The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum.

Dulneva A., Lee S., Oliver PL., Di Gleria K., Kessler BM., Davies KE., Becker EBE.

The Moonwalker (Mwk) mouse is a model of dominantly inherited cerebellar ataxia caused by a gain-of-function mutation in the transient receptor potential (TRP) channel TRPC3. Here, we report impairments in dendritic growth and synapse formation early on during Purkinje cell development in the Mwk cerebellum that are accompanied by alterations in calcium signaling. To elucidate the molecular effector pathways that regulate Purkinje cell dendritic arborization downstream of mutant TRPC3, we employed transcriptomic analysis of developing Purkinje cells isolated by laser-capture microdissection. We identified significant gene and protein expression changes in molecules involved in lipid metabolism. Consistently, lipid homeostasis in the Mwk cerebellum was found to be disturbed, and treatment of organotypic cerebellar slices with ceramide significantly improved dendritic outgrowth of Mwk Purkinje cells. These findings provide the first mechanistic insights into the TRPC3-dependent mechanisms, by which activated calcium signaling is coupled to lipid metabolism and the regulation of Purkinje cell development in the Mwk cerebellum.

DOI

10.1093/hmg/ddv150

Type

Journal article

Journal

Hum Mol Genet

Publication Date

15/07/2015

Volume

24

Pages

4114 - 4125

Keywords

Animals, Calcium Signaling, Cerebellar Ataxia, Cerebellum, Dendrites, Gene Expression Regulation, Lipid Metabolism, Mice, Purkinje Cells, TRPC Cation Channels, Transcriptome

Permalink Original publication