Proteomic Profiling of Exosomes Derived from Plasma of HIV-Infected Alcohol Drinkers and Cigarette Smokers

J Neuroimmune Pharmacol. 2020 Sep;15(3):501-519. doi: 10.1007/s11481-019-09853-2. Epub 2019 May 8.

Abstract

Abuse of alcohol and tobacco could exacerbate HIV pathogenesis by transferring materials through exosomes (small nanovesicles). Exosomes present a stable and accessible source of information concerning the health and/or disease status of patients, which can provide diagnostic and prognostic biomarkers for myriad conditions. Therefore, we aimed to study the specific exosomal proteins that are altered in both HIV-infected subjects and alcohol/tobacco users. Exosomes were isolated from plasma of the following subjects: a) HIV-negative subjects (healthy), b) HIV-positive subjects (HIV), c) HIV-negative alcohol drinkers (drinkers), d) HIV-negative tobacco smokers (smokers), e) HIV-positive drinkers (HIV + drinkers), and f) HIV-positive smokers (HIV + smokers). Quantitative proteomic profiling was then performed from these exosomes. Sixteen proteins were significantly altered in the HIV group, ten in drinkers, four in HIV + drinkers, and fifteen in smokers compared to healthy subjects. Only one protein, fibulin-1 (FBLN1), was significantly altered in HIV + smokers. Interestingly, hemopexin was not significantly altered in drinkers or HIV patients but was significantly altered in HIV + drinkers. Further, our study is the first to show properdin expression in plasma exosomes, which was decreased in HIV + smokers and HIV + drinkers compared to HIV patients. The present findings suggest that hemopexin and properdin show potential as markers for physiological effects that may arise in HIV-infected individuals who abuse alcohol and tobacco. Graphical abstract This study presents a proteomic analysis of plasma-derived exosomes from HIV-infected alcohol drinkers and smokers. Among the proteins altered due to drug-abuse, hemopexin and properdin were of highest significance. These proteins can be potential biomarkers for co-morbid conditions associated with drug abuse in HIV-patients.

Keywords: Alcohol; HIV; Plasma exosome; Proteomics; Smoking.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Alcohol Drinking / genetics*
  • Calcium-Binding Proteins / genetics
  • Exosomes / chemistry
  • Exosomes / genetics*
  • Female
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation
  • Gene Products, gag / genetics
  • HIV Infections / complications
  • HIV Infections / genetics*
  • Hemopexin / genetics
  • Humans
  • Male
  • Middle Aged
  • Properdin / genetics
  • Proteomics / methods*
  • Smokers*
  • Smoking / genetics*
  • tat Gene Products, Human Immunodeficiency Virus / genetics

Substances

  • Calcium-Binding Proteins
  • Gene Products, gag
  • fibulin
  • tat Gene Products, Human Immunodeficiency Virus
  • Properdin
  • Hemopexin