CYTOSOLIC CA2-PROTEINS DURING RAT-BRAIN AGING - LOSS OF CALBINDIN ANDCALRETININ IN THE HIPPOCAMPUS, WITH NO CHANGE IN THE CEREBELLUM( BINDING)

The expression of two cytosolic, high affinity Ca2+-binding proteins, calbindin-28 and calretinin, has been investigated in the cerebellum a nd hippocampus of young and old rats (from 12 days to 30 months) by co mbining immunofluorescence and Western blotting. Three markers, calret iculin (the major Ca2+ binding protein within the lumen of the endopla smic reticulum), MAP-2 (a microtubule binding protein concentrated in neuronal dendrites) and synaptophysin (an integral protein of synaptic vesicles), were studied in parallel. In the cerebellar cortex a rise from 12 to 60 days was observed with calbindin-28 and, especially, cal retinin, concentrated in the Purkinje and granule neurons, respectivel y. The level of expression of the two proteins subsequently remained h igh and the distribution was unchanged, even in the cerebellum of old animals. A completely different pattern was observed in the hippocampu s. Here calretinin, present especially in fibres and interneurons, was abundant in the young, decreased in the adult and reached low values in the old rats. Calbindin-28 accumulated during growth, especially in a subpopulation of CA1 pyramidal cells and in the messy fibres of CA3 , then declined, although irregularily, during ageing. These changes o f the two proteins were more marked in the dorsal and central parts th an in the ventral part of the hippocampus. In the same brain areas the levels of expression of the three additional markers and their distri bution within neurons and synapses were unchanged by ageing. These las t results demonstrate that ageing is not accompanied by a marked loss of hippocampal neurons, yet most of the latter cells appear to modify their general Ca2+ homeostasis as a consequence of the decreased level of cytosolic Ca2+ binding proteins. These events could contribute to the changes in neuronal functioning that have been reported in the age d hippocampus, whereas those of the cerebellum appear to be sustained by other mechanisms.