Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage

• Sudo, Atsushi

• Kanagawa, Motoi

• Kondo, Mai

• Ito, Chiyomi

• Kobayashi, Kazuhiro

• Endo, Mitsuharu

• Minami, Yasuhiro

• Aiba, Atsu

• Toda, Tatsushi

Abstract

Congenital muscular dystrophies (CMDs) are characterized by progressive weakness and degeneration of skeletal muscle. In several forms of CMD, abnormal glycosylation of α-dystroglycan (α-DG) results in conditions collectively known as dystroglycanopathies, which are associated with central nervous system involvement. We recently demonstrated that fukutin, the gene responsible for Fukuyama congenital muscular dystrophy, encodes the ribitol-phosphate transferase essential for dystroglycan function. Brain pathology in patients with dystroglycanopathy typically includes cobblestone lissencephaly, mental retardation, and refractory epilepsy; however, some patients exhibit average intelligence, with few or almost no structural defects. Currently, there is no effective treatment for dystroglycanopathy, and the mechanisms underlying the generation of this broad clinical spectrum remain unknown. Here, we analysed four distinct mouse models of dystroglycanopathy: two brain-selective fukutin conditional knockout strains (neuronal stem cell-selective Nestin-fukutin-cKO and forebrain-selective Emx1-fukutin-cKO), a Fukutin(Hp) strain with the founder retrotransposal insertion in the fukutin gene, and a spontaneous Large-mutant Large(myd) strain. These models exhibit variations in the severity of brain pathology, replicating the clinical heterogeneity of dystroglycanopathy. Immunofluorescence analysis of the developing cortex suggested that residual glycosylation of α-DG at embryonic day 13.5 (E13.5), when cortical dysplasia is not yet apparent, may contribute to subsequent phenotypic heterogeneity. Surprisingly, delivery of fukutin or Large into the brains of mice at E12.5 prevented severe brain malformation in Emx1-fukutin-cKO and Large(myd/myd) mice, respectively. These findings indicate that spatiotem-poral persistence of functionally glycosylated α-DG may be crucial for brain development and modulation of glycosylation during the fetal stage could be a potential therapeutic strategy for dystroglycanopathy.

Journal

• Human Molecular Genetics

  Human Molecular Genetics 27 (7), 1174-1185, 2018-04-01

  Oxford University Press (OUP)

Keywords

• Genetics (clinical)
• Genetics
• Molecular Biology
• General Medicine

Details

• CRID: 1050575520347231232
• NII Article ID: 120006459805
• DOI: 10.1093/hmg/ddy032
• ISSN: 14602083
• ISSN: 09646906
• HANDLE: 20.500.14094/90004804
• Web Site: http://academic.oup.com/hmg/article-pdf/27/7/1174/24398868/ddy032.pdf
• Text Lang: en
• Article Type: journal article
• Data Source:
  • IRDB
  • Crossref
  • CiNii Articles
  • KAKEN