HIV-1 Tat alters neuronal intrinsic excitability

被引:4
|
作者
Francesconi W. [2 ,3 ]
Berton F. [2 ,3 ]
Marcondes M.C.G. [1 ,3 ]
机构
[1] San Diego Biomedical Research Institute, 10865 Road to the Cure, San Diego, 92121, CA
[2] Department of Anatomy and Cell Biology, College of Medicine, University of Illinois Chicago, 6068 COMRB MC 512, Chicago, 60612, IL
[3] Scripps Research Institute, 10550 North Torrey Pines Rd., San Diego, 92037, CA
基金
美国国家卫生研究院;
关键词
Electrophysiology; Hippocampal neurons; HIV Tat; neuroHIV; Synaptic transmission;
D O I
10.1186/s13104-018-3376-8
中图分类号
学科分类号
摘要
Objective: 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. Results: 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. © 2018 The Author(s).
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