In this study, we investigated whether alterations in the pattern of caspase activation could be found at the level of peripheral blood mononuclear cells (PBMCs) in patients with Alzheimer’s disease (AD). The results showed that in experimental conditions resembling a physiological stimulation, there was a statistically significant increase in the enzymatic activity of caspase-3, caspase-8, and caspase-9 in PBMCs from a small, but well-characterized, cohort of sporadic AD patients compared to those from a comparable control group of aged adults (AA). This was accompanied by a parallel, early increase in the cleavage activity of the same caspases. The higher level of caspase activity in PBMCs from AD compared to AAwas not associated with quantitative differences in cell subset profiles. Moreover, no increase in apoptosis level, in the same experimental conditions, was found in PBMCs from this cohort of AD patients compared to those from AA. Conversely, the higher proneness to caspase activation in PBMCs from AD patients in comparison with that from AA was associated with a higher proliferative response to PHA or CD3. These data show a new dysfunction in AD patients at the PBMCs level and suggest that increased proneness to caspase activation in lymphocytes could reflect an ongoing systemic response in neurodegenerative disease with pathogenetic implications.

Tacconi, S., Perri, R., Balestrieri, E., Grelli, S., Bernardini, S., Annichiarico, R., et al. (2004). Increased caspase activation in peripheral blood mononuclear cells of patients with Alzheimer’s disease. EXPERIMENTAL NEUROLOGY, 190(1), 254-262 [10.1016/j.expneurol.2004.07.009].

Increased caspase activation in peripheral blood mononuclear cells of patients with Alzheimer’s disease

BALESTRIERI, EMANUELA;GRELLI, SANDRO;BERNARDINI, SERGIO;CALTAGIRONE, CARLO;MACCHI, BEATRICE
2004-01-01

Abstract

In this study, we investigated whether alterations in the pattern of caspase activation could be found at the level of peripheral blood mononuclear cells (PBMCs) in patients with Alzheimer’s disease (AD). The results showed that in experimental conditions resembling a physiological stimulation, there was a statistically significant increase in the enzymatic activity of caspase-3, caspase-8, and caspase-9 in PBMCs from a small, but well-characterized, cohort of sporadic AD patients compared to those from a comparable control group of aged adults (AA). This was accompanied by a parallel, early increase in the cleavage activity of the same caspases. The higher level of caspase activity in PBMCs from AD compared to AAwas not associated with quantitative differences in cell subset profiles. Moreover, no increase in apoptosis level, in the same experimental conditions, was found in PBMCs from this cohort of AD patients compared to those from AA. Conversely, the higher proneness to caspase activation in PBMCs from AD patients in comparison with that from AA was associated with a higher proliferative response to PHA or CD3. These data show a new dysfunction in AD patients at the PBMCs level and suggest that increased proneness to caspase activation in lymphocytes could reflect an ongoing systemic response in neurodegenerative disease with pathogenetic implications.
2004
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/14 - FARMACOLOGIA
Settore MED/26 - NEUROLOGIA
English
Con Impact Factor ISI
Alzheimer’s disease; aging; caspases; lymphocytes; apoptosis; reference values; leukocytes, mononuclear; phytohemagglutinins; enzyme activation; humans; cell proliferation; antibodies, monoclonal; antigens, CD3; adult; cohort studies; middle aged; male; female
Tacconi, S., Perri, R., Balestrieri, E., Grelli, S., Bernardini, S., Annichiarico, R., et al. (2004). Increased caspase activation in peripheral blood mononuclear cells of patients with Alzheimer’s disease. EXPERIMENTAL NEUROLOGY, 190(1), 254-262 [10.1016/j.expneurol.2004.07.009].
Tacconi, S; Perri, R; Balestrieri, E; Grelli, S; Bernardini, S; Annichiarico, R; Mastino, A; Caltagirone, C; Macchi, B
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/40906
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