https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:46784 Wed 30 Nov 2022 13:21:59 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:43721 Wed 28 Sep 2022 10:29:52 AEST ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:37132 Wed 19 Aug 2020 14:02:44 AEST ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:48220 Sat 11 Mar 2023 12:36:58 AEDT ]]> https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:37687 90% purity. Properties of these cultured adult Sertoli cells were then compared with those of cultured Sertoli cells derived from 20-day-old mice (also > 90% purity). By cell counting, bromo-2-deoxyuridine incorporation, and metaphase plate detection, we demonstrated that only adult Sertoli cells did not proliferate throughout 12 culture days. In contrast, Sertoli cells derived from 20-day-old mice still proliferated until Day 10 in culture. The morphology and profiles of intracellular lipidomics and spent medium proteomics of the 2 cultures were also different. Cultured adult Sertoli cells were larger in size and contained higher levels of triacylglycerols, cholesteryl esters, and seminolipid, and the proteins in their spent medium were mainly engaged in cellular metabolism. In contrast, proteins involved in cell division, including anti-Mullerian hormone, cell division cycle protein 42 (CDC42), and collagen isoforms, were at higher levels in Sertoli cell cultures derived from 20-day-old mice. Therefore, cultured Sertoli cells derived from 10-week-old mice, rather than those from 20-day-old animals, should be used for studies on properties of adult Sertoli cells.]]> Mon 15 Mar 2021 15:08:53 AEDT ]]>