Apoptosis is essential for normal human neurodevelopment and is increasingl
y recognized for its role in various neurodegenerative diseases such as Alz
heimer's and Parkinson's diseases. Bcl-2 is a 26 kDa membrane-associated pr
otein known to protect neurons against apoptosis. Interestingly, Bcl-2 prot
ein levels are altered in certain neurodegenerative disorders that reveal i
ncreased apoptosis. However, little is known about the normal expression of
Bcl-2 protein in human brain. Bcl-2 protein levels were determined by ELIS
A and semiquantitative Western Blotting in the frontal cortex of 20 human p
ost-mortem brains, separated into three groups: six infants (age. 0.83 +/-
1.0 years, mean +/- S.D.), five adolescents (age: 17.4 +/- 1.7 years), and
nine adults (age: 41.0 +/- 9.6 years). All subjects died of non-CNS related
illness and had no history of psychiatric illness. Bcl-2 increased signifi
cantly across the age groups in the ELISA (p = 0.0058) and the Western Blot
(p = 0.002) experiments. The ELISA demonstrated significant differences in
Bcl-2 levels between infant and adolescent cortex (p < 0.05), and between
infant and adult cortex (p < 0.01) using a post-hoc Tukey's multiple compar
ison test. The Western blots demonstrated a similar significant increase in
Bcl-2 between infant and adult cortex (p < 0.01). A secondary analysis sho
wed significant correlation between individual ages and Bcl-2 levels (r(2)
= 0.4933, p = 0.0006). This study demonstrates that Bcl-2 protein expressio
n in human cortex is developmentally regulated and supports the hypothesis
that Bcl-2 is involved in normal aging. (C) 2000 Elsevier Science B.V. All
rights reserved.