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Caspase-1 Activity in Microglia Stimulated by Pro-Inflammagen Nanocrystals
Author(s) -
Alexandre Moquin,
Eliza Hutter,
Angela O. Choi,
Armen Khatchadourian,
Annie Castonguay,
Françoise M. Winnik,
Dušica Maysinger
Publication year - 2013
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/nn404473g
Subject(s) - microglia , lipopolysaccharide , inflammation , microbiology and biotechnology , caspase 1 , caspase 3 , in vivo , chemistry , inflammasome , apoptosis , biochemistry , programmed cell death , biology , immunology
Although caspase-1 is a key participant in inflammation, there is no sensitive assay to measure its enzymatic activity in real time in cells or animals. Here we describe a nanosensor for caspase-1 ratiometric measurements, consisting of a rhodamine-labeled, caspase-1 cleavable peptide linked to quantum dots (QDs). Microglia cells were stimulated by lipopolysaccharide (LPS) and by hybrid nanoparticles LPS-QDs. These stimuli activated caspase-1 in microglia monolayers and in the mouse brain, while a selected caspase inhibitor markedly reduced it. LPS-QDs entered into the lysosomal compartment and led to an enlargement of these cellular organelles in the exposed microglia. Both lysosomal swelling and mitochondrial impairment contributed to caspase-1 activation and to the consequent interleukin-1β release. The results from these studies highlight how the unique properties of QDs can be used to create versatile biotools in the study of inflammation in real time in vivo.

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