Peripheral inflammation promotes brain tau transmission via disrupting blood-brain barrier

Biosci Rep. 2020 Feb 28;40(2):BSR20193629. doi: 10.1042/BSR20193629.

Abstract

Abnormal aggregation of pathological tau protein is a neuropathological feature of Alzheimer's disease (AD). In the AD patients, the abnormal tau accumulation first appeared in entorhinal cortex (EC) and then propagated to the hippocampus with microglia activation and inflammation, but the mechanism is elusive. Here, we studied the role and mechanisms underlying periphery inflammation on brain tau transmission. By intraperitoneal injection of lipopolysaccharide (LPS) with brain medial entorhinal cortex (MEC)-specific overexpressing P301L human tau (P301L-hTau), we found that both acute and chronic administration of LPS remarkably promoted P301L-hTau transmission from MEC to the hippocampal subsets. Interestingly, the chronic LPS-induced P301L-hTau transmission was still apparent after blocking microglia activation. Further studies demonstrated that LPS disrupted the integrity of blood-brain barrier (BBB) and simultaneous intraperitoneal administration of glucocorticoid (GC) attenuated LPS-promoted P301L-hTau transmission. These data together suggest that a non-microglia-dependent BBB disruption contributes to peripheral LPS-promoted brain P301L-hTau transmission, therefore, maintaining the integrity of BBB can be a novel strategy for preventing pathological tau propagation in AD and other tauopathies.

Keywords: Alzheimers disease; blood brain barrier; lipopolysaccharides; microglia; tau transmission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology
  • Animals
  • Behavior, Animal
  • Blood-Brain Barrier / metabolism*
  • Blood-Brain Barrier / pathology
  • Cognition
  • Disease Models, Animal
  • Elevated Plus Maze Test
  • Entorhinal Cortex / metabolism*
  • Entorhinal Cortex / pathology
  • Entorhinal Cortex / physiopathology
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Hippocampus / physiopathology
  • Inflammation / chemically induced
  • Inflammation / genetics
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Lipopolysaccharides
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Morris Water Maze Test
  • Motor Activity
  • Open Field Test
  • Protein Transport
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism
  • tau Proteins / genetics
  • tau Proteins / metabolism*

Substances

  • Lipopolysaccharides
  • MAPT protein, human
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • tau Proteins