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Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos

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Abstract

Neural tube defects, including spina bifida, develop in the curly tail mutant mouse as a result of delayed closure of the posterior neuropore at 10.5 days of gestation. Affected embryos are characterized by increased ventral curvature of the caudal region. To determine whether closure of the neuropore could be affected by this angle of curvature, we experimentally enhanced the curvature of non-mutant embryos. The amnion was opened in 9.5 day embryos; after 20 h of culture, a proportion of the embryos exhibited a tightly wrapped amnion with enhanced curvature of the caudal region compared with the control embryos in which the opened amnion remained inflated. Enhanced curvature correlated with a higher frequency of embryos with an open posterior neuropore, irrespective of developmental stage within the range, 27–32 somites. Thus, within this somite range, caudal curvature is a more accurate determinant for normal spinal neurulation than the exact somite stage. Enhanced ventral curvature of the curly tail embryo correlates with an abnormal growth difference between the neuroepithelium and ventral structures (the notochord and hindgut). We experimentally corrected this imbalance by culturing under conditions of mild hyperthermia and subsequently determined whether the angle of curvature would also be corrected. The mean angle of curvature and length of the posterior neuropore were both reduced in embryos cultured at 40.5°C by comparison with control embryos cultured at 38°C. We conclude that the sequence of morphogenetic events leading to spinal neural tube defects in curly tail embryos involves an imbalance of growth rates, which leads to enhanced ventral curvature that, in turn, leads to delayed closure of the posterior neuropore.

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References

  • Armitage P, Berry G (1987) Statistical methods in medical research, 2nd edn. Blackwell, Oxford

    Google Scholar 

  • Beier DR, Dushkin H, Teile T (1995) Haplotype analysis of intraspecific backcross curly-tail mice confirms the localization of ct to chromosome 4. Mamm Genome 6: 269–272

    Google Scholar 

  • Brook FA, Shum ASW, Straaten HWM van, Copp AJ (1991) Curvature of the caudal region is responsible for failure of neural fold closure in the curly tail (ct) mouse embryo. Development 113: 671–678

    Google Scholar 

  • Brown NA (1990) Routine assessment of morphology and growth: scoring systems and measurements of size. In: Copp AJ, Cockroft DL (eds) Postimplantation mammalian embryos: a practical approach. IRL Press, Oxford, pp 15–40

    Google Scholar 

  • Chen WH, Morris-Kay GM, Copp AJ (1995) Genesis and prevention of spinal neural tube defects in the curly tail mutant mouse: involvement of retinoic acid and its nuclear receptors RAR-β and RAR-γ. Development 121: 681–691

    Google Scholar 

  • Cockroft DL (1988) Changes with gestational age in the nutritional requirements of postimplantation rat embryos in culture. Teratology 38: 281–290

    Google Scholar 

  • Cockroft DL (1990) Dissection and culture of postimplantation embryos. In: Copp AJ, Cockroft DL (eds) Postimplantation mammalian embryos: a practical approach. IRL Press, Oxford, pp 15–40

    Google Scholar 

  • Copp AJ (1985) Relationship between timing of posterior neuropore closure and development of spinal neural tube defects in mutant (curly tail) and normal mouse embryos in culture. J Embryol Exp Morphol 88: 39–54

    Google Scholar 

  • Copp AJ, Bernfield M (1988) Accumulation of basement membrane-associated hyaluronate is reduced in the posterior neuropore region of mutant (curly tail) mouse embryos developing spinal neural tube defects. Dev Biol 130: 583–590

    Google Scholar 

  • Copp AJ, Seller MJ, Polani PE (1982) Neural tube development in mutant (curly tail) and normal mouse embryos: the timing of posterior neuropore closure in vivo and in vitro. J Embryol Exp Morphol 69: 151–167

    Google Scholar 

  • Copp AJ, Brook FA, Roberts HJ (1988a) A cell-type-specific abnormality of cell proliferation in mutant (curly tail) mouse embryos developing spinal neural tube defects. Development 104: 285–295

    Google Scholar 

  • Copp AJ, Crolla JA, Brook FA (1988b) Prevention of spinal neural tube defects in the mouse embryo by growth retardation during neurulation. Development 104: 297–303

    Google Scholar 

  • Copp AJ, Brook FA, Estibeiro JP, Shum ASW, Cockroft DL (1990) The embryonic development of mammalian neural tube defects. Prog Neurobiol 35: 363–403

    Google Scholar 

  • Embury S, Seller MJ, Adinolfi M, Polani PE (1979) Neural tube defects in curly-tail mice. I. Incidence and expression. Proc R Soc Lond [Biol] 206: 85–94

    Google Scholar 

  • Freeman SJ, Lloyd JB (1983) Evidence that protein ingested by the rat visceral yolk sac yields amino acids for synthesis of embryonic protein. J Embryol Exp Morphol 73: 307–315

    Google Scholar 

  • Grüneberg H (1954) Genetical studies on the skeleton of the mouse. VIII. Curly tail. J Genet 52: 52–67

    Google Scholar 

  • Hanks JH, Wallace RE (1949) Relation of oxygen and temperature in the preservation of tissues by refrigeration. Proc Soc Exp Biol Med 71: 196

    Google Scholar 

  • Herken R (1980) Cell cycle phase specificity of hydroxyurea and its effects on the cell kinetics in embryonic spinal cord. Teratology 21: 9–14

    Google Scholar 

  • Higginbottom MC, Jones KL, Hall BD, Smith DW (1979) The amniotic band disruption complex: timing of amniotic rupture and variable spectra of consequent defects. J Pediatr 95: 544–549

    Google Scholar 

  • Hunter ES III, Sadler TW (1988) Embryonic metabolism of foetal fuels in whole-embryo culture. Toxicol In Vitro 2: 163–167

    Google Scholar 

  • Jacobson AG, Tam PPL (1982) Cephalic neurulation in the mouse embryo analysed by SEM and morphometry. Anat Rec 203: 341–359

    Google Scholar 

  • Langenbach RJ, Danenberg PV, Heidelberger C (1972) Thymidylate synthetase: mechanism of inhibition by 5-fluoro-2′-deoxyuridylate. Biochem Biophys Res Commun 48: 1565–1571

    Google Scholar 

  • Linder CC, Davisson MT (1994) Mouse models for studying neural tube defects. Neurology News; The Jackson Laboratory, Bar Harbor, Me

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265–275

    CAS  PubMed  Google Scholar 

  • McLone DG, Stephens FD (1990) Amniotic constraints as a cause of embryonic neural deformation. Concepts Pediatr Neurosurg 10: 22–29

    Google Scholar 

  • Neumann PE, Frankel WN, Letts VA, Coffin JM, Copp AJ, Bernfield M (1994) Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice. Nat Genet 6: 357–362

    Google Scholar 

  • New DAT, Coppola PT, Terry S (1973) Culture of explanted rat embryos in rotating tubes. J Reprod Fertil 35: 135–138

    Google Scholar 

  • Park HW, Shepard TH (1994) Volume and glucose concentration of rat amniotic fluid: effects on embryo nutrition and axis rotation. Teratology 49: 465–469

    Google Scholar 

  • Renfree MB, Hensleigh HC, McLaren A (1975) Developmental changes in the composition and amount of mouse fetal fluids. J Embryol Exp Morphol 33: 435–446

    Google Scholar 

  • Scott WJ, Ritter EJ, Wilson JG (1971) DNA synthesis inhibition and cell death associated with hydroxyurea teratogenesis in rat embryos. Dev Biol 26: 306–315

    Google Scholar 

  • Seller MJ (1983) The cause of neural tube defects: some experiments and a hypothesis. J Med Genet 20: 164–168

    Google Scholar 

  • Seller MJ, Perkins KJ (1983) Effect of hydroxyurea on neural tube defects in curly tail mouse. J Craniofac Genet Dev Biol 3: 11–17

    Google Scholar 

  • Seller MJ, Perkins KJ (1986) Effect of mitomycin C on the neural tube defects of curly tail mouse. Teratology 33: 305–309

    Google Scholar 

  • Shepard TH, Tanimura T, Robkin MA (1970) Energy metabolism in early mammalian embryos. Dev Biol [Suppl] 4: 42–58

    Google Scholar 

  • Straaten HWM van, Hekking JWM, Copp AJ, Bernfield M (1992) Deceleration and acceleration in the rate of posterior neuropore closure during neurulation in the curly tail (ct) mouse embryo. Anat Embryol 185: 169–174

    Google Scholar 

  • Straaten HWM van, Hekking JWM, Consten C, Copp AJ (1993) Intrinsic and extrinsic factors in the mechanism of neurulation: effect of curvature of the body axis in closure of the posterior neuropore. Development 117: 1163–1172

    Google Scholar 

  • Tanimura T (1968) Effects of mitomycin C administered at various stages of pregnancy upon mouse fetuses. Okajimas Folia Anat Jpn 44: 337–355

    Google Scholar 

  • Tanimura T, Shepard TH (1970) Glucose metabolism by rat embryos in vitro. Proc Soc Exp Biol Med 135: 51–54

    Google Scholar 

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Peeters, M.C.E., Hekking, J.W.M., van Straaten, H.W.M. et al. Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos. Anat Embryol 193, 123–130 (1996). https://doi.org/10.1007/BF00214703

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