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- W1480499782 abstract "Synaptodendritic pruning and alterations in neurotransmission are the main underlying causes of HIV-associated neurocognitive disorders (HAND). Our studies in humans and nonhuman primates indicated that the protein ferritin heavy chain (FHC) is a critical player in neuronal changes and ensuing cognitive deficit observed in these patients. Here we focus on the effect of HIV proteins and inflammatory cytokines implicated in HAND on neuronal FHC levels, dendritic changes, and neurocognitive behavior. In two well characterized models of HAND (HIV transgenic and gp120-treated rats), we report reductions in spine density and dendritic branches in prefrontal cortex pyramidal neurons compared with age-matched controls. FHC brain levels are elevated in these animals, which also show deficits in reversal learning. Moreover, IL-1β, TNF-α, and HIV gp120 upregulate FHC in rat cortical neurons. However, although the inflammatory cytokines directly altered neuronal FHC, gp120 only caused significant FHC upregulation in neuronal/glial cocultures, suggesting that glia are necessary for sustained elevation of neuronal FHC by the viral protein. Although the envelope protein induced secretion of IL-1β and TNF-α in cocultures, TNF-α blockade did not affect gp120-mediated induction of FHC. Conversely, studies with an IL-1β neutralizing antibody or specific IL-1 receptor antagonist revealed the primary involvement of IL-1β in gp120-induced FHC changes. Furthermore, silencing of neuronal FHC abrogates the effect of gp120 on spines, and spine density correlates negatively with FHC levels or cognitive deficit. These results demonstrate that viral and host components of HIV infection increase brain expression of FHC, leading to cellular and functional changes, and point to IL-1β-targeted strategies for prevention of these alterations. Significance statement: This work demonstrates the key role of the cytokine IL-1β in the regulation of a novel intracellular mediator [i.e., the protein ferritin heavy chain (FHC)] of HIV-induced dendritic damage and the resulting neurocognitive impairment. This is also the first study that systematically investigates dendritic damage in layer II/III prefrontal cortex neurons of two different non-infectious models of HIV-associated neurocognitive disorders (HAND) and reveals a precise correlation of these structural changes with specific biochemical and functional alterations also reported in HIV patients. Overall, these data suggest that targeting the IL-1β-dependent FHC increase may represent a valid strategy for neuroprotective adjuvant therapies in HAND." @default.
- W1480499782 created "2016-06-24" @default.
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- W1480499782 date "2015-07-22" @default.
- W1480499782 modified "2023-10-10" @default.
- W1480499782 title "Induction of Interleukin-1 by Human Immunodeficiency Virus-1 Viral Proteins Leads to Increased Levels of Neuronal Ferritin Heavy Chain, Synaptic Injury, and Deficits in Flexible Attention" @default.
- W1480499782 cites W1522823711 @default.
- W1480499782 cites W1710867374 @default.
- W1480499782 cites W1913367972 @default.
- W1480499782 cites W1964526292 @default.
- W1480499782 cites W1969296748 @default.
- W1480499782 cites W1973929699 @default.
- W1480499782 cites W1975622423 @default.
- W1480499782 cites W1976434061 @default.
- W1480499782 cites W1976686309 @default.
- W1480499782 cites W1979334603 @default.
- W1480499782 cites W1994809873 @default.
- W1480499782 cites W1995746794 @default.
- W1480499782 cites W1996767517 @default.
- W1480499782 cites W1997753515 @default.
- W1480499782 cites W1999613356 @default.
- W1480499782 cites W2003556530 @default.
- W1480499782 cites W2005077425 @default.
- W1480499782 cites W2005804545 @default.
- W1480499782 cites W2009222844 @default.
- W1480499782 cites W2011884125 @default.
- W1480499782 cites W2016762244 @default.
- W1480499782 cites W2019249853 @default.
- W1480499782 cites W2025503583 @default.
- W1480499782 cites W2029843028 @default.
- W1480499782 cites W2038968007 @default.
- W1480499782 cites W2039662811 @default.
- W1480499782 cites W2039990777 @default.
- W1480499782 cites W2045145531 @default.
- W1480499782 cites W2045304025 @default.
- W1480499782 cites W2050175870 @default.
- W1480499782 cites W2050328515 @default.
- W1480499782 cites W2051348697 @default.
- W1480499782 cites W2053618924 @default.
- W1480499782 cites W2054841967 @default.
- W1480499782 cites W2055558890 @default.
- W1480499782 cites W2057109954 @default.
- W1480499782 cites W2062012741 @default.
- W1480499782 cites W2065104437 @default.
- W1480499782 cites W2065400194 @default.
- W1480499782 cites W2070524933 @default.
- W1480499782 cites W2070640704 @default.
- W1480499782 cites W2082920313 @default.
- W1480499782 cites W2084758662 @default.
- W1480499782 cites W2085718084 @default.
- W1480499782 cites W2088875934 @default.
- W1480499782 cites W2093190968 @default.
- W1480499782 cites W2093352510 @default.
- W1480499782 cites W2097082866 @default.
- W1480499782 cites W2098550298 @default.
- W1480499782 cites W2098736996 @default.
- W1480499782 cites W2119392695 @default.
- W1480499782 cites W2133655326 @default.
- W1480499782 cites W2134581110 @default.
- W1480499782 cites W2135349758 @default.
- W1480499782 cites W2138902434 @default.
- W1480499782 cites W2139117500 @default.
- W1480499782 cites W2144414931 @default.
- W1480499782 cites W2148095890 @default.
- W1480499782 cites W2148923308 @default.
- W1480499782 cites W2158052449 @default.
- W1480499782 cites W2158703764 @default.
- W1480499782 cites W2165727006 @default.
- W1480499782 cites W2169607015 @default.
- W1480499782 cites W2172058091 @default.
- W1480499782 cites W2444353434 @default.
- W1480499782 doi "https://doi.org/10.1523/jneurosci.4403-14.2015" @default.
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