Intravenous immunoglobulin suppresses NLRP1 and NLRP3 inflammasome-mediated neuronal death in ischemic stroke

David Y. Fann(The University of Queensland), S-Y Lee(The University of Queensland), Silvia Manzanero(The University of Queensland), S-C Tang(National Taiwan University), Mathias Gelderblom(Universität Hamburg), Prasad Chunduri(The University of Queensland), Christian Bernreuther(Universität Hamburg), Markus Glatzel(Universität Hamburg), Y-L Cheng(The University of Queensland), John Thundyil(The University of Queensland), Alexander Widiapradja(The University of Queensland), K-Z Lok(The University of Queensland), Sok Lin Foo(The University of Queensland), YC Wang(National Taiwan University), Yu‐I Li(National Taiwan University), Grant R. Drummond(Monash University), Milan Bašta(BioInVision (United States)), Tim Magnus(Universität Hamburg), Dong‐Gyu Jo(Sungkyunkwan University), Mark P. Mattson(Institute on Aging), Christopher G. Sobey(Monash University), Thiruma V. Arumugam(The University of Queensland)
Cell Death and Disease
September 5, 2013
Cited by 490Open Access
Full Text

Abstract

Multi-protein complexes called inflammasomes have recently been identified and shown to contribute to cell death in tissue injury. Intravenous immunoglobulin (IVIg) is an FDA-approved therapeutic modality used for various inflammatory diseases. The objective of this study is to investigate dynamic responses of the NLRP1 and NLRP3 inflammasomes in stroke and to determine whether the NLRP1 and NLRP3 inflammasomes can be targeted with IVIg for therapeutic intervention. Primary cortical neurons were subjected to glucose deprivation (GD), oxygen-glucose deprivation (OGD) or simulated ischemia-reperfusion (I/R). Ischemic stroke was induced in C57BL/6J mice by middle cerebral artery occlusion, followed by reperfusion. Neurological assessment was performed, brain tissue damage was quantified, and NLRP1 and NLRP3 inflammasome protein levels were evaluated. NLRP1 and NLRP3 inflammasome components were also analyzed in postmortem brain tissue samples from stroke patients. Ischemia-like conditions increased the levels of NLRP1 and NLRP3 inflammasome proteins, and IL-1β and IL-18, in primary cortical neurons. Similarly, levels of NLRP1 and NLRP3 inflammasome proteins, IL-1β and IL-18 were elevated in ipsilateral brain tissues of cerebral I/R mice and stroke patients. Caspase-1 inhibitor treatment protected cultured cortical neurons and brain cells in vivo in experimental stroke models. IVIg treatment protected neurons in experimental stroke models by a mechanism involving suppression of NLRP1 and NLRP3 inflammasome activity. Our findings provide evidence that the NLRP1 and NLRP3 inflammasomes have a major role in neuronal cell death and behavioral deficits in stroke. We also identified NLRP1 and NLRP3 inflammasome inhibition as a novel mechanism by which IVIg can protect brain cells against ischemic damage, suggesting a potential clinical benefit of therapeutic interventions that target inflammasome assembly and activity.


Related Papers

No related papers found

Powered by citation graph analysis