Lithium rescues the impaired autophagy process in CbCln3 δex7/8/δex7/8 cerebellar cells and reduces neuronal vulnerability to cell death via IMPase inhibition

Jae Woong Chang, Hyunwoo Choi, Susan L. Cotman, Yong Keun Jung

Research output: Contribution to journalArticle

25 Scopus citations

Abstract

Juvenile neuronal ceroid lipofuscinosis (Batten disease) is a neurodegenerative disorder caused by mutation in CLN3. Defective autophagy and concomitant accumulation of autofluorescence enriched with mitochondrial ATP synthase subunit c were previously discovered in Cln3 mutant knock-in mice. In this study, we show that treatment with lithium reduces numbers of LC3-positive autophagosomes and accumulation of LC3-II in Cln3 mutant knock-in cerebellar cells (CbCln3δex7/8/δex7/8). Lithium, an inhibitor of GSK3 and IMPase, reduces the accumulation of mitochondrial ATP synthase subunit c and autofluorescence in CbCln3δex7/8/δex7/8 cells, and mitigates the abnormal subcellular distribution of acidic vesicles in the cells. L690,330, an IMPase inhibitor, is as effective as lithium in restoring autophagy in CbCln3δex7/8/δex7/8 cells. Moreover, lithium or down-regulation of IMPase expression protects CbCln3 δex7/8/δex7/8 cells from cell death induced by amino acid deprivation. These results suggest that lithium overcomes the autophagic defect in CbCln3δex7/8/δex7/8 cerebellar cells probably through IMPase, thereby reducing their vulnerability to cell death.

Original languageEnglish (US)
Pages (from-to)659-668
Number of pages10
JournalJournal of Neurochemistry
Volume116
Issue number4
DOIs
StatePublished - Feb 1 2011

Keywords

  • Batten disease
  • IMPase
  • autophagy
  • lithium

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