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Cell Dev. Biol."],"abstract":"<jats:p>\n                    Neural progenitor cell differentiation is a complex process requiring the proper integration of instructive and permissive factors. Instructive cues including signaling molecules and transcription factor networks have been well studied in this context, but permissive factors such as cell homeostasis have not. Cell homeostasis is critical to support the health and stability of a cell and enable the cell to act on instructive differentiation cues. Our study investigates a homeostasis protein, FAF2, and its function in neural progenitor cells. FAF2 is an adaptor protein involved in endoplasmic reticulum (ER) associated degradation to remove misfolded proteins and restore ER homeostasis. Here we show that knocking out\n                    <jats:italic>Faf2<\/jats:italic>\n                    in neural progenitor cells results in increased ER stress signature at the protein and transcription level, indicating a conserved functional role in neural progenitor cells. Induced neural differentiation of FAF2 deletion cells shows a failure of neurite development but RNA-seq indicates genes that support neural differentiation are induced. Reducing ER stress in FAF2 knockout cells with a small molecule inhibitor can rescue neural differentiation, providing evidence that excess ER stress contributes to the inhibited differentiation. Taken together, these results reveal that FAF2 is a critical protein in neural progenitor cells for the maintenance of ER homeostasis and execution of neural differentiation.\n                  <\/jats:p>","DOI":"10.3389\/fcell.2026.1935883","type":"journal-article","created":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T06:04:49Z","timestamp":1787724289000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Faf2 is required for neural differentiation in embryonic neural progenitor cells"],"prefix":"10.3389","volume":"14","author":[{"given":"Anneke Dixie","family":"Kakebeen","sequence":"first","affiliation":[{"name":"Department of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder","place":["Boulder, CO, United States"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Leon","family":"Dunphy","sequence":"additional","affiliation":[{"name":"Department of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder","place":["Boulder, CO, United States"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Heather K.","family":"Hazen","sequence":"additional","affiliation":[{"name":"Department of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder","place":["Boulder, CO, United States"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lee A.","family":"Niswander","sequence":"additional","affiliation":[{"name":"Department of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder","place":["Boulder, CO, United States"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2026,8,26]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"2293","DOI":"10.1016\/j.bbamcr.2013.05.020","article-title":"Detection and quantification of endoplasmic reticulum stress in living cells using the fluorescent compound, thioflavin T","volume":"1833","author":"Beriault","year":"2013","journal-title":"Biochim. 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