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The community effect and ectoderm-mesoderm interaction inXenopus muscle differentiation

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Abstract

Community effects are believed to play an important role in the patterning of many tissues during development. They involve an interaction between neighbouring equivalent cells that is necessary for them to proceed to their fully differentiated state. However, the mechanisms underlying these effects remain unclear. In this paper, diffusion-based mathematical models are constructed and analysed in order to study possible mechanisms for the community effect inXenopus muscle differentiation. These models differ from each other in the assumptions that are made about the nature of an inhibitory effect that ectodermal tissue has been observed to have on muscle differentiation. It is possible to construct consistent models based on all the forms of inhibition considered. However, each model requires the diffusible factors on which it is based to have different properties. The current data from tissues reaggregate experiments are insufficient to determine the mechanisms underlying the community effect; the work presented here suggests that quantitative analysis of a further series of reaggregate experiments will make it possible to distinguish between the proposed mechanisms.

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References

  • Altshuler, D. and C. Cepko. 1992. A temporally regulated, diffusible activity is required for rod photoreceptor development in vitro.Development 114, 947–957.

    Google Scholar 

  • Altshuler, D., J. J. Turco, J. Rush and C. Cepko. 1993. Taurine promotes the differentiation of a vertebrate retinal cell type in vitro.Development 119, 1317–1328.

    Google Scholar 

  • Babloyantz, A. 1977. Self-organization phenomena resulting from cell-cell contact.J. Theor. Biol. 68, 551–561.

    Article  Google Scholar 

  • Cooke, J., K. Symes and E. J. Smith. 1989. Potentiation by the lithium ion of morphogenetic responses to aXenopus inducing factor.Development 105, 549–558.

    Google Scholar 

  • Cooke, J. 1995. Morphogens in vertebrate development: how do they work?BioEssays 17, 93–96.

    Article  Google Scholar 

  • Cossu, G., R. Kelly, S. Di Donna, E. Vivarelli and M. Buckingham. 1995. Myoblast differentiation during mammalian somitogenesis is dependent upon a community effect.Proc. Natl. Acad. Sci. U.S.A. 92, 2254–2258.

    Article  Google Scholar 

  • Crick, F. H. C. 1970. Diffusion in embryogenesis.Nature 225, 420–422.

    Article  Google Scholar 

  • Green, J. B. A., J. C. Smith and J. C. Gerhart. 1994. Slow emergence of a multithreshold response to activin requires cell-contact-dependent sharpending but not prepattern.Development 120, 2271–2278.

    Google Scholar 

  • Gurdon, J. B. 1988. A community effect in animal development.Nature 336, 772–774.

    Article  Google Scholar 

  • Gurdon, J. B., K. Kao, K. Kato and N. D. Hopwood. 1992. Muscle gene activation inXenopus requires intercellular communication during gastrula as well as blastula stages.Development 116, 137–142 (Suppl.).

    Google Scholar 

  • Gurdon, J. B., K. Kato and P. Lemaire. 1993a. The community effect, dorsalization and mesoderm induction.Curr. Opin. Gen. Dev. 3, 662–667.

    Article  Google Scholar 

  • Gurdon, J. B., P. Lemaire and K. Kato. 1993b. Community effects and related phenomena in development.Cell 75, 831–834.

    Article  Google Scholar 

  • Gurdon, J. B., E. Tiller, J. Roberts and K. Kato. 1993c. A community effect in muscle development.Current Biology 3, 1–11.

    Article  Google Scholar 

  • Hemmati-Brivanlou, A. and D. A. Melton. 1994a. Inhibition of activin receptor signaling promotes neuralization inXenopus.Cell 77, 273–281.

    Article  Google Scholar 

  • Hemmati-Brivanlou, A., O. G. Kelly and D. A. Melton. 1994b. Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity.Cell 77, 283–295.

    Article  Google Scholar 

  • Ho, R. K. 1992. Cell movements and cell fate during zebrafish gastrulation.Development 116, 65–73 (Suppl.).

    Google Scholar 

  • Hopwood, N. D., A. Pluck, J. B. Gurdon and S. M. Dilworth. 1992. Expression of XMyoD protein in earlyXenopus laevis embryos.Development 114, 31–38.

    Google Scholar 

  • Jouanneau, J., G. Moens, Y. Bourgeois, M. F. Poupon and J. P. Thiery. 1994. A minority of carcinoma cells producing acidic fibroblast growth factor induces a community effect for tumor progression.Proc. Natl. Acad. Sci. U.S.A. 91, 286–290.

    Article  Google Scholar 

  • Kato, K. and J. B. Gurdon. 1994. An inhibitory effect ofXenopus gastrula ectoderm on muscle cell differentiation and its role for dorsoventral patterning of mesoderm.Developmental Biology 163, 222–229.

    Article  Google Scholar 

  • Lewis, J., J. M. W. Slack and L. Wolpert. 1977. Thresholds in development.J. Theor. Biol. 65, 579–590.

    Article  Google Scholar 

  • Saxon, L. and S. Toivonen. 1962.Primary Embryonic Induction, London: Logos Press.

    Google Scholar 

  • Shymko, R. M. and L. Glass. 1976. Cellular and geometric control of tissue growth and mitotic instability.J. Theor. Biol. 63, 355–374.

    Article  Google Scholar 

  • Slack, J. M. W. 1991. The nature of the mesoderm inducing signal inXenopus. A transfilter study.Development 113, 661–669.

    Google Scholar 

  • Smith, J. C., V. Cunliffe, M-A. J. O'Reilly, S. Schulte-Merker and M. Umbhauer. 1995.Xenopus Brachyury.Sem. Dev. Biol. 6, 405–410.

    Google Scholar 

  • Stüttem, I. and J. A. Campos-Ortega. 1991. Cell commitment and cell interactions in the ectoderm ofDrosophila melanogaster.Development 113, 39–46 (Suppl. 2).

    Google Scholar 

  • Symes, K., C. Yordán and M. Mercola. 1994. Morphological differences inXenopus embryonic mesodermal cells are specified as an early response to distinct threshold concentrations of activin.Development 120, 2339–2346.

    Google Scholar 

  • Weintraub, H. 1993. The MyoD family and myogenesis: redundancy, networks and thresholds.Cell 75, 1241–1244.

    Article  Google Scholar 

  • Weston, M. J. D., K. Kato and J. B. Gurdon. 1994. A community effect is required for amphibian notochord differentiation.Roux's Arch. Dev. Biol. 203, 250–253.

    Article  Google Scholar 

  • Wilkinson, D. G. 1995. Genetic control of segmentation in the vertebrate hindbrain.Persp. Dev. Neurobiol. 3, 29–38.

    MathSciNet  Google Scholar 

  • Wilson, P. A. and D. A. Melton. 1994. Mesodermal patterning by an inducer gradient depends on secondary cell-cell communication.Current Biology 4, 676–686.

    Article  Google Scholar 

  • Yuen, I. S. and R. H. Gomer. 1994. Cell density-sensing inDictyostelium by means of the accumulation rate, diffusion coefficient and activity thresholds of a protein secreted by starved cells.J. Theor. Biol. 167, 273–282.

    Article  Google Scholar 

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Monk, N.A.M. The community effect and ectoderm-mesoderm interaction inXenopus muscle differentiation. Bltn Mathcal Biology 59, 409–425 (1997). https://doi.org/10.1007/BF02459458

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  • DOI: https://doi.org/10.1007/BF02459458

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