In order to study whether phosphokinases might be involved in the neur
opathology of Down Syndrome (DS) and Alzheimer disease (AD), cyclin de
pendent kinase (CDK) activity and protein, phosphokinase C (PKC) and p
hosphokinase A (PKA) activities have been determined in frontal lobes
of DS, AD and control brains. An enzyme linked immunosorbent assay (EL
ISA) technique for CDK protein, and commercially available enzyme assa
ys for CDK, PKC and PKA activities have been used. The major finding o
f our study was the remarkable and significant decrease of CDK protein
and activity in DS brains in comparison to AD and controls. PKC and P
KA were unaffected in both, AD and DS. As CDK controls cell division a
nd differentiation, lowered CDK levels could reflect impaired prolifer
ation and differentiation in DS.