Neurons in motion: same principles for different shapes?

Marín, Oscar; Valdeolmillos, Miguel; Moya, Fernando

doi:10.1016/j.tins.2006.10.001

Cited by 71Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene RegulationAxon Guidance and Neuronal Signaling

Neurons in motion: same principles for different shapes?

Marín, Oscar, Valdeolmillos, Miguel, Moya, Fernando·2006·Trends in Neurosciences

DOI 10.1016/j.tins.2006.10.001

Open this paper in CoChat — free account

Abstract

The special conformation of the developing nervous system, in which progenitor zones are largely confined to the lumen of the neural tube, places neuronal migration as one of the most fundamental processes in brain development. Previous studies have shown that different neuronal types adopt distinct morphological modes of migration in the developing brain, indicating that neuronal migration might be a diverse process. Here, we review recent data on the molecular mechanisms underlying neuronal migration that suggest that similar signaling principles are responsible for the frequently variable morphology of different types of migrating neuron. According to this idea, the same basic molecular mechanisms found in other cell types, such as fibroblasts, might have been adapted to the special morphological needs of migrating neurons in different regions of the developing brain.

Integrity signals

Registry

Crossref · 10.1016/j.tins.2006.10.001

Cites

56 of 56 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Interneurons born in the MGE, CGE and preoptic region use largely the same cellular mechanisms to move to the cortex and show strong transcriptional similarity at that stage.
“Interneurons from the MGE, CGE and preoptic region use essentially the same cellular mechanisms to translocate to the cortex (Marín et al., 2006; Martini et al., 2009; Yanagida et al., 2012), and it is therefore perhaps not surprising that they exhibit great transcriptional similarity at this stage (Mayer et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Marín et al., 2006

Cell Migration: Integrating Signals from Front to Back
Ridley, A. J., Schwartz, M. A., Burridge, K., Firtel, R., Ginsberg, M. H., Borisy, G. G., Parsons, J. T., & Horwitz, A. R. (2003) · Science · doi:10.1126/science.1092053 · Cited by 4,929 · see citing works
Disruption of two novel genes by a translocation co-segregating with schizophrenia
Millar, J. K. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.9.1415 · Cited by 1,254 · see citing works
Integrin-Mediated Activation of Cdc42 Controls Cell Polarity in Migrating Astrocytes through PKCζ
Etienne‐Manneville, S., & Hall, A. K. (2001) · Cell · doi:10.1016/s0092-8674(01)00471-8 · Cited by 1,025 · see citing works
Spatial and Temporal Regulation of 3-Phosphoinositides by PI 3-Kinase and PTEN Mediates Chemotaxis
Funamoto, S., Meili, R., Lee, S. D., Parry, L. A., & Firtel, R. (2002) · Cell · doi:10.1016/s0092-8674(02)00755-9 · Cited by 746 · see citing works
Modes of neuronal migration in the developing cerebral cortex
Nadarajah, B., & Parnavelas, J. G. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn845 · Cited by 683 · see citing works
Patterns of neuronal migration in the embryonic cortex
Kriegstein, A. R., & Noctor, S. C. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.05.001 · Cited by 648 · see citing works
Nuclear Movement Regulated by Cdc42, MRCK, Myosin, and Actin Flow Establishes MTOC Polarization in Migrating Cells
Gomes, E. R., Jani, S., & Gundersen, G. G. (2005) · Cell · doi:10.1016/j.cell.2005.02.022 · Cited by 609 · see citing works
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
Hirotsune, S., Fleck, M. W., Gambello, M. J., Bix, G. J., Chen, A. Y.-C., Clark, G., Ledbetter, D. H., McBain, C. J., & Wynshaw-Boris, A. J. (1998) · Nature Genetics · doi:10.1038/1221 · Cited by 575 · see citing works
Signal Transduction in Neuronal Migration
Wong, K., Ren, X.-R., Huang, Y.-Z., Xie, Y., Liu, G., Saito, H., Tang, H., Wen, L., Brady‐Kalnay, S. M., Mei, L., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00530-x · Cited by 550 · see citing works
A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development
Kamiya, A., Kubo, K., Tomoda, T., Takaki, M., Youn, R., Ozeki, Y., Sawamura, N., Park, U., Kudo, C., Okawa, M., et al. (2005) · Nature Cell Biology · doi:10.1038/ncb1328 · Cited by 531 · see citing works
Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
Wilhelmsen, K., Litjens, S. H. M., Kuikman, I., Tshimbalanga, N., Janssen, H., van den Bout, I., Raymond, K., & Sonnenberg, A. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200506083 · Cited by 483 · see citing works
Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration
Tanaka, T., Serneo, F. F., Higgins, C., Gambello, M. J., Wynshaw-Boris, A. J., & Gleeson, J. G. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200309025 · Cited by 436 · see citing works
Cellular and genetic regulation of the development of the cerebellar system
Sotelo, C. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.004 · Cited by 432 · see citing works
LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages
Tsai, J., Chen, Y., Kriegstein, A. R., & Vallee, R. B. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200505166 · Cited by 401 · see citing works
Disrupted-in-Schizophrenia-1 (DISC-1): Mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth
Ozeki, Y., Tomoda, T., Kleiderlein, J. J., Kamiya, A., Bord, L., Fujii, K., Okawa, M., Yamada, N., Hatten, M. E., Snyder, S. H., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0136913100 · Cited by 388 · see citing works
p27 kip1 independently promotes neuronal differentiation and migration in the cerebral cortexPreprint
Nguyen, L., Besson, A., Heng, J. I., Schuurmans, C. J., Teboul, L., Parras, C. M., Philpott, A., Roberts, J. M., & Guillemot, F. (2006) · Genes & Development · doi:10.1101/gad.377106 · Cited by 367 · see citing works
Cytoskeletal coordination during neuronal migration
Schaar, B. T., & McConnell, S. K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506008102 · Cited by 364 · see citing works
Control of cortical interneuron migration by neurotrophins and PI3-kinase signaling
Polleux, F., Whitford, K. L., Dijkhuizen, P. A., Vitalis, T., & Ghosh, A. (2002) · Development · doi:10.1242/dev.129.13.3147 · Cited by 361 · see citing works
Ndel1 Operates in a Common Pathway with LIS1 and Cytoplasmic Dynein to Regulate Cortical Neuronal Positioning
Shu, T., Ayala, R., Nguyen, M.-D., Xie, Z., Gleeson, J. G., & Tsai, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.030 · Cited by 361 · see citing works
Nucleokinesis in Neuronal Migration
Tsai, L., & Gleeson, J. G. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.013 · Cited by 357 · see citing works
Nucleokinesis in Tangentially Migrating Neurons Comprises Two Alternating Phases: Forward Migration of the Golgi/Centrosome Associated with Centrosome Splitting and Myosin Contraction at the Rear
Bellion, A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1030-05.2005 · Cited by 354 · see citing works
Critical Role of Ena/VASP Proteins for Filopodia Formation in Neurons and in Function Downstream of Netrin-1
Lebrand, C., Dent, E. W., Strasser, G. A., Lanier, L. M., Krause, M., Svitkina, T., Borisy, G. G., & Gertler, F. B. (2004) · Neuron · doi:10.1016/s0896-6273(04)00108-4 · Cited by 351 · see citing works
Phosphorylation of Neurogenin2 Specifies the Migration Properties and the Dendritic Morphology of Pyramidal Neurons in the Neocortex
Hand, R., Bortone, D. S., Mattar, P. A., Nguyen, L., Heng, J. I., Guerrier, S., Boutt, E., Peters, E. C., Barnes, A. P., Parras, C. M., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.032 · Cited by 350 · see citing works
Doublecortin Is Required in Mice for Lamination of the Hippocampus But Not the Neocortex
Corbo, J. C., Deuel, T. A., Long, J. M., LaPorte, P., Tsai, E., Wynshaw-Boris, A. J., & Walsh, C. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07548.2002 · Cited by 324 · see citing works
New Directions in Neuronal Migration
Hatten, M. E. (2002) · Science · doi:10.1126/science.1074572 · Cited by 321 · see citing works
Reelin-mediated Signaling Locally Regulates Protein Kinase B/Akt and Glycogen Synthase Kinase 3β
Beffert, U., Morfini, G., Bock, H. H., Reyna, H., Brady, S. T., & Herz, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209205200 · Cited by 306 · see citing works
Serine 732 Phosphorylation of FAK by Cdk5 Is Important for Microtubule Organization, Nuclear Movement, and Neuronal Migration
Xie, Z., Sanada, K., Samuels, B. A., Shih, H. H., & Tsai, L. (2003) · Cell · doi:10.1016/s0092-8674(03)00605-6 · Cited by 305 · see citing works
The in vivo roles of STEF/Tiam1, Rac1 and JNK in cortical neuronal migration
Kawauchi, T., Chihama, K., Nabeshima, Y., & Hoshino, M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg413 · Cited by 297 · see citing works
Genetic Interactions between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth
Deuel, T. A., Liu, J. S.-H., Corbo, J. C., Yoo, S.-Y., Rorke-Adams, L. B., & Walsh, C. A. (2006) · Neuron · doi:10.1016/j.neuron.2005.10.038 · Cited by 287 · see citing works
Regulation of cell polarity during eukaryotic chemotaxis: the chemotactic compass
Weiner, O. D. (2002) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00310-1 · Cited by 284 · see citing works
Par6α signaling controls glial-guided neuronal migration
Solecki, D. J., Model, L. S., Gaetz, J., Kapoor, T. M., & Hatten, M. E. (2004) · Nature Neuroscience · doi:10.1038/nn1332 · Cited by 281 · see citing works
Motility and cytoskeletal organization of migrating cerebellar granule neurons
Rivas, R., & Hatten, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-02-00981.1995 · Cited by 279 · see citing works
Cdk5 phosphorylates and stabilizes p27kip1 contributing to actin organization and cortical neuronal migration
Kawauchi, T., Chihama, K., Nabeshima, Y., & Hoshino, M. (2005) · Nature Cell Biology · doi:10.1038/ncb1338 · Cited by 273 · see citing works
Extension of Long Leading Processes and Neuronal Migration in the Mammalian Brain Directed by the Chemoattractant Netrin-1
Yee, K. T., Simon, H. H., Tessier‐Lavigne, M., & O’Leary, D. D. M. (1999) · Neuron · doi:10.1016/s0896-6273(00)81116-2 · Cited by 262 · see citing works
doublecortin-like kinase Functions with doublecortin to Mediate Fiber Tract Decussation and Neuronal Migration
Koizumi, H., Tanaka, T., & Gleeson, J. G. (2006) · Neuron · doi:10.1016/j.neuron.2005.10.040 · Cited by 259 · see citing works
The actin depolymerizing factor n-cofilin is essential for neural tube morphogenesis and neural crest cell migration
Gurniak, C. B., Perlas, E., & Witke, W. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.11.010 · Cited by 230 · see citing works
Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility
Kholmanskikh, S., Koeller, H. B., Wynshaw-Boris, A., Gómez, T. M., Letourneau, P. C., & Ross, M. (2006) · Nature Neuroscience · doi:10.1038/nn1619 · Cited by 182 · see citing works
The Functions of Klarsicht and Nuclear Lamin in Developmentally Regulated Nuclear Migrations of Photoreceptor Cells in theDrosophilaEye
Patterson, K. D., Molofsky, A. B., Robinson, C. M., Acosta, S., Cater, C., & Fischer, J. A. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-06-0374 · Cited by 164 · see citing works
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice
Kappeler, C., Saillour, Y., Baudoin, J., Tuy, F. P. D., Alvarez, C., Houbron, C., Gaspar, P., Hamard, G., Chelly, J., Métin, C., et al. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl062 · Cited by 163 · see citing works
Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization
Cahana, A., Escámez, T., Nowakowski, R. S., Hayes, N. L., Giacobini, M., von Holst, A., Shmueli, O., Sapir, T., McConnell, S. K., Wurst, W., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101122598 · Cited by 156 · see citing works
Ca2+ transients control CNS neuronal migration
Komuro, H., & Kumada, T. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.006 · Cited by 147 · see citing works
Disregulated RhoGTPases and Actin Cytoskeleton Contribute to the Migration Defect in Lis1-Deficient Neurons
Kholmanskikh, S. S., Dobrin, J. S., Wynshaw-Boris, A. J., Letourneau, P. C., & Ross, M. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08673.2003 · Cited by 114 · see citing works
Involvement of a Rac Activator, P-Rex1, in Neurotrophin-Derived Signaling and Neuronal Migration
Yoshizawa, M., Kawauchi, T., Sone, M., Nishimura, Y. V., Terao, M., Chihama, K., Nabeshima, Y., & Hoshino, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4955-04.2005 · Cited by 112 · see citing works
Combined Signaling through ERK, PI3K/AKT, and RAC1/p38 Is Required for Met-triggered Cortical Neuron Migration
Segarra, J., Balenci, L., Drenth, T., Maina, F., & Lamballe, F. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508298200 · Cited by 101 · see citing works
PTEN regulation of neural development and CNS stem cells
Li, L., Liu, F., & Ross, A. H. (2002) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10312 · Cited by 99 · see citing works
Regulation of actin cytoskeleton by mDab1 through N-WASP and ubiquitination of mDab1
Suetsugu, S., Tezuka, T., Morimura, T., Hattori, M., Mikoshiba, K., Yamamoto, T. S., & Takenawa, T. (2004) · Biochemical Journal · doi:10.1042/bj20041103 · Cited by 94 · see citing works
Distinct roles of Rac1/Cdc42 and Rho/Rock for axon outgrowth and nucleokinesis of precerebellar neurons toward netrin 1
Causeret, F., Hidalgo‐Sánchez, M., Fort, P., Backer, S., Popoff, M. R., Gauthier‐Rouvière, C., & Bloch‐Gallego, E. (2004) · Development · doi:10.1242/dev.01162 · Cited by 93 · see citing works
Nuclear positioning: the means is at the ends
Morris, N. R. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00004-2 · Cited by 92 · see citing works
Proteomic and immunochemical characterization of a role for stathmin in adult neurogenesis
Jin, K., Mao, X. O., Cottrell, B. A., Schilling, B., Xie, L., Row, R. H., Sun, Y., Peel, A. L., Childs, J., Gendeh, G., et al. (2004) · The FASEB Journal · doi:10.1096/fj.03-0973com · Cited by 88 · see citing works
Ena/VASP Proteins Regulate Cortical Neuronal Positioning
Goh, K. L., Cai, L., Cepko, C. L., & Gertler, F. B. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00725-x · Cited by 85 · see citing works
Involvement of the Phosphatidylinositol 3-Kinase/Rac1 and Cdc42 Pathways in Radial Migration of Cortical Neurons
Konno, D., Yoshimura, S., Hori, K., Maruoka, H., & Sobue, K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408251200 · Cited by 79 · see citing works
GSK3β and PKCζ function in centrosome localization and process stabilization during Slit-mediated neuronal repolarization
Higginbotham, H., Tanaka, T., Brinkman, B. C., & Gleeson, J. G. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.03.003 · Cited by 68 · see citing works
Calcium signaling in chemorepellant Slit2-dependent regulation of neuronal migration
Xu, H., Yuan, X., Guan, C.-B., Duan, S., Wu, C.-P., & Feng, L. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0303893101 · Cited by 64 · see citing works
Polarized Increase of Calcium and Nucleokinesis in Tangentially Migrating Neurons
Moya, F., & Valdeolmillos, M. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh022 · Cited by 38 · see citing works
Self-citation
Analysis of non-radial interneuron migration dynamics and its disruption inLis1+/− mice
Nasrallah, I. M., McManus, M. F., Pancoast, M. M., Wynshaw-Boris, A. J., & Golden, J. A. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20966 · Cited by 36 · see citing works
Distribution of the microtubule-related protein ninein in developing neurons
Baird, D. H., Myers, K. A., Mogensen, M. M., Moss, D. K., & Baas, P. W. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.07.016 · Cited by 34 · see citing works

Flagged first, then by citations

Sorted by citations

Development and Functional Diversification of Cortical Interneurons
Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714 · see citing works
Guiding Neuronal Cell Migrations
Marin, O., Valiente, M., Ge, X., & Tsai, L.-H. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001834 · Cited by 417 · see citing works
Neuronal migration mechanisms in development and disease
Valiente, M., & Marín, Ó. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.12.003 · Cited by 255 · see citing works
Proneural Transcription Factors Regulate Different Steps of Cortical Neuron Migration through Rnd-Mediated Inhibition of RhoA Signaling
Pacary, E., Heng, J. I., Azzarelli, R., Riou, P., Castro, D. S., Lebel, M., Parras, C. M., Bell, D. M., Ridley, A. J., Parsons, M., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.018 · Cited by 216 · see citing works
Cellular and molecular mechanisms controlling the migration of neocortical interneurons
Marín, Ó. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12225 · Cited by 206 · see citing works
Cellular and molecular introduction to brain development
Jiang, X., & Nardelli, J. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.07.007 · Cited by 199 · see citing works
Orphan G Protein-coupled Receptor GPR56 Regulates Neural Progenitor Cell Migration via a Gα12/13 and Rho Pathway
Iguchi, T., Sakata, K., Yoshizaki, K., Tago, K., Mizuno, N., & Itoh, H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708919200 · Cited by 195 · see citing works
Reaction‐Diffusion Systems in Intracellular Molecular Transport and Control
Soh, S., Byrska, M., Kandere‐Grzybowska, K., & Grzybowski, B. A. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905513 · Cited by 194 · see citing works
A role for mDia, a Rho-regulated actin nucleator, in tangential migration of interneuron precursors
Shinohara, R., Thumkeo, D., Kamijo, H., Kaneko, N., Sawamoto, K., Watanabe, K., Takebayashi, H., Kiyonari, H., Ishizaki, T., Furuyashiki, T., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3020 · Cited by 131 · see citing works
The centrosome neither persistently leads migration nor determines the site of axonogenesis in migrating neurons in vivo
Distel, M., Hocking, J. C., Volkmann, K., & Köster, R. W. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201004154 · Cited by 129 · see citing works
Quantification of Cell Edge Velocities and Traction Forces Reveals Distinct Motility Modules during Cell Spreading
Dubin‐Thaler, B. J., Hofman, J. M., Cai, Y., Xenias, H. S., Spielman, I., Shneidman, A. V., David, L. A., Döbereiner, J., Wiggins, C. H., & Sheetz, M. P. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003735 · Cited by 127 · see citing works
Actomyosin Contraction at the Cell Rear Drives Nuclear Translocation in Migrating Cortical Interneurons
Martini, F. J., & Valdeolmillos, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1962-10.2010 · Cited by 125 · see citing works
Self-citation
Proneural genes in neocortical development
Wilkinson, G., Dennis, D. J., & Schuurmans, C. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.029 · Cited by 122 · see citing works
The physiological role of the amyloid precursor protein as an adhesion molecule in the developing nervous system
Sosa, L. J., Cáceres, A., Dupraz, S., Oksdath, M., Quiroga, S., & Lorenzo, A. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14122 · Cited by 105 · see citing works
Dental pulp stem cells as a multifaceted tool for bioengineering and the regeneration of craniomaxillofacial tissues
Aurrekoetxea, M., García-Gallastegui, P., Irastorza, I., Luzuriaga, J., Uribe‐Etxebarria, V., Unda, F. J., & Ibarretxe, G. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00289 · Cited by 102 · see citing works
Molecular Pathways Regulating Cytoskeletal Organization and Morphological Changes in Migrating Neurons
Kawauchi, T., & Hoshino, M. (2007) · Developmental Neuroscience · doi:10.1159/000109850 · Cited by 96 · see citing works
Optimization of interneuron function by direct coupling of cell migration and axonal targeting
Lim, L., Pakan, J. M. P., Selten, M. M., Marques-Smith, A., Llorca, A., Bae, S. E., Rochefort, N. L., & Marín, O. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0162-9 · Cited by 93 · see citing works
Human striatal neuroblasts develop and build a striatal-like structure into the brain of Huntington's disease patients after transplantation
Gallina, P., Paganini, M., Lombardini, L., Mascalchi, M., Porfirio, B., Gadda, D., Marini, M., Pinzani, P., Salvianti, F., Crescioli, C., et al. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.12.005 · Cited by 82 · see citing works
Differential Mitochondrial Requirements for Radially and Non-radially Migrating Cortical Neurons: Implications for Mitochondrial Disorders
Lin-Hendel, E. G., McManus, M. J., Wallace, D. C., Anderson, S. A., & Golden, J. A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.03.024 · Cited by 76 · see citing works
An antagonistic interaction between PlexinB2 and Rnd3 controls RhoA activity and cortical neuron migration
Azzarelli, R., Pacary, E., Garg, R., Garcez, P. P., van den Berg, D. L. C., Riou, P., Ridley, A. J., Friedel, R. H., Parsons, M., & Guillemot, F. (2014) · Nature Communications · doi:10.1038/ncomms4405 · Cited by 73 · see citing works
Focal Adhesion Kinase Modulates Radial Glia-Dependent Neuronal Migration through Connexin-26
Valiente, M., Ciceri, G., Rico, B., & Marín, Ó. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2678-11.2011 · Cited by 73 · see citing works
Cenpj/CPAP regulates progenitor divisions and neuronal migration in the cerebral cortex downstream of Ascl1
Garcez, P. P., Díaz-Alonso, J., Crespo‐Enríquez, I., Castro, D. S., Bell, D. M., & Guillemot, F. (2015) · Nature Communications · doi:10.1038/ncomms7474 · Cited by 62 · see citing works
CAMDI, a Novel Disrupted in Schizophrenia 1 (DISC1)-binding Protein, Is Required for Radial Migration
Fukuda, T., Sugita, S., Inatome, R., & Yanagi, S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.179481 · Cited by 62 · see citing works
Pax6 transcription factor is required for the interkinetic nuclear movement of neuroepithelial cells
Tamai, H., Shinohara, H. M., Miyata, T., Saito, K., Nishizawa, Y., Nomura, T., & Osumi, N. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01113.x · Cited by 58 · see citing works
Endocytosis Regulates Cell Soma Translocation and the Distribution of Adhesion Proteins in Migrating Neurons
Shieh, J. C., Schaar, B. T., Srinivasan, K., Brodsky, F. M., & McConnell, S. K. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017802 · Cited by 55 · see citing works
CDYL Deficiency Disrupts Neuronal Migration and Increases Susceptibility to Epilepsy
Qin, R., Cao, S., Lyu, T., Qi, C., Zhang, W., & Wang, Y. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.043 · Cited by 54 · see citing works
Prickle1b mediates interpretation of migratory cues during zebrafish facial branchiomotor neuron migration
Mapp, O. M., Wanner, S. J., Rohrschneider, M. R., & Prince, V. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22283 · Cited by 49 · see citing works
Calm1 signaling pathway is essential for the migration of mouse precerebellar neurons
Kobayashi, H., Saragai, S., Naito, A., Ichio, K., Kawauchi, D., & Murakami, F. (2014) · Development · doi:10.1242/dev.112680 · Cited by 47 · see citing works
Functional Genomics and Schizophrenia: Endophenotypes and Mutant Models
Waddington, J. L., Corvin, A. P., Donohoe, G. J., O’Tuathaigh, C. M. P., Mitchell, K. J., & Gill, M. (2007) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2007.04.011 · Cited by 44 · see citing works
Chloride Influx Provokes Lamellipodium Formation in Microglial Cells
Zierler, S., Frei, E., Grissmer, S., & Kerschbaum, H. (2008) · Cellular Physiology and Biochemistry · doi:10.1159/000113747 · Cited by 42 · see citing works
Differential gene expression in migrating cortical interneurons during mouse forebrain development
Faux, C. H., Rakić, S., Andrews, W. D., Yanagawa, Y., Obata, K., & Parnavelas, J. G. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22271 · Cited by 41 · see citing works
Scratch2 Modulates Neurogenesis and Cell Migration Through Antagonism of bHLH Proteins in the Developing Neocortex
Paul, V., Tonchev, A. B., Henningfeld, K. A., Pavlakis, E., Rust, B., Pieler, T., & Stoykova, A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs356 · Cited by 41 · see citing works
Sun1 deficiency leads to cerebellar ataxia in mice
Wang, J., Yu, I., Huang, C.-C., Chen, C., Wang, W.-P., Lin, S., Jeang, K., & Chi, Y. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.019240 · Cited by 41 · see citing works
Critical aspects of neurodevelopment
Chakraborty, R., Kumar, M., & Clement, J. P. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107415 · Cited by 38 · see citing works
Forces to Drive Neuronal Migration Steps
Minegishi, T., & Inagaki, N. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00863 · Cited by 37 · see citing works
Reaktions‐Diffusions‐Systeme für intrazellulären Transport und Kontrolle
Soh, S., Byrska, M., Kandere‐Grzybowska, K., & Grzybowski, B. A. (2010) · Angewandte Chemie · doi:10.1002/ange.200905513 · Cited by 30 · see citing works
Untitled work
(2012) · doi:10.1002/cne.22696 · Cited by 28 · see citing works
Control of neuronal network organization by chemical surface functionalization of multi-walled carbon nanotube arrays
Liu, J., Appaix, F., Bibari, O., Marchand, G., Benabid, A., Sauter-Starace, F., & WAARD, M. M. D. (2011) · Nanotechnology · doi:10.1088/0957-4484/22/19/195101 · Cited by 26 · see citing works
Src controls neuronal migration by regulating the activity of FAK and cofilin
Wang, J. T., Song, L., Li, L. L., Zhang, W., Chai, X., An, L., Chen, S. L., Frotscher, M., & Zhao, S. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.02.025 · Cited by 22 · see citing works
The WWOX Gene Influences Cellular Pathways in the Neuronal Differentiation of Human Neural Progenitor Cells
Kośla, K., Płuciennik, E., Styczeń-Binkowska, E., Nowakowska, M., Orzechowska, M., & Bednarek, A. K. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00391 · Cited by 20 · see citing works
Neuronal soma migration is determined by neurite tension
Hanein, Y., Tadmor, O., Anava, S., & Ayali, A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.10.022 · Cited by 18 · see citing works
Balloon cells associated with granule cell dispersion in the dentate gyrus in hippocampal sclerosis
Thom, M., Martinian, L., Caboclo, L. O. S. F., McEvoy, A. W., & Sisodiya, S. M. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0341-y · Cited by 18 · see citing works
The Emergence of Network Activity Patterns in the Somatosensory Cortex – An Early Window to Autism Spectrum Disorders
Iannone, A. F., & García, N. V. D. M. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.04.005 · Cited by 17 · see citing works
RhoE deficiency alters postnatal subventricular zone development and the number of calbindin-expressing neurons in the olfactory bulb of mouse
Ballester‐Lurbe, B., González-Granero, S., Mocholí, E., Poch, E., García‐Manzanares, M., Dierssen, M., Pérez‐Roger, I., García‐Verdugo, J. M., Guasch, R. M., & Terrado, J. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0846-1 · Cited by 15 · see citing works
The Nkx5/HMX homeodomain protein MLS-2 is required for proper tube cell shape in the C. elegans excretory system
Abdus-Saboor, I., Stone, C. E., Murray, J. I., & Sundaram, M. V. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.03.015 · Cited by 14 · see citing works
The abdomen of Drosophila: does planar cell polarity orient the neurons of mechanosensory bristles?
Fabre, C. C. G., Casal, J., & Lawrence, P. A. (2008) · Neural Development · doi:10.1186/1749-8104-3-12 · Cited by 14 · see citing works
Nose-to-brain translocation and nervous system injury in response to indium tin oxide nanoparticles of long-term low-dose exposures
Pang, Y., Qu, J. T., Zhang, H., Cao, Y., Ma, X., Wang, S., Wang, J., Wu, J., & Zhang, T. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.167314 · Cited by 12 · see citing works
Novel Functions of Core Cell Cycle Regulators in Neuronal Migration
Godin, J. D., & Nguyen, L. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-7687-6_4 · Cited by 11 · see citing works
Rest represses maturation within migrating facial branchiomotor neurons
Love, C. E., & Prince, V. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.02.021 · Cited by 11 · see citing works
Aberrant expression of LIMK1 impairs neuronal migration during neocortex development
Xie, J., Li, X., Zhang, W., Chai, X., Huang, Y., Li, K., Cheng, X., & Zhao, S. (2016) · Histochemistry and Cell Biology · doi:10.1007/s00418-016-1514-8 · Cited by 10 · see citing works
Inhibition of glycogen synthase kinase-3 reduces extension of the axonal leading process by destabilizing microtubules in cerebellar granule neurons
Inami, Y., Omura, M., Kubota, K., & Konishi, Y. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.011 · Cited by 9 · see citing works
Setting up presynaptic structures at specific positions
Ou, C.-Y., & Shen, K. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.04.011 · Cited by 8 · see citing works
Tailor-Made Electrospun Culture Scaffolds Control Human Neural Progenitor Cell Behavior—Studies on Cellular Migration and Phenotypic Differentiation
Englund-Johansson, U., Netanyah, E., & Johansson, F. (2016) · Journal of Biomaterials and Nanobiotechnology · doi:10.4236/jbnb.2017.81001 · Cited by 8 · see citing works
Research Advances in Neuroblast Migration in Traumatic Brain Injury
Wu, N., Li, W., Chen, Q., Chen, M., Chen, S., Cheng, C.-J., & Xie, Y.-M. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04117-4 · Cited by 6 · see citing works
The Role of Intracellular Calcium and RhoA in Neuronal Migration
Faux, C. H., & Parnavelas, J. G. (2007) · Science s STKE · doi:10.1126/stke.4122007pe62 · Cited by 7 · see citing works
Identification of genes differentially expressed in dorsal and ventral chick midbrain during early Development
Chittka, A., Volff, J., & Wizenmann, A. (2009) · BMC Developmental Biology · doi:10.1186/1471-213x-9-29 · Cited by 3 · see citing works
Further studies about Coactosin-like protein-1 affecting the migration of mouse neocortical neurons
Liu, M., Li, G., Wang, M., Cheng, X., Huang, Y., Xu, M., Li, K., Chen, J., Zhu, X., & Zhao, S. (2018) · Journal of Molecular Histology · doi:10.1007/s10735-018-9790-3 · Cited by 4 · see citing works
Contact and Encirclement of Glioma Cells In Vitro Is an Intrinsic Behavior of a Clonal Human Neural Stem Cell Line
Khosh, N., Brown, C. E., Aboody, K. S., & Barish, M. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051859 · Cited by 4 · see citing works
Optimization of interneuron function by direct coupling of cell migration and axonal targeting
Lim, L. (2018) · doi:10.26226/morressier.5b31ec402afeeb0013459ca6 · Cited by 4 · see citing works
Leading Process Dynamics During Neuronal Migration
Valdeolmillos, M., & Moya, F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00025-9 · Cited by 3 · see citing works
Self-citation
PHACTRing in actin: actin deregulation in genetic epilepsies
Eid, L., Raju, P. K., & Rossignol, E. (2018) · Brain · doi:10.1093/brain/awy272 · Cited by 2 · see citing works
Transcriptional Regulation of Tangential Neuronal Migration in the Vertebrate Hindbrain
Meglio, T. D., & Rijli, F. M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00033-8 · Cited by 2 · see citing works
Imaging the Cell Biology of Neuronal Migration in Zebrafish
Distel, M., Hocking, J. C., & Köster, R. W. (2010) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814307352_0003 · Cited by 2 · see citing works
Cortical Interneurons Refuse to Follow the PAK
Guillemot, F. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.009 · Cited by 1 · see citing works
Analysis of Branchiomotor Neuron Migration in the Zebrafish
Stockinger, P., & Heisenberg, C. (2010) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814307352_0001 · Cited by 1 · see citing works
The interplay of JNK and SCG10 during cortical development and in excitotoxic responses in brain
Zdrojewska, J. (2014) · Doria (University of Helsinki)
Toward a Modular Analysis of Cell Mechanosensing and Mechanotransduction
Dubin‐Thaler, B. J., & Sheetz, M. P. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195874.008
Differentiation of neural stem cells in fragile X syndrome
Tervonen, T. A. (2008) · Työväentutkimus Vuosikirja
Quantification of Cell Movement Reveals Distinct Edge Motility Types During Cell SpreadingPreprint
Dubin‐Thaler, B. J., Hofman, J. M., Xenias, H. S., Spielman, I., Shneidman, A. V., David, L. A., Dobereiner, H.-G., Wiggins, C. H., & Sheetz, M. P. (2007) · Nature Precedings · doi:10.1038/npre.2007.391.1
THE ROLE OF PROTEIN KINASE D IN NEURONAL TRANSPORT PROCESSES AND IN DENDRITIC DEVELOPMENT
Czöndör, K., Schlett, K., Erdei, A., & Détári, L. (2009)
Actin Cytoskeletal Regulation in Neuronal Migration
Ross, M. E., & Kholmanskikh, S. S. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_8

Authors: Marín, O., Valdeolmillos, M., & Moya, F.
Affiliations: Instituto de Neurociencias (ES)
ORCID: Valdeolmillos, Miguel
Venue: Trends in Neurosciences
Publisher: Elsevier BV
Published: 2006-12
Volume: 29
Issue: 12
Pages: 655-661
ISSN: 0166-2236 (ISSN-L)
DOI: 10.1016/j.tins.2006.10.001
OpenAlex: W2051394348
Cited by: 71
References: 56
Citations by year: 2024: 1 · 2023: 1 · 2021: 2 · 2020: 1 · 2019: 1 · 2018: 6 · 2017: 2 · 2016: 3 · 2015: 6 · 2014: 4 · 2013: 5 · 2012: 4
FWCI: 0.38
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Neurosciences (publishedVersion)
PubMed (publishedVersion)
DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
Funders: National Alliance for Research on Schizophrenia and Depression
European Commission
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
Keywords: neuronal migration, neural tube, cell shape, brain development, fibroblast migration, signaling pathways
MeSH terms: Animals, Brain, Cell Movement, Humans, Neurons, Cell Shape

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Neurons in motion: same principles for different shapes?

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks