HIV-1 Tat alters neuronal intrinsic excitability
BMC Research Notes volume 11, Article number: 275 (2018)
In HIV+ individuals, the virus enters the central nervous system and invades innate immune cells, producing important changes that result in neurological deficits. We aimed to determine whether HIV plays a direct role in neuronal excitability. Of the HIV peptides, Tat is secreted and acts in other cells. In order to examine whether the HIV Tat can modify neuronal excitability, we exposed primary murine hippocampal neurons to that peptide, and tested its effects on the intrinsic membrane properties, 4 and 24 h after exposure.
The exposure of hippocampal pyramidal neurons to Tat for 4 h did not alter intrinsic membrane properties. However, we found a strong increase in intrinsic excitability, characterized by increase of the slope (Gain) of the input–output function, in cells treated with Tat for 24 h. Nevertheless, Tat treatment for 24 h did not alter the resting membrane potential, input resistance, rheobase and action potential threshold. Thus, neuronal adaptability to Tat exposure for 24 h is not applicable to basic neuronal properties. A restricted but significant effect on coupling the inputs to the outputs may have implications to our knowledge of Tat biophysical firing capability, and its involvement in neuronal hyperexcitability in neuroHIV.
Neuronal plasticity and regeneration are interrelated phenomena, tightly dependent on the normal functioning of the Central Nervous System (CNS). Changes in glia drastically affect neuronal capacity to recover and rewire [1,2,3]. Microglia invade the CNS at prenatal stages, increasing density during the first weeks of postnatal life, reaching a maximum by P18, concomitant to an intense synaptogenesis period [4,5,6]. Microglia express cytokines, neurotrophins [7, 8], glutamate and NO [9,10,11,12], which regulate synaptic properties. Importantly, microglia are critical during Human Immunodeficiency Virus (HIV) infection, because they get infected by virus carried into the brain by macrophages at early time points [13, 14].
The consequences of HIV in the brain include high incidence of neurological dysfunctions, even in the post-antiretroviral age . Of all HIV-1 peptides, Tat is involved in viral transcription, and is unconventionally secreted by infected targets [15,16,17,18], with consequences to neighboring cells, including neurons. HIV-Tat has been linked to impaired learning and memory, and gray matter deficits [19, 20], suggesting its involvement in the development of HIV-associated neurological disorders (HAND).
The hippocampus is a brain region involved in cognition, and memory formation, organization, and retrieval, where the main cell type is the excitatory glutamatergic pyramidal neuron, integrating spatial, contextual, and emotional information, while transmitting all outputs to cellular targets throughout the brain, in response to glutamate, a key neurotransmitter . Pyramidal cells in the CA1 and subiculum regions carry output by firing individual or high frequency bursts of action potentials (AP), increasing synaptic communication through evoking a postsynaptic spike [22, 23]. They also participate in plasticity and place field development [24, 25]. Excitatory synaptic transmission in hippocampal neurons is susceptible to changes, contributing to cognitive impairments. Due to the abundance of these neurons, the hippocampus is crucial for recalling when and where an event occurred, or ‘episodic memory’ , one of the first functions lost in HAND and in aging [27, 28]. Importantly, we have demonstrated that HIV Tat prevents long-term potentiation in the hippocampal CA1 region . Our goal was to further characterize the neuronal response to HIV Tat in primary cultures.
Neuronal membrane properties are characterized by means of the input–output response function, giving the rate of AP discharge as a function of the injected current strength. The linear relationship between neuronal input and output is defined by the rheobase (minimum synaptic input that generates an AP), and by the slope (gain). The gain control is a central feature of neural information processing . Changes in gain control, associated with alterations in the conductance of voltage-gated channels such as the A-type (IA), the delayed-rectifier K+ (Id) and L-type voltage-gated Ca2+ (IKCa) channels, are critical in several pathophysiological conditions. An increase in IA, Id and IKCa reduces neuronal gain. In contrast, increases in the slow voltage-gated Ca2+ channel conductance (GCaS) increase neuronal gain. The hyperpolarization-activated inward channel (Ih) is ‘gain neutral’. The functional relevance of such changes include protecting neurons from over-excitation during ischemia, infection, or aging, and for making neurons more excitable during associative learning [31,32,33,34,35,36].
We used the slope of the fitted linear function (gain, I–O slope) as a quantitative measure of biophysical firing capabilities under DC step stimulation , to examine whether HIV-1 Tat can modulate hippocampal neuron properties, explaining changes in memory functions experienced by HIV+ subjects. In neuronal primary cultures we modeled Tat exposure, and tested its effects on excitability.
In cell line studies, Tat internalization by neurons was detected at 4 h . Effects on molecular functions and morphology were detected at 24 h [39, 40], preceding neurotoxicity at 48 h . The ability of Tat to modify neuronal excitability in the primary hippocampal neuron culture system was tested on whole cell patch electrophysiological testing paradigms, at 4 and 24-h time points. We found a significant effect of Tat at 24 h after exposure.
Animal use was approved by Institutional Animal Care and Use Committees of The Scripps Research Institute (TSRI) and San Diego Biomedical Research Institute. In three independent experiments, two pregnant C57Bl/6 females, 5–8 weeks old, were purchased from TSRI Department of Animal Resources. E17 pups  (~ 7/experiment) were sacrificed by CO2 inhalation. Hippocampi were dissected in Ca2+/Mg2+-free, HEPES-buffered Hank’s balanced salt solution (HBSS), pH7.45, dissociated through flame-narrowed Pasteur pipettes of decreasing aperture, and resuspended in DMEM without glutamine, 10% fetal bovine serum and penicillin/streptomycin (100 U/ml and 100 μg/ml, respectively). Cells were plated (120,000/dish) onto 25 mm round Matrigel (200 μl, 0.2 mg/ml; BD Biosciences) pre-coated cover glass glued to cover a 19-mm-diameter opening drilled through the bottom of a 35 mm Petri dish. Neurons were grown in 10% CO2, at 37 °C, and fed on days 1 and 6, by exchanging 75% of the media with DMEM containing 10% horse serum and penicillin/streptomycin. In all experiments, pyramidal-shaped neurons behaved as such in patch-clamp.
Recombinant HIV-1 Tat (Clade B) was from the National Institutes of Health AIDS Research and Reference Reagent Program, Division of AIDS, National Institute of Allergy and Infectious Diseases. In control experiments, Tat was heat-inactivated at 85 °C for 30 min. The cells were incubated with Tat 10 ng/ml (6.4 nM). Tat (or inactivated Tat) was added to the media 4 or 24 h prior to recordings. Coded cultures were removed from 37 °C, and a 95% O2/5% CO2 injector was placed in wells, under a differential interference contrast microscope (Leica). Electrophysiology was performed in randomized cultures, in a blinded manner.
Whole-cell patch clamp recordings and intracellular stimulation
Patch clamp recordings and intracellular stimulation were performed and captured using Multiclamp 700B amplifier (Axon Instruments). Stimulus waveforms were generated using data acquisition software DASYLab11.0 (National Instruments) in Windows computer equipped with National Instruments PCI-MIO-16-E4 board. We used rectangular hyperpolarizing and depolarizing current pulses as stimuli for physiological characterization. Specifically, 350 ms current pulses starting from − 200 pA, were incremented by 10 pA. Voltage responses were analyzed using software developed by Delphi, 2009, using the following parameters: Resting membrane potential, Resting input resistance, Rheobase, AP Threshold, AP amplitude and duration, AP after hyperpolarization, and the I-O function (gain). The spontaneous excitatory postsynaptic currents (sEPSCs) were recorded in voltage clamp mode at − 70 mV holding potential. The spontaneous inhibitory postsynaptic current (sIPSC) was recorded in voltage clamp mode at − 40 mV holding potential.
Using Prism5 (GraphPad Software Inc, La Jolla, CA), we examined deviations from normality in the data using Kolmogorov–Smirnov test. Slopes were tested using Pearson’s correlation coefficient (r) (p < 0.01), and linear regression. The mean of input–output relationship  was compared by ANOVA, and Bonferroni’s post hoc test (p < 0.05). Individual parameters between controls and Tat 24 h were compared using Student’s t test.
We examined whether dysfunctional properties are detectable in hippocampal neurons exposed to HIV-1 Tat for 4 and 24 h. We measured electrophysiological properties in the pyramidal subset, in comparison to cultures treated with inactivated Tat. In both time-points, control cultures showed similar behaviors and thus measurements were pooled.
Figure 1 summarizes the parameters characterizing neuronal subsets. Baseline recordings showed that hippocampal neuronal subsets in primary cultures exhibit expected behaviors, and are a valid system for studying the direct effects of HIV peptides such as Tat, or neuroimmune factors. In control cultures, pyramidal Glutamatergic neurons (Fig. 1, red lines) differed from GABAergic interneurons (Fig. 1, blue lines), in recording patterns during whole cell patch-clamp assays. Pyramidal neurons displayed characteristic voltage sag during hyperpolarizing pulse, and strong adaptation (Fig. 1a, upper trace), while interneurons fired at higher frequency without signs of adaptation (Fig. 1a, lower trace). Regarding AP evoked by a short depolarizing current pulse, pyramidal neurons showed depolarizing potential during the repolarization phase (Fig. 1b, upper trace), while in interneurons, AP was followed by a fast after-hyperpolarization (fAHP) (Fig. 1b, lower trace). The AP width was shorter in interneurons (Fig. 1c, blue line) compared to pyramidal neurons (Fig. 1c, red line). All parameters were according to predicted results for these subsets.
Using this system, we tested the hypothesis that Tat can directly affect neuronal performance, detectable by increase or decrease in pulse current intensity necessary to elicit an AP. We have focused on glutamatergic pyramidal neurons, due to their excitatory role in circuitry architecture, and due to their consistent pattern of Tat-elicited changes, compared to control neurons. All cultures showed a linear relationship between the injected current and the number of spikes, determined by Pearson’s coefficient (Control r2 = 0.9969, p = 0.0031; Tat 4 h r2 = 0.9989, p = 0.0011; Tat 24 h r2 = 0.9827, p = 0.0004). Compared to control cultures, Tat did not alter neuronal behaviors at 4 h. However, a strong increase of the gain function was seen at 24 h (Fig. 2). The slope comparison by linear regression revealed a significant difference, with F = 16.4446, DFn = 2, DFd = 8, and p = 0.001465, and with a 0.15% chance of randomly choosing data points exhibiting these differences. The comparison of the mean of the slopes input–output (I/O) relationship within the tested interval showed a significant difference between Control and Tat 24 h (p = 0.002, Bonferroni’s p < 0.05). Yet, pyramidal neurons treated with Tat did not alter the RMP, input resistance, rheobase (or the minimal depolarizing current input that generates an AP), and AP threshold at 24 h (Table 1).
We found that Tat critically affects neuronal intrinsic excitability in cultured hippocampal pyramidal neurons, as a result of a lower reactive threshold to current. This effect was not observed at 4 h after HIV-1 Tat exposure, but only at the 24 h time point.
In cell line studies, conflicting results relate to the diversity of models. In a neuro-epithelial-like stem (NES) cell line from human fetal hindbrain, Tat at 10 times lower doses than in our study caused deep changes in gene expression and cytoskeletal structure at 24 h, and a reduction of output excitability at 48 h , likely due to neurotoxicity.
In primary cultures, Tat-induced changes are subset, dose and time-depend. For instance, in rat dorsal root ganglion small diameter capsaicin-sensory neurons, Tat at 20 nM greatly enhanced excitability, suggesting a direct role in pain . On the other hand, studies in rat hippocampal neurons show Tat-induced biphasic changes in NMDA-evoked increases in intracellular Ca2+, with consequences to spontaneous activity [42, 44]. Tat (at 5-fold higher concentrations than in our study) acutely reduced spontaneous spike frequencies while increasing AP bursts amplitude and duration, followed by attenuation, and adaptation at 24 h. These changes were hypothesized to result from aberrant network activity, attributed to changes in NMDA-gated intracellular Ca2+, mediated by Src kinase and NO signaling [42, 45]. Our results complement those, suggesting that neuronal adaptability to lower Tat concentrations may be relative, or not applicable to all aspects of neuronal function. Our findings are in agreement with the excitatory effect of Tat on cultured human fetal neurons, and rat hippocampal slices [46,47,48].
The neuronal ability to receive and transmit information depends on neurotransmitter concentrations in presynaptic terminals, numbers and intrinsic properties of postsynaptic receptors on dendritic trees, and receiving synaptic inputs, which depend on the type of voltage-dependent membrane ionic channels. These channels, upon inputs and AP, allow ionic movement, changing the excitability. We observed that Tat increases neuronal excitability, or the slope of the input–output relationship. Tat may enhance firing via Ca2+ influx [49, 50], by prolonging Ca2+ potentials mediated by L-channels. Importantly, neuronal voltage-gated K+ channels (Kv) are involved in memory processes [51, 52], and in acquired neuronal channelopathies observed in HIV-associated neurocognitive disorders . Further studies must determine what conductance is affected by Tat exposure, and whether these findings apply to neuroHIV models in vivo. If so, these may have consequences to how HIV in the brain affects perception, reactivity to sensory stimulation, and memory, in part explaining HIV-associated neurobehavioral changes.
HIV-Tat acts on hippocampal pyramidal neurons by lowering the current pulse intensity threshold that elicits an action potential response, and increases gain slope 24 h following exposure, indicating an enhanced intrinsic neuronal excitability.
This study was in isolated neurons in culture, not subjected to neuroimmune changes, or active infection, differing from the HIV-infected brain. Yet, it is a system for the examination of direct effects of HIV and its peptides, and that can accommodate complexities from neuroimmune cells. More studies are need for identifying mechanisms by which Tat affects excitability, without affecting other functions.
trans-activator of Transcription
central Nervous System
pre-natal day 18
human immunodeficiency virus
HIV-associated neurocognitive disorders
cornu ammonis layer 1
resting membrane potential
A-type voltage gated channel
delayed rectifier K+ gated channel
L-type voltage-gated Ca2+ channel
voltage-gated Ca2+ channel conductance
embryonic day 17
Hank’s balanced salt solution
San Diego Biomedical Research Institute
The Scripps Research Institute
Dulbecco’s modified Eagle’s medium
acquired immunodeficiency syndrome
inhibitory post synaptic current
analysis of variance
fast after hyperpolarization
neuro-epithelial-like stem cell
voltage-gated K+ channels
Barreto GE, Gonzalez J, Torres Y, Morales L. Astrocytic-neuronal crosstalk: implications for neuroprotection from brain injury. Neurosci Res. 2011;71(2):107–13.
Bechade C, Cantaut-Belarif Y, Bessis A. Microglial control of neuronal activity. Front Cell Neurosci. 2013;7:32.
Bessis A, Bechade C, Bernard D, Roumier A. Microglial control of neuronal death and synaptic properties. Glia. 2007;55(3):233–8.
Dalmau I, Finsen B, Tonder N, Zimmer J, Gonzalez B, Castellano B. Development of microglia in the prenatal rat hippocampus. J Comp Neurol. 1997;377(1):70–84.
Dalmau I, Finsen B, Zimmer J, Gonzalez B, Castellano B. Development of microglia in the postnatal rat hippocampus. Hippocampus. 1998;8(5):458–74.
Dalmau I, Vela JM, Gonzalez B, Finsen B, Castellano B. Dynamics of microglia in the developing rat brain. J Comp Neurol. 2003;458(2):144–57.
Elkabes S, DiCicco-Bloom EM, Black IB. Brain microglia/macrophages express neurotrophins that selectively regulate microglial proliferation and function. J Neurosci. 1996;16(8):2508–21.
Hanisch UK. Microglia as a source and target of cytokines. Glia. 2002;40(2):140–55.
Barger SW, Basile AS. Activation of microglia by secreted amyloid precursor protein evokes release of glutamate by cystine exchange and attenuates synaptic function. J Neurochem. 2001;76(3):846–54.
Chao CC, Hu S, Molitor TW, Shaskan EG, Peterson PK. Activated microglia mediate neuronal cell injury via a nitric oxide mechanism. J Immunol. 1992;149(8):2736–41.
Floden AM, Li S, Combs CK. Beta-amyloid-stimulated microglia induce neuron death via synergistic stimulation of tumor necrosis factor alpha and NMDA receptors. J Neurosci. 2005;25(10):2566–75.
Piani D, Frei K, Do KQ, Cuenod M, Fontana A. Murine brain macrophages induced NMDA receptor mediated neurotoxicity in vitro by secreting glutamate. Neurosci Lett. 1991;133(2):159–62.
An SF, Groves M, Gray F, Scaravilli F. Early entry and widespread cellular involvement of HIV-1 DNA in brains of HIV-1 positive asymptomatic individuals. J Neuropathol Exp Neurol. 1999;58(11):1156–62.
Burdo TH, Lo J, Abbara S, Wei J, DeLelys ME, Preffer F, Rosenberg ES, Williams KC, Grinspoon S. Soluble CD163, a novel marker of activated macrophages, is elevated and associated with noncalcified coronary plaque in HIV-infected patients. J Infect Dis. 2011;204(8):1227–36.
Debaisieux S, Rayne F, Yezid H, Beaumelle B. The ins and outs of HIV-1 Tat. Traffic. 2012;13(3):355–63.
Rayne F, Debaisieux S, Bonhoure A, Beaumelle B. HIV-1 Tat is unconventionally secreted through the plasma membrane. Cell Biol Int. 2010;34(4):409–13.
Rayne F, Debaisieux S, Tu A, Chopard C, Tryoen-Toth P, Beaumelle B. Detecting HIV-1 Tat in cell culture supernatants by ELISA or Western Blot. Methods Mol Biol. 2016;1354:329–42.
Vendeville A, Rayne F, Bonhoure A, Bettache N, Montcourrier P, Beaumelle B. HIV-1 Tat enters T cells using coated pits before translocating from acidified endosomes and eliciting biological responses. Mol Biol Cell. 2004;15(5):2347–60.
Carey AN, Liu X, Mintzopoulos D, Paris JJ, Muschamp JW, McLaughlin JP, Kaufman MJ. Conditional Tat protein expression in the GT-tg bigenic mouse brain induces gray matter density reductions. Prog Neuropsychopharmacol Biol Psychiatry. 2013;43:49–54.
Carey AN, Sypek EI, Singh HD, Kaufman MJ, McLaughlin JP. Expression of HIV-Tat protein is associated with learning and memory deficits in the mouse. Behav Brain Res. 2012;229(1):48–56.
Pettit DL, Augustine GJ. Distribution of functional glutamate and GABA receptors on hippocampal pyramidal cells and interneurons. J Neurophysiol. 2000;84(1):28–38.
Lisman JE. Bursts as a unit of neural information: making unreliable synapses reliable. Trends Neurosci. 1997;20(1):38–43.
Williams SR, Stuart GJ. Mechanisms and consequences of action potential burst firing in rat neocortical pyramidal neurons. J Physiol. 1999;521(Pt 2):467–82.
Epsztein J, Brecht M, Lee AK. Intracellular determinants of hippocampal CA1 place and silent cell activity in a novel environment. Neuron. 2011;70(1):109–20.
Golding NL, Staff NP, Spruston N. Dendritic spikes as a mechanism for cooperative long-term potentiation. Nature. 2002;418(6895):326–31.
Moscovitch M, Nadel L, Winocur G, Gilboa A, Rosenbaum RS. The cognitive neuroscience of remote episodic, semantic and spatial memory. Curr Opin Neurobiol. 2006;16(2):179–90.
Castelo JM, Sherman SJ, Courtney MG, Melrose RJ, Stern CE. Altered hippocampal-prefrontal activation in HIV patients during episodic memory encoding. Neurology. 2006;66(11):1688–95.
Winocur G, Moscovitch M, Rosenbaum RS, Sekeres M. A study of remote spatial memory in aged rats. Neurobiol Aging. 2010;31(1):143–50.
Behnisch T, Francesconi W, Sanna PP. HIV secreted protein Tat prevents long-term potentiation in the hippocampal CA1 region. Brain Res. 2004;1012(1–2):187–9.
Silver RA. Neuronal arithmetic. Nat Rev Neurosci. 2010;11(7):474–89.
Disterhoft JF, Oh MM. Learning, aging and intrinsic neuronal plasticity. Trends Neurosci. 2006;29(10):587–99.
Disterhoft JF, Oh MM. Pharmacological and molecular enhancement of learning in aging and Alzheimer’s disease. J physiol Paris. 2006;99(2–3):180–92.
Disterhoft JF, Oh MM. Alterations in intrinsic neuronal excitability during normal aging. Aging Cell. 2007;6(3):327–36.
Kim JR, Ahn SY, Jeong SW, Kim LS, Park JS, Chung SH, Oh MK. Cortical auditory evoked potential in aging: effects of stimulus intensity and noise. Otol Neurotol. 2012;33(7):1105–12.
Oh MM, Disterhoft JF. Cellular mechanisms for altered learning in aging. Future neurology. 2010;5(1):147–55.
Oh MM, Oliveira FA, Disterhoft JF. Learning and aging related changes in intrinsic neuronal excitability. Front Aging Neurosci. 2010;2:2.
Szucs A, Berton F, Sanna PP, Francesconi W. Excitability of jcBNST neurons is reduced in alcohol-dependent animals during protracted alcohol withdrawal. PLoS ONE. 2012;7(8):e42313.
Tryoen-Toth P, Chasserot-Golaz S, Tu A, Gherib P, Bader MF, Beaumelle B, Vitale N. HIV-1 Tat protein inhibits neurosecretion by binding to phosphatidylinositol 4,5-bisphosphate. J Cell Sci. 2013;126(Pt 2):454–63.
Ganief T, Gqamana P, Garnett S, Hoare J, Stein DJ, Joska J, Soares N, Blackburn JM. Quantitative proteomic analysis of HIV-1 Tat-induced dysregulation in SH-SY5Y neuroblastoma cells. Proteomics. 2017;17(6):1600236.
Gurwitz KT, Burman RJ, Murugan BD, Garnett S, Ganief T, Soares NC, Raimondo JV, Blackburn JM. Time-dependent, HIV-Tat-induced perturbation of human neurons in vitro: towards a model for the molecular pathology of HIV-associated neurocognitive disorders. Front Mol Neurosci. 2017;10:163.
Falzone TL, Stokin GB, Lillo C, Rodrigues EM, Westerman EL, Williams DS, Goldstein LS. Axonal stress kinase activation and tau misbehavior induced by kinesin-1 transport defects. J Neurosci. 2009;29(18):5758–67.
Krogh KA, Wydeven N, Wickman K, Thayer SA. HIV-1 protein Tat produces biphasic changes in NMDA-evoked increases in intracellular Ca2 + concentration via activation of Src kinase and nitric oxide signaling pathways. J Neurochem. 2014;130(5):642–56.
Chi X, Amet T, Byrd D, Chang KH, Shah K, Hu N, Grantham A, Hu S, Duan J, Tao F, et al. Direct effects of HIV-1 Tat on excitability and survival of primary dorsal root ganglion neurons: possible contribution to HIV-1-associated pain. PLoS ONE. 2011;6(9):e24412.
Krogh KA, Green MV, Thayer SA. HIV-1 Tat-induced changes in synaptically-driven network activity adapt during prolonged exposure. Curr HIV Res. 2015;12(6):406–14.
Krogh KA, Green MV, Thayer SA. HIV-1 Tat-induced changes in synaptically-driven network activity adapt during prolonged exposure. Curr HIV Res. 2014;12(6):406–14.
Cheng J, Nath A, Knudsen B, Hochman S, Geiger JD, Ma M, Magnuson DS. Neuronal excitatory properties of human immunodeficiency virus type 1 Tat protein. Neuroscience. 1998;82(1):97–106.
Magnuson DS, Knudsen BE, Geiger JD, Brownstone RM, Nath A. Human immunodeficiency virus type 1 tat activates non-N-methyl-d-aspartate excitatory amino acid receptors and causes neurotoxicity. Ann Neurol. 1995;37(3):373–80.
Nath A, Psooy K, Martin C, Knudsen B, Magnuson DS, Haughey N, Geiger JD. Identification of a human immunodeficiency virus type 1 Tat epitope that is neuroexcitatory and neurotoxic. J Virol. 1996;70(3):1475–80.
Brailoiu GC, Brailoiu E, Chang JK, Dun NJ. Excitatory effects of human immunodeficiency virus 1 Tat on cultured rat cerebral cortical neurons. Neuroscience. 2008;151(3):701–10.
Napier TC, Chen L, Kashanchi F, Hu XT. Repeated cocaine treatment enhances HIV-1 Tat-induced cortical excitability via over-activation of l-type calcium channels. J Neuroimmune Pharmacol. 2014;9(3):354–68.
Giese KP, Storm JF, Reuter D, Fedorov NB, Shao LR, Leicher T, Pongs O, Silva AJ. Reduced K+ channel inactivation, spike broadening, and after-hyperpolarization in Kvbeta1.1-deficient mice with impaired learning. Learn Mem. 1998;5(4–5):257–73.
Solntseva EI, Bukanova IuV, Skrebitskii VG. Memory and potassium channels. Usp Fiziol Nauk. 2003;34(4):16–25.
Gelman BB, Soukup VM, Schuenke KW, Keherly MJ, Holzer C 3rd, Richey FJ, Lahart CJ. Acquired neuronal channelopathies in HIV-associated dementia. J Neuroimmunol. 2004;157(1–2):111–9.
MCGM: study concept and design, data analysis and interpretation, manuscript writing, editing and submission; WF and FB: study concept and design, performance of electrophysiology techniques, data analysis and interpretation, manuscript writing. All authors read and approved the final manuscript.
The authors wish to thank Dr. Sandra Encalada, The Scripps Research Institute, La Jolla, CA, for providing the neuronal cultures used in this study, and Dr. Bruno Conti for the space and amazing support. We also thank Daniel Ryan (SDBRI) for critically reviewing our manuscript.
The authors declare that they have no competing of interests.
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Data are all contained within the paper. The datasets from the analyses are available from the corresponding author on reasonable request.
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All animal use was reviewed and approved by the Institutional Animal Care and Use Committee of The Scripps Research Institute and of the San Diego Biomedical Research Institute.
The authors declare that this experiment was partially funded by the R01DA036164 to MCGM.
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Francesconi, W., Berton, F. & Marcondes, M.C.G. HIV-1 Tat alters neuronal intrinsic excitability. BMC Res Notes 11, 275 (2018). https://doi.org/10.1186/s13104-018-3376-8