium18. Moreover, the expression and up-regulation of Rarβ2 was recently reported in the regenerating limb and tail of N. viridescens, and their function in limb regeneration was demonstrated by using the specific RARβ2 inhibitor LE13519.
Because the loss of function of CYP26 by R115866 preferentially avoids at-RA catabolism8, it is reasonable to speculate that levels of free at-RA may increase within the blastema. On this basis, at-RA may be an endogenous ligand during Xenopus limb regeneration. However, though in vitro experiments show that 4-oxo-RA is one of the catabolic products of CYP2620, in vivo it is detected at high levels in the Xenopus embryo6. It also activates RARβ and is known to be as potent as RA7. Therefore, 4 oxo-RA should not be excluded as the retinoid that may activate RARβ2 in vivo, particularly considering the existence of several CYP26 and P450 enzymes. In addition, the possibility that RA could be transformed into other as yet unexplored active retinoids should not be ruled out.
Based on the literature and on present results, the main role of CYP26 during limb development could be to protect against the teratogenic effect of RA21,22, but in the regeneration process it would be to protect the blastema from re-specification and change of positional information. On the basis of gene expression pattern of Raldh2, Cyp26b and Crabp2 during Xenopus limb regeneration, it has been suggested that a dynamic and concentric RA gradient is formed during this process17. Cyp26b is expressed in the early blastema at 3 days of regeneration, in principle a time window sensitive to CYP26 enzyme inhibitors. We suggest that in our experiments the treatment with R115866 would be able to break that RA gradient, giving rise to re-specification of E51-51.5 blastema during its formation. Thus it would be possible to consider that low doses of the inhibitor, or treatment at later stages may result in mild proximalized phenotypes.
A remarkable result of the present work were the B-L duplications obtained after chemical activation with RARβ, no previously reported with any retinoid assayed, representing a bona fide homeotic transformation: one secondary pelvic girdle developed bearing two symmetric legs that maintained a constant position with regard to the stump from which they emerged (see Fig. 3). Several reports have shown the effects of different regimes of exogenously applied vitamin A and derived retinoids in regenerating limbs and tails in developing embryos10,23,24. From our point of view, the two most striking phenotypes obtained are the homeotic transformation of amputated tails into limbs in two anuran species12,25 and the RA homeotic transformation induced in mouse embryos resulting in multiple ectopic hindlimbs and lower-body duplication26. The experimental design proposed here suggests that blastema must change its coordinate system and re-specify the axes at a very early stage post-amputation, within a narrow time window of less than 24 h. This early specification27 implies that the instructive/permissive action of RA must occur before a distinguishable blastema forms. Fate maps and transplantation experiments have shown that the blastema specifies its P-D axis and is already divided into growth zones as early as 3 days post amputation28. Also, the blastema is more sensitive to retinoids during early blastema formation, when cells actively proliferate29.
We speculate that B-L limb duplication observed in this study arises because a new dorso-ventral axis in the blastema forms and as a consequence a new left-right axis emerges in the regenerating limb (Fig. 2E, Fig. 3). Importantly, this dorso-ventral axis maintains a constant orientation with respect the main body axis as shown in Fig. 3. This constant position is not observed in the case of incomplete duplicates that show a heterogeneous orientation with respect the main body axis. It is known that RARβ is expressed and up regulated in blastema after amputation of the limb in adult newt19. It is possible that over activation of RARβ may intensify the phenomenon of proximalization by RA on limb regeneration4.
RA has been proposed to act as a morphogen in development and regeneration, specifically as an instructive molecule. It has also been stated that RA may act as a permissive molecule21,30. Regardless of the mechanism of action, RA has been demonstrated as a necessary signaling molecule in the generation and maintenance of blastema in regenerating zebrafish fins and as the diffusive signal arising from the trunk that together with FGF establishes the identity of P-D axis in the developing limb31,32. Investigating the dynamics between RA and FGFs signaling33,34 with the use of transcriptome strategies could contribute to our understanding of regulatory hierarchies and elusive unidentified molecules controlling axial patterning. Also of interest is whether the activation of RARβ in blastema regulates a mechanism similar to that occurring in bilateral symmetry establishment during somitogenesis by RA35. Based on the B-L duplication, we propose that the mirror-limb duplications generated in several animal models may also be interpreted as a partial bilateral duplication that will be evident as more and more proximal bones become duplicated.
Methods
Larvae hindlimb amputation
Xenopus laevis were injected with chorionic gonadotropin to induce spawning. Larvae were fed with powdered staple fish food. Stage 51–51.5 larvae were anesthetized by immersion in cool water and hindlimbs were unilaterally amputated using tungsten needles and leaving intact the proximal third. Contralateral limbs were left as developing internal control. Five cm-long juvenile axolotls were maintained in aquaria and fed daily with Artemia salina. Forelimb amputations were performed at the mid-stylopod with nail clippers and treated with R115866 as described below. This research protocol was reviewed and approved by the Institutional Review Board for the Care and Use of Laboratory Animals of Instituto de Investigaciones Biomedicas, UNAM.
CYP-26 inhibitor and RARβ agonist treatment
Amputated larvae were left to recover for 8 h. They were then transferred in groups of 3 to glass containers with 100 ml of aquarium water and treated with R115866 (obtained from Janssen Research Foundation) from a 50 mM stock solution in DMSO, or with AC-55649 (BIOMOL) from a 50 mM stock solution in DMSO, or added with vehicle control (v/v DMSO). DMSO treated larvae regenerate and develop normal limbs in all cases assessed (16/16). Containers were covered with aluminum foil to protect them from light. Treatment with the CYP26 inhibitor lasted for 72 h, while with the RARβ2 agonist treatment it lasted only for 18 h. Following treatment, regeneration and development was allowed to continue until early metamorphosis, around stage 629, when all treated larvae died.
Skeletal staining, histology and cell death detection
Pre-metamorphic larvae were euthanized with an overdose of tricaine, then fixed and dehydrated overnight (O/N) in 100% ethanol. Thereafter they were incubated in acetone for 24 h and stained for 3 h at 37°C and then O/N at room temperature in Alcian Blue and Alizarin red in 70% ethanol with 5% acetic acid. Finally, they were rinsed in tap water before clearing in 1% KOH and 20% glycerol for 24 h and then placed in graded glycerol.
References
Sikes, J. M. & Bely, A. E. Making heads from tails: development of a reversed anterior-posterior axis during budding in an acoel. Dev Biol 338, 86–97 (2010).
Allard, P. & Tabin, C. J. Achieving bilateral symmetry during vertebrate limb development. Semin Cell Dev Biol 20, 479–484 (2009).
Niazi, I. A. & Saxena, S. Abnormal hind limb regeneration in tadpoles of the toad, Bufo andersoni, exposed to excess vitamin A. Folia Biol (Krakow) 26, 3–8 (1978).
Maden, M. Vitamin A and pattern formation in the regenerating limb. Nature 295, 672–675 (1982).
Fujii, H. et al. Metabolic inactivation of retinoic acid by a novel P450 differentially expressed in developing mouse embryos. Embo J 16, 4163–4173 (1997).
Blumberg, B. et al. Novel retinoic acid receptor ligands in Xenopus embryos. Proc Natl Acad Sci U S A 93, 4873–4878 (1996).
Pijnappel, W. W. et al. The retinoid ligand 4-oxo-retinoic acid is a highly active modulator of positional specification. Nature 366, 340–344 (1993).
Stoppie, P. et al. R115866 inhibits all-trans-retinoic acid metabolism and exerts retinoidal effects in rodents. J Pharmacol Exp Ther 293, 304–312 (2000).
Nieukoop, P. D. & Faber, J. Normal Table of Xenopus laevis (Daudin). (1967).
Scadding, S. R. & Maden, M. Comparison of the effects of vitamin A on limb development and regeneration in Xenopus laevis tadpoles. J Embryol Exp Morphol 91, 35–53 (1986).
Lund, B. W. et al. Discovery of a potent, orally available and isoform-selective retinoic acid beta2 receptor agonist. J Med Chem 48, 7517–7519 (2005).
Maden, M. The homeotic transformation of tails into limbs in Rana temporaria by retinoids. Dev Biol 159, 379–391 (1993).
Maden, M. Retinoids as endogenous components of the regenerating limb and tail. Wound Repair Regen 6, 358–365 (1998).
Scadding, S. R. Citral, an inhibitor of retinoic acid synthesis, modifies pattern formation during limb regeneration in the axolotl Ambystoma mexicanum. Canadian Journal of Zoology 77, 1835–1837 (1999).
Scadding, S. R. & Maden, M. Comparison of the effects of vitamin A on limb development and regeneration in the axolotl, Ambystoma mexicanum. J Embryol Exp Morphol 91, 19–34 (1986).
Scadding, S. R. & Maden, M. Retinoic acid gradients during limb regeneration. Dev Biol 162, 608–617 (1994).
McEwan, J., Lynch, J. & Beck, C. W. Expression of key retinoic acid modulating genes suggests active regulation during development and regeneration of the amphibian limb. Dev Dyn 240, 1259–1270 (2011).
Monaghan, J. R. & Maden, M. Visualization of retinoic acid signaling in transgenic axolotls during limb development and regeneration. Dev Biol 368, 63–75 (2012).
Carter, C., Clark, A., Spencer, G. & Carlone, R. Cloning and expression of a retinoic acid receptor beta2 subtype from the adult newt: evidence for an early role in tail and caudal spinal cord regeneration. Dev Dyn 240, 2613–2625 (2011).
Abu-Abed, S. S. et al. Mouse P450RAI (CYP26) expression and retinoic acid-inducible retinoic acid metabolism in F9 cells are regulated by retinoic acid receptor gamma and retinoid X receptor alpha. J Biol Chem 273, 2409–2415 (1998).
Zhao, X. et al. Retinoic acid promotes limb induction through effects on body axis extension but is unnecessary for limb patterning. Curr Biol 19, 1050–1057 (2009).
Pennimpede, T. et al. The role of CYP26 enzymes in defining appropriate retinoic acid exposure during embryogenesis. Birth Defects Res A Clin Mol Teratol 88, 883–894 (2010).
Niazi, I. A., Pescitelli, M. J. & Stocum, D. Stage-dependent effects of retinoic acid on regenerating urodele limbs. Roux's Arch Dev Biol 194, 355–363 (1985).
Scadding, S. R. & Maden, M. Comparison of the effects of vitamin A on limb development and regeneration in Xenopus laevis tadpoles. J Embryol Exp Morphol 91, 19–34 (1986).
Mohanty-Hejmadi, P., Dutta, S. K. & Mahapatra, P. Limbs generated at site of tail amputation in marbled balloon frog after vitamin A treatment. Nature 355, 352–353 (1992).
Rutledge, J. C. et al. Limb and lower-body duplications induced by retinoic acid in mice. Proc Natl Acad Sci U S A 91, 5436–5440 (1994).
Dudley, A. T., Ros, M. A. & Tabin, C. J. A re-examination of proximodistal patterning during vertebrate limb development. Nature 418, 539–544 (2002).
Echeverri, K. & Tanaka, E. M. Proximodistal patterning during limb regeneration. Dev Biol 279, 391–401 (2005).
Maden, M. The effect of vitamin A on limb regeneration in Rana temporaria. Dev Biol 98, 409–416 (1983).
Gibert, Y., Gajewski, A., Meyer, A. & Begemann, G. Induction and prepatterning of the zebrafish pectoral fin bud requires axial retinoic acid signaling. Development 133, 2649–2659 (2006).
Blum, N. & Begemann, G. Retinoic acid signaling controls the formation, proliferation and survival of the blastema during adult zebrafish fin regeneration. Development 139, 107–116 (2012).
Rosello-Diez, A., Ros, M. A. & Torres, M. Diffusible signals, not autonomous mechanisms, determine the main proximodistal limb subdivision. Science 332, 1086–1088 (2011).
Mercader, N., Tanaka, E. M. & Torres, M. Proximodistal identity during vertebrate limb regeneration is regulated by Meis homeodomain proteins. Development 132, 4131–4142 (2005).
Mariani, F. V., Ahn, C. P. & Martin, G. R. Genetic evidence that FGFs have an instructive role in limb proximal-distal patterning. Nature 453, 401–405 (2008).
Vilhais-Neto, G. C. et al. Rere controls retinoic acid signalling and somite bilateral symmetry. Nature 463, 953–957 (2010).
Acknowledgements
The authors thank Marcia Bustamante and Fernando Rosales for technical assistance and Dr. Christopher Wood, Dr. David Stocum, Dr. Katia del Rio-Tsonis and Dr. Panagiotis Tsonis for careful reading of the manuscript. We thank Dionisio Slava of the biological station Umbral Axochiatl A.C. for supplying the axolotl larvae. This study was partially supported by CONACyT grants 53484 and 168642, DGAPA-UNAM grants IN214511 and IN220808. RC thanks for the fellowship Estancias Posdoctorales by grant 53484 from CONACyT. Isabel Pérez Montfort corrected the English version of this manuscript.
Author information
Authors and Affiliations
Contributions
Study conception and design: R.C., J.C.-M. Acquisition of data: R.C. Analysis and interpretation of data: R.C., J.C.-M. Wrote the paper: R.C., J.C.-M.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Rights and permissions
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
About this article
Cite this article
Cuervo, R., Chimal-Monroy, J. Chemical activation of RARβ induces post-embryonically bilateral limb duplication during Xenopus limb regeneration. Sci Rep 3, 1886 (2013). https://doi.org/10.1038/srep01886
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/srep01886
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.