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Reduced expression of the Ca 2+ transporter protein PMCA2 slows Ca 2+ dynamics in mouse cerebellar Purkinje neurones and alters the precision of motor coordination
Author(s) -
Empson Ruth M.,
Turner Paul R.,
Nagaraja Raghavendra Y.,
Beesley Philip W.,
Knöpfel Thomas
Publication year - 2010
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2009.182196
Subject(s) - cerebellum , chemistry , transporter , motor coordination , biophysics , neuroscience , biochemistry , biology , gene
Cerebellar Purkinje neurones (PNs) express high levels of the plasma membrane calcium ATPase, PMCA2, a transporter protein critical for the clearance of calcium from excitable cells. Genetic deletion of one PMCA2 encoding gene in heterozygous PMCA2 knock‐out (PMCA2 +/− ) mice enabled us to determine how PMCA2 influences PN calcium regulation without the complication of the severe morphological changes associated with complete PMCA2 knock‐out (PMCA2 −/− ) in these cells. The PMCA2 +/− cerebellum expressed half the normal levels of PMCA2 and this nearly doubled the time taken for PN dendritic calcium transients to recover (mean fast and slow recovery times increased from 70 ms to 110 ms and from 600 ms to 1100 ms). The slower calcium recovery had distinct consequences for PMCA2 +/− PN physiology. The PNs exhibited weaker climbing fibre responses, prolonged outward Ca 2+ ‐dependent K + current (mean fast and slow recovery times increased from 136 ms to 192 ms and from 595 ms to 1423 ms) and a slower mean frequency of action potential firing (7.4 Hz compared with 15.8 Hz). Our findings were consistent with prolonged calcium accumulation in the cytosol of PMCA2 +/− Purkinje neurones. Although PMCA2 +/− mice exhibited outwardly normal behaviour and little change in their gait pattern, when challenged to run on a narrow beam they exhibited clear deficits in hindlimb coordination. Training improved the motor performance of both PMCA2 +/− and wild‐type mice, although PMCA2 +/− mice were always impaired. We conclude that reduced calcium clearance perturbs calcium dynamics in PN dendrites and that this is sufficient to disrupt the accuracy of cerebellar processing and motor coordination.