HIV-1 Tat-induced diarrhea evokes an enteric glia-dependent neuroinflammatory response in the central nervous system

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Giuseppe Esposito
Elena Capoccia
Stefano Gigli
Marcella Pesce
Eugenia Bruzzese
Alessandra D’Alessandro
Carla Cirillo
Alessandro di Cerbo
Rosario Cuomo
Luisa Seguella
Luca Steardo
Giovanni Sarnelli
机构
[1] “La Sapienza” University of Rome,Department of Physiology and Pharmacology
[2] University of Naples “Federico II”,Department of Clinical Medicine and Surgery, Section of Gastroenterology
[3] University of Naples “Federico II”,Department of Translational Medical Science, Section of Pediatrics
[4] TARGID,Laboratory for Enteric Neuroscience (LENS)
[5] University of Leuven,Department of Biomedical Science
[6] “G. D’Annunzio” University,undefined
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Despite the effectiveness of combined anti-retroviral therapy, human immunodeficiency virus (HIV) infected-patients frequently report diarrhea and neuropsychological deficits. It is claimed that the viral HIV-1 Trans activating factor (HIV-1 Tat) protein is responsible for both diarrhea and neurotoxic effects, but the underlying mechanisms are not known. We hypothesize that colonic application of HIV-1 Tat activates glial cells of the enteric nervous system (EGCs), leading to a neuroinflammatory response able to propagate to the central nervous system. We demonstrated that HIV-1 Tat-induced diarrhea was associated with a significant activation of glial cells within the colonic wall, the spinal cord and the frontal cortex, and caused a consistent impairment of the cognitive performances. The inhibition of glial cells activity by lidocaine, completely abolished the above-described effects. These observations point out the role of glial cells as putative effectors in HIV-1 Tat-associated gastrointestinal and neurological manifestations and key regulators of gut-brain signaling.
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