Abstract |
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.
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Authors | 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 |
Journal | EMBO molecular medicine
(EMBO Mol Med)
Vol. 3
Issue 11
Pg. 667-81
(Nov 2011)
ISSN: 1757-4684 [Electronic] England |
PMID | 21882344
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 EMBO Molecular Medicine. |
Chemical References |
- Glycogen
- Glycogen Synthase
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Topics |
- Animals
- Astrocytes
(enzymology)
- Disease Models, Animal
- Female
- Glycogen
(metabolism)
- Glycogen Synthase
(genetics, metabolism)
- Hippocampus
(enzymology)
- Humans
- Inclusion Bodies
(enzymology, genetics)
- Lafora Disease
(enzymology, genetics, pathology, physiopathology)
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Nerve Degeneration
(enzymology, genetics, pathology, physiopathology)
- Neurons
(enzymology)
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