Literature DB >> 15834957

Differential expression of CRMP1, CRMP2A, CRMP2B, and CRMP5 in axons or dendrites of distinct neurons in the mouse brain.

Sylvie Bretin1, Sophie Reibel, Emmanuelle Charrier, Marion Maus-Moatti, Nathalie Auvergnon, Anne Thevenoux, Jacques Glowinski, Véronique Rogemond, Joël Prémont, Jérôme Honnorat, Christian Gauchy.   

Abstract

CRMP1, CRMP2, and CRMP5 have been identified as cytosolic proteins relaying semaphorin 3A signalling, one of the molecular cues conducting axon and dendrite growth and guidance. They are highly expressed during brain ontogenesis, but, because of their lower levels in the adult, their distribution in the mature brain is poorly documented. By using specific antibodies, we investigated the cellular distribution of these CRMPs in different adult brain structures and in neural cell cultures with a special focus on the splice variants CRMP2A and CRMP2B. In brain sections of adult mouse, CRMP1, CRMP2B, and CRMP5 were located predominantly in dendrites of specific neuronal populations, such as cortical pyramidal neurons, hippocampal CA1 pyramidal cells, or Purkinje cerebellar cells. On the contrary, CRMP2A was specifically associated with axons of the corpus callosum, bundles of the striatum, and mossy fibers of the hippocampus. In cultures of cortical neurons, CRMP1, CRMP2A, CRMP2B, and CRMP5 were equally distributed throughout cell bodies, axons, or dendrites of neurons, whereas CRMP2A and CRMP5 were completely absent from Purkinje cerebellar cells in 12-day-old animals. By comparison, oligodendrocytes exclusively express CRMP2B and CRMP5 in cell bodies and processes both in situ in the adult brain and in primary cultures. Overall, our results demonstrate specific subcellular localizations of CRMP1, CRMP2A, CRMP2B, and CRMP5 depending on cell types, neuronal compartment, and developmental stage. This study suggests that, beyond their signalling function in axon outgrowth and guidance, CRMPs also play a role in mature neurons both in axons and in dendrites. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15834957     DOI: 10.1002/cne.20465

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  35 in total

1.  Preconditioning with Ginkgo biloba (EGb 761®) provides neuroprotection through HO1 and CRMP2.

Authors:  Shadia E Nada; Zahoor A Shah
Journal:  Neurobiol Dis       Date:  2012-01-24       Impact factor: 5.996

Review 2.  Collapsin response mediator proteins regulate neuronal development and plasticity by switching their phosphorylation status.

Authors:  Naoya Yamashita; Yoshio Goshima
Journal:  Mol Neurobiol       Date:  2012-02-18       Impact factor: 5.590

3.  CRMP5 interacts with tubulin to inhibit neurite outgrowth, thereby modulating the function of CRMP2.

Authors:  Sébastien Brot; Véronique Rogemond; Valérie Perrot; Naura Chounlamountri; Carole Auger; Jérôme Honnorat; Mahnaz Moradi-Améli
Journal:  J Neurosci       Date:  2010-08-11       Impact factor: 6.167

Review 4.  Early life nutrition and neural plasticity.

Authors:  Michael K Georgieff; Katya E Brunette; Phu V Tran
Journal:  Dev Psychopathol       Date:  2015-05

Review 5.  CRMPs: critical molecules for neurite morphogenesis and neuropsychiatric diseases.

Authors:  T T Quach; J Honnorat; P E Kolattukudy; R Khanna; A M Duchemin
Journal:  Mol Psychiatry       Date:  2015-06-16       Impact factor: 15.992

6.  Collapsin response mediator protein-2 phosphorylation promotes the reversible retraction of oligodendrocyte processes in response to non-lethal oxidative stress.

Authors:  Agata Fernández-Gamba; María Celeste Leal; Chera L Maarouf; Christiane Richter-Landsberg; Terence Wu; Laura Morelli; Alex E Roher; Eduardo M Castaño
Journal:  J Neurochem       Date:  2012-04-27       Impact factor: 5.372

7.  Enhanced Peptide Detection Toward Single-Neuron Proteomics by Reversed-Phase Fractionation Capillary Electrophoresis Mass Spectrometry.

Authors:  Sam B Choi; Camille Lombard-Banek; Pablo Muñoz-LLancao; M Chiara Manzini; Peter Nemes
Journal:  J Am Soc Mass Spectrom       Date:  2017-11-16       Impact factor: 3.109

8.  Tat-collapsin response mediator protein 2 (CRMP2) increases the survival of neurons after NMDA excitotoxity by reducing the cleavage of CRMP2.

Authors:  Yanling Yin; Yansong Wang; Lumian Chen; Song Han; Li Zhao; Yanlin Luo; Junfa Li
Journal:  Neurochem Res       Date:  2013-08-02       Impact factor: 3.996

9.  Downstream targets of methyl CpG binding protein 2 and their abnormal expression in the frontal cortex of the human Rett syndrome brain.

Authors:  Joanne H Gibson; Barry Slobedman; Harikrishnan K N; Sarah L Williamson; Dimitri Minchenko; Assam El-Osta; Joshua L Stern; John Christodoulou
Journal:  BMC Neurosci       Date:  2010-04-26       Impact factor: 3.288

10.  Identification and structural analysis of C-terminally truncated collapsin response mediator protein-2 in a murine model of prion diseases.

Authors:  Fumiko Shinkai-Ouchi; Yoshio Yamakawa; Hideyuki Hara; Minoru Tobiume; Masahiro Nishijima; Kentaro Hanada; Ken'ichi Hagiwara
Journal:  Proteome Sci       Date:  2010-10-20       Impact factor: 2.480

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