Microbiota-derived short chain fatty acids modulate microglia and promote A beta plaque deposition

Colombo, A.V.; Sadler, R.K.; Llovera, G.; Singh, V.; Roth, S.; Heindl, S.; Monasor, L.S.; Verhoeven, A.; Peters, F.; Parhizkar, S.; Kamp, F.; Aguero, M.G. de; MacPherson, A.J.; Winkler, E.; Herms, J.; Benakis, C.; Dichgans, M.; Steiner, H.; Giera, M.; Haass, C.; Tahirovic, S.; Liesz, A.

doi:doi:10.7554/eLife.59826

Previous studies have identified a crucial role of the gut microbiome in modifying Alzheimer's disease (AD) progression. However, the mechanisms of microbiome-brain interaction in AD were so far unknown. Here, we identify microbiota-derived short chain fatty acids (SCFA) as microbial metabolites which promote A beta deposition. Germ-free (GF) AD mice exhibit a substantially reduced A beta plaque load and markedly reduced SCFA plasma concentrations; conversely, SCFA supplementation to GF AD mice increased the Al3 plaque load to levels of conventionally colonized (specific pathogen-free [SPF]) animals and SCFA supplementation to SPF mice even further exacerbated plaque load. This was accompanied by the pronounced alterations in microglial transcriptomic profile, including upregulation of ApoE. Despite increased microglial recruitment to A beta plaques upon SCFA supplementation, microglia contained less intracellular A beta. Taken together, our results demonstrate that microbiota...Show morePrevious studies have identified a crucial role of the gut microbiome in modifying Alzheimer's disease (AD) progression. However, the mechanisms of microbiome-brain interaction in AD were so far unknown. Here, we identify microbiota-derived short chain fatty acids (SCFA) as microbial metabolites which promote A beta deposition. Germ-free (GF) AD mice exhibit a substantially reduced A beta plaque load and markedly reduced SCFA plasma concentrations; conversely, SCFA supplementation to GF AD mice increased the Al3 plaque load to levels of conventionally colonized (specific pathogen-free [SPF]) animals and SCFA supplementation to SPF mice even further exacerbated plaque load. This was accompanied by the pronounced alterations in microglial transcriptomic profile, including upregulation of ApoE. Despite increased microglial recruitment to A beta plaques upon SCFA supplementation, microglia contained less intracellular A beta. Taken together, our results demonstrate that microbiota-derived SCFA are critical mediators along the gut-brain axis which promote A beta deposition likely via modulation of the microglial phenotype.Show less

Leiden University Scholarly Publications

View statistics

Documents

In Collections

Microbiota-derived short chain fatty acids modulate microglia and promote A beta plaque deposition