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Publication : Impaired motor coordination and Purkinje cell excitability in mice lacking calretinin.

First Author  Schiffmann SN Year  1999
Journal  Proc Natl Acad Sci U S A Volume  96
Issue  9 Pages  5257-62
PubMed ID  10220453 Mgi Jnum  J:54517
Mgi Id  MGI:1336424 Doi  10.1073/pnas.96.9.5257
Citation  Schiffmann SN, et al. (1999) Impaired motor coordination and Purkinje cell excitability in mice lacking calretinin. Proc Natl Acad Sci U S A 96(9):5257-62
abstractText  In the cerebellum, the parallel fiber-Purkinje cell synapse can undergo long-term synaptic plasticity suggested to underlie motor learning and resulting from variations in intracellular calcium concentration ([Ca2+]i). Ca2+ binding proteins are enriched in the cerebellum, but their role in information processing is not clear. Here, we show that mice deficient in calretinin (Cr-/-) are impaired in tests of motor coordination. An impairment in Ca2+ homeostasis in Cr-/- Purkinje cells was supported by the high Ca2+-saturation of calbindin-D28k in these cells. The firing behavior of Purkinje cells is severely affected in Cr-/- alert mice, with alterations of simple spike firing rate, complex spike duration, and simple spike pause. In contrast, in slices, transmission at parallel fiber- or climbing fiber-Purkinje cell synapses is unaltered, indicating that marked modifications of the firing behavior in vivo can be undetectable in slice. Thus, these results show that calretinin plays a major role at the network level in cerebellar physiology.
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