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Here, we study this process by leveraging the heightened susceptibility to seizure kindling of Angelman syndrome (AS) model mice, which lack the maternal\n                  <jats:italic>Ube3a<\/jats:italic>\n                  (\n                  <jats:italic>mUbe3a<\/jats:italic>\n                  ) allele. We identify parvalbumin-expressing (PV+) interneurons as critical gatekeepers; selective\n                  <jats:italic>mUbe3a<\/jats:italic>\n                  deletion in PV+ neurons phenocopies enhanced AS epileptogenesis, whereas restoring UBE3A broadly in GABAergic neurons confers seizure resistance. Further, pathological remodeling of the extracellular matrix in the dentate gyrus faithfully tracks with post-kindling seizure susceptibility, highlighting this region\u2019s particular relevance to enhanced epileptogenesis. Mechanistically, we uncover a \u2018two-hit\u2019 electrophysiologic phenomenon in AS model mice: kindling fails to recruit compensatory inhibition onto dentate granule cells and instead drives their maladaptive intrinsic hyperexcitability. Together, these findings link cell type-specific inhibitory dysfunction and altered homeostatic plasticity to epileptogenesis, suggesting future circuit-based treatment strategies.\n                <\/jats:p>","DOI":"10.64898\/2026.09.17.752419","type":"posted-content","created":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T09:10:12Z","timestamp":1789809012000},"source":"Crossref","is-referenced-by-count":1,"title":["Parvalbumin interneurons and dentate gyrus homeostatic dysregulation shape epileptogenesis in Angelman syndrome model mice"],"prefix":"10.64898","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5665-5776","authenticated-orcid":false,"given":"Nicholas W.","family":"Ringelberg","sequence":"first","affiliation":[{"name":"Neuroscience Curriculum"},{"name":"Neuroscience Center"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-3534-5889","authenticated-orcid":false,"given":"David W.","family":"Kipp","sequence":"additional","affiliation":[{"name":"Department of Cell Biology and Physiology"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ren\u00e9e E.","family":"Mayfield","sequence":"additional","affiliation":[{"name":"Carolina Institute for Developmental Disabilities"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0499-9299","authenticated-orcid":false,"given":"Lucas M.","family":"James","sequence":"additional","affiliation":[{"name":"Neuroscience Center"},{"name":"Department of Cell Biology and Physiology"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0002-5982-463X","authenticated-orcid":false,"given":"Audrey L.","family":"Smith","sequence":"additional","affiliation":[{"name":"Neuroscience Curriculum"},{"name":"Neuroscience Center"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0131-8961","authenticated-orcid":false,"given":"Paul B.","family":"Manis","sequence":"additional","affiliation":[{"name":"Department of Cell Biology and Physiology"},{"name":"Department of Otolaryngology\/Head and Neck Surgery"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8926-8606","authenticated-orcid":false,"given":"Alain C.","family":"Burette","sequence":"additional","affiliation":[{"name":"Neuroscience Center"},{"name":"Department of Cell Biology and Physiology"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3942-5036","authenticated-orcid":false,"given":"Michael R.","family":"Kasten","sequence":"additional","affiliation":[{"name":"Department of Otolaryngology\/Head and Neck Surgery"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2746-9143","authenticated-orcid":false,"given":"Benjamin D.","family":"Philpot","sequence":"additional","affiliation":[{"name":"Neuroscience Center"},{"name":"Department of Cell Biology and Physiology"},{"name":"Carolina Institute for Developmental Disabilities"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"54368","reference":[{"key":"2026092314300544000_2026.09.17.752419v1.1","doi-asserted-by":"publisher","DOI":"10.1007\/s00232-021-00192-3"},{"key":"2026092314300544000_2026.09.17.752419v1.2","doi-asserted-by":"publisher","DOI":"10.1016\/S0079-6123(07)63001-5"},{"key":"2026092314300544000_2026.09.17.752419v1.3","doi-asserted-by":"publisher","DOI":"10.1016\/J.NEURON.2018.12.026"},{"key":"2026092314300544000_2026.09.17.752419v1.4","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.2011.226175"},{"key":"2026092314300544000_2026.09.17.752419v1.5","doi-asserted-by":"crossref","unstructured":"Bebin EM et al. 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