Literature DB >> 18448089

Lamination of the cerebral cortex is disturbed in Gli3 mutant mice.

Melanie Friedrichs1, Osmany Larralde, Thomas Skutella, Thomas Theil.   

Abstract

The layered organization of the cerebral cortex develops in an inside-out pattern, a process which is controlled by the secreted protein reelin. Here we report on cortical lamination in the Gli3 hypomorphic mouse mutant Xt(J)/Pdn which lacks the cortical hem, a major source of reelin(+) Cajal Retzius cells in the cerebral cortex. Unlike other previously described mouse mutants with hem defects, cortical lamination is disturbed in Xt(J)/Pdn animals. Surprisingly, these layering defects occur in the presence of reelin(+) cells which are probably derived from an expanded Dbx1(+) progenitor pool in the mutant. However, while these reelin(+) neurons and also Calretinin(+) cells are initially evenly distributed over the cortical surface they form clusters later during development suggesting a novel role for Gli3 in maintaining the proper arrangement of these cells in the marginal zone. Moreover, the radial glial network is disturbed in the regions of these clusters. In addition, the differentiation of subplate cells is affected which serve as a framework for developing a properly laminated cortex.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18448089     DOI: 10.1016/j.ydbio.2008.03.032

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  9 in total

1.  The doublesex homolog Dmrt5 is required for the development of the caudomedial cerebral cortex in mammals.

Authors:  Amandine Saulnier; Marc Keruzore; Sarah De Clercq; Isabelle Bar; Virginie Moers; Dario Magnani; Tessa Walcher; Carol Filippis; Sadia Kricha; Damien Parlier; Laurène Viviani; Clinton K Matson; Yasushi Nakagawa; Thomas Theil; Magdalena Götz; Antonello Mallamaci; Jean-Christophe Marine; David Zarkower; Eric J Bellefroid
Journal:  Cereb Cortex       Date:  2012-08-23       Impact factor: 5.357

2.  The Gli3 hypomorphic mutation Pdn causes selective impairment in the growth, patterning, and axon guidance capability of the lateral ganglionic eminence.

Authors:  Dario Magnani; Kerstin Hasenpusch-Theil; Erin C Jacobs; Anthony T Campagnoni; David J Price; Thomas Theil
Journal:  J Neurosci       Date:  2010-10-13       Impact factor: 6.167

3.  Homeobox genes in obsessive-compulsive disorder.

Authors:  G Nestadt; Y Wang; M A Grados; M A Riddle; B D Greenberg; J A Knowles; A J Fyer; J T McCracken; S L Rauch; D L Murphy; S A Rasmussen; B Cullen; J Piacentini; D Geller; D Pauls; O J Bienvenu; Y Chen; K Y Liang; F S Goes; B Maher; A E Pulver; Y Y Shugart; D Valle; J F Samuels; Y C Chang
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2011-11-16       Impact factor: 3.568

4.  Gli3 is required for maintenance and fate specification of cortical progenitors.

Authors:  Hui Wang; Guannan Ge; Yutaka Uchida; Brian Luu; Sohyun Ahn
Journal:  J Neurosci       Date:  2011-04-27       Impact factor: 6.167

5.  Role of Fgf8 signalling in the specification of rostral Cajal-Retzius cells.

Authors:  Céline Zimmer; Jun Lee; Amélie Griveau; Silvia Arber; Alessandra Pierani; Sonia Garel; François Guillemot
Journal:  Development       Date:  2010-01       Impact factor: 6.868

6.  Lateral Thalamic Eminence: A Novel Origin for mGluR1/Lot Cells.

Authors:  Nuria Ruiz-Reig; Belén Andrés; Dhananjay Huilgol; Elizabeth A Grove; Fadel Tissir; Shubha Tole; Thomas Theil; Eloisa Herrera; Alfonso Fairén
Journal:  Cereb Cortex       Date:  2017-05-01       Impact factor: 5.357

7.  A focused in situ hybridization screen identifies candidate transcriptional regulators of thymic epithelial cell development and function.

Authors:  Qiaozhi Wei; Brian G Condie
Journal:  PLoS One       Date:  2011-11-07       Impact factor: 3.240

8.  Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility.

Authors:  Hyejung Won; Jerry Huang; Carli K Opland; Chris L Hartl; Daniel H Geschwind
Journal:  Nat Commun       Date:  2019-06-03       Impact factor: 14.919

9.  Unraveling the disease pathogenesis behind lethal hydrolethalus syndrome revealed multiple changes in molecular and cellular level.

Authors:  Heli Honkala; Jenni Lahtela; Heli Fox; Massimiliano Gentile; Niklas Pakkasjärvi; Riitta Salonen; Kirmo Wartiovaara; Matti Jauhiainen; Marjo Kestilä
Journal:  Pathogenetics       Date:  2009-04-28
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.