{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T22:29:13Z","timestamp":1789770553737,"version":"4.0.1"},"reference-count":87,"publisher":"The Company of Biologists","issue":"2","license":[{"start":{"date-parts":[[2022,2,17]],"date-time":"2022-02-17T00:00:00Z","timestamp":1645056000000},"content-version":"vor","delay-in-days":289,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"name":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","award":["HD083157"],"award-info":[{"award-number":["HD083157"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,2,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:p>22q11.2 Deletion Syndrome (22q11DS) is a neurodevelopmental disorder associated with cranial nerve anomalies and disordered oropharyngeal function, including pediatric dysphagia. Using the LgDel 22q11DS mouse model, we investigated whether sensory neuron differentiation in the trigeminal ganglion (CNgV), which is essential for normal orofacial function, is disrupted. We did not detect changes in cranial placode cell translocation or neural crest migration at early stages of LgDel CNgV development. However, as the ganglion coalesces, proportions of placode-derived LgDel CNgV cells increase relative to neural crest cells. In addition, local aggregation of placode-derived cells increases and aggregation of neural crest-derived cells decreases in LgDel CNgV. This change in cell-cell relationships was accompanied by altered proliferation of placode-derived cells at embryonic day (E)9.5, and premature neurogenesis from neural crest-derived precursors, reflected by an increased frequency of asymmetric neurogenic divisions for neural crest-derived precursors by E10.5. These early differences in LgDel CNgV genesis prefigure changes in sensory neuron differentiation and gene expression by postnatal day 8, when early signs of cranial nerve dysfunction associated with pediatric dysphagia are observed in LgDel mice. Apparently, 22q11 deletion destabilizes CNgV sensory neuron genesis and differentiation by increasing variability in cell-cell interaction, proliferation and sensory neuron differentiation. This early developmental divergence and its consequences may contribute to oropharyngeal dysfunction, including suckling, feeding and swallowing disruptions at birth, and additional orofacial sensory\/motor deficits throughout life.<\/jats:p>","DOI":"10.1242\/dmm.047357","type":"journal-article","created":{"date-parts":[[2021,3,15]],"date-time":"2021-03-15T10:55:32Z","timestamp":1615805732000},"source":"Crossref","is-referenced-by-count":14,"title":["Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome"],"prefix":"10.1242","volume":"15","author":[{"given":"Beverly A.","family":"Karpinski","sequence":"first","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 1 Department of Anatomy and Cell Biology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas M.","family":"Maynard","sequence":"additional","affiliation":[{"name":"The Fralin Biomedical Research Institute, Virginia Tech Carilion School of Medicine 2 , Roanoke, VA 24014 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Corey A.","family":"Bryan","sequence":"additional","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 1 Department of Anatomy and Cell Biology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gelila","family":"Yitsege","sequence":"additional","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 1 Department of Anatomy and Cell Biology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anelia","family":"Horvath","sequence":"additional","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 3 Department of Pharmacology and Physiology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norman H.","family":"Lee","sequence":"additional","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 3 Department of Pharmacology and Physiology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sally A.","family":"Moody","sequence":"additional","affiliation":[{"name":"The George Washington School of Medicine and Health Sciences 1 Department of Anatomy and Cell Biology , , Washington DC, 20037 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9458-5534","authenticated-orcid":false,"given":"Anthony-Samuel","family":"LaMantia","sequence":"additional","affiliation":[{"name":"The Fralin Biomedical Research Institute, Virginia Tech Carilion School of Medicine 2 , Roanoke, VA 24014 , USA"},{"name":"Virginia Tech 4 Department of Biological Sciences , , Blacksburg, VA 24060 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2021,5,4]]},"reference":[{"key":"2024061306460232700_DMM047357C1","doi-asserted-by":"publisher","first-page":"33","DOI":"10.1016\/bs.mcb.2016.01.002","article-title":"Patterning, morphogenesis, and neurogenesis of zebrafish cranial sensory placodes","volume":"134","author":"Aguillon","year":"2016","journal-title":"Methods Cell Biol."},{"key":"2024061306460232700_DMM047357C200","doi-asserted-by":"publisher","first-page":"603","DOI":"10.1038\/s41598-017-19093-0","article-title":"Phenotypic and functional characterization of peripheral sensory neurons derived from human embryonic stem cells","volume":"8","author":"Alshawaf","year":"2018","journal-title":"Sci. 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