Effects of HIV gp120 on Neuroinflammation in Immunodeficient vs. Immunocompetent States.
Effects of HIV gp120 on Neuroinflammation in Immunodeficient vs. Immunocompetent States.
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HIV gp120对免疫缺陷与免疫活性状态下神经炎症的影响
DOI:
10.1007/s11481-020-09936-5
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发表时间:
2021-06
期刊:
影响因子:
--
通讯作者:
Cao L
中科院分区:
文献类型:
--
作者:
Arabatzis TJ;Wakley AA;McLane VD;Canonico D;Cao L
HIV affects 37 million people worldwide, 25-69% of which develop HIV-associated neurocognitive disorders (HAND) regardless of antiviral treatment. HIV infection of the brain decreases cognitive function, disrupts/impairs learning and memory, and reduces quality of life for those affected. HIV-induced neuroinflammation has been associated with viral proteins such as gp120 and Tat, which remain elevated in the CNS even in patients with low peripheral viremia counts. In this study, we examined the effects of gp120 on neuroinflammation in immunodeficient vs. immunocompetent states by examining neuroinflammatory markers in gp120tg mice with or without systemic immunodeficiency caused by murine retroviral administration (LP-BM5 murine AIDS). Changes in inflammatory cytokine/chemokine mRNA expression was complex and dependent upon expression of gp120 protein, immunodeficiency status, brain region (hippocampus, frontal lobe, or striatum), and age. Gp120 expression reduced hippocampal synaptophysin expression but did not affect animals’ learning/memory on the spontaneous T-maze test in our experimental conditions. Our results emphasize the critical role of the neuroinflammatory micro-environment and the peripheral immune system context in which gp120 acts. Multiple factors, particularly system-level differences in the immune response of different brain regions, need to be considered when developing treatment for HAND.
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