Literature DB >> 21569831

CCM2 expression during prenatal development and adult human neocortex.

Gamze Tanriover1, Berna Sozen, Murat Gunel, Necdet Demir.   

Abstract

Cerebral cavernous malformation (CCM) is one of the most common types of vascular malformations of the central nervous system, affecting nearly one in 200 people. CCM lesions are characterized by grossly dilated vascular channels lined by a single layer of endothelium. Genetic linkage analyses have mapped three CCM loci to CCM1, CCM2 and CCM3. All three causative genes have now been identified allowing new insights into CCM pathophysiology. We focused on the CCM2 protein that might take place in blood vessel formation; we report here the expression patterns of CCM2 in prenatal development and adult human neocortex by means of immunohistochemistry and Western blot analysis. CCM2 was obviously detected in vascular endothelium and neuroglial precursor cells during development and also observed in arterial endothelium, neurons, some of the glial cells in adult neocortex. The expression patterns suggest that it could be one of the arterial markers whether this is a cause or a consequence of an altered vascular identity. CCM2 might play a role during vasculogenesis and angiogenesis during human brain development. Furthermore, with this study, CCM2 have been described for the first time in developing human neocortex.
Copyright © 2011 ISDN. All rights reserved.

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Year:  2011        PMID: 21569831     DOI: 10.1016/j.ijdevneu.2011.04.006

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  1 in total

1.  De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations.

Authors:  Lorena Mosca; Silvana Pileggi; Francesca Avemaria; Claudia Tarlarini; Maria Sole Cigoli; Valeria Capra; Patrizia De Marco; Marco Pavanello; Alessandro Marocchi; Silvana Penco
Journal:  J Mol Neurosci       Date:  2012-03-14       Impact factor: 3.444

  1 in total

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