Literature DB >> 27732850

Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.

Ilan Gobius1, Laura Morcom2, Rodrigo Suárez2, Jens Bunt2, Polina Bukshpun3, William Reardon4, William B Dobyns5, John L R Rubenstein6, A James Barkovich7, Elliott H Sherr3, Linda J Richards8.   

Abstract

The corpus callosum is the major axon tract that connects and integrates neural activity between the two cerebral hemispheres. Although ∼1:4,000 children are born with developmental absence of the corpus callosum, the primary etiology of this condition remains unknown. Here, we demonstrate that midline crossing of callosal axons is dependent upon the prior remodeling and degradation of the intervening interhemispheric fissure. This remodeling event is initiated by astroglia on either side of the interhemispheric fissure, which intercalate with one another and degrade the intervening leptomeninges. Callosal axons then preferentially extend over these specialized astroglial cells to cross the midline. A key regulatory step in interhemispheric remodeling is the differentiation of these astroglia from radial glia, which is initiated by Fgf8 signaling to downstream Nfi transcription factors. Crucially, our findings from human neuroimaging studies reveal that developmental defects in interhemispheric remodeling are likely to be a primary etiology underlying human callosal agenesis.
Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Fgf8; Nfia; Nfib; astrocyte; callosal agenesis; interhemispheric fissure

Mesh:

Substances:

Year:  2016        PMID: 27732850      PMCID: PMC5094913          DOI: 10.1016/j.celrep.2016.09.033

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  54 in total

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Journal:  Eur J Pediatr       Date:  2009-09-08       Impact factor: 3.183

2.  Appropriate Bmp7 levels are required for the differentiation of midline guidepost cells involved in corpus callosum formation.

Authors:  Cristina Sánchez-Camacho; Juan Alberto Ortega; Inmaculada Ocaña; Soledad Alcántara; Paola Bovolenta
Journal:  Dev Neurobiol       Date:  2011-05       Impact factor: 3.964

3.  Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

Authors:  Catherine Dodé; Jacqueline Levilliers; Jean-Michel Dupont; Anne De Paepe; Nathalie Le Dû; Nadia Soussi-Yanicostas; Roney S Coimbra; Sedigheh Delmaghani; Sylvie Compain-Nouaille; Françoise Baverel; Christophe Pêcheux; Dominique Le Tessier; Corinne Cruaud; Marc Delpech; Frank Speleman; Stefan Vermeulen; Andrea Amalfitano; Yvan Bachelot; Philippe Bouchard; Sylvie Cabrol; Jean-Claude Carel; Henriette Delemarre-van de Waal; Barbara Goulet-Salmon; Marie-Laure Kottler; Odile Richard; Franco Sanchez-Franco; Robert Saura; Jacques Young; Christine Petit; Jean-Pierre Hardelin
Journal:  Nat Genet       Date:  2003-03-10       Impact factor: 38.330

4.  NFIA controls telencephalic progenitor cell differentiation through repression of the Notch effector Hes1.

Authors:  Michael Piper; Guy Barry; John Hawkins; Sharon Mason; Charlotta Lindwall; Erica Little; Anindita Sarkar; Aaron G Smith; Randal X Moldrich; Glen M Boyle; Shubha Tole; Richard M Gronostajski; Timothy L Bailey; Linda J Richards
Journal:  J Neurosci       Date:  2010-07-07       Impact factor: 6.167

5.  Molecular regulation of the developing commissural plate.

Authors:  Randal X Moldrich; Ilan Gobius; Thomas Pollak; Jiangyang Zhang; Tianbo Ren; Lucia Brown; Susumu Mori; Camino De Juan Romero; Olga Britanova; Victor Tarabykin; Linda J Richards
Journal:  J Comp Neurol       Date:  2010-09-15       Impact factor: 3.215

6.  Multiple Eph receptors and B-class ephrins regulate midline crossing of corpus callosum fibers in the developing mouse forebrain.

Authors:  Shannon W Mendes; Mark Henkemeyer; Daniel J Liebl
Journal:  J Neurosci       Date:  2006-01-18       Impact factor: 6.167

7.  Midline radial glia translocation and corpus callosum formation require FGF signaling.

Authors:  Karen Müller Smith; Yasushi Ohkubo; Maria Elisabetta Maragnoli; Mladen-Roko Rasin; Michael L Schwartz; Nenad Sestan; Flora M Vaccarino
Journal:  Nat Neurosci       Date:  2006-05-21       Impact factor: 24.884

8.  An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.

Authors:  Anupam Rao; Sheridan O'Donnell; Nicole Bain; Cliff Meldrum; Damon Shorter; Himanshu Goel
Journal:  Eur J Med Genet       Date:  2014-01-22       Impact factor: 2.708

9.  Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning.

Authors:  Dario Magnani; Kerstin Hasenpusch-Theil; Carine Benadiba; Tian Yu; M Albert Basson; David J Price; Cécile Lebrand; Thomas Theil
Journal:  Cereb Cortex       Date:  2012-10-04       Impact factor: 5.357

10.  Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Authors:  A O Wilkie; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

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  24 in total

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Authors:  Kok-Siong Chen; Caitlin R Bridges; Zorana Lynton; Jonathan W C Lim; Brett W Stringer; Revathi Rajagopal; Kum-Thong Wong; Dharmendra Ganesan; Hany Ariffin; Bryan W Day; Linda J Richards; Jens Bunt
Journal:  J Neurooncol       Date:  2019-11-23       Impact factor: 4.130

2.  FGF Signaling Directs the Cell Fate Switch from Neurons to Astrocytes in the Developing Mouse Cerebral Cortex.

Authors:  Tung Anh Dinh Duong; Yoshio Hoshiba; Kengo Saito; Kanji Kawasaki; Yoshie Ichikawa; Naoyuki Matsumoto; Yohei Shinmyo; Hiroshi Kawasaki
Journal:  J Neurosci       Date:  2019-06-07       Impact factor: 6.167

3.  Neurog2 and Ascl1 together regulate a postmitotic derepression circuit to govern laminar fate specification in the murine neocortex.

Authors:  Daniel J Dennis; Grey Wilkinson; Saiqun Li; Rajiv Dixit; Lata Adnani; Anjali Balakrishnan; Sisu Han; Christopher Kovach; Nicole Gruenig; Deborah M Kurrasch; Richard H Dyck; Carol Schuurmans
Journal:  Proc Natl Acad Sci U S A       Date:  2017-06-05       Impact factor: 11.205

4.  A pan-mammalian map of interhemispheric brain connections predates the evolution of the corpus callosum.

Authors:  Rodrigo Suárez; Annalisa Paolino; Laura R Fenlon; Laura R Morcom; Peter Kozulin; Nyoman D Kurniawan; Linda J Richards
Journal:  Proc Natl Acad Sci U S A       Date:  2018-09-04       Impact factor: 11.205

5.  Tissue Injury and Astrocytic Reaction, But Not Cognitive Deficits, Are Dependent on Hypoxia Duration in Very Immature Rats Undergoing Neonatal Hypoxia-Ischemia.

Authors:  L E Durán-Carabali; E F Sanches; F K Odorcyk; F Nicola; R G Mestriner; L Reichert; D Aristimunha; A S Pagnussat; C A Netto
Journal:  Neurochem Res       Date:  2019-09-28       Impact factor: 3.996

Review 6.  DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

Authors:  Ashley P L Marsh; Timothy J Edwards; Charles Galea; Helen M Cooper; Elizabeth C Engle; Saumya S Jamuar; Aurélie Méneret; Marie-Laure Moutard; Caroline Nava; Agnès Rastetter; Gail Robinson; Guy Rouleau; Emmanuel Roze; Megan Spencer-Smith; Oriane Trouillard; Thierry Billette de Villemeur; Christopher A Walsh; Timothy W Yu; Delphine Heron; Elliott H Sherr; Linda J Richards; Christel Depienne; Richard J Leventer; Paul J Lockhart
Journal:  Hum Mutat       Date:  2017-11-11       Impact factor: 4.878

7.  NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

Authors:  Ina Schanze; Jens Bunt; Jonathan W C Lim; Denny Schanze; Ryan J Dean; Marielle Alders; Patricia Blanchet; Tania Attié-Bitach; Siren Berland; Steven Boogert; Sangamitra Boppudi; Caitlin J Bridges; Megan T Cho; William B Dobyns; Dian Donnai; Jessica Douglas; Dawn L Earl; Timothy J Edwards; Laurence Faivre; Brieana Fregeau; David Genevieve; Marion Gérard; Vincent Gatinois; Muriel Holder-Espinasse; Samuel F Huth; Kosuke Izumi; Bronwyn Kerr; Elodie Lacaze; Phillis Lakeman; Sonal Mahida; Ghayda M Mirzaa; Sian M Morgan; Catherine Nowak; Hilde Peeters; Florence Petit; Daniela T Pilz; Jacques Puechberty; Eyal Reinstein; Jean-Baptiste Rivière; Avni B Santani; Anouck Schneider; Elliott H Sherr; Constance Smith-Hicks; Ilse Wieland; Elaine Zackai; Xiaonan Zhao; Richard M Gronostajski; Martin Zenker; Linda J Richards
Journal:  Am J Hum Genet       Date:  2018-11-01       Impact factor: 11.025

8.  High Angular Resolution Diffusion MRI Reveals Conserved and Deviant Programs in the Paths that Guide Human Cortical Circuitry.

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9.  Recurrent NFIA K125E substitution represents a loss-of-function allele: Sensitive in vitro and in vivo assays for nontruncating alleles.

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10.  DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation.

Authors:  Laura Morcom; Timothy J Edwards; Eric Rider; Dorothy Jones-Davis; Jonathan Wc Lim; Kok-Siong Chen; Ryan J Dean; Jens Bunt; Yunan Ye; Ilan Gobius; Rodrigo Suárez; Simone Mandelstam; Elliott H Sherr; Linda J Richards
Journal:  Elife       Date:  2021-05-04       Impact factor: 8.713

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