Kurrasch, DeborahThornton, Hayley2017-08-102017-08-1020172017Thornton, H. (2017). Characterization of embryonic hypothalamic neurospheres and the role of sex steroids in the developing hypothalamus (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/25274http://hdl.handle.net/11023/4006There is emerging evidence indicating sex steroids may function as neurotrophic factors during brain development. Our objective was to determine whether sex steroids influence murine hypothalamic development during peak neurogenesis. We hypothesized during development hypothalamic neural stem and progenitor cells (NSPCs) respond to hormones to influence proliferation and/or self-renewal. Initially, we characterized the neurosphere assay as an in vitro model system to study hypothalamic NSPCs. We isolated hypothalamic NSPCs and assessed various culturing parameters such as media, density, growth factors, and extrinsic signals. We then utilized this assay to test whether exposure to androgens and estrogens alters their growth. Pharmacological treatment of DHT enhanced the sphere-forming capacity of primary neurospheres. Self-renewal capacity was also increased with physiologically-relevant doses of DHT and E2 exposed only as secondary cultures. Overall, we provide a working protocol for studying embryonic hypothalamic neurospheres and evidence that hypothalamic NSPC behaviour can be modulated by sex steroids.engUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.NeuroscienceHypothalamusDevelopmentneural stem cellshormonesneurospheresneurogenesisCharacterization of embryonic hypothalamic neurospheres and the role of sex steroids in the developing hypothalamusmaster thesis10.11575/PRISM/25274