Literature DB >> 9184664

Expression of NF2-encoded merlin and related ERM family proteins in the human central nervous system.

A O Stemmer-Rachamimov1, C Gonzalez-Agosti, L Xu, J A Burwick, R Beauchamp, D Pinney, D N Louis, V Ramesh.   

Abstract

Germline mutations of the neurofibromatosis 2 (NF2) gene are associated with an increased incidence of gliomas and glial harmartomas, suggesting a role for the NF2-encoded protein, merlin, in glial growth control. Using monoclonal and polyclonal anti-merlin antibodies for Western blotting and immunohistochemistry, we evaluated the cellular pattern of merlin expression in the normal human central nervous system (CNS), reactive gliosis; and NF2-associated glial hamartomas. In the normal CNS, merlin is widely expressed in coarse cytoplasmic granules in both glia and neurons, with less pronounced expression in other cells. Merlin is also expressed in reactive astrocytes and in the astrocytes of NF2-associated glial hamartomas. In reactive astrocytes, however, merlin is also present at the cell membrane and in cellular processes, suggesting redistribution of the protein in activated cells. Merlin is structurally related to ezrin, radixin and moesin, which are also expressed in the CNS, as demonstrated by Western blotting. The pattern of merlin expression, however, is distinct from that of ezrin, which has been previously described, and that of moesin, in which immunohistochemistry with an anti-moesin antibody showed expression in endothelial cells, glia and neurons in a membranous or diffuse cytoplasmic pattern. These findings imply that merlin has widespread and specific functions in the human central nervous system.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9184664

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  11 in total

1.  Functional analysis of the neurofibromatosis type 2 protein by means of disease-causing point mutations.

Authors:  R P Stokowski; D R Cox
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

2.  Cloning and characterization of SCHIP-1, a novel protein interacting specifically with spliced isoforms and naturally occurring mutant NF2 proteins.

Authors:  L Goutebroze; E Brault; C Muchardt; J Camonis; G Thomas
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

3.  Universal absence of merlin, but not other ERM family members, in schwannomas.

Authors:  A O Stemmer-Rachamimov; L Xu; C Gonzalez-Agosti; J A Burwick; D Pinney; R Beauchamp; L B Jacoby; J F Gusella; V Ramesh; D N Louis
Journal:  Am J Pathol       Date:  1997-12       Impact factor: 4.307

Review 4.  Molecular pathogenesis of meningiomas.

Authors:  Arie Perry; David H Gutmann; Guido Reifenberger
Journal:  J Neurooncol       Date:  2004-11       Impact factor: 4.130

5.  Overexpression of ezrin inactivates NF2 tumor suppressor in glioblastoma.

Authors:  Fabiana C Morales; Jennifer R Molina; Yuho Hayashi; Maria-Magdalena Georgescu
Journal:  Neuro Oncol       Date:  2010-02-14       Impact factor: 12.300

6.  Statistical considerations for immunohistochemistry panel development after gene expression profiling of human cancers.

Authors:  Rebecca A Betensky; Catherine L Nutt; Tracy T Batchelor; David N Louis
Journal:  J Mol Diagn       Date:  2005-05       Impact factor: 5.568

7.  The phosphorylation status of merlin in sporadic vestibular Schwannomas.

Authors:  Zhaoyan Wang; Yanjun Lu; Juanjuan Tang; Haojie Wang; Hao Wu
Journal:  Mol Cell Biochem       Date:  2009-01-14       Impact factor: 3.396

Review 8.  An update on the CNS manifestations of neurofibromatosis type 2.

Authors:  Shannon Coy; Rumana Rashid; Anat Stemmer-Rachamimov; Sandro Santagata
Journal:  Acta Neuropathol       Date:  2019-06-04       Impact factor: 17.088

Review 9.  A neuronal function of the tumor suppressor protein merlin.

Authors:  Alexander Schulz; Ansgar Zoch; Helen Morrison
Journal:  Acta Neuropathol Commun       Date:  2014-07-12       Impact factor: 7.801

10.  Neurofibromatosis type 2 tumor suppressor protein is expressed in oligodendrocytes and regulates cell proliferation and process formation.

Authors:  Andrea Toledo; Elena Grieger; Khalad Karram; Helen Morrison; Stephan L Baader
Journal:  PLoS One       Date:  2018-05-01       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.