CHARACTERISTIC TRANSKETOLASE ALTERATIONS IN DERMAL FIBROBLASTS OF ALZHEIMER PATIENTS ARE MODULATED BY CULTURE CONDITIONS

Citation
D. Tombaccini et al., CHARACTERISTIC TRANSKETOLASE ALTERATIONS IN DERMAL FIBROBLASTS OF ALZHEIMER PATIENTS ARE MODULATED BY CULTURE CONDITIONS, Experimental and molecular pathology, 60(2), 1994, pp. 140-146
Citations number
16
Categorie Soggetti
Pathology
ISSN journal
00144800
Volume
60
Issue
2
Year of publication
1994
Pages
140 - 146
Database
ISI
SICI code
0014-4800(1994)60:2<140:CTAIDF>2.0.ZU;2-P
Abstract
Cultured Alzheimer fibroblasts were found to present peculiar alterati ons of transketolase (TK) ascribed to enhanced proteolytic activities in these cells and tentatively proposed as a marker of the disease. TK abnormalities, consisting of enzyme forms (alkaline bands) with unusu ally high alkaline pI, were investigated with respect to the mechanism of their generation and modulation by culture conditions. Alzheimer f ibroblasts propagated at different pH, within a range of 7.3-7.8, exhi bited TK abnormalities whose expression correlated directly with incre ases in medium pH values. Alterations were mostly evident in cells gro wn at 5% CO2 saturation in the atmosphere and with 3.7 g/liter NaHCO3 in the medium to yield an initial pH of about 7.75. Alkaline bands wer e not detected in either Alzheimer fibroblasts incubated at 10% CO2 or in control cells under any of the other conditions tested. Changes in initial medium pH also affected the morphology of fibroblasts, which shifted from a relatively large to an elongated shape as the medium pH decreased. The formation of alkaline bands was abolished by the addit ion of E-64, a known cysteine protease inhibitor, to cells just prior to extraction. On the contrary, Alzheimer fibroblasts cultured for 2 d ays in the presence of the inhibitor maintained the typically altered TK pattern. The establishment of conditions suitable for the expressio n of TK alterations in Alzheimer fibroblasts might be of help for diag nostic purposes and provide information on still elusive pathogenetic mechanisms of the disease. (C) 1994 Academic Press, Inc.