Skip to main content
Log in

Stage-dependent effects of retinoic acid on regenerating urodele limbs

  • Published:
Wilhelm Roux's archives of developmental biology Aims and scope Submit manuscript

Summary

Following amputation through the distal zeugopodium, regenerating limbs of larvalAmbystoma mexicanum and pre and post-metamorphicPleurodeles waltlii were treated with 150 μg of retinoic acid (RA) per gram of body weight, at the dedifferentiation, early bud, medium bud, late bud or early redifferentiation stages of regeneration. The effect of RA on regenerate morphogenesis differed as a function of the stage at which it was administered. When given during dedifferentiation or at early bud stages, RA evoked proximodistal duplications of stump segments in the regenerates. The maximum duplication index (DI) inAbystoma was achieved when RA was injected at 4 days post-amputation, which corresponds to the stage of dedifferentiation; and inPleurodeles at 10 days post-amputation, which corresponds to a stage midway between early bud and medium bud. When RA was administered at later stages, the DI declined progressively to zero or nearly zero by the stage of early redifferentiation in both species. The decline in DI was due to a decreased frequency of duplication, not to a decrease in the magnitude of duplication in individual regenerates. At the same time, there was an increase in hypomorphism and aberrant morphogenesis of both duplicating and non-duplicating regenerates. These results indicate that regenerative cells are differentially sensitive to RA in a stage-dependent way.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Cope FO, Knox KL, Hall RC (1984) Retinoid binding to nuclei and microsomes of rat testes interstitial cells: I-Mediation of retinoid binding by cellular retinoid-binding proteins. Nutr Res 4: 289–304

    Google Scholar 

  • Connelly TG (1977) The relationship between growth, developmental stage and postamputation age of the regeneration blastema of the newt,Notophthalmus viridescens. J. Exp Zool 199: 33–40

    PubMed  Google Scholar 

  • Dhouailly D, Hardy MH, Sengel P (1980) Formation of feathers on foot scales a stage dependent morphogenetic response to retinoic acid. J Embryol Exp Morphol 58: 63–78

    PubMed  Google Scholar 

  • Elias PM, Chung J-C, Orozco-Topete R, Nemanic MK (1983) Membrane glycoconjugate visualization and biosynthesis in normal and retinoid-treated epidermis. J Invest Dermatol 81: 81–85

    Google Scholar 

  • Fell HB (1957) The effect of excess vitamin A on cultures of embryonic chicken skin explanted at different stages of differentiation. Proc R Soc B 146: 242–256

    Google Scholar 

  • Gallandre F, Kistler A (1980) Inhibition and reversion of chondrogenesis by retionoic acid in rat limb bud cell cultures. Wilhelm Roux's Arch 189: 25–33

    Google Scholar 

  • Hardy MH (1983) Vitamin A and the epithelial-mesenchymal interactions in skin differentiation. In: Sawyer RH, Fallon JF (eds) Epithelial-mesenchymal interactions in development. Praeger, New York, pp 163–188

    Google Scholar 

  • Jangir OP, Niazi IA (1978) Stage dependent effects of vitamin A excess on limbs during ontogenesis and regeneration in tadpoles of the toadBufo melanostictus (Schneider). Indian J Exp Biol 16: 438–445

    Google Scholar 

  • Jetten AM (1984) Modulation of cell growth by retinoids and their possible mechanisms of action. Fed Proc 43: 134–139

    PubMed  Google Scholar 

  • Kistler A (1984) Reversible suppression by ionophore A21387 of retinoic acid-induced cartilage resorption in cultured fetal rat bones. Wilhelm Roux's Arch 193: 121–126

    Google Scholar 

  • Kochbar DM (1973) Limb development in mouse embryos: Analysis of teratogenic effects of retinoic acid. Teratol 7: 289–298

    Google Scholar 

  • Kochhar DM (1977) Cellular basis of congenital limb deformity induced in mice by vitamin A. Birth Defects: Original Article Series 13: 111–154

    Google Scholar 

  • Kraft AS, Anderson WB (1983) Characterization of cytosolic calcium-activated phospholipid-dependent protein kinase activity in embryonal carcinoma cells. J Biol Chem 258: 9178–9183

    PubMed  Google Scholar 

  • Kwasigroch TE, Kochhar DM (1980) Production of congenital limb defects with retinoic acid: phenomenological evidence of progressive differentiation during limb morphogenesis. Anat Embryol 161: 105–113

    PubMed  Google Scholar 

  • Levin LV, Clark JN, Quill HR, Newberne PM, Wolf G (1983) Effect of retinoic acid on the synthesis of glycoproteins of mouse skin tumors during progression from promoted skin through papillomas to carcinomas. Cancer Res 43: 1724–1732

    PubMed  Google Scholar 

  • Lewis CA, Pratt RM, Pennypacker JP, Hassel JR (1978) Inhibition of limb chondrogenesisin vitro by vitamin A: Alterations in cell surface characteristics. Dev Biol 64: 31–47

    PubMed  Google Scholar 

  • Liau G, Ong DE, Chytil F (1981) Interaction of the retinol/cellular retinol-binding protein complex with isolated nuclei and nuclear components. J Cell Biol 91: 63–68

    PubMed  Google Scholar 

  • Lotan R (1980) Effects of vitamin A and its analogs (retinoids) on normal and neoplastic cells. Biochim Biophys Acta 605: 33–91

    PubMed  Google Scholar 

  • Maden M (1982) Vitamin A and pattern formation in the regenerating limb. Nature 295: 672–675

    PubMed  Google Scholar 

  • Maden M (1983a) The effect of vitamin A on limb regeneration inRana temporaria. Dev Biol 98: 409–416

    PubMed  Google Scholar 

  • Maden M (1983b) The effect of vitamin A on the regenerating axolotl limb. J Embryol Exp Morphol 77: 273–295

    PubMed  Google Scholar 

  • Niazi IA, Alam S (1984) Regeneration of whole limbs from shank stumps in toad tadpoles treated with vitamin A. Wilhelm Roux's Arch 193: 111–116

    Google Scholar 

  • Niazi IA, Ratnasamy CS (1984) Regeneration of whole limbs in toad tadpoles treated with retinol palmitate after the wound healing stage. J Exp Zool 230: 501–505

    Google Scholar 

  • Niazi IA, Saxena S (1978) Abnormal hind limb regeneration in tadpoles of the toad,Bufo andersoni, exposed to excess vitamin A. Folia Biol [Krakow] 26: 3–11

    Google Scholar 

  • Robinson J, Freinkel RK, Gotschalk R (1984) Effect of retinoic acid and low calcium conditions on surface glycoconjugates defined by differential lectin labeling in mouse epidermal cell celture. Br J Dermatol 110: 17–27

    PubMed  Google Scholar 

  • Sporn MB, Roberts AB (1983) Role of retinoids in differentiation and carcinogenesis. Cancer Res 43: 3034–3040

    PubMed  Google Scholar 

  • Stocum DL (1979) Stages of forelimb regeneration inAmbystoma maculatum. J Exp Zool 209: 395–416

    PubMed  Google Scholar 

  • Strickland S, Mahdavi V (1978) The induction of differentiation in teratocarcinoma stem cells by retinoic acid. Cell 15: 393–403

    Article  PubMed  Google Scholar 

  • Thoms SD, Stocum DL (1984) Retinoic acid-induced pattern duplication in regenerating urodele limbs. Dev Biol 103: 319–328

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Niazi, I.A., Pescitelli, M.J. & Stocum, D.L. Stage-dependent effects of retinoic acid on regenerating urodele limbs. Wilhelm Roux' Archiv 194, 355–363 (1985). https://doi.org/10.1007/BF00877373

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00877373

Key words

Navigation