Neurodegeneration and functional impairments associated with glycogen synthase accumulation in a mouse model of Lafora disease

Jordi Valles-Ortega, Jordi Duran, Mar Garcia-Rocha, Carles Bosch, Isabel Saez, Lluís Pujadas, Anna Serafin, Xavier Cañas, Eduardo Soriano, José M. Delgado-García, Agnès Gruart, Joan J. Guinovart

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94 Citations (Scopus)


Lafora disease (LD) is caused by mutations in either the laforin or malin gene. The hallmark of the disease is the accumulation of polyglucosan inclusions called Lafora Bodies (LBs). Malin knockout (KO) mice present polyglucosan accumulations in several brain areas, as do patients of LD. These structures are abundant in the cerebellum and hippocampus. Here, we report a large increase in glycogen synthase (GS) in these mice, in which the enzyme accumulates in LBs. Our study focused on the hippocampus where, under physiological conditions, astrocytes and parvalbumin-positive (PV +) interneurons expressed GS and malin. Although LBs have been described only in neurons, we found this polyglucosan accumulation in the astrocytes of the KO mice. They also had LBs in the soma and some processes of PV + interneurons. This phenomenon was accompanied by the progressive loss of these neuronal cells and, importantly, neurophysiological alterations potentially related to impairment of hippocampal function. Our results emphasize the relevance of the laforin-malin complex in the control of glycogen metabolism and highlight altered glycogen accumulation as a key contributor to neurodegeneration in LD.

Original languageEnglish
Pages (from-to)667-681
Number of pages15
JournalEMBO Molecular Medicine
Issue number11
Publication statusPublished - Nov 2011
Externally publishedYes


  • Glycogen
  • Glycogen synthase
  • Lafora
  • Malin
  • Neurodegeneration


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