Akkermansia muciniphila-derived small extracellular vesicles attenuate intestinal ischemia-reperfusion-induced postoperative cognitive dysfunction by suppressing microglia activation via the TLR2/4 signaling

Biochim Biophys Acta Mol Cell Res. 2024 Feb;1871(2):119630. doi: 10.1016/j.bbamcr.2023.119630. Epub 2023 Nov 13.

Abstract

Akkermansia muciniphila (AKK) bacteria improve the functions of theere intestinal and blood-brain barriers (BBB) via their extracellular vesicles (AmEvs). However, their role in postoperative cognitive dysfunction (POCD) and its underlying mechanisms remain unclear. To investigate, we used C57BL/6 J mice divided into five groups: Sham, POCD, POCD+Akk, POCD+Evs, and POCD+Evs + PLX5622. POCD was induced through intestinal ischemia-reperfusion (I/R). The mice's cognitive function was assessed using behavioral tests, and possible mechanisms were explored by examining gut and BBB permeability, inflammation, and microglial function. Toll-like receptor (TLR) 2/4 pathway-related proteins were also investigated both in vitro and in vivo. PLX5622 chow was employed to eliminate microglial cells. Our findings revealed a negative correlation between AKK abundance and POCD symptoms. Supplementation with either AKK or AmEvs improved cognitive function, improved the performance of the intestinal barrier and BBB, and decreased inflammation and microglial activation in POCD mice compared to controls. Moreover, AmEvs treatment inhibited TLR2/4 signaling in the brains of POCD mice and LPS-treated microglial cells. In microglial-ablated POCD mice, however, AmEvs failed to protect BBB integrity. Overall, AmEvs is a potential therapeutic strategy for managing POCD by enhancing gut and BBB integrity and inhibiting microglial-mediated TLR2/4 signaling.

Keywords: Akkermansia muciniphila (AKK); Akkermansia muciniphila-derived extracellular vesicles; Blood–brain barrier (BBB); Inflammation; Postoperative cognitive dysfunction (POCD).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Akkermansia
  • Animals
  • Extracellular Vesicles*
  • Inflammation / metabolism
  • Ischemia
  • Mice
  • Mice, Inbred C57BL
  • Microglia / metabolism
  • Organic Chemicals*
  • Postoperative Cognitive Complications* / metabolism
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 2 / metabolism
  • Verrucomicrobia / physiology

Substances

  • PLX5622
  • Toll-Like Receptor 2
  • Organic Chemicals

Supplementary concepts

  • Akkermansia muciniphila