| Literature DB >> 28506993 |
Scott Haston1, Sara Pozzi2, Gabriela Carreno2, Saba Manshaei2, Leonidas Panousopoulos2, Jose Mario Gonzalez-Meljem2, John R Apps2, Alex Virasami3, Selvam Thavaraj4, Alice Gutteridge5, Tim Forshew5, Richard Marais6, Sebastian Brandner7,8, Thomas S Jacques2,3, Cynthia L Andoniadou9,10, Juan Pedro Martinez-Barbera1.
Abstract
Despite the importance of the RAS-RAF-MAPK pathway in normal physiology and disease of numerous organs, its role during pituitary development and tumourigenesis remains largely unknown. Here, we show that the over-activation of the MAPK pathway, through conditional expression of the gain-of-function alleles BrafV600E and KrasG12D in the developing mouse pituitary, results in severe hyperplasia and abnormal morphogenesis of the gland by the end of gestation. Cell-lineage commitment and terminal differentiation are disrupted, leading to a significant reduction in numbers of most of the hormone-producing cells before birth, with the exception of corticotrophs. Of note, Sox2+ stem cells and clonogenic potential are drastically increased in the mutant pituitaries. Finally, we reveal that papillary craniopharyngioma (PCP), a benign human pituitary tumour harbouring BRAF p.V600E also contains Sox2+ cells with sustained proliferative capacity and disrupted pituitary differentiation. Together, our data demonstrate a crucial function of the MAPK pathway in controlling the balance between proliferation and differentiation of Sox2+ cells and suggest that persistent proliferative capacity of Sox2+ cells may underlie the pathogenesis of PCP.Entities:
Keywords: Mouse; Papillary craniopharyngioma; Pituitary development; Sox2; Tumour
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Year: 2017 PMID: 28506993 PMCID: PMC5482995 DOI: 10.1242/dev.150490
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868