Brain-derived neurotrophic factor (BDNF) is known to have trophic effects o
n various neurons, throughout the brain and spinal cord, via its high-affin
ity tyrosine kinase receptor TrkB. It has been reported that the mRNA for t
his neurotrophin is reduced in Alzheimer's disease (AD) brain. We have exam
ined, by Western blotting, the catalytic (p145) and noncatalytic or truncat
ed (p95) forms of TrkB and find that, in both the temporal and frontal cort
ex, there is a selective loss of immunoreactive-positive staining for the c
atalytic or kinase form compared with the truncated form. This may have imp
ortant consequences for the neurotrophic support of vulnerable neurons in A
D. (C) 1999 Academic Press.