| Autor: |
Fattakhov N; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Ngo A; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Torices S; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Joseph JA; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Okoro A; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Moore C; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Naranjo O; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Becker S; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States., Toborek M; Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida, United States. |
| Abstrakt: |
Blood-brain barrier (BBB) breakdown is one of the pathophysiological characteristics of ischemic stroke, which may contribute to the progression of brain tissue damage and subsequent neurological impairment. Human immunodeficiency virus (HIV)-infected individuals are at greater risk for ischemic stroke due to diminished immune function and HIV-associated vasculopathy. Studies have shown that astrocytes are involved in maintaining BBB integrity and facilitating HIV-1 infection in the brain. The present study investigated whether targeting astrocyte-endothelial cell signaling with cenicriviroc (CVC), a dual chemokine receptor (CCR)2 and CCR5 antagonist, may protect against dysregulation of cross talk between these cells after oxygen-glucose deprivation/reoxygenation (OGD/R) combined with HIV-1 infection. Permeability assay with 10 kDa fluorescein isothiocyanate (FITC)-dextran demonstrated that CVC alleviated endothelial barrier disruption in noncontact coculture of human brain microvascular endothelial cells (HBMECs) with HIV-1-infected human astrocytes, and reversed downregulation of tight junction protein claudin-5 induced by OGD/R- and HIV-1. Moreover, CVC attenuated OGD/R- and HIV-1-triggered upregulation of the NOD-like receptor protein-3 (NLRP3) inflammasome and IL-1β secretion. Treatment with CVC also suppressed astrocyte pyroptosis by attenuating cleaved caspase-1 levels and the formation of cleaved N-terminal GSDMD (N-GSDMD). Secretome profiling revealed that CVC ameliorated secretion levels of chemokine CC chemokine ligand 17 (CCL17), adhesion molecule intercellular adhesion molecule-1 (ICAM-1), and T cell activation modulator T cell immunoglobulin and mucin domain 3 (TIM-3) by astrocytes synergistically induced by OGD/R and HIV-1. Overall, these results suggest that CVC contributes to restoring astrocyte-endothelial cross interactions in an astrocyte-dependent manner via protection against NLRP3 activation and pyroptosis. NEW & NOTEWORTHY The present study reveals the role of astrocytic NOD-like receptor protein-3 (NLRP3) inflammasome in dysfunctional astrocyte-endothelial cross interactions triggered in response to oxygen/glucose deprivation injury associated with human immunodeficiency virus type 1 (HIV-1) infection. Our results suggest that blocking NLRP3 inflammasome activation and pyroptosis-mediated inflammation with cenicriviroc (CVC) may constitute a potentially effective therapeutic strategy for blood-brain barrier (BBB) protection during HIV-1-associated ischemic stroke. |
