Affiliations: Neurochemical Laboratory, Department of Biochemistry, Medical
University. Lodz, Poland
Note: [] Address for correspondence: Ludmila Zylinska Neurochemical
Laboratory Department of Biochemistry Medical University 6 Lindley Street
90-131 Lodz, Poland phone : (+48.42) 679.00.35 fax : (+48.42) 678.62.45 E-mail
: luska@psk2.am.lodz.pl
Abstract: During the last decade the mechanisms of Ca2+ regulation in the
brain have been extensively investigated in a variety of neural cells. These
investigations demonstrate that intraneuronal Ca2+ participate in the multiple
controls of important neural functions, like excitability, neurotransmitters
release or long-term changes in synaptic efficacy. Moreover, there is a
significant number of data confirming that the impairment of calcium
homeostasis is closely linked with aging and several brain disorders. The
plasma membrane Ca2+-ATPase (PMCA) is a ubiquitously expressed protein, which
constitutes a high affinity system extruding Ca2+ outside the cell and
maintains the intracellular Ca2+ in the submicromolar range in a resting state.
In neuronal tissues more than 26 transcripts of the four separate PMCA genes
are distributed in a region specific manner. Differences in the structure and
localization of PMCA variants are thought to correlate with specific regulatory
properties and may have consequences for proper Ca2+ signaling or for the
response to the brain malfunction. Below some new aspects of the Ca2+-ATPase
modulation in physiological and pathological conditions will be discussed which
may influence neuronal calcium signaling.