Impact of Suramin on Key Pathological Features of Sporadic Alzheimer's Disease-Derived Forebrain Neurons

J Alzheimers Dis. 2024;98(1):301-318. doi: 10.3233/JAD-230600.

Abstract

Background: Alzheimer's disease (AD) is characterized by disrupted proteostasis and macroautophagy (hereafter "autophagy"). The pharmacological agent suramin has known autophagy modulation properties with potential efficacy in mitigating AD neuronal pathology.

Objective: In the present work, we investigate the impact of forebrain neuron exposure to suramin on the Akt/mTOR signaling pathway, a major regulator of autophagy, in comparison with rapamycin and chloroquine. We further investigate the effect of suramin on several AD-related biomarkers in sporadic AD (sAD)-derived forebrain neurons.

Methods: Neurons differentiated from ReNcell neural progenitors were used to assess the impact of suramin on the Akt/mTOR signaling pathway relative to the autophagy inducer rapamycin and autophagy inhibitor chloroquine. Mature forebrain neurons were differentiated from induced pluripotent stem cells (iPSCs) sourced from a late-onset sAD patient and treated with 100μM suramin for 72 h, followed by assessments for amyloid-β, phosphorylated tau, oxidative/nitrosative stress, and synaptic puncta density.

Results: Suramin treatment of sAD-derived neurons partially ameliorated the increased p-Tau(S199)/Tau ratio, and fully remediated the increased glutathione to oxidized nitric oxide ratio, observed in untreated sAD-derived neurons relative to healthy controls. These positive results may be due in part to the distinct increases in Akt/mTOR pathway mediator p-p70S6K noted with suramin treatment of both ReNcell-derived and iPSC-derived neurons. Longer term neuronal markers, such as synaptic puncta density, were unaffected by suramin treatment.

Conclusions: These findings provide initial evidence supporting the potential of suramin to reduce the degree of dysregulation in sAD-derived forebrain neurons in part via the modulation of autophagy.

Keywords: Alzheimer’s disease; autophagy; induced pluripotent stem cells; neurons; suramin.

MeSH terms

  • Alzheimer Disease* / pathology
  • Amyloid beta-Peptides / metabolism
  • Chloroquine / metabolism
  • Chloroquine / pharmacology
  • Humans
  • Induced Pluripotent Stem Cells* / metabolism
  • Neurons / metabolism
  • Prosencephalon / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Sirolimus / pharmacology
  • Suramin / metabolism
  • Suramin / pharmacology
  • TOR Serine-Threonine Kinases / metabolism
  • tau Proteins / metabolism

Substances

  • Suramin
  • tau Proteins
  • Proto-Oncogene Proteins c-akt
  • Amyloid beta-Peptides
  • TOR Serine-Threonine Kinases
  • Sirolimus
  • Chloroquine