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Junctional Neural Tube Defect

  • Eibach, Sebastian (Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University) ;
  • Pang, Dachling (Department of Paediatric Neurosurgery, Great Ormond Street Hospital for Children, NHS Trust)
  • Received : 2020.01.22
  • Accepted : 2020.03.09
  • Published : 2020.05.01

Abstract

Junctional neurulation represents the most recent adjunct to the well-known sequential embryological processes of primary and secondary neurulation. While its exact molecular processes, occurring at the end of primary and the beginning of secondary neurulation, are still being actively investigated, its pathological counterpart -junctional neural tube defect (JNTD)- had been described in 2017 based on three patients whose well-formed secondary neural tube, the conus, is widely separated from its corresponding primary neural tube and functionally disconnected from corticospinal control from above. Several other cases conforming to this bizarre neural tube arrangement have since appeared in the literature, reinforcing the validity of this entity. The cardinal clinical, neuroimaging, and electrophysiological features of JNTD, and the hypothesis of its embryogenetic mechanism, form part of this review.

Keywords

References

  1. Ali M, McNeely PD : Junctional neural tube defect: a supporting case report. Childs Nerv Syst 34 : 1447-1448, 2018 https://doi.org/10.1007/s00381-018-3855-1
  2. Beck CW, Slack JM : A developmental pathway controlling outgrowth of the Xenopus tail bud. Development 126 : 1611-1620, 1999 https://doi.org/10.1242/dev.126.8.1611
  3. Catala M, Teillet MA, De Robertis EM, Le Douarin NM : A spinal cord fate map in the avian embryo: while regressing, Hensen's node lays down the notochord and floor plate thus joining the spinal cord lateral walls. Development 122 : 2599-2610, 1996 https://doi.org/10.1242/dev.122.9.2599
  4. Colas JF, Schoenwolf GC : Towards a cellular and molecular understanding of neurulation. Dev Dyn 221 : 117-145, 2001 https://doi.org/10.1002/dvdy.1144
  5. Cooper O, Sweetman D, Wagstaff L, Munsterberg A : Expression of avian prickle genes during early development and organogenesis. Dev Dyn 237 : 1442-1448, 2008 https://doi.org/10.1002/dvdy.21490
  6. Copp AJ, Greene ND : Genetics and development of neural tube defects. J Pathol 220 : 217-230, 2010 https://doi.org/10.1002/path.2643
  7. Copp AJ, Greene ND, Murdoch JN : The genetic basis of mammalian neurulation. Nat Rev Genet 4 : 784-793, 2003 https://doi.org/10.1038/nrg1181
  8. Criley BB : Analysis of the embryonic sources and mechanisms of development of posterior levels of chick neural tubes. J Morphol 128 : 465-501, 1969 https://doi.org/10.1002/jmor.1051280406
  9. Dady A, Blavet C, Duband JL : Timing and kinetics of E- to N-cadherin switch during neurulation in the avian embryo. Dev Dyn 241 : 1333-1349, 2012. https://doi.org/10.1002/dvdy.23813
  10. Dady A, Havis E, Escriou V, Catala M, Duband JL : Junctional neurulation: a unique developmental program shaping a discrete region of the spinal cord highly susceptible to neural tube defects. J Neurosci 34 : 13208-13221, 2014 https://doi.org/10.1523/JNEUROSCI.1850-14.2014
  11. Doudney K, Ybot-Gonzalez P, Paternotte C, Stevenson RE, Greene ND, Moore GE, et al. : Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients. Am J Med Genet A 136 : 90-92, 2005
  12. Dzamba BJ, Jakab KR, Marsden M, Schwartz MA, DeSimone DW : Cadherin adhesion, tissue tension, and noncanonical wnt signaling regulate fibronectin matrix organization. Dev Cell 16 : 421-432, 2009 https://doi.org/10.1016/j.devcel.2009.01.008
  13. Eibach S, Moes G, Hou YJ, Zovickian J, Pang D : Unjoined primary and secondary neural tubes: junctional neural tube defect, a new form of spinal dysraphism caused by disturbance of junctional neurulation. Childs Nerv Syst 33 : 1633-1647, 2017 https://doi.org/10.1007/s00381-016-3288-7
  14. Eibach S, Moes G, Zovickian J, Pang D : Limited dorsal myeloschisis associated with dermoid elements. Childs Nerv Syst 33 : 55-67, 2017 https://doi.org/10.1007/s00381-016-3207-y
  15. Florea SM, Faure A, Brunel H, Girard N, Scavarda D : A case of junctional neural tube defect associated with a lipoma of the filum terminale: a new subtype of junctional neural tube defect? J Neurosurg Pediatr 21 : 601-605, 2018 https://doi.org/10.3171/2018.1.PEDS17492
  16. Goto T, Davidson L, Asashima M, Keller R : Planar cell polarity genes regulate polarized extracellular matrix deposition during frog gastrulation. Curr Biol 15 : 787-793, 2005 https://doi.org/10.1016/j.cub.2005.03.040
  17. Griffith CM, Wiley MJ, Sanders EJ : The vertebrate tail bud: three germ layers from one tissue. Anat Embryol (Berl) 185 : 101-113, 1992 https://doi.org/10.1007/BF00185911
  18. Hamburger V, Hamilton HL : A series of normal stages in the development of the chick embryo. J Morphol 88 : 49-92, 1951 https://doi.org/10.1002/jmor.1050880104
  19. Hughes AF, Freeman RB : Comparative remarks on the development of the tail cord among higher vertebrates. J Embryol Exp Morphol 32 : 355-363, 1974
  20. Kostovic-Knezevic L, Gajovic S, Svajger A : Morphogenetic features in the tail region of the rat embryo. Int J Dev Biol 35 : 191-195, 1991
  21. Lowery LA, Sive H : Strategies of vertebrate neurulation and a re-evaluation of teleost neural tube formation. Mech Dev 121 : 1189-1197, 2004 https://doi.org/10.1016/j.mod.2004.04.022
  22. Mills CL, Bellairs R : Mitosis and cell death in the tail of the chick embryo. Anat Embryol (Berl) 180 : 301-308, 1989 https://doi.org/10.1007/BF00315888
  23. Muller F, O'Rahilly R : The primitive streak, the caudal eminence and related structures in staged human embryos. Cells Tissues Organs 177 : 2-20, 2004 https://doi.org/10.1159/000078423
  24. Nakaya Y, Kuroda S, Katagiri YT, Kaibuchi K, Takahashi Y : Mesenchymal-epithelial transition during somitic segmentation is regulated by differential roles of Cdc42 and Rac1. Dev Cell 7 : 425-438, 2004 https://doi.org/10.1016/j.devcel.2004.08.003
  25. Nievelstein RA, Hartwig NG, Vermeij-Keers C, Valk J : Embryonic development of the mammalian caudal neural tube. Teratology 48 : 21-31, 1993 https://doi.org/10.1002/tera.1420480106
  26. O'Rahilly R, Muller F : Somites, spinal ganglia, and centra. Enumeration and interrelationships in staged human embryos, and implications for neural tube defects. Cells Tissues Organs 173 : 75-92, 2003 https://doi.org/10.1159/000068948
  27. Pang D : Sacral agenesis and caudal spinal cord malformations. Neurosurgery 32 : 755-779; discussion 778-779, 1993 https://doi.org/10.1227/00006123-199305000-00009
  28. Pang D, Zovickian J, Lee JY, Moes GS, Wang KC : Terminal myelocystocele: surgical observations and theory of embryogenesis. Neurosurgery 70 : 1383-1404; discussion 1404-1405, 2012 https://doi.org/10.1227/NEU.0b013e31824c02c0
  29. Pang D, Zovickian J, Moes GS : Retained medullary cord in humans: late arrest of secondary neurulation. Neurosurgery 68 : 1500-1519; discussion 1519, 2011 https://doi.org/10.1227/NEU.0b013e31820ee282
  30. Pang D, Zovickian J, Oviedo A : Long-term outcome of total and neartotal resection of spinal cord lipomas and radical reconstruction of the neural placode: part I-surgical technique. Neurosurgery 65 : 511-528; discussion 528-529, 2009 https://doi.org/10.1227/01.NEU.0000350879.02128.80
  31. Pang D, Zovickian J, Oviedo A, Moes GS : Limited dorsal myeloschisis: a distinctive clinicopathological entity. Neurosurgery 67 : 1555-1579; discussion 1579-1580, 2010 https://doi.org/10.1227/NEU.0b013e3181f93e5a
  32. Pang D, Zovickian J, Wong ST, Hou YJ, Moes GS : Limited dorsal myeloschisis: a not-so-rare form of primary neurulation defect. Childs Nerv Syst 29 : 1459-1484, 2013 https://doi.org/10.1007/s00381-013-2189-2
  33. Saitsu H, Yamada S, Uwabe C, Ishibashi M, Shiota K : Development of the posterior neural tube in human embryos. Anat Embryol (Berl) 209 : 107-117, 2004 https://doi.org/10.1007/s00429-004-0421-2
  34. Saraga-Babic M, Krolo M, Sapunar D, Terzic J, Biocic M : Differences in origin and fate between the cranial and caudal spinal cord during normal and disturbed human development. Acta Neuropathol 91 : 194- 199, 1996 https://doi.org/10.1007/s004010050413
  35. Schmidt C, Voin V, Iwanaga J, Alonso F, Oskouian RJ, Topale N, et al. : Junctional neural tube defect in a newborn: report of a fourth case. Childs Nerv Syst 33 : 873-875, 2017 https://doi.org/10.1007/s00381-017-3353-x
  36. Schoenwolf GC : Histological and ultrastructural studies of secondary neurulation in mouse embryos. Am J Anat 169 : 361-376, 1984 https://doi.org/10.1002/aja.1001690402
  37. Schoenwolf GC, Delongo J : Ultrastructure of secondary neurulation in the chick embryo. Am J Anat 158 : 43-63, 1980 https://doi.org/10.1002/aja.1001580106
  38. Schoenwolf GC, Smith JL : Mechanisms of neurulation. Methods Mol Biol 136 : 125-134, 2000
  39. Shimokita E, Takahashi Y : Secondary neurulation: fate-mapping and gene manipulation of the neural tube in tail bud. Dev Growth Differ 53 : 401-410, 2011 https://doi.org/10.1111/j.1440-169X.2011.01260.x
  40. Tam PP : The histogenetic capacity of tissues in the caudal end of the embryonic axis of the mouse. J Embryol Exp Morphol 82 : 253-266, 1984
  41. Tao H, Suzuki M, Kiyonari H, Abe T, Sasaoka T, Ueno N : Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity. Proc Natl Acad Sci U S A 106 : 14426-14431, 2009 https://doi.org/10.1073/pnas.0901332106
  42. Thiery JP, Sleeman JP : Complex networks orchestrate epithelial-mesenchymal transitions. Nat Rev Mol Cell Biol 7 : 131-142, 2006 https://doi.org/10.1038/nrm1835
  43. Wang KC, Lee JS, Kim K, Im YJ, Park K, Kim KH, et al. : Do junctional neural tube defect and segmental spinal dysgenesis have the same pathoembryological background? Childs Nerv Syst 36 : 241-250, 2020 https://doi.org/10.1007/s00381-019-04425-4
  44. Yang HJ, Wang KC, Chi JG, Lee MS, Lee YJ, Kim SK, et al. : Cytokinetics of secondary neurulation in chick embryos: Hamburger and Hamilton stages 16-45. Childs Nerv Syst 22 : 567-571, 2006 https://doi.org/10.1007/s00381-006-0087-6
  45. Ybot-Gonzalez P, Savery D, Gerrelli D, Signore M, Mitchell CE, Faux CH, et al. : Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development 134 : 789-799, 2007 https://doi.org/10.1242/dev.000380

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