HIV Protein Nef Induces Cardiomyopathy Through Induction of Bcl2 and p21

Int J Mol Sci. 2024 Oct 23;25(21):11401. doi: 10.3390/ijms252111401.

Abstract

HIV-associated cardiovascular diseases remain a leading cause of death in people living with HIV/AIDS (PLWHA). Although antiretroviral drugs suppress the viral load, they fail to remove the virus entirely. HIV-1 Nef protein is known to play a role in viral virulence and HIV latency. Expression of Nef protein can be detected in different organs, including cardiac tissue. Despite the established role of Nef protein in HIV-1 replication, its impact on organ function inside the human body is not clear. To understand the effect of Nef at the organ level, we created a new Nef-transgenic (Nef-TG) mouse that expresses Nef protein in the heart. Our study found that Nef expression caused inhibition of cardiac function and pathological changes in the heart with increased fibrosis, leading to heart failure and early mortality. Further, we found that cellular autophagy is significantly inhibited in the cardiac tissue of Nef-TG mice. Mechanistically, we found that Nef protein causes the accumulation of Bcl2 and Beclin-1 proteins in the tissue, which may affect the cellular autophagy system. Additionally, we found Nef expression causes upregulation of the cellular senescence marker p21 and senescence-associated β-galactosidase expression. Our findings suggest that the Nef-mediated inhibition of autophagy and induction of senescence markers may promote aging in PLWHA. Our mouse model could help us to understand the effect of Nef protein on organ function during latent HIV infection.

Keywords: Bcl2; Beclin-1; HIV; Nef; P21; autophagy; cardiomyopathy; fibrosis.

MeSH terms

  • Animals
  • Autophagy*
  • Cardiomyopathies* / etiology
  • Cardiomyopathies* / genetics
  • Cardiomyopathies* / metabolism
  • Cardiomyopathies* / pathology
  • Cardiomyopathies* / virology
  • Cyclin-Dependent Kinase Inhibitor p21 / genetics
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • HIV Infections / complications
  • HIV Infections / metabolism
  • HIV Infections / virology
  • HIV-1 / metabolism
  • Humans
  • Mice
  • Mice, Transgenic*
  • Myocardium / metabolism
  • Myocardium / pathology
  • Proto-Oncogene Proteins c-bcl-2* / genetics
  • Proto-Oncogene Proteins c-bcl-2* / metabolism
  • nef Gene Products, Human Immunodeficiency Virus* / genetics
  • nef Gene Products, Human Immunodeficiency Virus* / metabolism

Substances

  • nef Gene Products, Human Immunodeficiency Virus
  • Proto-Oncogene Proteins c-bcl-2
  • nef protein, Human immunodeficiency virus 1
  • Cyclin-Dependent Kinase Inhibitor p21
  • Bcl2 protein, mouse