5-HT7R Deficiency Alleviates ADP-Heptose-Induced Cognitive Impairment via Inhibiting Ferroptosis and Neuroinflammation in Mice

CNS Neurosci Ther. 2025 Jun;31(6):e70455. doi: 10.1111/cns.70455.

Abstract

Background: ADP-heptose (ADP-hep), a soluble intermediate in the biosynthesis of lipopolysaccharide in Gram-negative bacteria, is known to trigger inflammation. Our research suggests that 5-hydroxytryptamine receptor 7 (5-HT7R) could serve as a potential pattern recognition receptor (PRR) for ADP-hep, yet the precise mechanism of ADP-hep's regulation on 5-HT7R remains unclear.

Aims: Based on the results of mRNA sequencing analysis, this study took ferroptosis of neurons and microglia as a starting point to explore the role and underlying mechanisms of ADP-hep/5-HT7R signaling in mediating neuroinflammation and cognitive impairment in mice.

Results: We found that 5-HT7R may act as a potential PRR for ADP-hep and potentially bind to ADP-hep. 5-HT7R deficiency significantly ameliorated cognitive dysfunction induced by ADP-hep in mice, as well as ferroptosis mediated by the p53/cystine-glutamate antiporter (xCT)/glutathione peroxidase 4 (GPX4) signaling pathway and its associated key markers. Furthermore, 5-HT7R deficiency inhibited ferroptosis in neurons and M2-type microglia, mitigated the decline in the proportion of M2-type microglia, and subsequently suppressed the inflammatory microenvironment to promote neuronal survival, thereby exerting neuroprotective effects.

Conclusion: In summary, 5-HT7R deficiency promotes cognitive recovery by alleviating the neuronal and microglial ferroptosis triggered by ADP-hep, subsequently dampening the inflammatory microenvironment to support neuronal viability. These findings provide a novel perspective and approach for the development of innovative therapeutic strategies for the treatment of cognitive impairment-related diseases.

Keywords: 5‐HT7R; ADP‐heptose; cognitive impairment; ferroptosis; microglia polarization; neuroinflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cognitive Dysfunction* / chemically induced
  • Cognitive Dysfunction* / metabolism
  • Ferroptosis* / drug effects
  • Ferroptosis* / physiology
  • Heptoses
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / metabolism
  • Neuroinflammatory Diseases* / chemically induced
  • Neuroinflammatory Diseases* / metabolism
  • Neurons / metabolism
  • Pathogen-Associated Molecular Pattern Molecules
  • Receptors, Serotonin* / deficiency
  • Receptors, Serotonin* / genetics
  • Receptors, Serotonin* / metabolism

Substances

  • serotonin 7 receptor
  • Receptors, Serotonin
  • ADP-heptose
  • Pathogen-Associated Molecular Pattern Molecules
  • Heptoses