Literature DB >> 3941326

Pathogenesis of neural dysraphism in the mouse mutant vacuolated lens (vl).

D B Wilson, D P Wyatt.   

Abstract

The pathogenesis and expression of caudal neural dysraphism were studied by means of tritiated thymidine autoradiography in the mouse mutant vacuolated lens (vl) at 11-13 days of gestation. In homozygous litters, all of the embryos microscopically exhibited spinal cord defects, even though dysraphism could be detected grossly only in the most severely affected ones. The defects ranged from extreme eversion of widely open neural folds to a dorsally expanded neurocoel with an attenuated or distorted roof plate. Incorporation of tritiated thymidine occurred in cells in the defective roof plates, in severely distorted areas of the neural tube where cellular disaggregation occurred, and in isolated areas within the developing intermediate layer, as well as in normal sites of cellular proliferation. The frequently observed central mass of distorted but proliferating neural tissue associated with bilateral attenuations of the roof plate suggests a failure of, or defect in, the normal process of apposition and fusion of the neural folds, rather than a failure in opposition. The range in severity and the gross and microscopic manifestations of neuropathological lesions in the homozygous vl embryos indicate that this heretofore unexplored mutant has considerable potential as an experimental model for analyzing the origins and mechanisms of human neural dysraphism.

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Year:  1986        PMID: 3941326     DOI: 10.1097/00005072-198601000-00004

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  7 in total

Review 1.  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

2.  Immunofluorescent analysis of fibronectin and laminin distribution in the vl mutant mouse.

Authors:  D B Wilson; D P Wyatt
Journal:  Histochem J       Date:  1989-07

3.  Closure of the posterior neuropore in the vl mutant mouse.

Authors:  D B Wilson; D P Wyatt
Journal:  Anat Embryol (Berl)       Date:  1988

4.  Ultrastructural defects in the apical neural folds in mutant embryos with spina bifida.

Authors:  D B Wilson; D P Wyatt
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

5.  The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.

Authors:  Paul G Matteson; Jigar Desai; Ron Korstanje; Gloria Lazar; Tanya E Borsuk; Jarod Rollins; Sindhuja Kadambi; Jamie Joseph; Taslima Rahman; Jason Wink; Rym Benayed; Beverly Paigen; James H Millonig
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205

Review 6.  Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans.

Authors:  Siti W Mohd-Zin; Ahmed I Marwan; Mohamad K Abou Chaar; Azlina Ahmad-Annuar; Noraishah M Abdul-Aziz
Journal:  Scientifica (Cairo)       Date:  2017-02-13

7.  Wnt1 Lineage Specific Deletion of Gpr161 Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal Development.

Authors:  Sung-Eun Kim; Karla Robles-Lopez; Xuanye Cao; Kristyn Liu; Pooja J Chothani; Nikitha Bhavani; Lauren Rahman; Saikat Mukhopadhyay; Bogdan J Wlodarczyk; Richard H Finnell
Journal:  Front Genet       Date:  2021-11-23       Impact factor: 4.599

  7 in total

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