Literature DB >> 15926912

Expression of collapsin response mediator proteins 1, 2 and 5 is differentially regulated in newly generated and mature neurons of the adult olfactory system.

Alexandra Veyrac1, Nathalie Giannetti, Emmanuelle Charrier, Isabelle Reymond-Marron, Michèle Aguera, Veronique Rogemond, Jérôme Honnorat, François Jourdan.   

Abstract

Collapsin-response mediator proteins (CRMPs) are highly expressed in the developing brain where they take part in several aspects of neuronal differentiation. CRMPs are still present postnatally, but their function remains speculative in the adult brain. We studied the expression and localization of CRMP1, CRMP2 and CRMP5 in two areas of the nervous system with persistent neurogenesis in adult mice, the olfactory mucosa and the olfactory bulb. In the olfactory mucosa, we have established that CRMP expression is restricted to postmitotic cells of the olfactory neurons lineage. CRMP5 is coexpressed with growth associated protein of 43 kDa (GAP43) in immature olfactory neurons and is down-regulated in olfactory marker protein-positive mature neurons. In contrast, CRMP1 and CRMP2 persist at all stages of differentiation from immature GAP43-positive to fully mature olfactory neurons. In the olfactory bulb, CRMP1, CRMP2 and CRMP5 are abundant in neuronal progenitors of the subependymal layer and in differentiating interneurons. In both areas, the subcellular distribution of CRMP1 or CRMP2 is different in mature vs. immature neurons, suggesting that these proteins are sequentially involved in various cellular events during neuronal lifetime. The variations of CRMP expression following axotomy are consistent with their differential localization and functional involvement in immature vs. mature neurons of the olfactory system. Our data bring new insight to the putative functions of CRMPs within areas of the adult nervous system with permanent neurogenesis, some related to differentiation of newly generated neurons but others occurring in mature neurons with a limited lifespan.

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Year:  2005        PMID: 15926912     DOI: 10.1111/j.1460-9568.2005.04112.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  15 in total

1.  Age-related proteomic changes in the subventricular zone and their association with neural stem/progenitor cell proliferation.

Authors:  Melissa J McGinn; Raymond J Colello; Dong Sun
Journal:  J Neurosci Res       Date:  2012-02-16       Impact factor: 4.164

Review 2.  Neuronal networks in mental diseases and neuropathic pain: Beyond brain derived neurotrophic factor and collapsin response mediator proteins.

Authors:  Tam T Quach; Jessica K Lerch; Jerome Honnorat; Rajesh Khanna; Anne-Marie Duchemin
Journal:  World J Psychiatry       Date:  2016-03-22

3.  CRMP-2 is involved in axon growth inhibition induced by RGMa in vitro and in vivo.

Authors:  Tianzhu Wang; Xiaohui Wu; Cheng Yin; Damon Klebe; John H Zhang; Xinyue Qin
Journal:  Mol Neurobiol       Date:  2012-12-30       Impact factor: 5.590

4.  Combined age- and trauma-related proteomic changes in rat neocortex: a basis for brain vulnerability.

Authors:  Neal D Mehan; Kenneth I Strauss
Journal:  Neurobiol Aging       Date:  2011-11-16       Impact factor: 4.673

5.  Insight into the role of CRMP2 (collapsin response mediator protein 2) in T lymphocyte migration: the particular context of virus infection.

Authors:  Pascale Giraudon; Adeline Nicolle; Sylvie Cavagna; Claire Benetollo; Romain Marignier; Michel Varrin-Doyer
Journal:  Cell Adh Migr       Date:  2012-10-17       Impact factor: 3.405

6.  Deletion of collapsin response mediator protein 4 results in abnormal layer thickness and elongation of mitral cell apical dendrites in the neonatal olfactory bulb.

Authors:  Atsuhiro Tsutiya; Hikaru Watanabe; Yui Nakano; Masugi Nishihara; Yoshio Goshima; Ritsuko Ohtani-Kaneko
Journal:  J Anat       Date:  2016-01-06       Impact factor: 2.610

7.  Behavioral and quantitative mitochondrial proteome analyses of the effects of simvastatin: implications for models of neural degeneration.

Authors:  Ilse S Pienaar; Timothy Schallert; Suzél Hattingh; William M U Daniels
Journal:  J Neural Transm (Vienna)       Date:  2009-06-06       Impact factor: 3.575

Review 8.  The CRMP family of proteins and their role in Sema3A signaling.

Authors:  Eric F Schmidt; Stephen M Strittmatter
Journal:  Adv Exp Med Biol       Date:  2007       Impact factor: 2.622

9.  CRMP5 regulates generation and survival of newborn neurons in olfactory and hippocampal neurogenic areas of the adult mouse brain.

Authors:  Alexandra Veyrac; Sophie Reibel; Joëlle Sacquet; Mireille Mutin; Jean-Philippe Camdessanche; Pappachan Kolattukudy; Jérôme Honnorat; François Jourdan
Journal:  PLoS One       Date:  2011-10-04       Impact factor: 3.240

10.  CRMP1 Inhibits Proliferation of Medulloblastoma and Is Regulated by HMGA1.

Authors:  Kay Ka-Wai Li; Yan Qi; Tian Xia; Yu Yao; Liangfu Zhou; Kin-Mang Lau; Ho-Keung Ng
Journal:  PLoS One       Date:  2015-05-26       Impact factor: 3.240

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