M1-Type Microglia-Derived Extracellular Vesicles Overexpressing IL-1R1 Promote Postoperative Cognitive Dysfunction by Regulating Neuronal Inflammation

Inflammation. 2023 Dec;46(6):2254-2269. doi: 10.1007/s10753-023-01875-6. Epub 2023 Jul 28.

Abstract

Postoperative cognitive dysfunction (POCD) is a common complication after surgical anesthesia, mainly manifested as memory impairment, decreased attention, and cognitive function with mood and personality changes. Activated microglia (M1-type microglia) have been demonstrated to release inflammatory substances (IL-1β, TNF-α, etc.) that cause neuronal degeneration and death by activating the NF-κB signaling pathway and upregulating Caspase-3 and Bax. However, the pathogenesis of POCD is still not fully understood and needs further research. In the present study, we investigated the effect of M1-type microglia-derived extracellular vesicles (EVsM1-Microglia) in the pathological process of POCD. The levels of NF-κB phosphorylation and IL-1β protein expression in hippocampal neurons were significantly increased in the Surgery group, while PSD95 and MAP2 were significantly decreased. Surgery induced microglia activation, synapse-associated protein decrease, and neuronal degeneration in hippocampus. And the amount of spine and mushroom spine significantly decreased in surgical mice, which was reverted in the presence of IL-1R1 siRNA. In addition, EVsM1-Microglia promoted synaptic loss and neuron degeneration independent of surgery and microglia activation. Furthermore, EVsM1-Microglia promoted memory defects in surgical mice. We demonstrated that EVsM1-Microglia with high expression of IL-1R1 promote POCD development by regulating neuronal inflammation.

Keywords: anesthesia; extracellular vesicles; postoperative cognitive dysfunction; surgery.

MeSH terms

  • Animals
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / metabolism
  • Extracellular Vesicles* / metabolism
  • Inflammation / metabolism
  • Mice
  • Microglia / metabolism
  • NF-kappa B / metabolism
  • Neurons / metabolism
  • Postoperative Cognitive Complications* / genetics
  • Postoperative Cognitive Complications* / metabolism
  • Postoperative Cognitive Complications* / pathology

Substances

  • NF-kappa B
  • IL1R1 protein, mouse