Postzygotic mosaicism in cerebral cavernous malformation. Issue 3 (24th August 2019)

• Record Type: Journal Article
• Authors: Rath, Matthias; Pagenstecher, Axel; Hoischen, Alexander; Felbor, Ute
• Is Part Of: Journal of medical genetics. Volume 57:Issue 3(2020)
• Page Start: 212
• Page End: 216
• Publication Date: 2019-08-24
• Subjects: cerebral cavernous malformations -- postzygotic mosaicism -- two-hit model of knudson -- late postzygotic mutation -- smmips; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmedgenet-2019-106182
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : Background: Cerebral cavernous malformations (CCMs) can cause severe neurological morbidity but our understanding of the mechanisms that drive CCM formation and growth is still incomplete. Recent experimental data suggest that dysfunctional CCM3-deficient endothelial cell clones form cavernous lesions in conjunction with normal endothelial cells. Objective: In this study, we addressed the question whether endothelial cell mosaicism can be found in human cavernous tissue of CCM1 germline mutation carriers. Methods and results: Bringing together single-molecule molecular inversion probes in an ultra-sensitive sequencing approach with immunostaining to visualise the lack of CCM1 protein at single cell resolution, we identified a novel late postzygotic CCM1 loss-of-function variant in the cavernous tissue of a de novo CCM1 germline mutation carrier. The extended unilateral CCM had been located in the right central sulcus causing progressive proximal paresis of the left arm at the age of 15 years. Immunohistochemical analyses revealed that individual caverns are lined by both heterozygous ( CCM1 +/− ) and compound heterozygous ( CCM1 −/− ) endothelial cells. Conclusion: We here demonstrate endothelial cell mosaicism within single caverns of human CCM tissue. In line with recent in vitro data on CCM1-deficient endothelial cells, our results provide further evidence for clonal evolution in human CCM1 pathogenesis.