AXONAL ATROPHY IN AGING IS ASSOCIATED WITH A DECLINE IN NEUROFILAMENTGENE-EXPRESSION

Citation
Im. Parhad et al., AXONAL ATROPHY IN AGING IS ASSOCIATED WITH A DECLINE IN NEUROFILAMENTGENE-EXPRESSION, Journal of neuroscience research, 41(3), 1995, pp. 355-366
Citations number
84
Categorie Soggetti
Neurosciences
ISSN journal
03604012
Volume
41
Issue
3
Year of publication
1995
Pages
355 - 366
Database
ISI
SICI code
0360-4012(1995)41:3<355:AAIAIA>2.0.ZU;2-S
Abstract
Neurofilaments (Nfs) are major determinants of axonal caliber, Nf tran script levels increase during development and maturation, and are asso ciated with an increase in Nf protein, Nf numbers, and caliber of axon s, With aging there is axonal atrophy, In this study we asked whether the axonal atrophy of aging was associated with a decline in Nf transc ript expression, Nf protein levels, and Nf numbers, Expression of tran scripts for the three Nf subunits was evaluated in dorsal root ganglia (DRG) of Fischer-344 rats aged 3-32 months by Northern and in situ hy bridization. There was an approximately 50% decrease in Nf subunit mRN A levels in DRG of aged (>23 months) as compared to young and mature ( 3 and 12 months) rats, whereas expression of another neuronal mRNA, GA P-43, showed no decline, Western analysis showed a corresponding decre ase in Nf subunit proteins and no decline in GAP-43, Morphometric anal ysis showed a 50% decrease in Nf numbers within axons, The decrease in Nf gene expression and Nf numbers was accompanied by a decrease in cr oss-sectional area and circularity of all myelinated fibers, with the largest fibers showing the most marked changes, and a shrinkage in the perikaryal area of large neurons. Furthermore, we found a concomitant decrease in the expression of transcripts for the nerve growth factor receptors trkA and p75 with aging, Although the mechanisms leading to the decrease in Nf gene expression with aging are not known, a decrea se in the availability of growth factors, or the neuron's ability to r espond to them, may play a role in this process, (C) 1995 Wiley-Liss, Inc.