Submit Manuscript  

Article Details


HIV-1 Tat-Induced Changes in Synaptically-Driven Network Activity Adapt During Prolonged Exposure

[ Vol. 12 , Issue. 6 ]

Author(s):

Kelly A. Krogh, Matthew V. Green and Stanley A. Thayer   Pages 406 - 414 ( 9 )

Abstract:


HIV-associated neurocognitive disorders (HAND) afflict approximately half of HIVinfected patients. The HIV-1 transactivator of transcription (Tat) protein is released by infected cells and contributes to the pathogenesis of HAND, but many of the underlying mechanisms remain poorly understood. Here we used fura-2-based Ca2+ imaging and whole-cell patch-clamp recording to study the effects of Tat on the spontaneous synaptic activity that occurs in networked rat hippocampal neurons in culture. Tat triggered aberrant network activity that exhibited a decrease in the frequency of spontaneous action potential bursts and Ca2+ spikes with a simultaneous increase in burst duration and Ca2+ spike amplitude. These network changes were apparent after 4 h treatment with Tat and required the low-density lipoprotein receptor-related protein (LRP). Interestingly, Tat-induced changes in network activity adapted during 24 h exposure. The activity returned to control levels in the maintained presence of Tat for 24 h. These observations indicate that Tat causes aberrant network activity, which is dependent on LRP, and adapts following prolonged exposure. Changes in network excitability may contribute to Tat-induced neurotoxicity in vitro and seizure disorders in vivo. Adaptation of neural networks may be a neuroprotective response to the sustained presence of the neurotoxic protein Tat and could underlie the behavioral and electrophysiological changes observed in HAND.

Keywords:

Adaptation, Ca2+ signaling, excitotoxicity, fura-2, hippocampal culture, HIV associated neurocognitive disorders (HAND), lipoprotein receptor, synaptic network.

Affiliation:

Department of Pharmacology, University of Minnesota, 6-120 Jackson Hall, 321 Church Street SE, Minneapolis, MN 55455, USA.

Graphical Abstract:



Read Full-Text article