Polygenic risk scores have identified that genetic variants without genome-wide significance still add to the genetic risk of developing Alzheimers disease (AD). Whether and how subthreshold risk loci translate into relevant disease pathways, is unknown. We investigate here the involvement of AD risk variants in the transcriptional responses of two mouse models: APPswe/PS1L166P and Thy-TAU22. A unique gene expression module, highly enriched for AD risk genes, is specifically responsive to A but not TAU pathology. We identify in this module 7 established AD risk genes (APOE, CLU, INPP5D, CD33, PLCG2, SPI1 and FCER1G) and 11 AD GWAS genes below the genome-wide significance threshold (GPC2, TREML2, SYK, GRN, SLC2A5, SAMSN1, PYDC1, HEXB, RRBP1, LYN and BLNK), that become significantly upregulated when exposed to A. Single microglia sequencing confirms that A, not TAU, pathology induces marked transcriptional changes in microglia, including increased proportions of activated microglia. We conclude that genetic risk of AD functionally translates into different microglia pathway responses to A pathology, placing AD genetic risk downstream of the amyloid pathway but upstream of TAU pathology. SOURCE: Bart De Strooper (bart.destrooper@kuleuven.vib.be) - Laboratory for the research of neurodegenerative diseases VIB - KU Leuven

Pluto Bioinformatics

GSE110741: Novel Alzheimer risk genes determine the microglia response to amyloid- but not to TAU pathology