Development of floor plate, neurons and axonal outgrowth pattern in the early spinal cord of the notochord-deficient chick embryo (original) (raw)

• Boloventa P, Dodd J (1990) Guidance of commissural growth cones at the floor plate in embryonic rat spinal cord. Development 109:435–447
  PubMed Google Scholar
• Fontaine-Pérus JC, Chanconie M, Ledouarin NM, Gershon MD, Rothman TP (1989) Mitogenic effect of muscle on the neuroepithelium of the developing spinal cord. Development 107:413–422
  PubMed Google Scholar
• Fraser S, Keynes R, Lumsden A (1990) Segmentation in the chick embryo hindbrain is defined by cell lineage restrictions. Nature 344:431–435
  PubMed Google Scholar
• Grabowski CT (1956) The effects of the excision of Hensen's node on the early development of the chick embryo. J Exp Zool 133:301–343
  Google Scholar
• Hamburger V, Hamilton HGA (1951) A series of normal stages in the development of the chick embryo. J Morphol 88:49–92
  Google Scholar
• Karnovsky MJ an Roots L (1964) A “direct coloring” thiocholin method for cholinesterase. J Histochem Cytochem 12:219
  PubMed Google Scholar
• Kosher RA, Lash JW (1975) Notochordal stimulation of in-vitro somite chondrogenesis before and after enzymatic removal of perinotochordal materials. Dev Biol 42:362–378
  PubMed Google Scholar
• Layer PG, Alber R, Rathjen FG (1988) Sequential activation of butyrylcholinsterease in rostral half somites and acetylcholinesterase in motoneurones and myotomes preceding growth of motor axons. Development 102:387–396
  PubMed Google Scholar
• Lyser KM (1964) Early differentiation of motor neuroblasts in the chick embryo as studied by electron microscopy. I. General aspects. Dev Biol 10:433–466
  PubMed Google Scholar
• Lyser KM (1970) Early differentiation of the chick embryo spinal cord in organ culture: light and electron microscopy. Anat Rec 169:45–64
  Google Scholar
• Malacinski GM, Youn BW (1981) Neural plate morphogenesis and axial stretching in notochord-defective_Xenopus laevis_ embryos. Dev Biol 88:352–357
  PubMed Google Scholar
• Miki A, Atoji Y, Mizoguti H (1981) Time of origin of the neuroblasts in the neural tube of the chick embryo determined by histochemical observation of acetylcholinesterase. Acta Histochem Cytochem 14:641–653
  Google Scholar
• Mizoguti H, Miki A (1985) Interrelationship among the proliferating ability, morphological development and acetylcholinesterase activity of the neural tube cells in early chick embryos. Acta Histoch Cytochem 18:85–95
  Google Scholar
• Nagele RG, Hunter E, Bush K, Lee HY (1987) Studies on the mechanisms of neurulation in the chick: morphometric analysis of force distribution within the neuroepithelium during neural tube formation. J Exp Zool 244:425–436
  PubMed Google Scholar
• Newgreen DF, Scheel M, Kastner V (1986) Morphogenesis of sclerotome and neural crest in avian embryos. In vivo and in vitro studies on the role of notochordal extracellular material. Cell Tissue Res 244:299–313
  PubMed Google Scholar
• Pettway Z, Guillory G, Bronner-Fraser M (1990) Absence of neural crest cells from the region surrounding implanted notochords in situ. Dev Biol 142:335–345
  PubMed Google Scholar
• Placzek M, Tessier-Lavigne M, Yamada T, Jessell T, Dodd J (1990) Mesodermal control of neural cell identity — floor plate induction by the notochord. Science 250:985–988
  PubMed Google Scholar
• Rothman TP, Gershon MD, Fontaine-Perus JC, Chanconie M, Le Douarin NM (1987) The effect of back-transplants of the embryonic gut wall on growth of the neural tube. Dev Biol 124:331–346
  PubMed Google Scholar
• Schoenwolf GC (1985) Shaping and bending of the avian neuroepithelium: morphometric analyses. Dev Biol 109:127–139
  PubMed Google Scholar
• Schoenwolf GC (1988) Microsurgical analyses of avian neurulation: separation of medial and lateral tissues. J Comp Neurol 276:498–507
  PubMed Google Scholar
• Schoenwolf GC, Franks MV (1984) Quantitative analyses of changes in cell shapes during bending of the avian neural plate. Dev Biol 105:257–272
  PubMed Google Scholar
• Schoenwolf GC, Sheard P (1990) Fate mapping the avian epiblast with focal injections of a fluorescent-histochemical marker: ectodermal derivatives. J Exp Zool 255:323–339
  PubMed Google Scholar
• Smith JL, Schoenwolf GC (1987) Cell cycle and neuroepithelial cell shape during bending of the chick neural plate. Anat Rec 218:196–206
  PubMed Google Scholar
• Smith JL, Schoenwolf GC (1988) Role of cell-cycle in regulating neuroepithelial cell shape during bending of the chick neural plate. Cell Tissue Res 252:491–500
  PubMed Google Scholar
• Smith JL, Schoenwolf GC (1989) Notochordal induction of cell wedging in the chick neural plate and its role in neural tube formation. J Exp Zool 250:49–62
  PubMed Google Scholar
• Straaten HWM van, Drukker J (1987) Influence of the notochord on the morphogenesis of the neural tube. In: Wolff JR et al. (eds) Mesenchymal-epithelial interactions in neural development. NATO ASI series. Springer, Berlin Heidelberg, pp 153–162
  Google Scholar
• Straaten HWM van, Hekking JWM, Thors F, Wiertz-Hoessels EL, Drukker J (1985a) Induction of an additional floor plate in the neural tube. Acta Morphol Neerl Scand 23:91–97
  PubMed Google Scholar
• Straaten HWM van, Thors F, Wiertz-Hoessels ELJM, Hekking JWM, Drukker J (1985b) Effect of a notochordal implant on the early morphogenesis of the neural tube and neuroblasts: histometrical and histological results. Dev Biol 110:247–254
  PubMed Google Scholar
• Straaten HWM van, Hekking JWM, Drukker J (1986) The demonstration of acetylcholinesterase in plastic sections. Its application as a marker of early neuronal development. Acta Histochem Jena 32 suppl:185–190
  Google Scholar
• Straaten HWM van, Hekking JWM, Wiertz-Hoessels EL, Thors F, Drukker J (1988a) Effect of the notochord on the differentiation of a floor plate area in the neural tube of the chick embryo. Anat Embryol 177:317–324
  PubMed Google Scholar
• Straaten HWM van, Hekking JWM, Drukker J (1988b) A HCltoluidine blue staining procedure specific for nuclei, mitotic figures and axons in GMA embedded embryonic neural tissue. Stain Technol 65:360–362
  Google Scholar
• Straaten HWM van, Hekking JWM, Beursgens JPWM, Terwindt-Rouwenhorst E, Drukker J (1989) Effect of the notochord on proliferation and differentiation in the neural tube of the chick embryo. Development 107:793–803
  PubMed Google Scholar
• Tessier-Lavigne M, Placzek M, Lumsden AGS, Dodd J, Jessell TM (1988) Chemotropic guidance of developing axons in the mammalian central nervous system. Nature 336:775–776
  PubMed Google Scholar
• Tosney KW (1988) Proximal tissues and patterned neurite outgrowth at the lumbosacral level of the chick embryo: partial and complete deletion of the somite. Dev Biol 127:266–286
  PubMed Google Scholar
• Vasan NS (1983) Analysis of perinotochordal materials. 2. Studies on the influence of proteoglycans in somite chondrogenesis. J Embryol Exp Morphol 73:263–274
  PubMed Google Scholar
• Wagner M, Thaller C, Jessell T, Eichele G (1990) Polarizing activity and retinoid synthesis in the floor plate of the neural tube. Nature 345:819–822
  PubMed Google Scholar
• Watterson RL (1965) Structure and mitotic behavior of the early neural tube. In: Haan R, Ursprung H (eds) Organogenesis. Holt, Rinehart and Winston, New York, pp 129–159
  Google Scholar
• Yaginuma H, Shiga T, Homma S, Ishihara R, Oppenheim RW (1990) Identification of early developing axon projections from spinal interneurons in the chick embryo with a neuron specific_β_-tubulin antibody: evidence for a new pioneer pathway in the spinal cord. Development 108:705–716
  PubMed Google Scholar
• Youn BW, Malacinski GM (1981) Axial structure development in ultraviolet-irradiated (notochord-defective) amphibian embryos. Dev Biol 83:339–352
  PubMed Google Scholar