The NLRP3 and NLRP1 inflammasomes are activated in Alzheimer's disease.
The NLRP3 and NLRP1 inflammasomes are activated in Alzheimer's disease.
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DOI:
10.1186/s13024-016-0088-1
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发表时间:
2016-03-03
影响因子:
15.1
通讯作者:
Clerici M
中科院分区:
文献类型:
--
作者:
Saresella M;La Rosa F;Piancone F;Zoppis M;Marventano I;Calabrese E;Rainone V;Nemni R;Mancuso R;Clerici M
Interleukin-1 beta (IL-1β) and its key regulator, the inflammasome, are suspected to play a role in the neuroinflammation observed in Alzheimer’s disease (AD); no conclusive data are nevertheless available in AD patients. mRNA for inflammasome components (NLRP1, NLRP3, PYCARD, caspase 1, 5 and 8) and downstream effectors (IL-1β, IL-18) was up-regulated in severe and MILD AD. Monocytes co-expressing NLRP3 with caspase 1 or caspase 8 were significantly increased in severe AD alone, whereas those co-expressing NLRP1 and NLRP3 with PYCARD were augmented in both severe and MILD AD. Activation of the NLRP1 and NLRP3 inflammasomes in AD was confirmed by confocal microscopy proteins co-localization and by the significantly higher amounts of the pro-inflammatory cytokines IL-1β and IL-18 being produced by monocytes. In MCI, the expression of NLRP3, but not the one of PYCARD or caspase 1 was increased, indicating that functional inflammasomes are not assembled in these individuals: this was confirmed by lack of co-localization and of proinflammatory cytokines production. The activation of at least two different inflammasome complexes explains AD-associated neuroinflammation. Strategies targeting inflammasome activation could be useful in the therapy of AD.