Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer's Disease.
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IF: 66.850
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Cited by: 395
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Abstract

Although complex inflammatory-like alterations are observed around the amyloid plaques of Alzheimer's disease (AD), little is known about the molecular changes and cellular interactions that characterize this response. We investigate here, in an AD mouse model, the transcriptional changes occurring in tissue domains in a 100-μm diameter around amyloid plaques using spatial transcriptomics. We demonstrate early alterations in a gene co-expression network enriched for myelin and oligodendrocyte genes (OLIGs), whereas a multicellular gene co-expression network of plaque-induced genes (PIGs) involving the complement system, oxidative stress, lysosomes, and inflammation is prominent in the later phase of the disease. We confirm the majority of the observed alterations at the cellular level using in situ sequencing on mouse and human brain sections. Genome-wide spatial transcriptomics analysis provides an unprecedented approach to untangle the dysregulated cellular network in the vicinity of pathogenic hallmarks of AD and other brain diseases.

Keywords

ISS
Spatial Transcriptomics
Alzheimer’s disease
amyloid plaque
astrocyte
cellular phase
complement cascade
in situ sequencing
microglia
myelination
oligodendrocyte
spatial transcriptomics

MeSH terms

Alzheimer Disease
Amyloid
Amyloid beta-Peptides
Animals
Brain
Complement System Proteins
Disease Models, Animal
Gene Expression Profiling
Humans
Lysosomes
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Myelin Sheath
Oxidative Stress
Sequence Analysis, DNA
Transcriptome

Authors

Chen, Wei-Ting
Lu, Ashley
Craessaerts, Katleen
Pavie, Benjamin
Sala Frigerio, Carlo
Corthout, Nikky
Qian, Xiaoyan
Laláková, Jana
Kühnemund, Malte
Voytyuk, Iryna
Wolfs, Leen
Mancuso, Renzo
Salta, Evgenia
Balusu, Sriram
Snellinx, An
Munck, Sebastian
Jurek, Aleksandra
Fernandez Navarro, Jose
Saido, Takaomi C
Huitinga, Inge
Lundeberg, Joakim
Fiers, Mark
De Strooper, Bart

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