| Literature DB >> 26586559 |
Joshua J White1, Marife Arancillo2, Annesha King2, Tao Lin2, Lauren N Miterko3, Samrawit A Gebre2, Roy V Sillitoe4.
Abstract
Neurological diseases are especially devastating when they involve neurodegeneration. Neuronal destruction is widespread in cognitive disorders such as Alzheimer's and regionally localized in motor disorders such as Parkinson's, Huntington's, and ataxia. But, surprisingly, the onset and progression of these diseases can occur without neurodegeneration. To understand the origins of diseases that do not have an obvious neuropathology, we tested how loss of CAR8, a regulator of IP3R1-mediated Ca(2+)-signaling, influences cerebellar circuit formation and neural function as movement deteriorates. We found that faulty molecular patterning, which shapes functional circuits called zones, leads to alterations in cerebellar wiring and Purkinje cell activity, but not to degeneration. Rescuing Purkinje cell function improved movement and reducing their Ca(2+) influx eliminated ectopic zones. Our findings in Car8(wdl) mutant mice unveil a pathophysiological mechanism that may operate broadly to impact motor and non-motor conditions that do not involve degeneration.Entities:
Keywords: Ataxia; Behavior; Cerebellum; In vivo electrophysiology; Neurodegeneration; Tremor
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Year: 2015 PMID: 26586559 PMCID: PMC4778569 DOI: 10.1016/j.nbd.2015.11.008
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996