Cell-type specific profiling of human entorhinal cortex at the onset of Alzheimer's disease neuropathology
Rodriguez-Rodriguez, P.; Wang, W.; Tsagkogianni, C.; Feng, I.; Morello-Megias, A.; Jain, K.; Alanko, V.; Kahvecioglu, H.; Mohammadi, E.; Li, X.; Flajolet, M.; Sandebring-Matton, A.; Maioli, S.; Vidal, N.; Milosevic, A.; Roussarie, J.-P.
Show abstract
Neurons located in layer II of the entorhinal cortex (ECII) are the primary site of pathological tau accumulation and neurodegeneration at preclinical stages of Alzheimers disease (AD). Exploring the alterations that underlie the early degeneration of these cells is essential to develop therapies that curb the disease before symptom onset. Here we performed cell-type specific profiling of human EC at the onset of AD neuropathology. We identify an early response to amyloid pathology by microglia and oligodendrocytes. Importantly, we provide the first insight into neuronal alterations that coincide with incipient tau pathology: the signaling pathway for Reelin, recently shown to be a major AD resilience gene is dysregulated in ECII neurons, while the secreted synaptic organizer molecules NPTX2 and CBLN4, emerging AD biomarkers, are downregulated in surrounding neurons. By uncovering the complex multicellular landscape of EC at these early AD stages, this study paves the way for detailed characterization of the mechanisms governing NFT formation and opens long-needed novel therapeutic avenues.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Molecular Signatures of Resilience to Alzheimer's Disease in Neocortical Layer 4 Neurons 99%
- A public resource of single cell transcriptomes and multiscale networks from persons with and without Alzheimer's disease 97%
- DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types 97%
Similar papers in this journal
- Diverse human astrocyte and microglial transcriptional responses to Alzheimer's pathology 98%
- Rare genetic variation in Fibronectin 1 (FN1) protects against APOEe4 in Alzheimer's disease 97%
- Dysregulated coordination of MAPT exon 2 and exon 10 splicing underlies different tau pathologies in PSP and AD 97%
Similar papers in this journal
- Natural genetic variation determines microglia heterogeneity in wild-derived mouse models of Alzheimer's disease 97%
- Applying high-resolution spatial transcriptomics to characterise the amyloid plaque cell niche in Alzheimer's Disease 96%
- Single cell spatial transcriptomic and translatomic profiling of dopaminergic neurons in health, aging and disease 96%
Similar papers in this journal
- Genome-wide consensus transcriptional signatures identify synaptic pruning linking Alzheimer's disease and epilepsy 96%
- Analyses of the Autism-associated Neuroligin-3 R451C Mutation in Human Neurons Reveals a Gain-of-Function Synaptic Mechanism 95%
- Loss of function of the mitochondrial peptidase PITRM1 induces proteotoxic stress and Alzheimer's disease-like pathology in human cerebral organoids 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.