Alpha7 nicotinic acetylcholine receptor is required for blood-brain barrier injury-related CNS disorders caused by Cryptococcus neoformans and HIV-1 associated comorbidity factors

BMC Infect Dis. 2015 Aug 19:15:352. doi: 10.1186/s12879-015-1075-9.

Abstract

Background: Cryptococcal meningitis is the most common fungal infection of the central nervous system (CNS) in HIV/AIDS. HIV-1 virotoxins (e.g., gp41) are able to induce disorders of the blood-brain barrier (BBB), which mainly consists of BMEC. Our recent study suggests that α7 nAChR is an essential regulator of inflammation, which contributes to regulation of NF-κB signaling, neuroinflammation and BBB disorders caused by microbial (e.g., HIV-1 gp120) and non-microbial [e.g., methamphetamine (METH)] factors. However, the underlying mechanisms for multiple comorbidities are unclear.

Methods: In this report, an aggravating role of α7 nAChR in host defense against CNS disorders caused by these comorbidities was demonstrated by chemical [inhibitor: methyllycaconitine (MLA)] and genetic (α7(-/-) mice) blockages of α7 nAChR.

Results: As shown in our in vivo studies, BBB injury was significantly reduced in α7(-/-) mice infected with C. neoformans. Stimulation by the gp41 ectodomain peptide (gp41-I90) and METH was abolished in the α7(-/-) animals. C. neoformans and gp41-I90 could activate NF-κB. Gp41-I90- and METH-induced monocyte transmigration and senescence were significantly inhibited by MLA and CAPE (caffeic acid phenethyl ester, an NF-κB inhibitor).

Conclusions: Collectively, our data suggest that α7 nAChR plays a detrimental role in the host defense against C. neoformans- and HIV-1 associated comorbidity factors-induced BBB injury and CNS disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aconitine / analogs & derivatives
  • Aconitine / pharmacology
  • Animals
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / metabolism*
  • Central Nervous System Stimulants / pharmacology
  • Coinfection
  • Cryptococcus neoformans*
  • HIV Envelope Protein gp41 / pharmacology
  • HIV Infections / metabolism
  • HIV-1 / metabolism
  • Inflammation
  • Meningitis, Cryptococcal / genetics*
  • Methamphetamine / pharmacology
  • Mice
  • Mice, Knockout
  • NF-kappa B / drug effects
  • Nicotinic Antagonists / pharmacology
  • alpha7 Nicotinic Acetylcholine Receptor / antagonists & inhibitors
  • alpha7 Nicotinic Acetylcholine Receptor / genetics*

Substances

  • Central Nervous System Stimulants
  • Chrna7 protein, mouse
  • HIV Envelope Protein gp41
  • NF-kappa B
  • Nicotinic Antagonists
  • alpha7 Nicotinic Acetylcholine Receptor
  • gp41 protein, Human immunodeficiency virus 1
  • methyllycaconitine
  • Methamphetamine
  • Aconitine