{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T20:29:37Z","timestamp":1768508977655,"version":"3.49.0"},"posted":{"date-parts":[[2023,11,6]]},"group-title":"Neuroscience","reference-count":159,"publisher":"openRxiv","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2024,7,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                <jats:p>\n                  Preventative treatment for Alzheimer\u2019s Disease is of dire importance, and yet, cellular mechanisms underlying early regional vulnerability in Alzheimer\u2019s Disease remain unknown. In human patients with Alzheimer\u2019s Disease, one of the earliest observed pathophysiological correlates to cognitive decline is hyperexcitability. In mouse models, early hyperexcitability has been shown in the entorhinal cortex, the first cortical region impacted by Alzheimer\u2019s Disease. The origin of hyperexcitability in early-stage disease and why it preferentially emerges in specific regions is unclear. Using cortical-region and cell-type-specific proteomics coupled with\n                  <jats:italic>ex vivo<\/jats:italic>\n                  and\n                  <jats:italic>in vivo<\/jats:italic>\n                  electrophysiology, we uncovered differential susceptibility to human-specific amyloid precursor protein (hAPP) in a model of sporadic Alzheimer\u2019s. Unexpectedly, our findings reveal that early entorhinal hyperexcitability may result from intrinsic vulnerability of parvalbumin (PV) interneurons, rather than the suspected layer II excitatory neurons. This vulnerability of entorhinal PV interneurons is specific to hAPP, as it could not be recapitulated with increased murine APP expression. However, partial replication of the findings could be seen after introduction of a murine APP chimera containing a humanized amyloid-beta sequence. Surprisingly, neurons in the Somatosensory Cortex showed no such vulnerability to adult-onset hAPP expression. hAPP-induced hyperexcitability in entorhinal cortex could be ameliorated by enhancing PV interneuron excitability\n                  <jats:italic>in vivo.<\/jats:italic>\n                  Co-expression of human Tau with hAPP decreased circuit hyperexcitability, but at the expense of increased pathological tau species. This study suggests early disease interventions targeting non-excitatory cell types may protect regions with early vulnerability to pathological symptoms of Alzheimer\u2019s Disease and downstream cognitive decline.\n                <\/jats:p>","DOI":"10.1101\/2023.11.06.565629","type":"posted-content","created":{"date-parts":[[2023,11,7]],"date-time":"2023-11-07T00:45:15Z","timestamp":1699317915000},"source":"Crossref","is-referenced-by-count":2,"title":["Entorhinal cortex vulnerability to human APP expression promotes hyperexcitability and tau pathology"],"prefix":"10.64898","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5004-3330","authenticated-orcid":false,"given":"Annie 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