Literature DB >> 16202709

Dual functional activity of semaphorin 3B is required for positioning the anterior commissure.

Julien Falk1, Falk Julien, Ahmad Bechara, Roberto Fiore, Homaira Nawabi, Heather Zhou, Carolina Hoyo-Becerra, Muriel Bozon, Geneviève Rougon, Martin Grumet, Andreas W Püschel, Joshua R Sanes, Valérie Castellani.   

Abstract

Chemorepulsion by semaphorins plays a critical role during the development of neuronal projections. Although semaphorin-induced chemoattraction has been reported in vitro, the contribution of this activity to axon pathfinding is still unclear. Using genetic and culture models, we provide evidence that both attraction and repulsion by Sema3B, a secreted semaphorin, are critical for the positioning of a major brain commissural projection, the anterior commissure (AC). NrCAM, an immunoglobulin superfamily adhesion molecule of the L1 subfamily, associates with neuropilin-2 and is a component of a receptor complex for Sema3B and Sema3F. Finally, we show that activation of the FAK/Src signaling cascade distinguishes Sema3B-mediated attractive from repulsive axonal responses of neurons forming the AC, revealing a mechanism underlying the dual activity of this guidance cue.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16202709     DOI: 10.1016/j.neuron.2005.08.033

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  86 in total

Review 1.  Semaphorin signaling in angiogenesis, lymphangiogenesis and cancer.

Authors:  Atsuko Sakurai; Colleen L Doçi; Colleen Doci; J Silvio Gutkind
Journal:  Cell Res       Date:  2011-12-13       Impact factor: 25.617

Review 2.  Spatial organization of transmembrane receptor signalling.

Authors:  Ioanna Bethani; Sigrid S Skånland; Ivan Dikic; Amparo Acker-Palmer
Journal:  EMBO J       Date:  2010-08-18       Impact factor: 11.598

3.  Expression by midbrain dopamine neurons of Sema3A and 3F receptors is associated with chemorepulsion in vitro but a mild in vivo phenotype.

Authors:  Enrique R Torre; Claire-Anne Gutekunst; Robert E Gross
Journal:  Mol Cell Neurosci       Date:  2010-03-16       Impact factor: 4.314

4.  Glial scar expression of CHL1, the close homolog of the adhesion molecule L1, limits recovery after spinal cord injury.

Authors:  Igor Jakovcevski; Junfang Wu; Nicole Karl; Iryna Leshchyns'ka; Vladimir Sytnyk; Jian Chen; Andrey Irintchev; Melitta Schachner
Journal:  J Neurosci       Date:  2007-07-04       Impact factor: 6.167

5.  Single-Base Resolution Mapping of 5-Hydroxymethylcytosine Modifications in Hippocampus of Alzheimer's Disease Subjects.

Authors:  Elizabeth M Ellison; Melissa A Bradley-Whitman; Mark A Lovell
Journal:  J Mol Neurosci       Date:  2017-09-02       Impact factor: 3.444

Review 6.  Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders.

Authors:  Carlos Bessa; Patrícia Maciel; Ana João Rodrigues
Journal:  Mol Neurobiol       Date:  2013-03-14       Impact factor: 5.590

Review 7.  Tyrosine phosphorylation in semaphorin signalling: shifting into overdrive.

Authors:  Mélanie Franco; Luca Tamagnone
Journal:  EMBO Rep       Date:  2008-07-25       Impact factor: 8.807

8.  Development of piriform cortex interhemispheric connections via the anterior commissure: progressive and regressive strategies.

Authors:  Eduardo Martin-Lopez; Sarah J Meller; Charles A Greer
Journal:  Brain Struct Funct       Date:  2018-08-24       Impact factor: 3.270

9.  Xenopus laevis neuronal cell adhesion molecule (nrcam): plasticity of a CAM in the developing nervous system.

Authors:  Ashwin Lokapally; Sanjeeva Metikala; Thomas Hollemann
Journal:  Dev Genes Evol       Date:  2016-12-10       Impact factor: 0.900

10.  Effects of moderate drinking during pregnancy on placental gene expression.

Authors:  Martina J Rosenberg; Christina R Wolff; Ahmed El-Emawy; Miranda C Staples; Nora I Perrone-Bizzozero; Daniel D Savage
Journal:  Alcohol       Date:  2010-01-06       Impact factor: 2.405

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.