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Basic fibroblast growth factor can induce exclusively neural tissue in Triturus ectoderm explants

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Abstract

Ectoderm was isolated from early gastrulae of Triturus alpestris and induced with recombinant basic fibroblast growth factor (b-FGF). Neural tissue differentiated in about 38% of the explants which were induced by 2,5 μg/ml FGF. These explants do not contain other tissues, or contain only small amounts of mesenchyme and melanophores which are probably derived from induced neural crest. It is therefore unlikely that these neural tissues are secondarily induced. The other explants contain predominantly blastema tissue, endothelium/ mesothelium, small amounts of skeletal muscle and, rarely, notochord besides neural tissues. The mitotic rate was enhanced in about 20% of the induced explants. Possible mechanisms for the unexpected neural-inducing activity of b-FGF in Triturus ectoderm are discussed.

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References

  • Ariizumi T, Moriya N, Uchiyama H, Asashima M (1991) Concentration dependent inducing activity of activin A. Roux's Arch Dev Biol 200:230–233

    Google Scholar 

  • Asashima M, Nakano H, Shimada K, Kinoshita K, Ishii K, Shibai H, Ueno N (1990a) Mesodermal induction in early amphibian embryos by activin A (erythroid differentiation factor). Roux's Arch Dev Biol 198:330–335

    Google Scholar 

  • Asashima M, Nakano H, Uchiyama H, Davids M, Plessow S, Loppnow-Blinde B, Hoppe P, Dan H, Tiedemann H (1990b) The vegetalizing factor belongs to a family of mesoderm-inducing proteins related to activin. Naturwissenschaften 77:389–391

    Google Scholar 

  • Asashima M, Uchiyama H, Nakano H, Eto Y, Eijima D, Sugino H, Davids M, Plessow S, Born J, Hoppe P, Tiedemann H, Tiedemann H(1991b) The vegetalizing factor from chicken embryos: its EDF (activin A)-like activity. Mech Dev 34:135–141

    Google Scholar 

  • Becker U, Tiedemann H, Tiedemann H (1959) Versuche zur Determination von embryonalem Amphibiengewebe durch Induktionsstoffe in Lösung. Z Naturforsch 14b:608–609

    Google Scholar 

  • Born J, Hoppe P, Janeczek J, Tiedemann H, Tiedemann H (1986) Covalent coupling of neuralizing factors from Xenopus to Sepharose beads: no decrease of inducing activity. Cell Differ 19:97–101

    Google Scholar 

  • Born J, Janeczek J, Schwarz W, Tiedemann H, Tiedemann H (1989) Activation of masked neural determinants in amphibian eggs and embryos and their release from the inducing tissue. Cell Differ Dev 27:1–7

    Google Scholar 

  • Charalambous BM, Wheeler KP (1985) Sodium-induced conformation changes in membrane transport proteins. FEBS Lett 189:163–166

    Google Scholar 

  • Davids M (1988) Protein kinases in amphibian ectoderm induced for neural differentiation. Roux's Arch Dev Biol 197:339–344

    Google Scholar 

  • Davids M, Loppnow B, Tiedemann H, Tiedemann H (1987) Neural differentiation of amphibian gastrula ectoderm exposed to phorbol ester. Roux's Arch Dev Biol 196:137–140

    Google Scholar 

  • Ding X, Mc Keehan WE, Xu J, Grunz H (1992) Spatial and temporal localization of FGF-receptors in Xenopus laevis. Roux's Arch Dev Biol 201:334–339

    Google Scholar 

  • Eijnden-van Raaij AJM van den, Zoelent EJJ van, Nimmen K van, Koster CH, Snoek GT, Durston AJ, Huylebroeck D (1990) Activin-like factor from a Xenopus laevis cell line responsible for mesoderm induction. Nature 345:732–734

    Google Scholar 

  • Flickinger RA (1949) A study of the metabolism of amphibian neural crest cells during their migration and pigmentation in vitro. J Exp Zool 112:465–484

    Google Scholar 

  • Friesel R, Dawid IB (1991) cDNA cloning and developmental expression of fibroblast growth factor receptors from Xenopus laevis. Mol Cell Biol 11:2481–2488

    Google Scholar 

  • Gillespie LL, Paterno GD, Slack JMW (1989) Analysis of competence: receptors for fibroblast growth factor in early Xenopus embryos. Development 106:203–208

    Google Scholar 

  • Gospodarowicz D, Cheng S, Lui GM, Baird A, Böhlen P (1984) Isolation of brain fibroblast growth factor by heparin-Sepharose affinity chromatography: Identity with pituitary fibroblast growth factor. Proc Natl Acad Sci USA 81:6963–6967

    Google Scholar 

  • Grunz H, Multier-Lajous AM, Herbst R, Arkenberg G (1975) The differentiations of isolated amphibian ectoderm with or without treatment with an inductor. Roux's Arch Dev Biol 178:277–284

    Google Scholar 

  • Grunz H, Born J, Tiedemann H, Tiedemann H (1986) The activation of a neuralizing factor in the neural plate is correlated with its homoiogenetic inducing activity. Roux's Arch Dev Biol 195:464–466

    Google Scholar 

  • Grunz H, McKeehan WL, Knöchel W, Born J, Tiedemann H, Tiedemann H (1988) Inductions of mesodermal tissues by acidic and basic heparin binding growth factors. Cell Differ 22:183–190

    Google Scholar 

  • Hamburger V (1962) A manual of experimental embryology. The University of Chicago Press, Chicago London, p 211

    Google Scholar 

  • Hart MJ, Eva A, Evans T, Aaronson StA, Cerione RA (1991) Catalysis of guanine nucleotide exchange on the CDC 42 Hs protein by the dbl oncogene product. Nature 354:311–314

    Google Scholar 

  • Hemmati-Brivanlou A, Melton DA (1992) A truncated activin receptor inhibits mesoderm induction and formation of axial structures in Xenopus embryos. Nature 359:609–614

    Google Scholar 

  • Holtfreter J (1933) Der Einfluβ von Wirtsalter und verschiedenen Organbezirken auf die Differenzierung von angelagertem Gastrulaektoderm. Arch Entwicklungsmech Org 127:619–775

    Google Scholar 

  • Hörstadius S (1950) The neural crest. Oxford University Press, Oxford London

    Google Scholar 

  • Janeczek J, Born J, Hoppe P, Tiedemann H (1992) Partial characterization of neural-inducing factors from Xenopus gastrulae. Evidence for a larger protein complex containing the factor. Roux's Arch Dev Biol 201:30–35

    Google Scholar 

  • Kimmelman D, Abraham JA, Haaparanta T, Palisi ThM, Kirschner MW (1988) The presence of fibroblast growth factor in the frog egg: its role as a natural inducer. Science 242:1053–1056

    Google Scholar 

  • Knöchel W, Born J, Hoppe P, Loppnow-Blinde B, Tiedemann H, Tiedemann H, McKeehan WE, Grunz H (1987) Mesoderm inducing factors. Their possible relationship to heparin-binding growth factors and transforming growth factor β. Naturwissenschaften 74:604–606

    Google Scholar 

  • Knöchel W, Grunz H, Loppnow-Blinde B, Tiedemann H, Tiedemann H (1989) Mesoderm induction and blood island formation of angiogenic growth factors and embryonic inducing factors. Blut 59:207–213

    Google Scholar 

  • Lobb RR, Harper JW, Fett JW (1986) Purification of heparin-binding growth factors: a review. Anal Biochem 154:1–14

    Google Scholar 

  • Lopashov GV, Selter H, Montenarh M, Knöchel W, Grunz H, Tiedemann H, Tiedemann H (1992) Neural inducing factors in neuroblastoma and retinoblastoma cell lines. Extraction with acid ethanol. Naturwissenschaften 79:365–367

    Google Scholar 

  • Moriarty TM, Padrell E, Carty DS, Omrj G, Landau EM, Iyengar R (1990) Go protein as signal transducer in the pertussis toxin-sensitive phosphatidylinositol pathway. Nature 343:79–82

    Google Scholar 

  • Moriya N, Asashima M (1992) Mesoderm and neural inductions in newt ectoderm by activin A. Dev Growth Differ 34:589–594

    Google Scholar 

  • Otte PA, Köster CH, Snoek GT, Durston AJ (1988) Proteinkinase C mediates neural induction in Xenopus laevis. Nature 334:618–620

    Google Scholar 

  • Pituello P, Homburger V, Saint-Jeannet JP, Audigier Y, Bockaert J, Duprat AM (1991) Expression of the guanine nucleotide-binding protein Go correlates with the state of neural competence in the amphibian embryo. Dev Biol 145:311–322

    Google Scholar 

  • Shi DL, Feige JJ, Rion JF, Simone DW de, Boucaut JC (1992) Differential expression and regulation of two distinct fibroblast growth factor receptors during early development of the urodele amphibian Pleurodeles waldii. Development 116:261–273

    Google Scholar 

  • Shu C, Farnsworth CL, Neel BG, Feig LA (1992) Molecular cloning of c-DNA's encoding a guanine-nucleotide-releasing factor for Ras p 21. Nature 358:351–354

    Google Scholar 

  • Siegel G, Grunz H, Grundmann H, Tiedemann H, Tiedemann H (1985) Embryonic induction and cation concentrations in amphibian embryos. Cell Differ 17:209–219

    Google Scholar 

  • Slack JMW, Darlington BG, Heath JK, Godsave SF (1987) Mesoderm induction in early Xenopus embryos by heparin-binding growth factors. Nature 326:197–200

    Google Scholar 

  • Smith JC, Price BMJ, Nimmen K van, Huylebroeck D (1990) Identification of a potent Xenopus mesoderm-inducing factor as a homologue of activin A. Nature 345:729–731

    Google Scholar 

  • Suzuki A, Kuwabara Y, Kuwana T (1976) Analysis of cell proliferation during early embryogenesis. Dev Growth Differ 18:447–455

    Google Scholar 

  • Suzuki A, Yashimura Y, Yano Y (1986) Neural-inducing activity of newly mesodermalized ectoderm. Roux's Arch Dev Biol 195:168–172

    Google Scholar 

  • Thomsen G, Woolf T, Whitman M, Sokol S, Vaughan J, Vale W, Melton DA (1990) Activins are expressed early in Xenopus embryogenesis and can induce axial mesoderm and anterior structures. Cell 63:485–493

    Google Scholar 

  • Tiedemann Hildegard (1986a) Test of embryonic inducing factors: Advantages and disadvantages of different procedures. In: Serrero G, Hayashi J (eds) Cellular endocrinology: Hormonal control of embryonic and cellular differentiation. Alan R. Liss, New York, pp 25–34

    Google Scholar 

  • Tiedemann Hildegard (1986b) The molecular mechanism of neural induction: neural differentiation of Triturus ectoderm exposed to Hepes buffer. Roux's Arch Dev Biol 195:399–402

    Google Scholar 

  • Tiedemann H (1990) Cellular and molecular aspects of embryonic induction. Zool Sci 7:171–186

    Google Scholar 

  • Tiedemann H, Lottspeich F, Davids M, Knochel S, Hoppe P, Tiedemann H (1992) The vegetalizing factor. A member of the evolutionary highly conserved activin family. FEBS Lett 300:123–126

    Google Scholar 

  • Tiedemann H, Grunz H, Knochel W, Tiedemann H (1993) Inducing factors and the molecular mechanism of differentiation in early amphibian development. Ontogenez 24:5–25

    Google Scholar 

  • Tiedemann-Waechter Hildegard (1960) Die Selbstdifferenzierungsfähigkeit und Induktionsfähigkeit medianer und lateraler Teile der Rumpfmedullarplatte bei Urodelen. Arch Entwicklungsmech Org 152:303–338

    Google Scholar 

  • Yamada T (1989) Cell type expression mediated by cell-cycle events, and signaled by mitogens and growth inhibitors. Int Rev Cytol 117:215–255

    Google Scholar 

  • Yamada T, Takata K (1961) A technique for testing macromolecular samples in solution for morphogenetic effects on the isolated ectoderm of the amphibian gastrula. Dev Biol 3:411–423

    Google Scholar 

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Tiedemann, H., Grunz, H., Loppnow-Blinde, B. et al. Basic fibroblast growth factor can induce exclusively neural tissue in Triturus ectoderm explants. Roux's Arch Dev Biol 203, 304–309 (1994). https://doi.org/10.1007/BF00457801

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