Literature DB >> 25037053

Cilia: traffic directors along the road of cortical development.

Christine Métin1, Maria Pedraza2.   

Abstract

While the presence of a primary cilium on neural progenitors and on post-mitotic neurons was noted long ago, a primary cilium has been observed on migrating cortical interneurons only recently. As in fibroblasts, the cilium of interneurons controls the directionality of migration. It plays an important role in the reorientation of cortical interneurons toward the cortical plate. The morphogen Shh, which is expressed in the migratory pathway of interneurons, is one of the signals that control this reorientation. After a short description of the migratory pathways of cortical interneurons, we focus on cellular mechanisms that allow interneurons to reorient their trajectory during their long-distance migration. Then we examine the role of the primary cilium in cell migration and how ciliogenesis might be related to the migration cycle in interneurons. Finally, we review the molecular mechanisms at the basis of the sensory function of the primary cilium and examine how Shh signals could influence the migratory behavior of cortical interneurons. These novel data provide a cellular basis to further understanding cognitive deficits associated with human ciliopathies.
© The Author(s) 2014.

Entities:  

Keywords:  ciliopathy; cortical interneuron; cytoskeleton; developing cortex; primary cilium; sonic hedgehog

Mesh:

Substances:

Year:  2014        PMID: 25037053     DOI: 10.1177/1073858414543151

Source DB:  PubMed          Journal:  Neuroscientist        ISSN: 1073-8584            Impact factor:   7.519


  7 in total

Review 1.  Sonic Hedgehog Signaling and Hippocampal Neuroplasticity.

Authors:  Pamela J Yao; Ronald S Petralia; Mark P Mattson
Journal:  Trends Neurosci       Date:  2016-11-16       Impact factor: 13.837

2.  Ciliopathy variant burden and developmental delay in children with hypoplastic left heart syndrome.

Authors:  Gabrielle C Geddes; Karl Stamm; Michael Mitchell; Kathleen A Mussatto; Aoy Tomita-Mitchell
Journal:  Genet Med       Date:  2016-10-27       Impact factor: 8.822

3.  A loss-of-function homozygous mutation in DDX59 implicates a conserved DEAD-box RNA helicase in nervous system development and function.

Authors:  Vincenzo Salpietro; Stephanie Efthymiou; Andreea Manole; Bhawana Maurya; Sarah Wiethoff; Balasubramaniem Ashokkumar; Maria Concetta Cutrupi; Valeria Dipasquale; Sara Manti; Juan A Botia; Mina Ryten; Jana Vandrovcova; Oscar D Bello; Conceicao Bettencourt; Kshitij Mankad; Ashim Mukherjee; Mousumi Mutsuddi; Henry Houlden
Journal:  Hum Mutat       Date:  2017-11-27       Impact factor: 4.878

4.  The familial dysautonomia disease gene IKBKAP is required in the developing and adult mouse central nervous system.

Authors:  Marta Chaverra; Lynn George; Marc Mergy; Hannah Waller; Katharine Kujawa; Connor Murnion; Ezekiel Sharples; Julian Thorne; Nathaniel Podgajny; Andrea Grindeland; Yumi Ueki; Steven Eiger; Cassie Cusick; A Michael Babcock; George A Carlson; Frances Lefcort
Journal:  Dis Model Mech       Date:  2017-02-06       Impact factor: 5.758

5.  Effects of chronic unpredictable mild stress induced prenatal stress on neurodevelopment of neonates: Role of GSK-3β.

Authors:  Mahino Fatima; Saurabh Srivastav; Mir Hilal Ahmad; Amal Chandra Mondal
Journal:  Sci Rep       Date:  2019-02-04       Impact factor: 4.379

Review 6.  KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders.

Authors:  Xinchen Teng; Abdel Aouacheria; Loïc Lionnard; Kyle A Metz; Lucian Soane; Atsushi Kamiya; J Marie Hardwick
Journal:  CNS Neurosci Ther       Date:  2019-07       Impact factor: 5.243

7.  Cortical interneurons migrating on a pure substrate of N-cadherin exhibit fast synchronous centrosomal and nuclear movements and reduced ciliogenesis.

Authors:  Camilla Luccardini; Claire Leclech; Lucie Viou; Jean-Paul Rio; Christine Métin
Journal:  Front Cell Neurosci       Date:  2015-08-03       Impact factor: 5.505

  7 in total

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