Literature DB >> 8800424

Regional differences in morphogenesis of the neuroepithelium suggest multiple mechanisms of spinal neurulation in the mouse.

A S Shum1, A J Copp.   

Abstract

A study of neuroepithelial morphogenesis in the mouse embryo has identified three modes of neural tube formation that occur consecutively as neurulation progresses along the spinal region. The three modes of neurulation differ in the extent to which the neuroepithelium exhibits formation of "hinge points', i.e. localised bending owing to reduction in apical surface area. In Mode 1, bending occurs only in the neuroepithelium overlying the notochord, creating a median hinge point. The neural folds remain straight along both apical and basal surfaces, resulting in a neural tube with a slitshaped lumen. In Mode 2, the neuroepithelium forms paired dorsolateral hinge points, as well as a median hinge point, whereas the remaining portions of the neuroepithelium do not bend. This produces a neural tube with a diamond-shaped lumen. In Mode 3 neurulation, the entire neuroepithelium exhibits bending, so that the cells specific hinge points are not discernible; the resulting neural tube has a circular lumen. The three modes of neurulation are present in all three strains of mice studied: C57BL/6, CBA/Ca and curly tail, a mutant predisposed to neural tube defects. However, curly tail embryos exhibit a delay in transition from Mode 2 to Mode 3, preceding faulty closure of the posterior neuropore. This heterogeneity of neurulation morphogenesis in the mouse embryo indicates that the underlying mechanisms may vary along the body axis. Specifically, we suggest that Mode 1 neurulation is driven largely by forces generated extrinsic to the neuroepithelium, in adjacent tissues, whereas Mode 3 neurulation is dependent primarily on forces generated intrinsic to the neuroepithelium. Down the body axis, there is a gradual decrease in the area of ectoderm involved in neural induction and, as neurulation reaches lower spinal levels, the newly induced neural plate exhibits marked indentation from the time of its first appearance. The transition from primary neurulation (neural folding of Mode 3 type) to secondary neurulation (neural tube formation by cavitation) appears to be a smooth continuation of this trend, with loss of contact between the newly induced neuroepithelium and the outside of the embryo.

Entities:  

Mesh:

Year:  1996        PMID: 8800424     DOI: 10.1007/bf00196316

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  34 in total

1.  Expansion of surface epithelium provides the major extrinsic force for bending of the neural plate.

Authors:  I S Alvarez; G C Schoenwolf
Journal:  J Exp Zool       Date:  1992-03-01

2.  Effect of the notochord on the differentiation of a floor plate area in the neural tube of the chick embryo.

Authors:  H W van Straaten; J W Hekking; E J Wiertz-Hoessels; F Thors; J Drukker
Journal:  Anat Embryol (Berl)       Date:  1988

3.  Notochordal induction of cell wedging in the chick neural plate and its role in neural tube formation.

Authors:  J L Smith; G C Schoenwolf
Journal:  J Exp Zool       Date:  1989-04

4.  Chemotropic guidance of developing axons in the mammalian central nervous system.

Authors:  M Tessier-Lavigne; M Placzek; A G Lumsden; J Dodd; T M Jessell
Journal:  Nature       Date:  1988 Dec 22-29       Impact factor: 49.962

Review 5.  Evidence for multi-site closure of the neural tube in humans.

Authors:  M I Van Allen; D K Kalousek; G F Chernoff; D Juriloff; M Harris; B C McGillivray; S L Yong; S Langlois; P M MacLeod; D Chitayat
Journal:  Am J Med Genet       Date:  1993-10-01

6.  Histological and ultrastructural studies of secondary neurulation in mouse embryos.

Authors:  G C Schoenwolf
Journal:  Am J Anat       Date:  1984-04

7.  Developmental study of neural tube closure in a mouse stock with a high incidence of exencephaly.

Authors:  K B Macdonald; D M Juriloff; M J Harris
Journal:  Teratology       Date:  1989-02

8.  Regional differences in mesenchymal cell morphology and glycosaminoglycans in early neural-fold stage rat embryos.

Authors:  G M Morriss; M Solursh
Journal:  J Embryol Exp Morphol       Date:  1978-08

Review 9.  Mechanisms of neurulation: traditional viewpoint and recent advances.

Authors:  G C Schoenwolf; J L Smith
Journal:  Development       Date:  1990-06       Impact factor: 6.868

10.  Genesis and prevention of spinal neural tube defects in the curly tail mutant mouse: involvement of retinoic acid and its nuclear receptors RAR-beta and RAR-gamma.

Authors:  W H Chen; G M Morriss-Kay; A J Copp
Journal:  Development       Date:  1995-03       Impact factor: 6.868

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  31 in total

Review 1.  Current perspectives on the genetic causes of neural tube defects.

Authors:  Patrizia De Marco; Elisa Merello; Samantha Mascelli; Valeria Capra
Journal:  Neurogenetics       Date:  2006-08-29       Impact factor: 2.660

2.  β-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation.

Authors:  Tianyu Zhao; Qini Gan; Arjun Stokes; Rhonda N T Lassiter; Yongping Wang; Jason Chan; Jane X Han; David E Pleasure; Jonathan A Epstein; Chengji J Zhou
Journal:  Development       Date:  2013-11-27       Impact factor: 6.868

3.  Formin homology 2 domain-containing 3 (Fhod3) controls neural plate morphogenesis in mouse cranial neurulation by regulating multidirectional apical constriction.

Authors:  Hikmawan Wahyu Sulistomo; Takayuki Nemoto; Toshihiko Yanagita; Ryu Takeya
Journal:  J Biol Chem       Date:  2018-12-20       Impact factor: 5.157

Review 4.  G-protein-coupled receptor signaling and neural tube closure defects.

Authors:  Issei S Shimada; Saikat Mukhopadhyay
Journal:  Birth Defects Res       Date:  2017-01-30       Impact factor: 2.344

Review 5.  Folate supplementation in three genetic models: implications for understanding folate-dependent developmental pathways.

Authors:  Claudia Kappen
Journal:  Am J Med Genet C Semin Med Genet       Date:  2005-05-15       Impact factor: 3.908

Review 6.  Human neural tube defects: developmental biology, epidemiology, and genetics.

Authors:  Eric R Detrait; Timothy M George; Heather C Etchevers; John R Gilbert; Michel Vekemans; Marcy C Speer
Journal:  Neurotoxicol Teratol       Date:  2005-03-05       Impact factor: 3.763

Review 7.  Curly tail: a 50-year history of the mouse spina bifida model.

Authors:  H W van Straaten; A J Copp
Journal:  Anat Embryol (Berl)       Date:  2001-04

8.  Apoptosis is not required for mammalian neural tube closure.

Authors:  Valentina Massa; Dawn Savery; Patricia Ybot-Gonzalez; Elisabetta Ferraro; Anthony Rongvaux; Francesco Cecconi; Richard Flavell; Nicholas D E Greene; Andrew J Copp
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-06       Impact factor: 11.205

Review 9.  Apical constriction: a cell shape change that can drive morphogenesis.

Authors:  Jacob M Sawyer; Jessica R Harrell; Gidi Shemer; Jessica Sullivan-Brown; Minna Roh-Johnson; Bob Goldstein
Journal:  Dev Biol       Date:  2009-09-12       Impact factor: 3.582

10.  Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.

Authors:  Victoria L Patterson; Christine Damrau; Anju Paudyal; Benjamin Reeve; Daniel T Grimes; Michelle E Stewart; Debbie J Williams; Pam Siggers; Andy Greenfield; Jennifer N Murdoch
Journal:  Hum Mol Genet       Date:  2009-02-17       Impact factor: 6.150

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