Neuronal migration in the CNS during development and disease: insights from in vivo and in vitro models

作者: Isabel Yasmin Buchsbaum , Silvia Cappello

DOI: 10.1242/DEV.163766

关键词:

摘要: Neuronal migration is a fundamental process that governs embryonic brain development. As such, mutations affect essential neuronal processes lead to severe malformations, which can cause complex and heterogeneous developmental disorders. Our fragmented knowledge about the aetiology of these disorders raises numerous issues. However, many now be addressed through studies in vivo vitro models attempt recapitulate human-specific mechanisms cortical In this Review, we discuss advantages limitations model systems suggest complementary approach, using combinations models, will broaden our molecular cellular underlie defective positioning human cerebral cortex.

参考文章(232)
Fiona Francis, Annette Koulakoff, Dominique Boucher, Philippe Chafey, Bruce Schaar, Marie-Claude Vinet, Gaëlle Friocourt, Nathalie McDonnell, Orly Reiner, Axel Kahn, Susan K McConnell, Yoheved Berwald-Netter, Philippe Denoulet, Jamel Chelly, Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons Neuron. ,vol. 23, pp. 247- 256 ,(1999) , 10.1016/S0896-6273(00)80777-1
Isabel Reillo, Camino de Juan Romero, Miguel Ángel García-Cabezas, Víctor Borrell, A Role for Intermediate Radial Glia in the Tangential Expansion of the Mammalian Cerebral Cortex Cerebral Cortex. ,vol. 21, pp. 1674- 1694 ,(2011) , 10.1093/CERCOR/BHQ238
Timothy W Yu, Ganeshwaran H Mochida, David J Tischfield, Sema K Sgaier, Laura Flores-Sarnat, Consolato M Sergi, Meral Topçu, Marie T McDonald, Brenda J Barry, Jillian M Felie, Christine Sunu, William B Dobyns, Rebecca D Folkerth, A James Barkovich, Christopher A Walsh, Mutations in WDR62 , encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture Nature Genetics. ,vol. 42, pp. 1015- 1020 ,(2010) , 10.1038/NG.683
Renzo Guerrini, William B Dobyns, Malformations of cortical development: clinical features and genetic causes Lancet Neurology. ,vol. 13, pp. 710- 726 ,(2014) , 10.1016/S1474-4422(14)70040-7
Karine Poirier, David A Keays, Fiona Francis, Yoann Saillour, Nadia Bahi, Sylvie Manouvrier, Catherine Fallet‐Bianco, Laurent Pasquier, Annick Toutain, Françoise Phan Dinh Tuy, Thierry Bienvenu, Sylvie Joriot, Sylvie Odent, Dorothée Ville, Isabelle Desguerre, Alice Goldenberg, Marie‐Laure Moutard, Jean‐Pierre Fryns, Hilde Van Esch, Robert J Harvey, Christian Siebold, Jonathan Flint, Chérif Beldjord, Jamel Chelly, None, Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). Human Mutation. ,vol. 28, pp. 1055- 1064 ,(2007) , 10.1002/HUMU.20572
F. Sicca, A. Kelemen, P. Genton, S. Das, D. Mei, F. Moro, W.B. Dobyns, R. Guerrini, Mosaic mutations of the LIS1 gene cause subcortical band heterotopia. Neurology. ,vol. 61, pp. 1042- 1046 ,(2003) , 10.1212/WNL.61.8.1042
Camino de Juan Romero, Carl Bruder, Ugo Tomasello, José Miguel Sanz‐Anquela, Víctor Borrell, Discrete domains of gene expression in germinal layers distinguish the development of gyrencephaly The EMBO Journal. ,vol. 34, pp. 1859- 1874 ,(2015) , 10.15252/EMBJ.201591176
S. Vuillaumier-Barrot, C. Bouchet-Seraphin, M. Chelbi, A. Eude-Caye, E. Charluteau, C. Besson, S. Quentin, L. Devisme, C. Le Bizec, P. Landrieu, A. Goldenberg, K. Maincent, P. Loget, O. Boute, B. Gilbert-Dussardier, F. Encha-Razavi, M. Gonzales, B. Grandchamp, N. Seta, Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies Neuromuscular Disorders. ,vol. 21, pp. 782- 790 ,(2011) , 10.1016/J.NMD.2011.06.001
David Horesh, Tamar Sapir, Fiona Francis, Sharon Grayer Wolf, Michal Caspi, Michael Elbaum, Jamel Chelly, Orly Reiner, Doublecortin, a Stabilizer of Microtubules Human Molecular Genetics. ,vol. 8, pp. 1599- 1610 ,(1999) , 10.1093/HMG/8.9.1599