Skip to main content
Top
Published in: Child's Nervous System 10/2017

01-10-2017 | A.J. RAIMONDI ISPN AWARD

Unjoined primary and secondary neural tubes: junctional neural tube defect, a new form of spinal dysraphism caused by disturbance of junctional neurulation

Authors: Sebastian Eibach, Greg Moes, Yong Jin Hou, John Zovickian, Dachling Pang

Published in: Child's Nervous System | Issue 10/2017

Login to get access

Abstract

Introduction

Primary and secondary neurulation are the two known processes that form the central neuraxis of vertebrates. Human phenotypes of neural tube defects (NTDs) mostly fall into two corresponding categories consistent with the two types of developmental sequence: primary NTD features an open skin defect, an exposed, unclosed neural plate (hence an open neural tube defect, or ONTD), and an unformed or poorly formed secondary neural tube, and secondary NTD with no skin abnormality (hence a closed NTD) and a malformed conus caudal to a well-developed primary neural tube.

Methods and results

We encountered three cases of a previously unrecorded form of spinal dysraphism in which the primary and secondary neural tubes are individually formed but are physically separated far apart and functionally disconnected from each other. One patient was operated on, in whom both the lumbosacral spinal cord from primary neurulation and the conus from secondary neurulation are each anatomically complete and endowed with functioning segmental motor roots tested by intraoperative triggered electromyography and direct spinal cord stimulation. The remarkable feature is that the two neural tubes are unjoined except by a functionally inert, probably non-neural band.

Conclusion

The developmental error of this peculiar malformation probably occurs during the critical transition between the end of primary and the beginning of secondary neurulation, in a stage aptly called junctional neurulation. We describe the current knowledge concerning junctional neurulation and speculate on the embryogenesis of this new class of spinal dysraphism, which we call junctional neural tube defect.
Literature
1.
go back to reference Beck CW, Slack JMW (1999) A developmental pathway controlling outgrowth of the Xenopus tail bud. Development 126(8):1611–1620PubMed Beck CW, Slack JMW (1999) A developmental pathway controlling outgrowth of the Xenopus tail bud. Development 126(8):1611–1620PubMed
2.
go back to reference Bosoi CM, Capra V, Allache R, Trinh VQ, De Marco P, Merello E, Drapeau P, Bassuk AG, Kibar Z (2011) Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects. Hum Mutat 32:1371–1375CrossRefPubMedPubMedCentral Bosoi CM, Capra V, Allache R, Trinh VQ, De Marco P, Merello E, Drapeau P, Bassuk AG, Kibar Z (2011) Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects. Hum Mutat 32:1371–1375CrossRefPubMedPubMedCentral
3.
go back to reference Cai C, Shi O (2014) Genetic evidence in planar cell polarity signaling pathway in human neural tube defects. Front Med 8:68–78CrossRefPubMed Cai C, Shi O (2014) Genetic evidence in planar cell polarity signaling pathway in human neural tube defects. Front Med 8:68–78CrossRefPubMed
4.
go back to reference Catala M, Teillet MA, De Robertis EM, Le Douarin ML (1996) 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 122:2599–2610PubMed Catala M, Teillet MA, De Robertis EM, Le Douarin ML (1996) 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 122:2599–2610PubMed
5.
go back to reference Catala M, Teillet MA, Le Douarin ML (1995) Organization and development of the tail bud analyzed with the quail-chick chimaera system. Mech Dev 51:51–65CrossRefPubMed Catala M, Teillet MA, Le Douarin ML (1995) Organization and development of the tail bud analyzed with the quail-chick chimaera system. Mech Dev 51:51–65CrossRefPubMed
6.
go back to reference Colas JF, Schoenwolf GC (2001) Towards a cellular and molecular understanding of neurulation. Dev Dyn 221:117–145CrossRefPubMed Colas JF, Schoenwolf GC (2001) Towards a cellular and molecular understanding of neurulation. Dev Dyn 221:117–145CrossRefPubMed
7.
go back to reference Cooper O, Sweetman D, Wagstaff L, Munsterberg A (2008) Expression of avian prickle genes during early development and organogenesis. Dev Dyn 237:1442–1448CrossRefPubMed Cooper O, Sweetman D, Wagstaff L, Munsterberg A (2008) Expression of avian prickle genes during early development and organogenesis. Dev Dyn 237:1442–1448CrossRefPubMed
9.
go back to reference Copp AJ, Greene ND, Murdoch JN (2003) The genetic basis of mammalian neurulation. Nat Rev Genet 4:784–793CrossRefPubMed Copp AJ, Greene ND, Murdoch JN (2003) The genetic basis of mammalian neurulation. Nat Rev Genet 4:784–793CrossRefPubMed
10.
11.
go back to reference Criley BB (1969) Analysis of embryonic sources and mechanisms of development of posterior levels of chick neural tubes. J Morphol 128:465–501CrossRefPubMed Criley BB (1969) Analysis of embryonic sources and mechanisms of development of posterior levels of chick neural tubes. J Morphol 128:465–501CrossRefPubMed
12.
go back to reference Dady A, Blavet C, Duband JL (2012) Timing and kinetics of E- to N-cadherin switch during neurulation in the avian embryo. Dev Dyn 241:1333–1349CrossRefPubMed Dady A, Blavet C, Duband JL (2012) Timing and kinetics of E- to N-cadherin switch during neurulation in the avian embryo. Dev Dyn 241:1333–1349CrossRefPubMed
13.
go back to reference Dady A, Havis E, Escriou V, Catala M, Duband J-L (2014) Junctional neurulation: a unique developmental program shaping a discrete region of the spinal cord highly susceptible to neural tube defects. J Neurosci 34:13208–13221CrossRefPubMed Dady A, Havis E, Escriou V, Catala M, Duband J-L (2014) Junctional neurulation: a unique developmental program shaping a discrete region of the spinal cord highly susceptible to neural tube defects. J Neurosci 34:13208–13221CrossRefPubMed
14.
go back to reference Doudney K, Ybot-Gonzalez P, Patemotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P (2005) Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients. Am J Med Genet A 136:90–92CrossRefPubMed Doudney K, Ybot-Gonzalez P, Patemotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P (2005) Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients. Am J Med Genet A 136:90–92CrossRefPubMed
15.
go back to reference Dzamba BJ, Jakab KR, Marsden M, Schwartz MA, DeSimone DW (2009) Cadherin adhesion, tissue tension, and noncanonical Wnt signaling regulate fibronectin matrix organization. Dev Cell 16:421–432CrossRefPubMedPubMedCentral Dzamba BJ, Jakab KR, Marsden M, Schwartz MA, DeSimone DW (2009) Cadherin adhesion, tissue tension, and noncanonical Wnt signaling regulate fibronectin matrix organization. Dev Cell 16:421–432CrossRefPubMedPubMedCentral
16.
go back to reference Eibach S, Moes G, Zovickian J, Pang D (2016) Limited dorsal myeloschisis associated with dermoid elements. Childs Nerv Syst. Eibach S, Moes G, Zovickian J, Pang D (2016) Limited dorsal myeloschisis associated with dermoid elements. Childs Nerv Syst.
17.
go back to reference Goto T, Davidson L, Asashima M, Keller R (2005) Planar cell polarity genes regulate polarized extracellular matrix deposition during frog gastrulation. Curr Biol 15:787–793CrossRefPubMed Goto T, Davidson L, Asashima M, Keller R (2005) Planar cell polarity genes regulate polarized extracellular matrix deposition during frog gastrulation. Curr Biol 15:787–793CrossRefPubMed
18.
go back to reference Griffith CM, Wiley MJ, Sanders EJ (1992) The vertebrate tail bud: three germ layers from one tissue. Anat Embryol 185:101–113CrossRefPubMed Griffith CM, Wiley MJ, Sanders EJ (1992) The vertebrate tail bud: three germ layers from one tissue. Anat Embryol 185:101–113CrossRefPubMed
19.
go back to reference Hamburger V, Hamilton HL (1951) A series of normal stages in the development of the chick embryo. J Morphol 88:49–92CrossRefPubMed Hamburger V, Hamilton HL (1951) A series of normal stages in the development of the chick embryo. J Morphol 88:49–92CrossRefPubMed
20.
go back to reference Harris MJ, Juriloff DM (2010) An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. Birth Defects Res A Clin Mol Teratol 88:653–669CrossRefPubMed Harris MJ, Juriloff DM (2010) An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. Birth Defects Res A Clin Mol Teratol 88:653–669CrossRefPubMed
21.
go back to reference Harris MJ, Juriloff DM (2007) Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Res A Clin Mol Teratol 79:187–210CrossRefPubMed Harris MJ, Juriloff DM (2007) Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Res A Clin Mol Teratol 79:187–210CrossRefPubMed
22.
go back to reference Hughes AF, Freeman RB (1974) Comparative remarks on the development of the tail cord among higher vertebrates. J Embryol Exp Morphol 32:355–363PubMed Hughes AF, Freeman RB (1974) Comparative remarks on the development of the tail cord among higher vertebrates. J Embryol Exp Morphol 32:355–363PubMed
23.
go back to reference Kostovic-Knezevic L, Gajovic S, Svajger A (1991) Morphogenetic features in the tail region of the rat embryo. Int J Dev Biol 35(3):191–195PubMed Kostovic-Knezevic L, Gajovic S, Svajger A (1991) Morphogenetic features in the tail region of the rat embryo. Int J Dev Biol 35(3):191–195PubMed
24.
go back to reference Lemire RJ, Shepard TH, Alvord EC Jr (1965) Caudal myeloschisis (lumbo-sacral spina bifida cystica) in a five millimeter (horizon xiv) human embryo. Anat Rec 152:9–16CrossRefPubMed Lemire RJ, Shepard TH, Alvord EC Jr (1965) Caudal myeloschisis (lumbo-sacral spina bifida cystica) in a five millimeter (horizon xiv) human embryo. Anat Rec 152:9–16CrossRefPubMed
25.
go back to reference Lowery LA, Sive H (2004) Strategies of vertebrate neurulation and re-evaluation of teleost neural tube formation. Mech Dev 121(10):1189–1197CrossRefPubMed Lowery LA, Sive H (2004) Strategies of vertebrate neurulation and re-evaluation of teleost neural tube formation. Mech Dev 121(10):1189–1197CrossRefPubMed
26.
go back to reference Mills CL, Bellairs R (1989) Mitosis and cell death in the tail of chick embryo. Anat Embryol 180(3):301–308CrossRefPubMed Mills CL, Bellairs R (1989) Mitosis and cell death in the tail of chick embryo. Anat Embryol 180(3):301–308CrossRefPubMed
27.
go back to reference Mueller F, O'Rahilly R (1987) The development of the human brain, the closure of the caudal neuropore, and the beginning of secondary neurulation at stage 12. Anat Embryol 176(4):413–430CrossRef Mueller F, O'Rahilly R (1987) The development of the human brain, the closure of the caudal neuropore, and the beginning of secondary neurulation at stage 12. Anat Embryol 176(4):413–430CrossRef
28.
go back to reference Mueller F, O'Rahilly R (2004) The primitive streak, the caudal eminence and related structures in staged human embryos. Cells Tissue Organs 177(1):2–20CrossRef Mueller F, O'Rahilly R (2004) The primitive streak, the caudal eminence and related structures in staged human embryos. Cells Tissue Organs 177(1):2–20CrossRef
29.
go back to reference Nakaya Y, Kuroda S, Katagiri YT, Kaibuchi K, Takahashi Y (2004) Mesenchymal-epithelial transition during somitic segmentation is regulated by differential roles of Cdc42 and Rac1. Dev Cell 7:425–438CrossRefPubMed Nakaya Y, Kuroda S, Katagiri YT, Kaibuchi K, Takahashi Y (2004) Mesenchymal-epithelial transition during somitic segmentation is regulated by differential roles of Cdc42 and Rac1. Dev Cell 7:425–438CrossRefPubMed
30.
go back to reference Nievelstein RA, Hartwig NG, Vermeij-Keers C, Valk J (1993) Embryonic development of the mammalian caudal neural tube. Teratology 48:21–31CrossRefPubMed Nievelstein RA, Hartwig NG, Vermeij-Keers C, Valk J (1993) Embryonic development of the mammalian caudal neural tube. Teratology 48:21–31CrossRefPubMed
31.
go back to reference O'Rahilly R, Muller F (1994) Neurulation in the normal human embryo. CIBA Found Symp 181:70–89PubMed O'Rahilly R, Muller F (1994) Neurulation in the normal human embryo. CIBA Found Symp 181:70–89PubMed
32.
go back to reference O'Rahilly R, Muller F (2003) Somites, spinal ganglia, and centra: enumeration and interrelationships in staged human embryos, and implications for neural tube defects. Cells Tiss Org 173:75–92CrossRef O'Rahilly R, Muller F (2003) Somites, spinal ganglia, and centra: enumeration and interrelationships in staged human embryos, and implications for neural tube defects. Cells Tiss Org 173:75–92CrossRef
33.
go back to reference Pang D, Zovickian J, Lee JY, Moes GS, Wang KC (2012) Terminal myelocystocele: surgical observations and theory of embryogenesis. Neurosurgery 70:1383–1405CrossRefPubMed Pang D, Zovickian J, Lee JY, Moes GS, Wang KC (2012) Terminal myelocystocele: surgical observations and theory of embryogenesis. Neurosurgery 70:1383–1405CrossRefPubMed
34.
go back to reference Pang D, Zovickian J, Moes GS (2011) Retained medullary cord in humans: late arrest of secondary neurulation. Neurosurgery 68:1500–1519CrossRefPubMed Pang D, Zovickian J, Moes GS (2011) Retained medullary cord in humans: late arrest of secondary neurulation. Neurosurgery 68:1500–1519CrossRefPubMed
35.
go back to reference Pang D, Zovickian J, Ovieda A (2009) Long term outcome of total and near total resection of spinal cord lipomas and radical reconstruction of the neural placode part I: surgical technique. Neurosurgery 65:511–529CrossRefPubMed Pang D, Zovickian J, Ovieda A (2009) Long term outcome of total and near total resection of spinal cord lipomas and radical reconstruction of the neural placode part I: surgical technique. Neurosurgery 65:511–529CrossRefPubMed
36.
go back to reference Pang D, Zovickian J, Oviedo A, Moes GS (2010) Limited dorsal myeloschisis: a distinctive clinicopathological entity. Neurosurgery 67:1555–1580CrossRefPubMed Pang D, Zovickian J, Oviedo A, Moes GS (2010) Limited dorsal myeloschisis: a distinctive clinicopathological entity. Neurosurgery 67:1555–1580CrossRefPubMed
37.
go back to reference Pang D, Zovickian Z, Wong ST, Hou YJ, Moes GS (2013) Limited dorsal myeloschisis: a not-so-rare form of primary neurulation defect. Childs Nerv Syst 29:1459–1484CrossRefPubMed Pang D, Zovickian Z, Wong ST, Hou YJ, Moes GS (2013) Limited dorsal myeloschisis: a not-so-rare form of primary neurulation defect. Childs Nerv Syst 29:1459–1484CrossRefPubMed
38.
go back to reference Pang D (2010) Electrophysiological monitoring for tethered cord surgery. In: Yamada S (ed) Tethered cord syndrome. Thieme Medical Publishers, New York, Stuttgart, pp. 199–209 Pang D (2010) Electrophysiological monitoring for tethered cord surgery. In: Yamada S (ed) Tethered cord syndrome. Thieme Medical Publishers, New York, Stuttgart, pp. 199–209
39.
go back to reference Pang D (2010) Intraoperative neurophysiology of the conus medullaris and cauda equina. Childs Nerv Syst 26:411–412CrossRefPubMed Pang D (2010) Intraoperative neurophysiology of the conus medullaris and cauda equina. Childs Nerv Syst 26:411–412CrossRefPubMed
40.
41.
go back to reference Saitsu H, Yamada S, Uwabe C (2007) Aberrant differentiation of the axially condensed tail bud mesenchyme in human embryos with lumbosacral myeloschisis. Anat Rec 290:251–258CrossRef Saitsu H, Yamada S, Uwabe C (2007) Aberrant differentiation of the axially condensed tail bud mesenchyme in human embryos with lumbosacral myeloschisis. Anat Rec 290:251–258CrossRef
42.
go back to reference Saitsu H, Yamada S, Uwabe C, Ishibashi M, Shiota K (2004) Development of the posterior neural tube in human embryos. Anat Embryol 209:107–117PubMed Saitsu H, Yamada S, Uwabe C, Ishibashi M, Shiota K (2004) Development of the posterior neural tube in human embryos. Anat Embryol 209:107–117PubMed
43.
go back to reference Saraga-Babic M, Krolo M, Sapunar D, Terzic J, Biocic M (1996) Differences in origin and fate between the cranial and caudal spinal cord during normal and disturbed human development. Acta Neuropathol 91(2):194–199CrossRefPubMed Saraga-Babic M, Krolo M, Sapunar D, Terzic J, Biocic M (1996) Differences in origin and fate between the cranial and caudal spinal cord during normal and disturbed human development. Acta Neuropathol 91(2):194–199CrossRefPubMed
44.
go back to reference Schoenwolf GC, Delongo J (1980) Ultrastructure of secondary neurulation in the chick embryo. Am J Anat 158:43–63CrossRefPubMed Schoenwolf GC, Delongo J (1980) Ultrastructure of secondary neurulation in the chick embryo. Am J Anat 158:43–63CrossRefPubMed
45.
go back to reference Schoenwolf GC, Smith JL (2000) Mechanisms of neurulation. Methods Mol Biol 136:125–134PubMed Schoenwolf GC, Smith JL (2000) Mechanisms of neurulation. Methods Mol Biol 136:125–134PubMed
46.
go back to reference Schoenwolf GC (1984) Histological and ultrastructure studies of secondary neurulation in mouse embryos. Am J Anat 169:361–376CrossRefPubMed Schoenwolf GC (1984) Histological and ultrastructure studies of secondary neurulation in mouse embryos. Am J Anat 169:361–376CrossRefPubMed
47.
go back to reference Shimokita E, Takahashi Y (2011) Secondary neurulation: fate-mapping and gene manipulation of the neural tube in tail bud. Develop Growth Differ 53:401–411CrossRef Shimokita E, Takahashi Y (2011) Secondary neurulation: fate-mapping and gene manipulation of the neural tube in tail bud. Develop Growth Differ 53:401–411CrossRef
48.
go back to reference Swalla BJ (1993) Mechanisms of gastrulation and tail formation in ascidians. Microsc Res Tech 26(4):274–284CrossRefPubMed Swalla BJ (1993) Mechanisms of gastrulation and tail formation in ascidians. Microsc Res Tech 26(4):274–284CrossRefPubMed
49.
go back to reference Tam PPL (1984) The histogenetic capacity of tissues in the caudal end of the embryonic axis of the mouse. J Embryol Exp Mophol 82:253–266 Tam PPL (1984) The histogenetic capacity of tissues in the caudal end of the embryonic axis of the mouse. J Embryol Exp Mophol 82:253–266
50.
go back to reference Tao H, Suzuki M, Kiyonari H, Abe T, Sasaoka T, Ueno N (2009) Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity. Proc Natl Acad Sci U S A 106:14426–14431CrossRefPubMedPubMedCentral Tao H, Suzuki M, Kiyonari H, Abe T, Sasaoka T, Ueno N (2009) Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity. Proc Natl Acad Sci U S A 106:14426–14431CrossRefPubMedPubMedCentral
51.
go back to reference Thiery JP, Sleeman JP (2006) Complex networks orchestrate epithelial-mesenchymal transitions. Nat Rev Mol Cell Biol 7:131–142CrossRefPubMed Thiery JP, Sleeman JP (2006) Complex networks orchestrate epithelial-mesenchymal transitions. Nat Rev Mol Cell Biol 7:131–142CrossRefPubMed
52.
go back to reference Wallingford JB, Niswander LA, Shaw GM, Finnel RH (2013) The continuing challenge of understanding, preventing and treating neural tube defects. Science 339:1222002CrossRefPubMedPubMedCentral Wallingford JB, Niswander LA, Shaw GM, Finnel RH (2013) The continuing challenge of understanding, preventing and treating neural tube defects. Science 339:1222002CrossRefPubMedPubMedCentral
53.
go back to reference Yang HJ, Wang KC, Chi JG, Lee MS, Lee YJ, Kim SK, Lee CS, Cho BK (2006) Cytokinetics of secondary neurulation in chick embryos: Hamburger and Hamilton stages 16-45. Childs Nerv Syst 22:567–571 Yang HJ, Wang KC, Chi JG, Lee MS, Lee YJ, Kim SK, Lee CS, Cho BK (2006) Cytokinetics of secondary neurulation in chick embryos: Hamburger and Hamilton stages 16-45. Childs Nerv Syst 22:567–571
54.
go back to reference Yang HJ, Wang KC, Chi JG, Lee YJ, Kim SK, Cho BK (2003) Neural differentiation of caudal cell mass (secondary neurulation) in chick embryos: Hamburger and Hamilton stages 16-45. Dev Brain Res 142:31–36CrossRef Yang HJ, Wang KC, Chi JG, Lee YJ, Kim SK, Cho BK (2003) Neural differentiation of caudal cell mass (secondary neurulation) in chick embryos: Hamburger and Hamilton stages 16-45. Dev Brain Res 142:31–36CrossRef
55.
go back to reference Ybot-Gonzalez P, Savery D, Gerrelli D, Signore M, Mitchell CE, Faux CH, Greene ND, Copp AJ (2007) Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development 134:789–799CrossRefPubMedPubMedCentral Ybot-Gonzalez P, Savery D, Gerrelli D, Signore M, Mitchell CE, Faux CH, Greene ND, Copp AJ (2007) Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development 134:789–799CrossRefPubMedPubMedCentral
Metadata
Title
Unjoined primary and secondary neural tubes: junctional neural tube defect, a new form of spinal dysraphism caused by disturbance of junctional neurulation
Authors
Sebastian Eibach
Greg Moes
Yong Jin Hou
John Zovickian
Dachling Pang
Publication date
01-10-2017
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 10/2017
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-016-3288-7

Other articles of this Issue 10/2017

Child's Nervous System 10/2017 Go to the issue